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Association between triglyceride glucose-body mass index and cardiovascular outcomes in patients undergoing percutaneous coronary intervention: a retrospective study

Abstract

Background

The triglyceride glucose-body mass index (TyG-BMI index) has been considered a reliable surrogate measure of insulin resistance; however, its ability to predict the incidence of cardiovascular disease in individuals with coronary artery disease (CAD) remains uncertain. The aim of this study was to demonstrate the correlation between the TyG-BMI index and cardiovascular incidence.

Methods

A total of 2533 consecutive participants who underwent percutaneous coronary intervention (PCI) and drug-eluting stent (DES) implantation were included. Data from 1438 patients was analyzed in the study. The endpoint was defined as a composite of acute myocardial infarction, repeat revascularization, stroke, and all-cause mortality (major adverse cardiac and cerebrovascular events, MACCEs) at 34-month follow-up. The formula for calculating the TyG-BMI index is ln [fasting triglyceride (mg/dL) × fasting blood glucose (mg/dL)/2] × BMI.

Results

Among the 1438 participants, 195 incident patient cases of MACCEs were ascertained. The incidence of MACCEs showed no statistically significant differences in the TyG-BMI index tertiles in the overall population. Further exploratory subgroup analysis and multivariable logistic regression analysis revealed a linear relationship between the TyG-BMI index (per 1 SD increased) and MACCEs in the elderly patients (OR = 1.22, 95% CI 1.011–1.467, p = 0.038) and in the female patients (OR = 1.33, 95% CI 1.004–1.764, p = 0.047). The addition of the TyG-BMI index to traditional risk factor models in elderly and female patients did not improve risk prediction for MACCEs.

Conclusion

A higher TyG-BMI index was proportionally related to an increased incidence of MACCEs in the elderly or female patients. However, the inclusion of the TyG-BMI index did not provide better predictive performance for MACCEs in the elderly, specifically in female patients.

Background

Coronary artery disease (CAD) has been considered the primary cause of death and is continuously raising the expense of health care and the burden on societal productivity not only in China but also all around the world [1, 2]. Although superior optimized strategies for revascularization and medication treatment have been developed and applied recently, there is still a high incidence of recurrent cardiovascular events [3, 4]. Therefore, it is of great clinical importance to improve the risk stratification to facilitate the management of patients with CAD, which is also a great challenge [5].

Insulin resistance (IR) means the diminished or impaired sensitivity to endogenous and exogenous insulin in insulin-dependent organs and tissues [6]. IR is also a critical hazard factor for the progress of type 2 diabetes mellitus (T2DM) and cardiovascular diseases [7, 8]. Multiple methods for IR assessment have been developed. However, the clinical application is limited [7, 9, 10]. Besides, the triglyceride glucose index (TyG index), which is calculated by considering both fasting triglycerides and fasting blood glucose level, has been shown as a symbol highly correlated to hyper-insulinemic euglycemic clamp (HEC) as well as the homeostatic model assessment of insulin resistance index (HOMA-IR) [11, 12]. Studies have revealed that the TyG index is related to pathophysiological processes including arterial stiffness and coronary artery calcification, which are associated with cardiovascular disorders like CAD and hypertension [13,14,15,16,17,18,19,20].

Obesity, identified by body mass index (BMI), is another principal factor linked to IR [21]. A combination of TyG and BMI (TyG-BMI index) was revealed to be in good accordance with HOMA-IR for IR assessment in the Korean population [6] and Chinese population [22]. Recently, one study showed that the TyG-BMI index was linearly linked with ischemic stroke [23]. These studies indicate that the TyG-BMI index may have a potential association with cardiovascular events in patients with CAD. However, very few studies focused on the influence of the TyG-BMI index on cardiovascular outcomes in those who underwent DES implantation. Consequently, current work aims to explore the impact of the baseline TyG-BMI index on cardiovascular outcomes in individuals with CAD undergoing PCI and to evaluate whether combining the TyG-BMI index with traditional risk indicators improves risk stratification.

Methods

Study population

Yao HM et al. provided the data used in the research [24], which is accessible through Dryad (https://doi.org/10.5061/dryad.13d31) [25]. The Ethics Committee at Zhengzhou University's First Affiliated Hospital authorized this research in line with the Declaration of Helsinki, and a waiver of informed consent was granted. Since research ethics has already approved the public policy statement underlying the dataset, no ethical declaration was necessary for the current study. The original study was designed to assess the prognosis of patients with coronary artery disease. All study participants who underwent PCI and were treated with DES between July 2009 and August 2011 (n = 2533) were included, and all completed a median of 29.8 months (quartiles, 25.6–34 months) of follow-up. Coronary angiography and PCI were conducted according to standard procedures and guidelines. All patients were administered loading doses of aspirin (300 mg) and clopidogrel (300 mg) before the coronary intervention, except those who had already been treated with antiplatelet medication. The surgeon decided the selection of procedure strategy, stenting techniques, stent type, and use of glycoprotein IIb/IIIa receptor inhibitors or intravascular ultrasound. All patients were treated with standard dual antiplatelet therapy (aspirin 100 mg/day and clopidogrel 75 mg/day) after PCI for at least one year, constantly [24]. After excluding confusing or missing data, data covering 1438 patients were used for the current analyses (Fig. 1).

Fig. 1
figure 1

Flowchart of participant selection. DBP diastolic blood pressure; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; SBP, systolic blood pressure; TC, total cholesterol; TG, triglyceride; TyG-BMI index, triglyceride glucose-body mass index

Data collection and definitions

Demographic data (age, gender, body mass index), comorbid diseases (heart failure, atrial fibrillation, previous acute myocardial infarction, previous stroke, PCI, hypertension, diabetes mellitus, smoking), and diagnostic information were obtained at admission. Routine laboratory tests, including glycemia, creatinine, uric acid, bilirubin, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), total cholesterol (TC), and triglyceride (TG), were performed using fasting blood samples. The laboratory data were gathered from medical records. The angiographic data, including the operative approach, number of diseased vessels, location of target lesions (left main coronary artery (LM), left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA)), characteristics of lesions (occlusion, chronic total occlusions (CTO), ostial lesion, and bifurcation lesion), number of stents, length and diameter of stents, and number of treated vessels, were also collected. Besides that, information about medications (aspirin, clopidogrel, beta blockers, angiotensin-converting enzyme inhibitors (ACEI), calcium channel blockers (CCB), and statins) was obtained. All data were collected retrospectively using a standardized data collection form. The follow-up information was gathered through the outpatient clinic, readmission, or phone contact.

The TyG-BMI index was ln [TG (mg/dL) × FBG (mg/dL)/2] × BMI [22]. The elderly patients were those aged over sixty years [26]. Smokers were defined as those who had smoked in the last decade. The history of diabetes mellitus was defined as treatment with diabetes medication or self-reported diabetes mellitus. The history of hypertension was defined as treatment with antihypertensive drugs or a self-reported hypertension. Repeat revascularization was revascularization with PCI or bypass surgery during the follow-up.

Endpoints

The endpoint of this study was major adverse cardiac and cerebrovascular events (MACCEs) at 34-month follow-up. The MACCEs included acute myocardial infarction, repeat revascularization, all-cause mortality, and stroke.

Statistical analysis

All participants were separated into tertiles according to the TyG-BMI index levels: tertile 1 (n = 479, TyG-BMI index < 195.26), tertile 2 (n = 479, 195.26 ≤ TyG-BMI index < 226.26), and tertile 3 (n = 480, TyG-BMI index ≥ 226.26), and the characteristics were depicted. Categorical variables were shown as numbers (n) and percentages (%) and were assessed using chi-square tests. Continuous variables were presented as the mean ± standard deviation for a normal distribution or the median (interquartile range) for a non-normal distribution. They were analyzed using one-way ANOVA and the Kruskal–Wallis test, respectively.

We standardized (Z-score) the TyG-BMI index, then included it in the univariate and multivariate logistic analyses to investigate the impact of an increase in the TyG-BMI per SD on MACCEs. Before constructing the multivariate model, we examined the collinearity between the TyG-BMI index and other variables by calculating the generalized variance inflation factor (GVIF). The variable was considered significant for collinearity if the GVIF^(1/2Df) was equal to or greater than 2 (Df, degrees of freedom). In the study, we selected the covariates based on the following principles: (1) if the variable was introduced into the basic model or was removed from the full model, the matched odds ratio would change more than 10%; (2) variables with a p-value < 0.1 in the univariate model; and (3) variables were considered based on previous findings, clinical significance, and the number of outcome events. Following the criteria above, we adjusted for age, heart failure, history of acute myocardial infarction (AMI), hypertension, diabetes, left ventricular ejection fraction (LVEF), ACEI, LM, CTO, number of stents, and diameter of stents in the multivariate logistic analyses for the overall population.

Additionally, subgroup analyses were done to explore if the association was modified by gender, age, hypertension, and diabetes mellitus. Interactions between the TyG-BMI index and the variables above were examined separately. Then we performed univariate and multivariate logistic analyses to describe the relationship between TyG-BMI per SD and MACCEs in the elderly patients and the female patients separately. According to the rules for covariate screening above, we adjusted for age, heart failure, history of AMI, ACEI, and uric acid (per 20 units) for elderly patients and controlled for age, history of AMI, diabetes mellitus, CTO, uric acid (per 20 units), and number of treated vessels for female patients in the multivariate model. Restricted cubic splines were applied to evaluate potential nonlinear associations between the TyG-BMI index and MACCEs in the gender and age subgroups. Ultimately, the receiver operating characteristic (ROC) curves were generated to assess whether adding the TyG-BMI index improves the predictive ability of the model containing traditional risk indicators. The area under the curve (AUC) comparisons between the models were evaluated with DeLong’s test. Furthermore, two other measures, net reclassification improvement (NRI) and integrated discrimination improvement (IDI), were computed to assess the additional predictive information of the TyG-BMI index.

Findings are reported by odds ratios (OR) and 95% confidence intervals (CI). All tests were two-tailed, and statistical significance was defined as P < 0.05. All analyses were conducted using the R Statistical Software (http://www.R-project.org, The R Foundation), Free Statistics software versions 1.7, and MedCalc version 20.0.22.

Results

Characteristics of the included and excluded patients

After excluding the confusing data, 1084 patients were excluded due to the missing data. Considering the high proportion of missing values, the characteristics of the included patients and the excluded patients were compared (Additional file 1: Table S1). There were no significant differences in the age and gender distributions between the two groups. The analyzed patients had a higher proportion of diabetes, smoking, and non-ST elevation acute coronary syndromes (NSTE-ACS); in contrast, the excluded patients had a higher percentage of previous PCI or CABG and stroke. No significant differences were observed in the angiographic characteristics except for the higher proportion of multi-vessel lesions. We also noticed that more patients in the excluded group received follow-up angiography, and cardiac death and repeat revascularization occurred more frequently in the group.

Characteristics of the population by TyG-BMI index

A total of 1438 patients were finally included, with a mean age of 60.1 ± 11.1 years, a gender ratio (male/female) of 2.18, and an average TyG-BMI index of 213.7. The characteristics of the patients by tertile of the TyG-BMI index are shown in Table 1. The percentage of females, those with a history of hypertension and diabetes, and those treated with ACEI or CCB increased in parallel with the TyG-BMI index. Patients with higher levels of the TyG-BMI index tended to have higher levels of BMI, TG, TC, and LDL-C and were more likely to have a lower proportion of smoking and a lower level of creatinine and HDL-C. The higher TyG-BMI index group presented with a larger proportion of NSTE-ACS, a higher frequency of multi-vessel lesions, RCA lesions, and more stent implantation; besides, the length of the stents was longer. However, no discernible variations were displayed in age, bilirubin, uric acid, medical history of heart failure, atrial fibrillation, AMI, stroke, or PCI.

Table 1 Baseline characteristics of the study population by tertiles of TyG-BMI index

TyG-BMI index and clinical outcomes in the overall population

The occurrence of MACCEs and individual events are summarized in Table 2. A total of 195 patients (13.6%) had at least one MACCE during follow-up, including 60 (12.5%) patients in the Tertile 1 group, 64 (13.4%) in the Tertile 2 group, and 71 (14.8%) in the Tertile 3 group. The incidence of MACCEs and the individual events showed no significant difference among the three groups. Univariate and multivariate logistic regression analyses were performed to determine the predictors for MACCEs in the overall population (Table 3). The rules of covariate screening were described in detail in the “Methods” section, and we presented the information for selection in Additional file 1: Table S2. The collinearity was assessed before the analyses (Additional file 1: Table S2). We excluded BMI, TC, TG, LDL-C, LCX, RCA, and length of the stents from analyses due to high collinearity with the TyG-BMI index. The risk factors for MACCEs were age, LVEF, the use of ACEI, CTO, LM, stent numbers, and stent diameters (all p < 0.05). However, no statistically significant connection between the TyG-BMI index (per 1 SD increase) and MACCEs was found either in univariate analysis (OR = 1.12, 95% CI 0.97–1.3, p = 0.134) or in multivariate analysis (OR = 1.11, 95% CI 0.91–1.37, p = 0.304). Additionally, we performed subgroup analyses to investigate the impacts of various potential confounding factors, including gender, age, hypertension, and diabetes mellitus (Table 4). We found significant interactions between the subgroups stratified by age and the effect of the TyG-BMI index on the MACCEs (p-value for interaction = 0.019). A similar result was also found in the female subgroup, though there was no statistical significance (p-value for interaction = 0.068).

Table 2 Incidence of clinical outcomes in the overall population during follow-up
Table 3 Univariate and multivariate analysis for predictors of MACCEs in overall population
Table 4 Subgroup analysis for association between TyG-BMI index (per 1 SD) and MACCEs

The linear relationship between the TyG-BMI index and MACCEs in the elderly population

Based on the findings in the subgroup analyses, we further analyzed the association between the TyG-BMI index and MACCEs in elderly patients. Similarly, we conducted collinearity analysis, variable screening (Additional file 1: Table S3), and logistic analyses. We found that the TyG-BMI index (per 1 SD increase) was correlated with a higher risk of MACCEs in the patients aged over 60 years old (OR = 1.21, 95% CI 1.02–1.44, p = 0.034), and the association remained significant (OR = 1.22, 95% CI 1.01–1.47, p = 0.038) even after controlling for the possible confounding variables (Table 5). A restricted cubic spline model was established to define the nonlinear relationship between the TyG-BMI index (per 1 unit) and MACCEs in elderly individuals. The model showed a linear association (p for non-linearity = 0.407) (Fig. 2A). There was no significant association between the TyG-BMI index and MACCEs in the nonelderly subgroup, though the restricted cubic splines model showed a linear relationship (p for non-linearity = 0.532) (Fig. 2B). In addition, we compared the individual outcomes between the lower TyG-BMI index group (< 210.76) and the higher TyG-BMI index group (≥ 210.76), however, no significance was found in all-cause death, cardiac death, AMI, repeat revascularization, or stroke (Table 6).

Table 5 Univariate and multivariate analysis for predictors of MACCEs in elderly patients
Fig. 2
figure 2

The relationship between the TyG-BMI index and MACCEs. A Relationship in the elderly patients. Adjusted for all covariates in Table 4. B Relationship in the nonelderly patients. C Relationship in the female patients. Adjusted for all covariates in Table 5. D Relationship in the male patients. Only 95% of the data is displayed. Odds ratios are indicated by solid lines and 95% CIs by shaded areas

Table 6 Incidence of clinical outcomes in elderly patients

The linear relationship between the TyG-BMI index and MACCEs in the female population

In the subgroup analyses, we observed the relationship between the TyG-BMI index (per 1 SD) and MACCEs in the female population. Then we constructed a logistic regression model to investigate the association further. The collinearity analysis and variable screening were shown in Additional file 1: Table S4. We included age, history of AMI, diabetes mellitus, CTO, uric acid (per 20 units), and number of treated vessels in the final model (Table 7). The results indicated that the baseline TyG-BMI index (per 1 SD) was significantly associated with MACCEs in the female population either in the univariate analyses (OR = 1.39, 95% CI 1.08–1.78, p = 0.010) or in the multivariate analyses (OR = 1.33, 95% CI 1.00–1.76, p = 0.047). Likewise, we fitted the restricted cubic spline model to assess the nonlinear relationship between the TyG-BMI index (per 1 unit) and MACCEs in female individuals. The model revealed a linear relationship (p for non-linearity = 0.938) (Fig. 2C). In the male patients, no association was observed between the TyG-BMI index and MACCEs (Fig. 2D). Furthermore, the incidence of single clinical outcomes was similar in the lower TyG-BMI index group (< 225.79) and the higher TyG-BMI index group (≥ 225.79) (Table 8).

Table 7 Univariate and multivariate analysis for predictors of MACCEs in female patients
Table 8 Incidence of clinical outcomes in female patients

Incremental effect of the TyG-BMI index for predicting MACCEs

In elderly participants, we assessed the ROC curves of the baseline risk model consisting of traditional risk factors (including age, heart failure, history of AMI, ACEI, and uric acid (per 20 units)) and the model fit based on the traditional risk factors and the TyG-BMI index (Fig. 3A). There is no significant difference between the baseline risk model (AUC: 0.687) and the model with the TyG-BMI index (AUC: 0.694) (p for comparison = 0.313). We further calculated the more sensitive category-free NRI of 0.221 (p = 0.020) and IDI of 0.006 (p = 0.059) (Table 9). The results showed limited ability to add the TyG-BMI index to the baseline model. In female patients, we assessed the ROC curves of the base model (including age, previous AMI, diabetes mellitus, CTO, uric acid (per 20 units), and the number of treated vessels) and the model consisting of traditional risk factors and the TyG-BMI index (Fig. 3B). No significant improvement was observed in the female patients considering the comparison of AUCs (base model 0.759 vs. base model + TyG-BMI index 0.765, p for comparison = 0.508). The category-free NRI of 0.222 (p = 0.106) and IDI of 0.012 (p = 0.102) indicated the addition of the TyG-BMI index had no significant incremental effect for predicting MACCEs as well (Table 10).

Fig. 3
figure 3

The receiver operating characteristic (ROC) curves of the TyG-BMI index as a marker to predict MACCEs. A Baseline risk model vs. + TyG-BMI index in the elderly patients. Baseline risk model includes age, heart failure, history of AMI, ACEI, and uric acid (per 20 units). B Baseline risk model vs. + TyG-BMI index in the female patients. Baseline risk model includes age, history of AMI, diabetes mellitus, CTO, uric acid (per 20 units), and number of treated vessels. AUC, area under curve

Table 9 NRI and IDI for the incremental predictive values of models in elderly patients
Table 10 NRI and IDI for the incremental predictive values of models in female patients

Discussion

Our research examined the correlation between the TyG-BMI index and MACCEs among CAD patients undergoing PCI with DES. The primary findings were as follows: (1) The TyG-BMI index was substantially linked with MACCEs in elderly patients and female patients; (2) a higher TyG-BMI index was proportionally related to a higher risk of MACCEs in the elderly patients and in the female patients, even when controlling for confounders rel ated to this research; and (3) the inclusion of the TyG-BMI index could not significantly improve the risk prediction for MACCEs either in the elderly patients or in the female patients.

It is well established that insulin resistance (IR) is a prominent risk factor for T2DM, dyslipidemias, obesity, and cardiovascular disease [27]. Previous studies have indicated that IR is associated with the progression of cardiovascular disorders and predicts cardiovascular outcomes [28]. Consequently, the TyG index was developed to assess IR [7, 11]. Moreover, BMI acts as an indicator of obesity and IR. Then, research in the Chinese population revealed that TyG-BMI was well associated with HOMA-IR in non-diabetic patients [22]. The Korean National Health and Nutrition Examination Survey (KNHANES) indicated the superiority of the TyG-BMI index over other parameters for IR assessed by HOMA-IR [6]. Subsequently, the TyG-BMI index was considered a marker of IR. Additionally, the TyG-BMI index was shown to be linked to hypertension and hyperuricemia [29,30,31,32]. A cross-sectional survey suggested that the TyG-BMI index and ischemic stroke seemed to be independently associated linearly among the general population, without a threshold or saturation effect [23]. And this implied a potential impact of the TyG-BMI index on MACCEs. Hence, we performed an analysis to obtain an accurate association.

In this study, we adjusted the conventional and possible risk factors initially described in our investigation. Intriguingly, we didn’t discover a remarkable link between the TyG-BMI index and MACCEs among the whole study population. It should be noted that the incidence of MACCEs in the study population was less frequent than that in the excluded population (13.6% vs. 21.2%) (Additional file 1: Table S1). The difference mainly resulted from cardiac death and repeat revascularization, possibly due to the lower proportion of follow-up coronary angiography in the study population (14.3% vs. 36.4%). Besides, the present study demonstrated a lower incidence of MACCEs compared to previous studies. Yang et al. and Zhang et al. reported 375 (34.4%) and 856 (27.0%) major adverse cardiovascular events during follow-up, respectively, in patients with AMI [33, 34]. In patients with both type 2 diabetes and acute coronary syndromes (ACS), 188 (24.2%) MACCEs were observed during follow-up [35]. Patients with stable angina or without diabetes were also included in this study, which may partially explain the lower frequency of MACCEs. Therefore, the result should be considered conservative.

A rising number of studies have focused on cardiovascular risk in the female population, demonstrating that the clinical features and prognosis of CAD patients vary by gender, with female patients likely to have worse clinical outcomes [36, 37]. The TyG index (another indicator of IR) was associated with the incidence of myocardial infarction in the general population after 11 years of follow-up, and the risk was considerably greater in women than in men [38]. Another study revealed gender disparities in the association between several IR evaluation parameters and atherosclerosis [39]. Age is generally accepted to be an independent risk factor for cardiovascular disease, and older patients with CAD have a higher risk of adverse cardiovascular outcomes, including ischemic and bleeding events [40]. The TyG-BMI index has been proven to be related to conventional risk factors, including hypertension and diabetes, and populations with combined hypertension and/or diabetes have a greater incidence of cardiovascular events [3, 4, 29, 41]. Thus, we performed an exploratory subgroup analysis focusing on gender, age, hypertension, and diabetes mellitus. The results demonstrated that higher TyG-BMI indexes were related to an increased risk of MACCEs in the older patients and female patients instead of the overall patients, though the precise mechanism remains unknown. Remarkably, the TyG-BMI index, which consists of three classic cardiovascular disease risk markers, lipid-related, glucose-related, and obesity-related components, is a reliable predictor of IR. Moreover, the TyG-BMI index is a valid indicator of IR, which may partially account for the connection seen in our research. IR can induce glucose metabolic disorders, leading to hyperglycemia and eventually triggering inflammation and oxidative stress [42]. Several studies have revealed that IR may contribute to the inactivation of nitric oxide (NO) and generate the overproduction of reactive oxidative stress (ROS) that damages endothelial function [43]. Furthermore, IR may lead to platelet hyperactivity and increase tissue factor (TF) synthesis, which are associated with thrombosis and inflammation [44]. Moreover, IR triggers inordinate glycosylation, promoting the proliferation of vascular smooth muscle cells and the crosslinking and deposition of collagen, ultimately resulting in diastolic left ventricular stiffness and cardiac fibrosis [28]. Finally, higher TG levels may induce raised plasma free fatty acid (FFA) levels, a major cause of obesity-associated IR and cardiovascular disease [21, 45].

Our findings indicated a relationship between the TyG-BMI index and MACCEs in the elderly population. On the one hand, the physiological functions of elderly people decline, and they become more susceptible to multiple metabolic disorders. This process is often accompanied by IR, which in turn exacerbates metabolic disorders, ultimately causing pathological and physiological changes such as endothelial dysfunction, inflammation, and excessive platelet activation, increasing the risk of cardiovascular disease [40]. On the other hand, compared to younger patients, elderly patients may have multiple risk factors and a worse prognosis. In this research, 137 (17.3%) MACCEs occurred in the elderly patients, which was much higher than the 58 (9%) MACCEs in the non-elderly patients. As a result, the conclusions may not be as definitive as they could be, and further research is needed to analyze the relationship between the TyG-BMI index and MACCEs in non-elderly patients. Meanwhile, we noticed similar effects in the gender subgroup. Further analysis revealed a linear association between TyG-BMI and MACCEs in female patients but not in male patients. Several studies about the relationship between IR and MACCEs have reported gender differences [38, 46]. In this study, the mean age of female patients was higher than that of male patients (63.2 years vs. 58.6 years). This may be due to the protective effects of estrogen on the cardiovascular system and insulin sensitivity [36]. Approximately 90% of the women in this study were in the menopausal transition or postmenopausal period, when the protective effects of estrogen were diminished or disappeared and the risk of abdominal fat gain, dyslipidemia, endothelial dysfunction, and IR was increased [47, 48]. Therefore, a higher variability of the TyG-BMI index was observed in the female patients, which may partly explain the findings in the gender subgroup. However, more studies are needed to verify the association and investigate the exact mechanism. Furthermore, we also investigated the association between the TyG-BMI index and individual cardiovascular events. However, no significant differences were observed between the lower and higher TyG-BMI index groups in the elderly and female patients. According to the original research, 11.4% of the patients with angina during the follow-up accepted conservative therapy with medication, and only 23.8% received follow-up coronary angiography [24]. As a result, the low incidence of the individual events was recorded, which limited the conclusions we could draw from our results. When added to the traditional models, no cumulative effects of the TyG-BMI index were observed according to the AUC, NRI, and IDI. The average age of both elderly and female patients in this study is over sixty, which is a time when multiple traditional cardiovascular risk factors are often combined. This weakens the predictive power of the TyG-BMI index.

As far as we know, this study explored the influence of the TyG-BMI index on the incidence of MACCEs in patients treated with DES for the first time. The current research revealed that the TyG-BMI index and MACCEs had a linear connection in elderly patients and female patients. However, there are several non-negligible limitations. Firstly, no conclusions can be drawn about causality due to the single-center observational design of the study. Secondly, the exclusion of a considerable number of patients due to missing data and the low incidence of cardiovascular events might have underestimated the effect. Therefore, further investigation and validation via large-sample, multicenter studies are needed. Thirdly, we couldn’t compare the TyG-BMI index with other current IR measuring techniques because of database restrictions. Fourthly, triglycerides, glucose, and other parameters were only tested at baseline, and they may have altered over follow-up owing to the participants’ lifestyles and medications. The residual or unmeasured confounding, especially the treatment for metabolic syndrome, dietary habits, and physical activities, were not included. Besides, the time-to-event analysis was not conducted due to the lack of a time variable in the data. These might weaken the results. Finally, the population covered in the study comes from a single site in China, limiting the applicability of the results to other communities. Hence, more research is required to verify these findings.

Conclusions

In summary, as a marker of IR, the TyG-BMI index was shown to be an independent prognostic factor of MACCEs in the elderly and female patients after DES implantation. A higher TyG-BMI index was proportionally related to an increased incidence of MACCEs in the elderly and female patients. However, the inclusion of the TyG-BMI index did not improve risk prediction over traditional risk factors in the elderly or female patients. Further investigation is needed to demonstrate the findings.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available in the Dryad repository https://doi.org/10.5061/dryad.13d31 [25].

Abbreviations

ACEI:

Angiotensin converting enzyme inhibitor

AMI:

Acute myocardial infarction

AVB:

Atrioventricular block

BMI:

Body mass index

CCB:

Calcium channel blocker

CABG:

Coronary artery bypass graft

COPD:

Chronic obstructive pulmonary disease

CTO:

Chronic total occlusions

DBP:

Diastolic blood pressure

HDL-C:

High density lipoprotein cholesterol

LAD:

Left anterior descending

LDL-C:

Low-density lipoprotein cholesterol

LM:

Left main coronary artery

LCX:

Left circumflex artery

LVEF:

Left ventricular ejection fraction

NSTE-ACS:

Non-ST elevation acute coronary syndromes

PCI:

Percutaneous coronary intervention

RCA:

Right coronary artery

SA:

Stable angina

SBP:

Systolic blood pressure

STEMI:

ST-segment myocardial infarction

TC:

Total cholesterol

TG:

Triglyceride

TyG-BMI index:

Triglyceride glucose-body mass index

References

  1. Vaduganathan M, Mensah GA, Turco JV, Fuster V, Roth GA. The global burden of cardiovascular diseases and risk: a compass for future health. J Am Coll Cardiol. 2022;80(25):2361–71.

    Article  PubMed  Google Scholar 

  2. The Writing Committee of the Report on Cardiovascular Health and Diseases in China. Report on cardiovascular health and diseases in China 2021: an updated summary. Biomed Environ Sci. 2022;35(7):573–603.

    Google Scholar 

  3. Zhao Q, Zhang TY, Cheng YJ, Ma Y, Xu YK, Yang JQ, Zhou YJ. Impacts of triglyceride-glucose index on prognosis of patients with type 2 diabetes mellitus and non-ST-segment elevation acute coronary syndrome: results from an observational cohort study in China. Cardiovasc Diabetol. 2020;19(1):108.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Zhang Y, Ding X, Hua B, Liu Q, Gao H, Chen H, Zhao X-Q, Li W, Li H. Predictive effect of triglyceride-glucose index on clinical events in patients with type 2 diabetes mellitus and acute myocardial infarction: results from an observational cohort study in China. Cardiovasc Diabetol. 2021;20(1):43.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  5. Li JJ, Liu HH, Li S. Landscape of cardiometabolic risk factors in Chinese population: a narrative review. Cardiovasc Diabetol. 2022;21(1):113.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  6. Lim J, Kim J, Koo SH, Kwon GC. Comparison of triglyceride glucose index, and related parameters to predict insulin resistance in Korean adults: an analysis of the 2007–2010 Korean national health and nutrition examination survey. PLoS ONE. 2019;14(3): e0212963.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  7. Tao LC, Xu JN, Wang TT, Hua F, Li JJ. Triglyceride-glucose index as a marker in cardiovascular diseases: landscape and limitations. Cardiovasc Diabetol. 2022;21(1):68.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  8. Yang J, Tang YD, Zheng Y, Li C, Zhou Q, Gao J, Meng X, Zhang K, Wang W, Shao C. The impact of the triglyceride-glucose index on poor prognosis in nondiabetic patients undergoing percutaneous coronary intervention. Front Endocrinol. 2021;12: 710240.

    Article  Google Scholar 

  9. Kim J, Shin SJ, Kang HT. The association between triglyceride-glucose index, cardio-cerebrovascular diseases, and death in Korean adults: a retrospective study based on the NHIS-HEALS cohort. PLoS ONE. 2021;16(11): e0259212.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  10. Wang L, Cong HL, Zhang JX, Hu YC, Wei A, Zhang YY, Yang H, Ren LB, Qi W, Li WY, et al. Triglyceride-glucose index predicts adverse cardiovascular events in patients with diabetes and acute coronary syndrome. Cardiovasc Diabetol. 2020;19(1):80.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  11. Guerrero-Romero F, Simental-Mendía LE, González-Ortiz M, Martínez-Abundis E, Ramos-Zavala MG, Hernández-González SO, Jacques-Camarena O, Rodríguez-Morán M. The product of triglycerides and glucose, a simple measure of insulin sensitivity. Comparison with the euglycemic-hyperinsulinemic clamp. J Clin Endocrinol Metab. 2010;95(7):3347–51.

    Article  CAS  PubMed  Google Scholar 

  12. Vasques AC, Novaes FS, de Oliveira MS, Souza JR, Yamanaka A, Pareja JC, Tambascia MA, Saad MJ, Geloneze B. TyG index performs better than HOMA in a Brazilian population: a hyperglycemic clamp validated study. Diabetes Res Clin Pract. 2011;93(3):e98–100.

    Article  CAS  PubMed  Google Scholar 

  13. Cui H, Liu Q, Wu Y, Cao L. Cumulative triglyceride-glucose index is a risk for CVD: a prospective cohort study. Cardiovasc Diabetol. 2022;21(1):22.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  14. Barzegar N, Tohidi M, Hasheminia M, Azizi F, Hadaegh F. The impact of triglyceride-glucose index on incident cardiovascular events during 16 years of follow-up: tehran lipid and glucose study. Cardiovasc Diabetol. 2020;19(1):155.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  15. Wang A, Tian X, Zuo Y, Chen S, Meng X, Wu S, Wang Y. Change in triglyceride-glucose index predicts the risk of cardiovascular disease in the general population: a prospective cohort study. Cardiovasc Diabetol. 2021;20(1):113.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  16. Zhang Y, Ren L, Ren M, Yang H, Li K, Cong H, Guo Z. Correlation between the triglyceride-glucose index and high risk of cardiovascular disease: a cohort study of 102,061 subjects from Tianjin, China. Risk Manag Healthc Policy. 2021;14:2803–10.

    Article  PubMed Central  PubMed  Google Scholar 

  17. Özkalaycı F, Karagöz A, Karabay CY, Tanboga İH, Türkyılmaz E, Saygı M, Oduncu V. Prognostic value of triglyceride/glucose index in patients with ST-segment elevation myocardial infarction. Biomark Med. 2022;16(8):613–22.

    Article  PubMed  Google Scholar 

  18. Zhang F, Kadierding R, Zhang S, Yang H, Ren L, Ren M, Ma Y, Wang L, Zhang R, Li W, et al. Triglyceride glucose index for predicting major adverse cardiovascular events in chinese patients with hypertension. Angiology. 2022. https://doi.org/10.1177/00033197221104559.

    Article  PubMed  Google Scholar 

  19. Won KB, Park GM, Lee SE, Cho IJ, Kim HC, Lee BK, Chang HJ. Relationship of insulin resistance estimated by triglyceride glucose index to arterial stiffness. Lipids Health Dis. 2018;17(1):268.

    Article  PubMed Central  PubMed  Google Scholar 

  20. Won KB, Park EJ, Han D, Lee JH, Choi SY, Chun EJ, Park SH, Han HW, Sung J, Jung HO, et al. Triglyceride glucose index is an independent predictor for the progression of coronary artery calcification in the absence of heavy coronary artery calcification at baseline. Cardiovasc Diabetol. 2020;19(1):34.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Boden G. Obesity, insulin resistance and free fatty acids. Curr Opin Endocrinol Diabetes Obes. 2011;18(2):139–43.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  22. Er LK, Wu S, Chou HH, Hsu LA, Teng MS, Sun YC, Ko YL. Triglyceride Glucose-Body Mass Index Is a simple and clinically useful surrogate marker for insulin resistance in nondiabetic individuals. PLoS ONE. 2016;11(3): e0149731.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Du Z, Xing L, Lin M, Sun Y. Estimate of prevalent ischemic stroke from triglyceride glucose-body mass index in the general population. BMC Cardiovasc Disord. 2020;20(1):483.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  24. Yao HM, Wan YD, Zhang XJ, Shen DL, Zhang JY, Li L, Zhao LS, Sun TW. Long-term follow-up results in patients undergoing percutaneous coronary intervention (PCI) with drug-eluting stents: results from a single high-volume PCI centre. BMJ Open. 2014;4(8): e004892.

    Article  PubMed Central  PubMed  Google Scholar 

  25. Data from: Long-term follow-up results in patients undergoing percutaneous coronary intervention (PCI) with drug-eluting stents: results from a single high-volume PCI center, Dryad, Dataset. https://doi.org/10.5061/dryad.13d31 Accessed 20 Jun 2022.

  26. Beard JR, Officer A, de Carvalho IA, Sadana R, Pot AM, Michel JP, Lloyd-Sherlock P, Epping-Jordan JE, Peeters G, Mahanani WR, et al. The World report on ageing and health: a policy framework for healthy ageing. Lancet. 2016;387(10033):2145–54.

    Article  PubMed  Google Scholar 

  27. Tello-Flores VA, Beltrán-Anaya FO, Ramírez-Vargas MA, Esteban-Casales BE, Navarro-Tito N, Alarcón-Romero LDC, Luciano-Villa CA, Ramírez M, Del Moral-Hernández Ó, Flores-Alfaro E. Role of long non-coding RNAs and the molecular mechanisms involved in insulin resistance. Int J Mol Sci. 2021;22(14):7256.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  28. Hill MA, Yang Y, Zhang L, Sun Z, Jia G, Parrish AR, Sowers JR. Insulin resistance, cardiovascular stiffening and cardiovascular disease. Metabolism. 2021;119: 154766.

    Article  CAS  PubMed  Google Scholar 

  29. Bala C, Gheorghe-Fronea O, Pop D, Pop C, Caloian B, Comsa H, Bozan C, Matei C, Dorobantu M. The association between six surrogate insulin resistance indexes and hypertension: a population-based study. Metab Syndr Relat Disord. 2019;17(6):328–33.

    Article  CAS  PubMed  Google Scholar 

  30. Gu Q, Hu X, Meng J, Ge J, Wang SJ, Liu XZ. Associations of triglyceride-glucose index and its derivatives with hyperuricemia risk: a cohort study in chinese general population. Int J Endocrinol. 2020;2020:3214716.

    Article  PubMed Central  PubMed  Google Scholar 

  31. Han R, Zhang Y, Jiang X. Relationship between four non-insulin-based indexes of insulin resistance and serum uric acid in patients with type 2 diabetes: a cross-sectional study. Diabetes Metab Syndr Obes. 2022;15:1461–71.

    Article  PubMed Central  PubMed  Google Scholar 

  32. Li Y, You A, Tomlinson B, Yue L, Zhao K, Fan H, Zheng L. Insulin resistance surrogates predict hypertension plus hyperuricemia. J Diabetes Investig. 2021;12(11):2046–53.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  33. Luo E, Wang D, Yan G, Qiao Y, Liu B, Hou J, Tang C. High triglyceride-glucose index is associated with poor prognosis in patients with acute ST-elevation myocardial infarction after percutaneous coronary intervention. Cardiovasc Diabetol. 2019;18(1):150.

    Article  PubMed Central  PubMed  Google Scholar 

  34. Zhang Y, Ding X, Hua B, Liu Q, Gao H, Chen H, Zhao XQ, Li W, Li H. High triglyceride-glucose index is associated with adverse cardiovascular outcomes in patients with acute myocardial infarction. Nutr Metab Cardiovasc Dis. 2020;30(12):2351–62.

    Article  CAS  PubMed  Google Scholar 

  35. Ma X, Dong L, Shao Q, Cheng Y, Lv S, Sun Y, Shen H, Wang Z, Zhou Y, Liu X. Triglyceride glucose index for predicting cardiovascular outcomes after percutaneous coronary intervention in patients with type 2 diabetes mellitus and acute coronary syndrome. Cardiovasc Diabetol. 2020;19(1):31.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  36. Wada H, Miyauchi K, Daida H. Gender differences in the clinical features and outcomes of patients with coronary artery disease. Expert Rev Cardiovasc Ther. 2019;17(2):127–33.

    Article  CAS  PubMed  Google Scholar 

  37. Montarello N, Chan WPA. Coronary artery disease in women. Aust Prescr. 2022;45(6):193–9.

    Article  PubMed Central  PubMed  Google Scholar 

  38. Tian X, Zuo Y, Chen S, Liu Q, Tao B, Wu S, Wang A. Triglyceride-glucose index is associated with the risk of myocardial infarction: an 11-year prospective study in the Kailuan cohort. Cardiovasc Diabetol. 2021;20(1):19.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  39. Nakagomi A, Sunami Y, Kawasaki Y, Fujisawa T, Kobayashi Y. Sex difference in the association between surrogate markers of insulin resistance and arterial stiffness. J Diabetes Complications. 2020;34(6): 107442.

    Article  PubMed  Google Scholar 

  40. Capranzano P, Angiolillo DJ. Antithrombotic management of elderly patients with coronary artery disease. JACC Cardiovasc Interv. 2021;14(7):723–38.

    Article  PubMed  Google Scholar 

  41. Wijeysundera HC, Machado M, Farahati F, Wang X, Witteman W, van der Velde G, Tu JV, Lee DS, Goodman SG, Petrella R, et al. Association of temporal trends in risk factors and treatment uptake with coronary heart disease mortality, 1994–2005. JAMA. 2010;303(18):1841–7.

    Article  CAS  PubMed  Google Scholar 

  42. Yang Q, Vijayakumar A, Kahn BB. Metabolites as regulators of insulin sensitivity and metabolism. Nat Rev Mol Cell Biol. 2018;19(10):654–72.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  43. Molina MN, Ferder L, Manucha W. Emerging role of nitric oxide and heat shock proteins in insulin resistance. Curr Hypertens Rep. 2016;18(1):1.

    Article  CAS  PubMed  Google Scholar 

  44. Gerrits AJ, Koekman CA, van Haeften TW, Akkerman JW. Platelet tissue factor synthesis in type 2 diabetic patients is resistant to inhibition by insulin. Diabetes. 2010;59(6):1487–95.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  45. Samuel VT, Shulman GI. The pathogenesis of insulin resistance: integrating signaling pathways and substrate flux. J Clin Invest. 2016;126(1):12–22.

    Article  PubMed Central  PubMed  Google Scholar 

  46. Wu Z, Liu L, Wang W, Cui H, Zhang Y, Xu J, Zhang W, Zheng T, Yang J. Triglyceride-glucose index in the prediction of adverse cardiovascular events in patients with premature coronary artery disease: a retrospective cohort study. Cardiovasc Diabetol. 2022;21(1):142.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  47. Lovejoy JC, Champagne CM, de Jonge L, Xie H, Smith SR. Increased visceral fat and decreased energy expenditure during the menopausal transition. Int J Obes (Lond). 2008;32(6):949–58.

    Article  CAS  PubMed  Google Scholar 

  48. The Lancet Diabetes. Menopause: a turning point for women’s health. Lancet Diabetes Endocrinol. 2022;10(6):373.

    Article  Google Scholar 

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Acknowledgements

We gratefully thank Haimu Yao (Department of Cardiology, The First Affiliated Hospital of Zhengzhou University) for providing the datasets. We are also grateful to Dr. Jie Liu (Department of Vascular and Endovascular Surgery, Chinese PLA General Hospital) for his contribution to the statistical support, and study design consultations.

Funding

This work was supported by the Social Development Project of Yangzhou (Grant No. YZ2021060).

Author information

Authors and Affiliations

Authors

Contributions

BX and SHH conceived and designed the study. YC, ZF, XXZ, YCW, and JQL performed the statistical analysis. YC drafted the article. BX and ZF performed manuscript revision. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Shenghu He or Bing Xu.

Ethics declarations

Ethics approval and consent to participate

This study was a secondary analysis of an observational cohort study. The study data collection was approved by the Ethics Committee of the First Affiliated Hospital of Zhengzhou University, and a waiver of informed consent was also granted. No ethic statement was required for the present research due to the dataset’s public policy statement.

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Not applicable.

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The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Table S1.

Characteristics of the included population and excluded population. Data are shown as mean ± standard deviation (SD) or median (IQR) for continuous variables and proportions (%) for categorical variables. P values in bold are < 0.05. ACEI, angiotensin converting enzyme inhibitor; AVB, atrioventricular block; BMI, body mass index; CCB, calcium channel blocker; CABG, coronary artery bypass graft; COPD, chronic obstructive pulmonary disease; CTO, chronic total occlusions; HDL-C, high density lipoprotein cholesterol; LAD, left anterior descending; LDL-C, low density lipoprotein cholesterol; LM, left main coronary artery; LCX, left circumflex artery; LVEF, left ventricular ejection fraction; NSTE-ACS, non-ST elevation acute coronary syndromes; AMI, acute myocardial infarction; PCI, percutaneous coronary intervention; RCA, right coronary artery; SA, stable angina; STEMI, ST-segment myocardial infarction; TC, total cholesterol; TG, triglyceride. Table S2. Selection of covariates and analysis of collinearity in overall patients. Dependent variable: TyG-BMI index. GVIF, generalized variance inflation factor; DF, degree of freedom. (GVIF^(1/(2*Df)) ≥ 2 indicates collinearity). Collinearity analysis showed that BMI, TC, TG, LDL-C, LCX, RCA, length of stents, and the TyG-BMI index had high collinearity. Abbreviations as in Additional file 1: Table S1. Table S3. Selection of covariates and analysis of collinearity in elderly patients. Dependent variable: TyG-BMI index. GVIF, generalized variance inflation factor; DF, degree of freedom. (GVIF^(1/(2*Df)) ≥ 2 indicates collinearity). Collinearity analysis showed that BMI, TC, TG, LDL-C, RCA, number of diseased vessels, length of stents, and the TyG-BMI index had high collinearity. Abbreviations as in Additional file 1: Table S1. Table S4. Selection of covariates and analysis of collinearity in female patients. Dependent variable: TyG-BMI index. GVIF, generalized variance inflation factor; DF, degree of freedom. (GVIF^(1/(2*Df)) ≥ 2 indicates collinearity). Collinearity analysis showed that BMI, glycemia, TC, TG, LDL-C, LAD, LCX, RCA, number of diseased vessels, length of stents, and the TyG-BMI index had high collinearity. Abbreviations as in Additional file 1: Table S1.

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Cheng, Y., Fang, Z., Zhang, X. et al. Association between triglyceride glucose-body mass index and cardiovascular outcomes in patients undergoing percutaneous coronary intervention: a retrospective study. Cardiovasc Diabetol 22, 75 (2023). https://doi.org/10.1186/s12933-023-01794-8

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