Stronger association of triglyceride glucose index than the HOMA-IR with arterial stiffness in patients with type 2 diabetes: a real-world single-centre study

1Studies have shown that arterial stiffness is an important risk discrimination for cardiovascular events, which remain leading causes of death worldwide. Diabetes, which is considered a risk equivalent for cardiovascular disease (CVD), affects 113.9 million people in China (prevalence 11.6%). Arterial stiffness is closely associated with the presence and progression of complications of diabetes, including CVD, retinopathy, neuropathy, and nephropathy. Brachial-ankle pulse wave velocity (baPWV) has been wildly used as an indicator of arterial stiffness in clinical setting and large population studies. Additionally large-scale studies have proved that the increased arterial stiffness, defined as elevated baPWV, is related to an increased risk of hypertension, stroke, and total and all-cause mortality and is positively associated with the risk of new-onset diabetes.

2Insulin resistance (IR) is an important cause of several metabolic disease, including diabetes and CVD. Pathophysiological studies suggest that IR promotes a pro‐inflammatory state and dyslipidemia, which may largely be responsible for arterial stiffness progress. The triglyceride-glucose index (TyG index), based on fasting glucose and triglycerides, has been proposed as a simple and reliable surrogate measure for the diagnosis of IR compared with the euglycaemic-hyperinsulinaemic clamp, which is the ‘gold standard’ for evaluating IR, but is expensive, complex, laborious and time-consuming. The homeostasis model assessment for IR (HOMA-IR) is the most frequently used index to evaluate IR and uses insulin and glucose level derived from the fasting state. However, the TyG index is more easily available and less cost-effective, and some studies revealed that the TyG index shows better performance for assessing IR than the HOMA-IR in clinical practice regardless of diabetes status.

3TyG index have been reported to precede and significantly predict diabetes and cardiovascular events in adults, older adults and hypertensive patients. Recent studies have demonstrated that the TyG index is positively associated with arterial stiffness in healthy population and hypertensive patients. Wang et al. reported that TyG index could predict the cardiovascular events in patients with diabetes. Arterial stiffness has been observed to be associated with IR, represented by the HOMA-IR in Chinese middle-aged adults. However, few studies have been conducted to evaluate the role of IR assessed by the TyG index and HOMA-IR, on arterial stiffness in a type 2 diabetes (T2D) population with a high risk of increased arterial stiffness. Accordingly, we aimed to investigate the association of the TyG index and HOMA-IR with arterial stiffness in patients with T2D.

4From June 2017 to November 2020, 4157 patients with T2D were screened at the National Metabolic Management Center (MMC) in Ruijin Hospital, Shanghai Jiao Tong University School of Medicine. Participants with a reported previous history of stroke (n = 162), heart failure (n = 10) or coronary heart disease (n = 393) and participants with missing BaPWV or TyG index measurements were excluded. In total, 3185 participants were finally included in the current study. All participants provided written informed consent, and the study protocol was approved by the Institutional Review Board of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine (ClinicalTrials. gov number, NCT03811470).

5An independent digital medical record systems described in our previous paper was used to collect information, including age, sex; the duration of diabetes; the history of previous cardiovascular diseases; smoking and drinking status; and the use of lipid lowering, antihypertensive or hypoglycemic agents. Smoking status was defined as ‘yes’ if the participants smoked daily or almost daily. Drinking status was defined as ‘yes’ if the participants drank weekly or almost weekly. Anthropometric information of each participant was measured by the trained investigators. Each participant’s body weight and height were measured in light clothing without shoes. Body mass index (BMI) was calculated as weight (kg)/height (m)2. Waist circumference was measured at the midpoint between the lower edge of the costal arch and the upper edge of the iliac crest. Blood pressure was measured with an automated electronic device (OMRON HBP-1100 U) in the seated position after resting for at least 5 min. The elbow of the arm used for measurement was supported at heart level.

6Fasting venous blood samples were collected from all participants after overnight fasting for 10–12 h. The postprandial blood samples were collected 120 min after having a steamed bread meal for the assessment of post load glucose. HbA1c was measured by high-performance liquid chromatography using the VARIANT II, a haemoglobin testing system (Bio-Rad Laboratories, Hercules, CA, USA). Serum insulin was measured by electrochemiluminescence immunoassay “ECLIA” on a Cobas e601 immunoassay analyzers (Roche Diagnostics Corp., Indianapolis, IN, USA). Plasma glucose was measured by using the glucose oxidase method, and total cholesterol (TC), triacylglycerols (TG), high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C) were measured by means of the cholesterol oxidase method, glycerophosphate oxidase–peroxidase (GPO–POD) method, polyanion polymer/detergent (PPD) method and solubilization (SOL) method with the auto-analyzer (AU5800; Beckman coulter, CA, USA). Urinary albumin and creatinine was determined by immunoturbidimetric method and sarcosine oxidase-PAP method on an automatic analyzer (Beckman coulter, CA, USA), respectively. Urinary albumin/creatinine ratio (UACR, mg/mmol) was calculated as the urinary albumin concentration divided by the urinary creatinine concentration. The white blood cell (WBC) counts were measured by blood cell analyzer (Beckman coulter, CA, USA). The TyG index was determined as ln (fasting triglycerides [mg/dL] × fasting glucose [mg/dL]/2), and the HOMA-IR was calculated as (fasting insulin [μIU/mL] × fasting glucose [mmol/L])/22.5.

7All the participants underwent baPWV measurements, with baPWV values determined by an automated recording apparatus (BP-203RPE III, form PWV/ABI, Omron Healthcare Co.). Briefly, cuffs were attached to participants around both arms and ankles after at least 5 min of rest at room temperature. Measurements from the brachial and tibial arteries were obtained simultaneously. Transit time, defined as the time interval between the initial increase in brachial and tibial waveforms, and transit distance between the arm and ankle were measured. The baPWV value was calculated as the transit distance divided by the transit time. We adopted the mean value of the right and left baPWV. As a previous study showed, elevated baPWV was defined as a value greater than the 75th percentile of the baPWV value in the present study, which was greater than 18.15 m/s.

8Eligible patients were diagnosed with T2D according to the 1999 World Health Organization criteria if they had a fasting plasma glucose ≥ 7.0 mmol/L or 2-h plasma glucose ≥ 11.1 mmol/L or a self-reported physician diagnosis. Increased arterial stiffness was defined as elevated baPWV, which was the fourth quartile of baPWV (18.15 m/s) in the current study. Albuminuria was defined as UACR ≥ 3.4 mg/mmol (30 mg/g).

9The characteristics of the participants were described according to the tertiles of the TyG index. Data are presented as mean ± standard deviation (SD) or median [interquartile range (IQR)] values for continuous variables and as the frequency (%) for categorical variables. P values for trend were calculated by using linear regression analyses and the Cochran–Armitage trend test for continuous and categorical variables across the three groups, respectively. The dose–response association between the TyG index or HOMA-IR and the baPWV was evaluated using a generalized additive model (GAM) and a fitted smoothing curve (penalized spline method). The independent association of the TyG index or HOMA-IR (independent variable) with baPWV (dependent variable) was evaluated using generalized linear models [beta coefficient (β) and 95% confidence interval (CI)]. Seemingly unrelated regression estimation (SUR) was applied to compare the regression coefficient (β) between the TyG index and the HOMA-IR. The independent association of the TyG index or HOMA-IR (independent variable) with increased arterial stiffness or albuminuria (dependent variable) was evaluated using multivariable logistic regression models [odds ratio (OR) and 95% CI]. We constructed three models with adjustments for major covariables: Model 1: adjusted for age and sex; Model 2: adjusted for variables in model 1 plus BMI, waist circumference, systolic blood pressure, LDL-C, HDL-C, WBC counts, HbA1c, and the duration of diabetes; and Model 3: adjusted for variables in model 2 plus smoking status, drinking status, the use of lipid lowering agents, the use of antihypertensive agents, the use of insulin therapy, and the use of non-insulin hypoglycaemic agents. In addition, we performed stratified analysis and interaction testing on the association between the TyG index and increased arterial stiffness to evaluate possible modifications by using multivariable logistic regression models with full adjustment in model 3.

10All analyses were performed using SAS version 9.4 (SAS Institute Inc, Cary, NC) and R software (version 3.6.3; R Foundation for Statistical Computing). A two-sided P value < 0.05 was considered statistically significant.

11The demographic and clinical characteristics of the 3185 participants according to TyG index tertiles are shown in Table 1. The mean age of the study participants was 54.6 (SD, 12.0) years, and 1954 were men (61.4%). The mean TyG index was 9.16 (SD, 0.7), and the mean baPWV was 16.20 (SD, 3.6) m/s. P for trend was calculated with each tertile of the TyG index taken as a unit. Compared to those in the lowest tertile of the TyG index, participants in the higher tertile were younger with shorter duration of diabetes; were more frequently men, smokers, drinkers; less frequently used non-insulin hypoglycaemic agents (all P for trend < 0.05); had lower levels of HDL-C; and had higher blood pressures, BMIs, waist circumferences, fasting and post load glucose levels, fasting insulin, HOMA-IR, HbA1c, TG, TC, LDL-C, UACR, and WBC counts (all P for trend < 0.001).

12GAM analysis revealed the significant positive linear associations of the TyG index and HOMA-IR with baPWV (Fig. 1, both P < 0.001). The generalized linear models showed that after full adjustments for the confounders (model 3), each 1-unit increase in the TyG and each 1-unit increase in the HOMA-IR were associated with a 0.38 m/s (95% CI 0.21–0.55, P < 0.001) and a 0.01 m/s (95% CI 0.001–0.01, P = 0.029) increase in baPWV (Table 2). We further explored the associations by categorizing TyG index levels and the HOMA-IR into tertiles and using the first tertile as a reference. Compared to the first tertile of the TyG index, the second and third tertiles of the TyG index were significantly associated with a 0.28 m/s (95% CI 0.02–0.54, P = 0.032) and 0.50 m/s (95% CI 0.21–0.79, P < 0.001) increase in baPWV, respectively. Similar linear associations were found for tertiles of the HOMA-IR and baPWV, but only with the third tertile of the HOMA-IR was associated with a 0.34 m/s (95% CI 0.06–0.62) increase in baPWV. Seemingly unrelated regression estimation analysis demonstrated that the TyG index showed stronger associations with baPWV than the HOMA-IR in all models (P < 0.001, Table 2, model 1–3).

13The prevalence rates of increased arterial stiffness were 22.1%, 26.6%, and 26.4% from the lowest to highest TyG tertile and 22.4%, 26.7%, and 26.5% from the lowest to highest HOMA-IR tertile, respectively. As shown in Table 3, after full adjustment, each one-unit increase in the TyG index was associated with a 1.40-fold (95% CI 1.16–1.70, P < 0.001) higher prevalence of increased arterial stiffness. Compared to the lowest tertile of the TyG index, the second and highest TyG index tertile were associated with a 40% [OR (95% CI) 1.40 (1.06, 1.83), P = 0.01] and 49% [OR (95% CI) 1.49 (1.09, 2.04), P = 0.003] higher prevalence of increased arterial stiffness, respectively (P for trend = 0.003). The prominent association of the HOMA-IR with the prevalence of increased arterial stiffness was not observed in full adjusted model (P = 0.89, model 3). Consistently, there were significant stronger associations of the TyG index with the prevalence of albuminuria than the HOMA-IR (Additional file 1: Table S1).

14In addition, we conducted a stratified analysis of the relationship between the TyG index and increased arterial stiffness according to the potential modifiers, including sex, age, HbA1c, duration of diabetes, SBP, and insulin therapy (Fig. 2). The model was fully adjusted anthropometric, clinical, socio-demographic variables. There were no significant associations between the TyG index and increased arterial stiffness participants aged less than 60 years (n = 1844), whose HbA1c was less than 7% (n = 1170), whose duration of diabetes was less than 5 years (n = 1498) and those with insulin therapy (n = 699), which may be because of the much smaller sample size (all P ≥ 0.05). On the other hand, the TyG index was significantly associated with a higher prevalence of increased arterial stiffness in a subgroup of women [OR (95% CI) 1.34 (1.08, 1.66)], men [OR (95% CI) 1.49 (1.14, 1.96)], those aged ≥ 60 years [OR (95% CI) 1.34 (1.07, 1.67)], those with HbA1c ≥ 7% [OR (95% CI) 1.55 (1.28, 1.88)], those with duration ≥ 5 years [OR (95% CI) 1.63 (1.31, 2.01)], those with SBP < 130 mmHg [OR (95% CI) 1.59 (1.20, 2.10)] or ≥ 130 mmHg [OR (95% CI) 1.40 (1.14, 1.71)], and those without insulin therapy [OR (95% CI) 1.43 (1.14, 1.78)] (all P < 0.05). No interactions were detected in the stratified analysis.

15This cross-sectional study confirms the significant positive association and a dose–response relation between the TyG index and arterial stiffness assessed by baPWV after adjusting for confounding factors in patients with T2D. Furthermore, the results provide evidence that the TyG index is independently and more strongly associated with arterial stiffness and the prevalence of increased arterial stiffness compared to the HOMA-IR, which elucidated the substantial role of TyG index in terms of arterial stiffness even for the patients with T2D.

16IR has proved to be the major feature of T2D and has been recognized to evaluate T2D-related cardiovascular risk, and the identification of IR has great clinical significance. Although euglycaemic hyperinsulinaemic clamp is the gold standard method and is closest to the real measure of IR, it is unavailable and impractical in clinical practice and is labour-and time-consuming. The TyG index, a simple and reliable alternative surrogate marker of IR, showed high sensitivity (96.5%) and specificity (85.0%) for the diagnosis of IR compared with the euglycaemic hyperinsulinaemic clamp, and can be widely used in clinical practice because measuring glucose and triglycerides are available in all clinical laboratories and quantification of insulin levels is not required. Compared with the HOMA-IR, the TyG index showed higher superiority in the patients with T2D regardless of the use of insulin related medication. Although there is no unambiguous explanation for the mechanisms behind the effectiveness of the TyG index as a marker of IR, it may be related to the metabolic inflexibility in IR conditions not limited to defects in glucose metabolism but also included fatty acid metabolism during excess triglyceride storage within skeletal muscle. Meanwhile, elevation of triglycerides is strongly related to a decrease in IR.

17Consistent with previous studies, our study also found the more severe metabolic impairment in the tertile with the highest TyG index. Intriguingly, both previous studies and our present study observed that insulin therapy and lipid lowering agents were not associated with the TyG index. The unexpected results might be due to the history of use of insulin therapy, and lipid lowering agents could not directly mirror the observational level of the TyG index. Further repeated-measures and longitudinal studies might be required to confirm the association of the TyG index with lipid lowering agents and insulin therapy in patients with T2D.

18Additionally, several studies have reported that the TyG index was strongly associated with arterial stiffness and coronary artery calcification in general adult Koreans. Li et al. recently conducted a cross-sectional study of 4718 Chinese hypertensive patients and demonstrated that the TyG index is independently positively associated with arterial stiffness, but they did not analyse the association between the HOMA-IR and arterial stiffness because insulin levels were not detected. T2D is characterized by increased arterial stiffness, and an elevated TyG index was also found to be an independent risk factor for the risk of T2D. In addition, TG and glucose are the classic markers of cardiometabolic risk in real clinical practice, particularly in patients with T2D. The subgroup analysis of 2560 relatively healthy Korean adults showed that the TyG index was independently related to baPWV in both nondiabetics participants and diabetics participants (n = 411). However, there is a lack of relatively large data on the role of the TyG index in terms of arterial stiffness in the T2D population. Considering that patients with T2D are a high-risk population for increased arterial stiffness as hypertensive patients, we thus defined increased arterial stiffness as elevated baPWV (> 75th percentile) in the present study based on the previous studies, which is higher than that of the relatively healthy population and could be a marker of target organ damage. The present study reported for the first time the independent and positive association of the TyG index with increased arterial stiffness in T2D participants. The subgroup analysis also confirmed that the TyG index was positively associated with increased arterial stiffness in the older participants with a longer duration of diabetes and poor glycaemic control, highlighting the importance of reducing the TyG index in patients with a high risk of arterial stiffness. Consistent with a study by Nakagomi et al., we found that the TyG index showed a stronger association with increased arterial stiffness in women than in men. However, Li et al. and Lee et al. found that the effect of the TyG index on the prevalence of increased arterial stiffness was greater in men than in women. A possible explanation for the conflicting results may be the difference in participant selection, and further research is needed to evaluate the sex difference in the association between the TyG index and arterial stiffness in different populations.

19We also found that the TyG index was better than the HOMA-IR at predicting increased arterial stiffness in T2D patients, which further confirmed that TyG index may serve as a low-cost and simple noninvasive biomarker to evaluate the prevalence of increased arterial stiffness for the patients with T2D. Several studies have reported that IR can promote endothelial dysfunction, activation and advanced plaque progression, and is associated with dyslipidaemia, hypertension and a proinflammatory state, all of which precipitate arterial stiffness. Although the mechanisms of the stronger association of the TyG index than the HOMA-IR with arterial stiffness have not yet been fully elucidated, it may be attributed to the TyG index performing better for assessing IR than the HOMA-IR even in the patients with T2D. Alternatively, compared with the HOMA-IR, which indicates IR in the liver, the TyG index may a better indicator of IR in muscle and may be a more useful marker of arterial stiffness. On the other hand, the TyG index, mirroring the physiological condition of glucose and lipid, plays a more important role in determining arterial stiffness than the HOMA-IR in the patients with T2D.

20The strengths of this study lie are its inclusion of a large number of participants with established T2D, standardized high-quality clinical characteristics and laboratory measurements, and adjustments for a relatively comprehensive set of metabolic confounders. Our study still has several limitations. First, the cross-sectional design limits the detection of causality, and further follow-up in the MMC may provide more precise evidence in future studies; second, we did not adjust for detailed food intake information, but overnight fasting can reduce its affection on the levels of glucose and TG. Last, the study population included Chinese patients with T2D, which may limit the generalizability of the results. Despite these limitations, this study first demonstrated the robustness of the association between the TyG index and arterial stiffness in patients with T2D.

21In this study of patients with T2D, we provided evidence that the TyG index is independently and more strongly associated with arterial stiffness than the HOMA-IR, elucidating the substantial role of the TyG index in determining arterial stiffness in patients with T2D. This finding lends support to the importance of controlling the TyG index in reducing the arterial stiffness risk for patients with T2D by targeting patients with a high risk of arterial stiffness and has important implications in real clinical settings and epidemiologic investigations.