Sex and Gender Driven Modifiers of Alzheimer’s: The Role for Estrogenic Control Across Age, Race, Medical, and Lifestyle Risks

1Alzheimer’s disease (AD) is a neurodegenerative disease marked by impairments in memory, attention, language, and daily living activities. While AD currently impacts 5.7 million Americans regardless of ethnic and cultural backgrounds, the prevalence is expected to triple by 2050, with nearly 14 million patients affected. Similar trends have been reported worldwide with a projected 130 million patients in the next 30 years.

2Alzheimer’s disease is an extremely debilitating condition currently falling within the top 10 causes of death across the world. This causes a severe fiscal burden on health services since AD is an extremely financially costly neurological disease to manage. Addressing the economic and social costs of AD is increasing in urgency as the Baby Boomer generation ages and life expectancy increases. Recent studies estimate that, from 2010 to 2050, annual costs will increase from $307 billion to $1.5 trillion in the United States alone. Medical advances that delay disease onset for 5 years or longer would result in a 41% lower prevalence and 40% lower cost of AD in 2050.

3To date, there has been a lack of therapeutics to prevent, delay, or reverse late-onset AD, resulting in a host of unsuccessful clinical trials. Research efforts over the past decade have prioritized therapeutic strategies that aim to remove beta-amyloid (Aβ) and tau pathology or prevent their accumulation, with limited success. Therefore, there exists an urgent and unmet need to develop novel strategies to prevent dementia, or at the very least delay its onset, or slow down progression. Several reasons underlie these past failures; among the most far-reaching are the stage at which therapeutic interventions are initiated, and the sex differences in the underlying mechanisms leading to AD.

4It has become widely accepted that the pathophysiological mechanisms of AD begin decades before the emergence of clinically detectable symptoms and contribute to a 15–20 year’s prodromal or “preclinical” disease stage starting in midlife. Failure to develop successful disease-modifying therapies may be because the majority of interventions have been tested in cohorts with clinically manifest disease and thus substantial synaptic and neuronal damage. Initiating therapies during the preclinical phase of AD will likely yield greater chances of success, a recognition that has effectively paved the way for primary and secondary AD prevention trials.

5There is also emerging evidence that several medical, environmental, and lifestyle risk factors that lead to AD development are modifiable. At least one out of three AD dementia cases can be linked to medical factors such as cardiovascular conditions, obesity, diabetes, and lifestyle factors such as physical activity, diet, social engagement, and educational attainment. Until disease-modifying treatment becomes available, risk reduction interventions could still drastically reduce the future burden of AD at the population level.

6In this context, it is being widely accepted that many of the above AD risk factors show gender effects, with female sex being more severely impacted. It has long been known that, after advanced age, female sex is the major risk factor for AD. Currently, two-thirds of AD patients are females. Postmenopausal women comprise over 60% of those patients. Increasing effort has thus been devoted to identifying sex-specific differences in disease etiology, manifestation, and progression as a crucial step toward gender-based disease prevention. Among putative biological mechanisms, it is becoming widely accepted that gonadal steroids contribute to the gender disparity in AD, as evidenced by the “estrogen hypothesis” presented herein. This posits that female sex hormones, 17β-estradiol in particular, exert a neuroprotective effect by buffering females’ brains against disease development. Hormonal changes in the years leading up to and after menopause are linked to the emergence of AD-related brain changes in females in contrast to males of the same age. In this review, we provide a comprehensive review of genetic, medical, societal, and lifestyle risk factors known to increase AD risk differently between the genders, with a focus on the role of gonadal hormones as key underlying mechanisms.

7It is has long been proposed that gonadal steroids contribute to gender differences in AD. Several reproductive hormones and their interactions may be implicated, including estrogen, progesterone, luteinizing hormone, and follicle stimulating hormones. All these so-called female hormones naturally fluctuate over endogenous hormonal cycles. Nonetheless, this review will focus primarily on estrogen since considerable evidence from molecular, animal, and clinical studies indicates that, of all gonadal hormones, estrogen may be particularly involved in the pathophysiology of AD-dementia in women. The “estrogen hypothesis” postulates that estrogen plays a protective role against AD-dementia, while that estrogen dysfunction seems to exacerbate, or perhaps precipitate the AD process in women.

8Even though it is present in both sexes, estrogen is often considered the primary female sex hormone. Reference to estrogen broadly refers to numerous compounds such as estrone (E1), estradiol (E2), and estriol (E3). The primary circulating estrogen during a woman’s reproductive years is 17β-estradiol, which is also the strongest form. For the purposes of this review, estrogen refers to 17β-estradiol, the endogenous form. 17β-estradiol plays a role in the formation of secondary sex characteristics in females and reproduction in males, and has peripheral effects in the liver and bone in both sexes. While it is primarily central to the ovaries for menstrual cycle coordination in women, it is also made by non-endocrine tissues, such as fat, breasts, and the brain.

9Estrogen affects several areas of the brain, thereby influencing cognitive function, affect, and behavior. Several lines of research have demonstrated that estrogen is a vital signaling molecule within the brain. It can not only go through the blood–brain barrier but the brain also produces estrogen endogenously from cholesterol. Estrogen utilizes a network of receptors and signaling pathways to initiate and regulate molecular and genomic responses required for survival at the level of the cells, genes, organs, and ultimately, the whole body (Figure 1; ). Estrogen receptors (ERs) are expressed by both sexes and are found on both neurons and glial cells throughout the brain. These receptors are conserved evolutionarily, with homologs present in all vertebrates. There are three types of ERs that have been discovered, to date: estrogen receptor 1 (ESR1 or ERα), estrogen receptor 2 (ESR2 or ERβ), and G-protein coupled estrogen receptor 1 (GPER). Binding of estrogen to these receptors activates several signaling pathways and cellular processes via both genomic and non-genomic processes.

10Of importance to the brain aging process, estrogen has known neuroprotective properties through its effects on spinogenesis, protecting the brain from age-related and toxic insults. Research using female rats in the early 1990s demonstrated that the density of dendritic spines on the CA1 region neurons of the hippocampus shifts over the ovarian cycle period and that surgical oophorectomy, the removal of one or both ovaries, contributes to a 30% loss in spine density that can be recovered neurons by estrogen replacement. This estrogen-led spinogenesis is followed by an equal increase in synapses pointing to potential integration of the new spines into the hippocampal network.

11Estrogen is also fundamental in metabolic regulation of the brain and body. For instance, it regulates glucose transport, aerobic glycolysis, and mitochondrial function to generate ATP in the brain. In animal models, oophorectomy causes a significant reduction in multiple brain glucose transporters, including GLUT-1, GLUT-3, and GLUT-4. Loss of ovarian hormones with reproductive aging leads to a significant reduction in brain glucose activity, which could be attributed to decreased neuronal glucose transporter expression, compromised hexokinase activity, inactivation of the pyruvate dehydrogenase complex (PDC), and eventually a functionally significant decrease in mitochondrial bioenergetic function. In addition to facilitating glucose transport, estrogen also promotes neuronal aerobic glycolysis and potentiates mitochondrial bioenergetics through its positive effects on pyruvate dehydrogenase (PDH), aconitase, and ATP synthase.

12Estrogen has also been shown to protect DNA against damage induced by hydrogen peroxide (H2O2) and arachidonic acid by increasing expression of a multitude of antioxidant enzymes, such as glutaredoxin, peroxiredoxin 5, and MnSOD. This estrogen-induced increase in antioxidants subsequently leads to a decrease in free radicals and oxidative damage to mitochondrial DNA and is potentially thought to contribute to the longer life span of women compared to men.

13Overall, these studies highlight the role of estrogen in brain aging and neurodegenerative diseases such as AD. More research is warranted to understand the effect of aging on brain estrogen activity, especially in the context of ERα and ERβ expression and signaling. So far, data suggest that in different parts of the brain, decreased ERα responsiveness may mediate cognitive decline and dementia risk. Although ERβ is at least partially receptive to E2 during aging, it may be unable to compensate for the lack of ERα. With aging, there is also an increase in particular ERα splice variants in some parts of the brain, especially the hippocampus, that cause most of the available ERα to be non-functional. Interestingly, research has shown that elderly women are more likely to have greater expression of ERα splice variants than elderly men. In addition to splice variants, there are numerous ERα polymorphisms that increase AD risk specifically in women, particularly when linked to the APOE ε4 allele which is a major AD genetic risk factor (discussed below).

14Further evidence for the “estrogen hypothesis” comes from studies that have implicated the menopause transition (MT) with the emergence of AD-related brain changes in women at risk for developing AD. The MT is associated with neurological symptoms such as disturbances of estrogen-regulated thermoregulation, sleep, onset of depression, and cognitive changes and ultimately results in reproductive senescence (; Figure 1). In the brain, ERs are widely found in the hypothalamic preoptic nucleus which serves as the primary thermoregulatory center; the suprachiasmatic nucleus of the hypothalamus which plays a central role in sleep and circadian rhythms regulation; the 5-hydroxy-tryptaminergic neurons of the raphe nucleus involved in affect and mood; and neurons in the locus coeruleus responsible for arousal and anxiety. In brain regions that are important for thinking, learning, and memory, ERs are present in the prefrontal cortex, medial temporal regions such as hippocampus and amygdala, and in the posterior cingulate and retrosplenial cortex. It has been proposed that during menopause, decline in circulating estrogen is coincident with decline in brain bioenergetics and shift toward a metabolically compromised phenotype in these brain regions. Inadequate or absent compensatory bioenergetic adaptations to lack of estrogenic activation would then trigger not only the signature symptoms of menopause (hot flashes, night sweats), insomnia, and depressive mood symptoms, but also cognitive changes, thereby increasing risk of late-onset AD in postmenopausal women.

15As later described in more detail, epidemiological data found an increased risk of dementia in women who underwent either unilateral or bilateral oophorectomy (surgical removal of the ovaries) before the onset of natural menopause. These findings have been confirmed and extended to include hysterectomy with and without oophorectomy. Additionally, brain imaging studies of women undergoing natural menopause provided evidence that the MT is related to a greater risk for AD-brain changes in middle-aged peri- and postmenopausal women compared to men of similar age. Further, the MT leads to an increased risk of depression, cardiovascular disease (CVD), type 2 diabetes mellitus (T2DM), and metabolic syndrome (MetS) in women, as well as a compromised response to head injuries – all of which serve as AD risk factors. Women exhibit increased vulnerability to a variety of environmental and lifestyle AD risk factors like physical inactivity, an imbalanced diet, disrupted sleep, and chronic stress. These findings highlight the higher susceptibility of women to AD and propose a potential window of opportunity for the implementation of AD risk reduction strategies.

16In the end, several lines of research provide support to the hypothesis that repeated hormone influxes in women confer protection against brain aging, while the onset of menopause may exacerbate an existing AD predisposition. An increasing number of studies have investigated estrogen therapy to potentially treat AD, as well as for CVD risk reduction in women. As reviewed below, earlier studies generally showed lack of benefits and even a potential harmful effect, whereas recent re-examinations indicate that the efficacy of estrogen in sustaining neurological health and function depends on several key factors, such as the time of initiation of estrogen therapy, the functioning of the brain at the time of therapy initiation, and the forms of hormones used. Additionally, both pharmacological and non-pharmacological therapies aimed at supporting hormonal levels in aging women may help attenuate the impact of modifiable AD risk factors on the brain.

17The aim of this review is to offer an updated review of the literature with respect to female-specific risk factors for AD (summarized in Table 1), and to put forth the estrogen hypothesis as a unifying mechanism of estrogen action on pre-existing and environmental risk. As previously discussed by, sex points to differences in biology such as chromosomal or hormonal factors, whereas gender refers to differences in the impact of psychosocial, cultural, and environmental influences on biological factors between men and women. Both sex- and gender-related risk factors are included below.

18As mentioned above, female sex is a major risk factor for late-onset AD. Approximately two-thirds of the more than 5 million Americans affected with AD are women and two-thirds of the more than 15 million Americans caring for someone with AD are women. As such, women find themselves at the epicenter of the impending AD epidemic. As grave a concern as breast cancer is to women’s health, women in their 1960s are almost two times more likely to develop AD over the rest of their lives as they are to develop breast cancer. A woman in her 1960s has an estimated lifetime risk of one in six for developing Alzheimer’s whereas the risk is 1 in 11 for a man of the same age.

19The prevailing view holds women’s greater longevity relative to men, which makes women more likely to reach the ages of greater risk, as the main reason for the increased AD prevalence. Studies in support of the increased longevity view have focused on estimates of incidence as well as prevalence. While it is well established that the prevalence of AD (i.e., the number of affected patients) is higher in females than in males, it is still not known whether incidence, i.e., the number of people who develop AD during a particular time period, also differs. The few studies investigating this issue found that in Europe and other areas, women also develop AD at a higher rate than men, especially at older ages. However, in the United States, the incidence seems to be similar across both genders. It is important to recognize that if men and women are developing AD at the same rate, but prevalence is ultimately higher in women, then the higher disease prevalence in women might indeed be attributed to their longer survival rates.

20Research on prevalence and incidence rates of mild cognitive impairment (MCI), an intermediary stage between cognitive changes associated with normal aging and dementia, has provided mixed results. Some studies report that men have a higher prevalence of MCI whereas others indicate greater prevalence in women. In terms of incidence, women tend to show an increased MCI incidence at older ages, while men consistently exhibit a higher incidence of the non-amnestic MCI, which is believed to be prodromal for other dementias, such as vascular dementia.

21While longevity is an important issue to consider, emerging evidence suggests that there are unique biological reasons for the increased AD prevalence in women beyond longevity alone. These biological, as well as social and lifestyle underpinnings contribute to differences in brain changes, progression, and symptom manifestation in AD between the genders.

22In fact, the longevity hypothesis does not take into account some important facts. First, the average life expectancy in the United States is currently 82 years for females and a little over 77 years for males, a difference of less than 5 years. As male survival rates have been steadily increasing, studies in Europe anticipate the longevity gap to be less than 2 years by 2030. Second, statistical models have shown that women exhibit a twofold higher incidence and lifetime AD risk even after accounting for gender-dependent mortality rates, age at death, and differences in lifespan.

23Further, there are well-documented differences in brain anatomy, function, and age-related brain changes between men and women. Recent studies found that women tend to accumulate greater tangle burden than do men with the same brain Aβ levels, but with no difference in lifetime AD risk, suggesting an earlier onset of AD pathophysiology. These observations are consistent with brain imaging findings of earlier emergence of AD-related brain changes in middle-aged women compared to age-matched men. Women also exhibit greater rates of neuropathological decline after an AD diagnosis, as evidenced by increased hippocampal atrophy and neurofibrillary tangles compared to men. In keeping with this, while women score generally higher on cognitive performance tests than men, female AD patients exhibit a faster rate of cognitive decline and loss of independence in comparison to male patients at the same level of dementia severity. Collectively, these data suggest an earlier start of AD pathogenesis in women, which might be masked by the female advantage in cognitive performance, resulting in females being diagnosed at a later stage than their male counterparts. Additionally, it highlights the importance of considering gender specific cut-offs in neuropsychological measures designed to detect AD-related cognitive impairments. Sex-adjusted cutoffs in the interpretation of verbal memory test results have led to improved diagnostic accuracy for both women and men.

24Furthermore, female sex may be associated with AD pathology seen in other conditions, like dementia with Lewy bodies, in which AD pathology occurs in a subset of patients. In one large study, while a composite AD biomarker profile was detected in 25% of all subjects, it was more frequent in women and was associated with worse cognitive performance. Given all these differences, further work into understanding sex differences in AD is an important step toward gender-based disease prevention.

25The APOE gene is currently the strongest genetic risk factor for late-onset AD. APOE codes for the Apolipoprotein E protein, an important cholesterol carrier that primarily coordinates transport of lipids in the brain. It consists of three major alleles: ε2, ε3, and ε4. APOE isoforms coordinate Aβ accumulation and removal in the brain, and play distinct roles in glucose metabolism, neuronal signaling, neuro inflammation, and mitochondrial function.

26Individuals with the ε4 allele are at a higher AD risk compared to those with the more common ε3 allele, whereas the ε2 allele has been associated with decreased risk. The ε4 allele is also associated with an earlier age onset in a gene dose-dependent manner. The frequency of AD and mean age at clinical onset for the different isoforms are as follows: 91% and 68 years of age in ε4 homozygotes, 47% and 76 years of age in ε4 heterozygotes, and 20% and 84 years in ε4 non-carriers. The ε4 allele is also related to an increased risk for cerebral amyloid angiopathy and age-related cognitive decline during normal aging.

27Sex differences in the effects of the ε4 allele have been well documented, with female carriers being more likely than male carriers to develop AD. AD risk increases nearly 4- and 10-fold in women with one and two ε4 alleles, whereas men exhibit essentially no increased risk with one ε4 allele and a fourfold increased risk with two ε4 alleles. A recent longitudinal study demonstrated that the conversion risk from normal aging to MCI or AD and from MCI to AD conferred by the ε4 allele is also significantly greater in women compared to men. However, a recent meta-analysis examining the relationship between APOE genotype and AD-dementia risk between men and women found no significant sex differences, except for a slightly increased risk for ε3/ε4 female carriers compared to male carriers within the ages of 65 and 75.

28Clearer evidence for negative associations of APOE ε4 genotype with female sex comes from biomarker studies showing that, among MCI patients, female ε4 carriers had significantly greater levels of CSF tau protein than male ε4 carriers. Among dementia-free individuals, female carriers exhibited greater brain hypometabolism, hippocampal volume reduction, and cortical thinning compared to male carriers Even in the absence of dementia, APOE ε4 significantly increases brain Aβ deposition and atrophy, and decreases brain connectivity in the default mode network much more effectively in women than in men.

29Given these findings, a greater comprehension of the APOE ε4 allele’s interaction with sex can have potential implications for AD treatment. To date, the few studies examining this issue have provided conflicting information. A research study investigating the efficacy of Tacrine, an FDA-approved cholinesterase inhibitor for AD treatment, found that female ε2/ε3 carriers showed greater improvements compared to female ε4 carriers. In contrast, men did not differ in their treatment responses based on APOE genotype. Another study assessing the efficacy of anticholinesterase therapy showed that female ε4 carriers derived the greatest cognitive benefit compared to non-carriers. A study examining the efficacy of intranasal insulin on cognitive function found that ε4 negative males demonstrated improvements but female non-carriers did not derive any benefits. Recent clinical trials of Aβ immunotherapy demonstrate that treatment was more effective in individuals with the ε4 genotype compared to non-carriers, though the data were not broken down by sex. More work is needed to systematically examine the differential response to pharmacological interventions by sex and APOE genotype.

30It is unclear why the APOE gene confers different risk in women, but some research suggests that it could be due to its interaction with estrogen. Studies in mice exhibited that APOE expression in different brain regions varied with the female reproductive cycle stages, consistent with the hypothesis that estradiol might induce APOE expression in the brain, as had already been demonstrated for APOE in blood. Moreover, trophic effects of estradiol on neurite growth in cultured mouse cerebral cortical neurons are reported to be highly dependent on APOE expression.

31Responses to estradiol are also in part dependent on APOE status: whereas estradiol is neurotrophic in the presence of human APOE ε2 or ε3, the ε4 variant does not support this response. In keeping with these findings, several lines of evidence indicate differential effects of estrogen replacement therapy dependent on APOE status, with ε4 positive women exhibiting worse rates of cognitive decline compared to non-carriers. Interestingly, a recent study found that transdermal estrogen therapy was associated with reduced Aβ deposition in postmenopausal women, particularly in ε4 carriers. In contrast, oral doses of conjugated equine estrogens (CEEs) was not associated with lower Aβ deposition. These results highlight the interaction of the APOE ε4 allele with estrogen and provide support for a biologically medicated relationship between APOE, estrogen use, and cognitive impairments.

32In general, older Hispanics and African Americans are at a higher AD risk in comparison to older whites. Differences in various health, lifestyle, and socioeconomic factors likely contribute to their higher AD risk. These include a greater prevalence of CVD, T2DM, hypertension, and early life adversity, as well as lower rates of education and physical activity.

33African American women in particular are twice more likely as white women to develop AD, strokes, and other forms of dementia. Likewise, women of Hispanic origin have a one and a half times greater risk for developing dementia, as well as CVD and T2DM than those who are white. This is of particular concern because in addition to a rapidly growing aging population, the United States is also becoming increasingly diverse. African Americans currently comprise 14.6% of the United States population and it is estimated that, by the year 2060, Hispanics who are currently the largest minority group will comprise over 28% of the United States population.

34Additionally, the caregiving burden among women within these communities is especially high. For instance, in some studies, Hispanic and African-American caregivers were more depressed and reported worse physical health than their white counterparts. While data on minority groups remain limited, there is an ongoing effort to produce high-quality data on large numbers of racial and ethnic minorities to better understand and treat possible AD-related risk factors.

35Cardiovascular disease, including coronary heart disease, stroke, atrial fibrillation, and heart failure, is the leading cause of death worldwide and a major risk factor for AD. The association between CVD and AD has been attributed to shared modifiable risk factors such as hypertension, obesity, diabetes mellitus, high cholesterol, and smoking. Several studies point to alterations in brain gray matter volume, increases in white matter lesions, and subcortical damage related to CVD as factors that could potentially increase AD-related neurodegeneration risk.

36Historically, CVD has been viewed as a typically “male” disease. The Framingham Heart study found that CVD related mortality and morbidity was two times higher in men than in women aged 50 and younger. However, even though CVD risk increases with age in both genders, it shows a steeper increase in risk in women after the age of 50 coinciding with the loss of estrogens occurring during and after menopause. Furthermore, coronary artery disease (CAD) is more prevalent in young females who underwent oophorectomy compared to those with intact ovaries.

37Several studies have documented the protective role of estrogen in CVD via its role in regulating LDL-cholesterol levels. During menopause, both natural and surgically induced, women experience an increase in LDL cholesterol levels. After age 50, LDL levels tend to increase at an average rate of 0.05 mmol/L per year in women aged 40–60 whereas they generally plateau in men. This postmenopause induced increase in LDL levels could be explained by declining estradiol levels that result in a downregulation of the activity of LDL receptors in the liver. This, in turn, leads to a reduction in the clearance of LDL from blood serum levels. Furthermore, estradiol’s interaction with ERα, ERβ, and GPER present in adult cardiomyocytes exerts a protective role by increasing angiogenesis (new blood vessels formation from older vessels), improving mitochondrial activity and reducing oxidative stress and fibrosis.

38Sex differences in terms of CVD risk and underlying pathology have also begun to emerge.

39Hypertension, a major risk factor for cognitive decline and a leading cause of cardiovascular morbidity, also increases significantly in women after menopause. A meta-analysis found that for every 10 mmHg increase in systolic blood pressure, there was a 25% and 15% increase in CVD risk for women and men, respectively. Sex differences in terms of CVD treatment have also been documented. For example, statins may be less effective at lowering cholesterol in women compared to men, although the complex relationship between statin exposure and sex-dependent risk reduction is complex and still remains to be understood. Additionally, some clinical trials found that angiotensin receptor blockers improve survival rates in men, but not in women with hypertension or CVD. The renin–angiotensin system is no an intense focus of research, given its potential association with risk of Alzheimer’s and interaction of estrogen with this system. Overall, hypertension seems to develop differently in women and men, and to respond differently to medications. The new guidelines by the American Heart Association for hypertension treatment will hopefully lead to better management of this risk factor in the future.

40Stroke has also been associated with an increased AD risk and earlier age of onset for dementia. Sex differences in terms of the underlying causes of stroke have been documented. The two major types of strokes are ischemic (caused by a blood clot that blocks a vessel in the brain) and hemorrhagic (caused either by a brain aneurysm burst or a weakened blood vessel leak). Hemorrhagic stroke is the lesser common of the two but often results in death. Aneurysmal subarachnoid hemorrhage (aSAH) is higher in women than in men, possibly as the result of female specific factors such as repeated childbirths and hormonal changes. Pregnancy-induced hypertension and vascular tension during delivery may lead to the formation of aneurysms. Several studies have shown that the increased aSAH prevalence in women occurs after the age of 50, coinciding with postmenopausal-related estrogen declines. However, a systematic review found that the role of hormone replacement therapy on the manifestation of aSAH is currently unclear.

41Finally, although sex differences in CAD have not been investigated adequately, there is some research indicating that women may be more prone to cardiac ischemia due to coronary microvascular obstruction than men. Women are also more affected by microvascular endothelial inflammation, a condition that contributes to heart failure. Compared to men, women who have experienced a myocardial infarction have a higher death rate, particularly evident in postmenopausal women, and experience more complications post-MRI such as stroke, congestive heart failure, cardiogenic shock, and depression.

42Diabetes mellitus, a common condition characterized by dysregulation of insulin and glucose levels, increases risk for incident AD, MCI, and cognitive impairment that posits a greater risk in women than men. For instance, women with type 1 diabetes mellitus (T1DM) exhibit a two times higher risk of cardiovascular events compared to men with T1DM. This increased CVD risk has been associated with significantly worse cardiac risk profiles, poorer diabetes management, and treatment options in women.

43Type 2 diabetes mellitus is also linked to an increased CVD and AD risk in women, especially after menopause. The prevalence of T2DM increases with age in a sex-specific manner. The Study of Women’s Health Across the Nation (SWAN) found that declining estrogen levels resulted in a 47% greater T2DM risk during the MT. The length of the reproductive lifetime, defined by age at last period and at menarche, has also been linked to women’s increased T2DM risk. The Women’s Health Initiative (WHI) showed that women with a reproductive lifetime of less than 30 years exhibited a nearly 40% increased T2DM risk than women with a lifetime reproductive span of 36–40 years.

44This menopausal-related increase in T2DM risk could be explained by biochemical and metabolic changes that take place during the MT. For instance, it is linked to an increase in fat deposition (especially in the abdominal region), reduction in lean body mass, and decline in overall energy expenditure. The increased visceral fat accumulation leads to the development of insulin resistance (IR) and the MetS, which play a major role in the development of T2DM. This finding is in accordance with previous data from experimental studies showing that reduced estrogen levels and decreased ERα activity is associated with IR development. Furthermore, T2DM and IR have been associated with atrophy of medial temporal regions such as the hippocampus and amygdala, which are particularly rich in ERs. These results provide further support to T2DM as a risk factor for AD via dysfunction of insulin signaling.

45Depression falls among the most common mental disorders in the elderly and is strongly linked to a higher risk for cognitive decline in both genders. However, women are two times more likely than men to experience depression. Studies have shown a rapid increase in depression rates starting at puberty and continuing through adulthood in women. Vulnerabilities to mood disorders in women tend to coincide with hormonal fluctuations experienced during and after pregnancy, as well as at the MT, suggesting a link between sex hormones and depression. For instance, women undergoing the MT experience a two- to threefold increase in major depressive disorder rates. It has been well documented that during the perimenopause period, women are two to three times more likely than men to experience a first episode of depression.

46The association among sex, depression, and AD risk needs to be more carefully considered. The data in terms of depressive symptoms and cognition stratified by sex have been mixed. Some studies demonstrate a stronger inverse relationship among depression and cognitive function in women, whereas other studies exhibit a stronger association in men. Furthermore, men with mild depressive symptoms exhibit an increased risk of amnestic MCI, while women with moderate or severe symptoms exhibit a higher AD risk. This suggests that symptoms might have to meet a higher severity threshold to increase clinical risk conversion in women compared to men.

47Several studies suggest a link between traumatic brain injury (TBI) and an increased AD risk. Emerging evidence indicates that even mild TBI is linked to cortical thinning in AD-sensitive areas and reduced memory performance in patients at risk for AD. Moreover, a history of TBI has been associated with AD neuropathology as evidenced by increased accumulation of Aβ and tau protein in patients with a history of TBI. TBI is also associated with chronic brain inflammation which has been shown to further accelerate AD disease progression.

48Some studies have highlighted sex-based differences in the context of recovery from TBI from sports-related head injuries. Female athletes are at a significantly higher risk of poorer outcomes, greater symptom severity, and lower recovery rate following mild TBI and concussions compared to their male counterparts. A recent MRI study focused on soccer related heading impacts found a sex-based association between heading and brain microstructure. In response to similar levels of heading, females had a fivefold greater volume of affected white matter than men, demonstrating a higher burden of microstructural consequences.

49The neuroprotective effects of estrogen in the context of recovery from TBI have been demonstrated in preclinical studies. Estrogen administration pre- and post-TBI is associated with increased neuronal survival, significant reductions in apoptosis, and improvements in functional outcomes. Estrogen is believed to be neuroprotective by increasing blood flow to ischemic regions after brain injuries, promoting antioxidant activity, and boosting the activity of astrocytes and microglia which provide neurons with metabolic support and elevate the immune response, respectively. Data from human studies show that mild TBI can potentially damage the anterior pituitary gland, which is responsible for producing FSH and LH. This reduction could significantly disrupt the production and circulation of endogenous estrogen levels. The decline of estrogen associated with menopause could potentially explain the poorer outcomes exhibited by females post-TBI compared to males.

50Systemic infections and related inflammation may potentially lead to a worsening of AD symptoms and increase the progression of AD-related neurodegeneration. A retrospective study found that the occurrence of two or more infections within a 4-year time period was linked to an almost twofold greater risk of developing AD in men and women. Following infections and injury, there is a heightened response of microglia and macrophages that lead to an increased inflammatory response.

51Emerging evidence suggests that chronic inflammation in the brain may be central to AD pathogenesis and that this may be triggered through Aβ accumulation. Postmortem brains examination of people with AD show increased expression of inflammatory mediators and complement factors, clusters of activated microglia, and cytokines in and near Aβ plaques. Although there is limited evidence that inflammation is a possible cause of late-onset AD, research on mouse models suggests that activation of inflammatory pathways is potent drivers of the disease. For instance, specific receptors on microglia and monocyte/macrophages are involved in determining whether Aβ clearance is carried out through non-inflammatory phagocytosis or via pro-inflammatory cytokine generation. Further, gene expression related to inflammation in brain is increased in aging, and this effect is heightened in patients with AD. Some epidemiological studies also link anti-inflammatory drugs usage with reduced risk for the disorder, although results are not always consistent.

52Sex differences in terms of response and prevalence to infections and inflammation have been documented, with females experiencing greater disease severity and worse outcomes than males, especially in the presence of reduced estradiol levels. For instance, women are at a greater risk for chronic inflammatory conditions such as lupus, rheumatic arthritis, and multiple sclerosis, especially after menopause. Additionally, preclinical studies demonstrate that the presence of influenza infection was associated with reduced reproductive functions in females. Furthermore, females treated with estradiol or an ERα receptor agonist had improved survival rates compared to females with either low levels or no estradiol.

53Overall, these findings suggest that sex differences in microglia activity in response to fluctuating hormone levels may lead to increased inflammatory responses, which may in turn increase women’s vulnerability to AD related neurodegeneration in later life stages.

54Thyroid function is routinely screened for in the clinical assessment of AD because thyroid dysfunction can cause symptoms that mimic those of dementia. Thyroid complications arise from an imbalance of triiodothyronine (T3) and thyroxine (T4) hormones, which regulate metabolism and vital functions. Hypothyroidism and hyperthyroidism result from an under and over production of T3 and T4 hormones, respectively. Among other potential causes, Graves’ disease and Hashimoto’s disease (two autoimmune conditions) are the most common causes of hyper- and hypothyroidism.

55It is widely reported that women are more likely to experience thyroid problems than men. One in eight women is expected to be affected by thyroid problems throughout their lifetimes. Some evidence shows that thyroid hormones can interfere with menstrual cycles and cause problems during pregnancy (discussed below) by reducing the clearance of estradiol and acting synergistically with FSH to increase the production of progesterone.

56Pregnancy and childbirth are characterized by obvious fluctuations in hormonal regulation that causes wide-ranged metabolic changes. Sometimes these can lead to a higher occurrence of IR and dyslipidemia, with a greater risk of future diabetes and obesity, all of which could potentially exacerbate AD risk later in life. There are mixed results on whether pregnancy increases AD risk later in life. Some studies report that a higher number of pregnancies are indeed linked to a higher risk and an earlier age of AD onset. For instance, one study estimated that women who had at least three pregnancies had a threefold greater risk of developing AD. The number of children born is also linked to increased neuropathological lesions of AD in women. However, a recent study reported the opposite trend, with a higher number of pregnancies linked to a lower AD risk in later life.

57Even though the data on pregnancy have been mixed, pregnancy-related conditions such as gestational diabetes and preeclampsia (pregnancy-related hypertension) can worsen CVD risk, and therefore risk of dementia. Further, hypertension due to pregnancy and vascular tension during delivery can potentially lead to aneurysms formation, which can contribute to an increased risk of stroke later in life.

58As mentioned throughout the article, the MT is the only known female-specific risk factor for AD to date. The effects of MT on AD risk have been highlighted by neuroimaging studies demonstrating a link between menopausal changes and emergence of AD pathology in midlife (,;; Figure 2). Among cognitively intact participants, postmenopausal and perimenopausal women exhibit higher AD-burden, as reflected by reduced glucose metabolism, increased Aβ deposition, gray matter volume loss (atrophy), and white matter volume loss than premenopausal women and age-matched men. Furthermore, a 3-year longitudinal study demonstrated that postmenopausal and perimenopausal women exhibited higher rates of AD biomarker progression, as evidenced by greater rates of metabolic declines and Aβ accumulation. These data point to the MT overlapping with the time course of preclinical AD. This is also supported by studies showing that estrogen depletion following oophorectomy is linked to an increased AD risk by up to 70%.

59Altogether, research provides support to the idea of the MT as an “optimal window of opportunity” for AD preventative interventions in women. The “critical window hypothesis,” also known as “the timing hypothesis” or “the critical period hypothesis,” says that the impact of hormonal replacement therapy (HRT) depends on the timing of treatment onset with respect to age and/or menopause onset, with benefits pertaining to early initiation.

60This is in stark contrast with the historical blanket use of high-dose HRT for treatment of menopause symptoms in postmenopausal women, which was common practice from the 1960s through 2003. In 2003, the primary results from the WHI study, a pivotal study investigating the effect of HRT on women’s health, were published. The WHI had two arms, one for hysterectomized women where the active treatment was estrogen-alone therapy (ET), and the other for postmenopausal women with a uterus where the active treatment was estrogen-plus-progestin therapy (EPT). Both trials were interrupted as early results showed a higher risk of CAD, stroke, and blood clots, with the EPT arm of the study also showing an increased risk of cancer.

61Further, the WHI included an additional arm, the WHI Memory Study (WHIMS), which investigated the outcome of HRT on dementia risk. In order to test whether HRT was effective in dementia prevention, the trial focused on postmenopausal women who were aged 65 or older at the time of enrollment. From a public health standpoint, it was thought that those women had the most to gain from the intervention since they were the most vulnerable to developing AD, as well as other conditions like CVD that could further increase AD risk. In the EPT arm, with a sample size of 4,532 women, there was a doubling of the risk of all-cause dementia with active treatment compared to placebo after an average follow-up of 4 years. The ET arm, with a sample size of 2,947 hysterectomized women followed over an average of 5 years, reported no significant impact of ET on dementia risk. These findings were in striking contrast to previous observational studies reporting a reduced risk of AD among women who had used HRT compared to those who had not as well as with smaller clinical trials showing no effects of HRT in AD patients.

62It is important to note several limitations pertaining to the WHI trials. First, the treatment administered was in the form of CEE tablets rather than 17 beta estradiol, with or without continuous medroxyprogesterone acetate, depending on the subject’s hysterectomy status. This might not have produced the same effects as oral or transdermal administration of estrogen or progesterone. Additionally, participants were already postmenopausal, generally older than 65 at the time of enrollment (therefore several years into menopause), possibly with pre-existing cardiovascular conditions. This raises the question of whether the results are applicable to younger post or peri-menopausal women. More work is needed to better examine effects of HRT dose, formulation, and mode of delivery on women’s brain health, especially for younger women without pre-existing conditions.

63Recent re-examination of results from the WHIMS indicates that treatment risks and benefits associated with HRT largely depend on three main factors: the patient’s chronological age, endocrine age (years to/from menopause), and hysterectomy status. Re-examination of the WHI data 18 years after they were interrupted reported that women who initiated HRT before the age of 60 or within 10 years after menopause had a lower mortality rate than placebo. Further, the Early versus Late Intervention Trial with Estradiol (ELITE) conducted with more than 600 postmenopausal women provided evidence that HRT reduced the progression of subclinical atherosclerosis when therapy was initiated right after menopause onset, which has been associated with a 30% reduced number of heart attacks and cardiac deaths.

64It is possible that early initiation of estrogen therapy may also provide protection against dementia later in life. Results on this topic have been mixed. On the one hand, meta-analysis of 18 studies demonstrated that among younger, 50–59-year-old women, those who used HRT had a 30–44% reduction in AD risk compared to those who did not use HRT, although these data need to be verified in formal clinical trials. In contrast, two recent randomized clinical trials – the ELITE study mentioned above and the Kronos Early Estrogen Prevention Study (KEEPS) – showed no cognitive improvements in women who started HRT within 6 years of menopause, but also no adverse effects of HRT. As both trials focused on women who were several years past menopause, more work is needed to systematically look at HRT effects in younger women, especially those of perimenopausal age.

65More persuasive evidence that HRT has value for dementia prevention comes from studies of hysterectomized women, particularly those who had their ovaries removed. A recent epidemiological study of 1,884 women showed that those who initiated ET within 5 years of surgery and continued until the natural age at menopause had a lower AD risk compared to those who did not take the drug. Additionally, randomized clinical trials of younger hysterectomized women showed that ET therapy had general beneficial effects on memory performance.

66Taken together, the majority of studies suggest that, for women with a uterus, EPT therapy initiated within 5 years of menopause onset or in the perimenopausal period may lower AD risk, whereas initiating therapy more than 5 years postmenopause may have the opposite effect. For women without a uterus, ET therapy started as close as possible after surgery and continuing until the natural age of menopause may offset the negative effects of the surgeries and also reduce AD risk. The value of initiating ET after the natural age at menopause is unclear.

67As previously discussed by, in medical research, the term “sex” refers to biological differences such as chromosomal or hormonal factors, whereas “gender” refers to differences in the impact of psychosocial, cultural, and environmental influences on biological factors between men and women. Gender-related risk factors for AD are discussed below.

68Low levels of educational achievement and occupation are associated with an increased AD risk in both genders. A possible explanation for this relationship lies in the idea of “cognitive reserve,” the brain’s ability to effectively utilize cognitive networks to allow individuals to normally perform cognitive activities despite sustaining pathological brain abnormalities such as increases in Aβ and tau levels. Higher education levels and cognitively stimulating occupations build more cognitive reserve. Likewise, several systematic reviews demonstrate that participation in cognitively stimulating activities is linked to a lower dementia risk.

69Historically, women had limited access to educational opportunities compared to men, which may have put them at a disadvantage in terms of their cognitive reserve build-up. This is especially relevant for people currently aged 70 years or older, who are at the greatest risk for AD. These findings suggest that lower educational achievement in women compared to men born early on in the 20th century could potentially play a role in women’s increased AD prevalence. However, according to the recent census, women had a higher educational attainment in the United States compared to men. There has been a significant change in occupational engagement with women taking on higher level positions and other roles that used to be men’s prerogatives. Hopefully these changing trends may help reduce the prevalence of Alzheimer’s in women in the future.

70Although studies that examined gender differences between cognitively engaging tasks and dementia risk are scarce, a recent study demonstrated that higher engagement in intellectual-cultural activities such as reading, radio and TV, and partaking in social and cultural activities were associated with improved verbal abilities in women, whereas higher engagement in self-improvement activities (playing sports, clubs and organizations, studies, outdoor activities) were associated with improved cognitive function in men. Despite the fact that women generally partake in more cognitive activities such as reading, arts and crafts, and social activities, the effect of these activities on cognitive reserve may be weaker than that of educational and occupational attainment.

71Low levels of physical activity are associated with a higher risk of dementia and greater cognitive decline among older adults. Physical activity can improve cognition through indirect effects on modifiable risk factors such as hypertension, obesity, IR, or via direct effects on neuronal activity. Increased physical activity has been shown to promote the formation, survival, and synaptic plasticity of new neurons in the hippocampus, and increase the production of brain-derived neurotrophic factor (BDNF) which play an important role in the formation, growth, and plasticity of neurons.

72Neuroimaging studies have also shown the beneficial effects of physical activity on brain structure and function. Individuals in a 3-month fitness training program showed increases in blood flow to the hippocampus, which was linked to improvements on memory and verbal learning tasks. Cross-sectional MRI studies report that increased fitness activity was related to larger anterior matter, prefrontal and temporal gray matter volumes. An fMRI study showed that individuals who underwent an aerobic fitness training program exhibited increased activity in the middle frontal gyrus, superior parietal cortex, and significant improvements in cognitive performance.

73Despite the well-known link between exercise and improved brain function, a gender gap exists in terms of physical activity engagement. For instance, women tend to engage in less physical activities than men. Research suggests that women’s societal roles can play a role, as parenthood and marital status may hinder women’s participation in physical activities. The prevalence of higher physical inactivity among women is concerning due to its association with T2DM, CVD, obesity, and hypertension.

74However, the relationship between long-term exercise and reduced cognitive impairment and AD dementia risk is more pronounced in women than men. For example, a meta-analysis examining the relationship between fitness training levels and cognition in older adults showed that fitness-related benefits on cognition were greater in women compared to men. A study conducted with over 9,000 women found that, although exercising in the teenage years was particularly brain-protective in the long term, being physically active reduced risk of cognitive impairment no matter their age. Elderly women with greater physical activity exhibit a reduced risk for AD dementia and are less likely to experience cognitive decline compared to women with lower physical activity levels. Importantly, exercise has been shown to ameliorate cognitive deficits even in women with a diagnosis of cognitive impairment and dementia.

75Specific dietary patterns like the Mediterranean (MeDi) diet and the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet have been associated with a reduced risk of dementia in both genders. Further, higher MeDi adherence is associated with a lower risk of AD biomarker abnormalities such as hypometabolism and Aβ deposition in AD-sensitive brain regions already in midlife.

76Both these dietary patterns focus on consumption of vegetables, fruit, whole grains, and legumes, with moderate amounts of fish and poultry, and limited amounts of dairy, red meat, and alcohol. Although results are not always consistent, several observational studies have shown that a MeDi-style diet is particularly protective for women, conferring a lower risk of AD, CVD, and diabetes. A study conducted exclusively in elderly women showed that higher MeDi adherence was also moderately related to better cognition and verbal memory. A recent study investigating the effect of a coconut oil enriched MeDi diet in mild to moderate AD patients found that women derived greater cognitive benefits than men.

77Higher whole grains and legumes consumption have also been related to reduced CVD risk, T2DM, obesity, and MetS in women which could be attributed to the fact that they contain high concentrations of phytoestrogens. Phytoestrogens are polyphenols which have similar molecular structure to endogenous estrogen. Evidence suggests that phytoestrogens exert their beneficial effects on female physiology via binding to ERs, activating epigenetic mechanisms, and increasing antioxidant activity. Furthermore, some preclinical studies have shown beneficial effects of phytoestrogens on cognitive function and AD. Perhaps as a result, increased intake of legumes and fish has been associated with a delayed menopause onset, whereas refined carbs, sugar, and processed foods resulted in an earlier onset of menopause and reduced ovulatory fertility.

78Other nutrients have also been associated with improved health outcomes in women, especially those past menopause. The Nurses’ Health Study conducted on over 75,000 women showed that replacement of saturated and trans-unsaturated fat for carbohydrates significantly reduced the risk of heart attack and stroke later in life. For each 5% energy intake increase from saturated fat, compared to the same energy intake from carbohydrates, a 17% increase in coronary disease risk was observed. Many other studies have shown that diets that favor carbohydrates, especially those with low glycemic load and high fiber content, also reduce T2DM risk and breast cancer in women. Further, replacement of 5% of energy from saturated fat with energy from unsaturated fats was estimated to reduce CVD risk in women by 42%, while replacement of 2% of energy from trans-fat with energy from un-hydrogenated, unsaturated fats would reduce risk by 53%. These data suggest that a similar nutritional pattern might be protective against AD in women as well, given that higher intakes of saturated fat and trans-fat have been linked to an almost doubled risk of dementia, whereas higher intake of unsaturated fat has been linked to a reduced risk.

79Poor sleep quality and circadian rhythm disruptions have been associated with an increased AD risk in the elderly. Preclinical and human studies have confirmed the beneficial effects of sleep via increases in cerebral blood flow and the clearing of Aβ plaques by microglial cells and astrocytes. Sleep deprivation leads to an increase in Aβ plaques accumulation. Subjective measures such as self-reports of sleep deterioration have also been linked to greater Aβ burden.

80When compared to men, women are generally at a greater risk for insomnia and experience greater age-dependent sleep quality deterioration, especially after menopause. Sleep apnea, a condition marked by recurring interruption of breathing during sleep, has been linked to cognitive decline and AD risk. Even though sleep apnea affects more men than women, its incidence significantly increases after menopause in women. Declining levels of estrogen and progesterone are thought to contribute to these findings. The Nurses’ Health Study II showed that women who underwent surgical menopause, which results in a shorter lifetime exposure to estrogen, had a 26% higher risk of experiencing obstructive sleep apnea (OSA). Even though the exact underlying biological mechanisms remain unclear, few studies have suggested that estrogen contributes to OSA risk by acting on upper airway dilatory pathways to coordinate ventilation. This sex-specific increase is concerning because women experiencing sleep disturbances are more prone to metabolic and cardiovascular dysfunction and mood disorders such as depression, previously established AD risk factors.

81Historically, women have been widely underrepresented in sleep studies which means that our current understanding of sleep-related disorders mostly comes from research conducted in men. This imbalance has significant implications for the efficacy of treatment interventions since strategies catered to men might not be effective or applicable to women.

82Cortisol dysregulation associated with repeated activation of the hypothalamic pituitary adrenal (HPA) axis in response to chronic stress is commonly found in patients with AD. It has been linked to memory impairments, cognitive decline, as well as brain atrophy.

83Sex-related differences in the HPA axis reactivity to early childhood and chronic stress have been previously reported. In response to early childhood trauma, women exhibit a significantly lower cortisol response compared to men later on in life. Moreover, this blunted HPA axis response occurs in a dose-dependent manner. The gender differences with regard to chronic stress could potentially be explained by the activity of gonadal hormones. An fMRI study demonstrated that brain circuitry activation patterns in response to stress in menis more similar to women in the early follicular phase of the menstrual cycle, during which estrogen and progesterone are low, compared to women in the late follicular/midcycle phase, during which estrogen is high and progesterone is still relatively low. Women demonstrated lower stress response circuitry activation compared to men, with differences being particularly evident as they progressed through their menstrual cycles. This finding implies that hormonal changes specifically estrogen or progesterone could potentially account for these activation differences. Additionally, it raises the question of whether stress impacts brain aging and neurodegeneration differently in women and men. A recent imaging study conducted in cognitively normal middle-aged adults demonstrated that increased cortisol levels were linked to brain volume reductions and impaired memory, with the brain shrinkage being only evident in women, which further highlights the link between hormonal changes and stress reactivity in sex differences.

84Research indicates that caregiving demands can severely tax the caregivers’ health and physical abilities, while compromising their immune response to stress, a condition known as “caregiver burden.” Caregiver burden has been associated with increased stress, sleep disturbances, depression, difficulties in social functioning, and declines in cognitive function. At the same time, the stress associated with caregiving can worsen existing chronic health conditions, with higher rates of cholesterol, blood pressure, and obesity. This has been associated with a greater risk of heart disease, stroke, and premature mortality, particularly under conditions of high strain. Moreover, perhaps due to all the reasons above, caregivers are at a greater risk for developing AD themselves. Approximately two-thirds of caregivers for AD dementia are women.

85In keeping with the notion that women’s reaction to stress is stronger than men’s, female caregivers report twice as more caregiver burden than their male counterparts. A study examining biological and emotional responses among spousal caregivers of patients with AD found that men reported significantly lower levels of stress, depression, subjective caregiver burden, and anxiety than women. Additionally, men reported higher levels of mental health functioning, sense of coherence, and social and physical well-being. The gender differences could be partly due to the fact that women tend to devote longer hours and perform a higher number of caregiving tasks than men.

86Longitudinal studies have demonstrated that unmarried or single individuals are at an increased risk for cognitive decline, MCI, and AD. Currently, marital status is the only AD risk factor that affects men more than women. While single people tend to have twice the risk of developing AD versus people with partners, non-cohabiting men are at a greater risk of experiencing cognitive impairment later in life compared with non-cohabitating women. Divorced men also exhibit a higher AD risk compared to divorced women. Interestingly, this difference was reduced after adjusting for socioeconomic (e.g., education and income) and demographic characteristics (e.g., age) suggesting that these factors could reduce risk in both genders. For instance, it has been shown that widowed women have a greater tendency be more socially active compared to widowed men which might reduce the negative effects of widowhood.

87In conclusion, AD is a neurodegenerative disorder that has shown strong sex and gender differences in several aspects of the disease, including a faster onset of AD pathology and disease progression after diagnosis, and different risk factors that may account for the increased female prevalence of AD. This review article focused on the research dedicated to understanding the effects of estradiol in terms of gender and sex differences in AD, and the negative effects of MT as a tipping point for middle-aged women. The research findings presented range from studies on molecular mechanisms and preclinical models that clearly highlight estradiol’s interactions with a number of signaling and transcriptional pathways involved in cognition and memory, to neuroimaging studies that visualized AD-related brain changes during the MT. Recent clinical trials and re-examinations of existing data lend support to the use of HRT as a possible risk reduction intervention in women at risk for AD, though more work is needed to examine this. Future research studies examining the underlying mechanism of estradiol’s neuroprotective action in AD are warranted.

88In order to address the growing AD epidemic, the field is shifting toward early detection and primary and secondary prevention efforts. It is crucial that these prevention and clinical trials take into account sex differences in AD biomarkers, disease progression, and gender differences with respect to modifiable risk factors to aid in the development of therapeutics for both men and women. Historically, women have been underrepresented in studies elucidating the underlying mechanisms of AD which has significantly impeded our understanding of gender differences. Women still remain underrepresented in clinical trials of CVD, a known AD risk factor. Future AD research studies should actively aim to increase women’s overall participation and analyze the influence of sex or gender on health outcomes. A better understanding of sex and gender differences is crucial toward the development of individualized AD risk reduction strategies and treatments.

89LM and AR discussed the concepts and wrote the manuscript. HJ, HH, RI, NS, TS, OE, CH, and RB reviewed the literature and provided critical revision of the manuscript for important intellectual content.

90The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.