key: cord-0915425-d3gbozef
authors: Gong, Rongpeng; Liu, Yuanyuan; Luo, Gang; Liu, Wenjing; Jin, Ziqi; Xu, Zixin; Li, Zheng; Yang, Lixin; Wei, Xiaoxing
title: Associations of TG/HDL Ratio with the Risk of Prediabetes and Diabetes in Chinese Adults: A Chinese Population Cohort Study Based on Open Data
date: 2021-07-08
journal: Int J Endocrinol
DOI: 10.1155/2021/9949579
sha: f5030f5395a1647b60903e46e9380a07c1478285
doc_id: 915425
cord_uid: d3gbozef

BACKGROUND: In the global chronic diseases, type 2 diabetes shows a significant upward trend, and there are more people before prediabetes (impaired glucose tolerance). Many patients with impaired glucose tolerance and undiagnosed diabetes do not know that their glucose metabolism system has been in a state of disorder. Every year, about 5% to 10% of prediabetics develop diabetes. One of the important achieving factors may be the increase in blood lipids. However, it is not clear whether the triglyceride/high-density lipoprotein ratio is associated with impaired glucose tolerance and diabetes in the Chinese population. Therefore, we investigated the relationship between triglyceride/high-density lipoprotein and impaired glucose tolerance and diabetes in the Chinese population. METHODS: We conducted a retrospective cohort study using data from the health screening program. The study included 116,855 participants from 32 locations in China, all of whom were adults over 20. Participants measured fasting blood glucose levels at each visit and collected information about their diabetes history. Impaired glucose tolerance was diagnosed as fasting blood glucose ≥6.00 mmol and self-reported diabetes mellitus. The patient was measured on the date of diagnosis or on his last visit (whichever comes first). RESULTS: The results showed that, after adjusting the potential confounding factors, the ratio of TG/HDL was positively correlated with the occurrence of prediabetes and diabetes, and there was a saturation effect. The inflection points were 1.04 and 1.33, respectively. The effect value and 95% confidence interval before and after the inflection point of impaired glucose tolerance patients were 1.57 and (1.42, 1.73) and 1.03 and (1.01, 1.05), respectively. The effect value and 95% confidence interval before and after the inflection point in patients with diabetes were 2.07 and (1.80, 2.39) and 1.08 and (1.04, 1.12).

Type 2 diabetes is a global chronic disease. In recent years, type 2 diabetes has been on the rise among chronic diseases worldwide [1] . As the most common chronic disease, diabetes puts a tremendous financial strain on both patients and healthcare systems. Simultaneously, some related studies have found that patients with diabetes have a worse prognosis and a higher mortality rate after being infected with COVID-19 [2] [3] [4] [5] . According to the International Diabetes Federation (IDF), there are about 425 million people (20-79 years old) with type 2 diabetes (T2DM) worldwide in 2019. By 2045, this number is expected to rise to 642 million, of which 140.2 million live in Asia [6] [7] [8] .

Prediabetes is the development of impaired glucose tolerance that does not meet the diagnostic criteria for type 2 diabetes [9] . In addition to type 2 diabetes, more people are currently prediabetic (impaired glucose tolerance), and these people are potentially at risk for type 2 diabetes [9, 10] . Many patients with prediabetes and untested and diagnosed diabetes are unaware of the disorder in their glucose metabolism and do not take preventive measures. As a result, approximately 5% to 10% of patients with prediabetes progress to diabetes each year [10] .

In recent years, patients with impaired glucose tolerance and type 2 diabetes have tended to be younger [1, 11] . Younger patients with impaired glucose tolerance and type 2 diabetes tend to have a poor prognosis and are associated with an increased risk of cardiovascular disease and microvascular complications [12] . e decline in the age of the initial onset of prediabetes and type 2 diabetes is unclear and complex. Some people speculate that this is related to the modern lifestyle. e increased probability of high-fat diet intake may be one reason for prediabetes, younger diabetic, and the number of people with diabetes [11, [13] [14] [15] [16] [17] [18] [19] .

erefore, it is of great significance to predict or screen out prediabetic patients (especially in the young population) to control the total number of diabetic population.

Related research shows that the onset of diabetes and age seem to have a critical connection [20] . Aging is itself a risk factor for diabetes: for every additional ten years a person spends, the risk of developing diabetes goes up by 50-70% [20] [21] [22] . However, the increase in the population's high-fat diets weakens the protective effect of age on diabetes incidence [23] . A high-fat diet can increase the amount of TG synthesis in the liver, lower the HDL relatively, and then increase the ratio of TG/HDL [24] [25] [26] [27] .

e population of diabetes in China ranks first globally, and there is an increasing trend year by year [8, [28] [29] [30] . is is closely related to China's rapid economic development and the change of the dietary structure. Among them, the high-fat and high-protein diet significantly increased during the same period. At present, some studies have reported the relationship between the TG/HDL ratio and the incidence of diabetes. For example, studies in Japan, South Korea, and the United States have shown that TG/HDL is an independent risk factor for the incidence of diabetes. However, the effect sizes of these results are inconsistent [31] [32] [33] . is may be due to the significant differences between ethnic groups. At the same time, these studies only analyzed the relationship between TG/HDL and diabetes and did not include patients with the prediabetic stage. erefore, it is of great significance to analyze whether the ratio of TG/HDL is correlated with the incidence of prediabetes and diabetes. In this study, based on the published data, we analyzed whether TG/HDL is a risk factor for prediabetes and diabetes in the Chinese population.

Our data come from Dryad public data (https://datadryad.org/stash), extracted by Chinese researchers (Chen et al.) from a computerized database set up by Ruiz Medical Group, covering 32 regions in China and 11 cities (Shanghai, Beijing, Shenzhen, Nanjing, Suzhou, Changzhou, Hefei, Wuhan, Chengdu, Guangzhou, and Nantong). e data include the medical records of all participants who received health checkups from 2010 to 2016. Participants initially included were at least 20 years of age and had undergone at least two health checkups between 2010 and 2016 (n � 685,277). At the time of inclusion, participants were excluded if they had no available weight and height measurements (n � 103946), no available information on gender (n � 1), an extreme BMI value (<15 kg/m 2 or >55 kg/m 2 ) (n � 152), no available TG or HDL indicators (n � 90124), or no available fasting glucose value (n � 31370). Participants with less than two years between visits (n � 324,233), participants diagnosed with diabetes at enrolment (2997 confirmed by self-report and 4115 diagnosed with fasting glucose ≥6.0 mmol), and participants with unknown diabetes status at follow-up (n � 6630) were further excluded. In the end, a total of 116,855 participants (62,868 men and 53,987 women) were included in the analysis ( Figure 1 ). e queue entry is defined as the date of the first access. Compared to the individuals excluded from this analysis, the individuals included in the analysis were similar in age (42.1 vs. 41.9 years), had a similar body mass index (23.2 vs. 23.3 kg/m 2 ), and had a relatively higher proportion of males (54.8% vs. 52.1%). Participants were asked to fill out a detailed questionnaire to assess demographics, lifestyle, medical history, and family history of chronic diseases at each visit to the health screening center. Height, weight, and blood pressure are measured by trained staff. Weight is measured without shoes and wearing light clothing, with weight measured to one decimal point and height measured to one decimal point. BMI is calculated by dividing weight in kilograms by height in meters squared. Blood pressure is measured with a standard mercury sphygmomanometer. Fasting venous blood samples were collected after a minimum of 10 hours of fasting for each examination. Serum triglyceride (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were measured by the Beckman 5800 automatic analyzer. Glucose oxidase assay was used to measure blood glucose levels on a Beckman 5800 automatic analyzer.

e study was a retrospective cohort study. Participants were divided into two ratio groups based on saturation effects, with impaired glucose tolerance being divided into N1 (TG/HDL < 1.04) and N2 (TG/HDL ≥ 1.04), and diabetes is divided into N1 (TG/HDL < 1.33) and N2 (TG/ HDL ≥ 1.33).

e diagnostic criteria of impaired diabetes were fasting blood glucose ≥6.00 mmoL/L and self-reported diabetes at follow-up. e diagnostic criteria of diabetes were fasting blood glucose ≥7.00 and self-exposed diabetes. Patients with prediabetes were reexamined on the date of diagnosis or on their last visit (whichever appears first).

Statistical analysis was performed using R statistical software (R 4.0.3). Bilateral P, values less than 0.05 were considered statistically significant. Data from the descriptive analysis were reported as mean (SD) or median (IQR) or scale. Cox proportional regression model was used to analyze the interaction between TG/HDL, impaired glucose tolerance, and underage diabetes, sex, smoking, alcohol consumption, and other groups. Cox proportional hazard regression model was used to estimate the relationship between TG/HDL ratio and impaired glucose tolerance and diabetes incidence (HR) (95% CI). e N1 group was selected as the control group, and the effect of the N2 group on the risk of prediabetes and diabetes was analyzed (HR, 95% CI). Covariates in the multivariate model included age, sex, smoking status, alcohol consumption status, BMI, biochemical markers, and a family history of diabetes. e effects of age on TG/HDL, impaired glucose tolerance, and diabetes incidence were further investigated. Because of the saturation effect between TG/HDL and impaired glucose tolerance and the risk of diabetes, we describe the risk scores of different groups in two segments, representing the increase of each unit of TG/HDL, the increased risk of impaired glucose tolerance, and diabetes. Curative effects of age, BMI, gender, and TG/ HDL interactions were assessed in a Cox model.

In this study, the median follow-up time of 3.1 years, a total of 116,855 participants were included in the final participants of impaired glucose tolerance and diabetes is respectively 9773 and 2689, including impaired glucose tolerance (6536 cases, 66.9%), diabetes (1579 cases, 72.7%) of male participants which was higher than female impaired glucose tolerance (3237 cases, 33.1%), and diabetes (594 cases, 27.3%) of participants. e mean age and standard deviation of participants with diabetes (55.7 ± 12.6 years) were higher than those of participants with impaired glucose tolerance (54.2 ± 13.0 years) and nondiabetic participants (43.8 ± 12.8 years). e proportion of smoking in the total population and the proportion of people with impaired glucose tolerance and diabetes were 20.4%, 30.6%, and 34.7%, respectively, and these proportions gradually increased. e proportion of participants with alcohol consumption, impaired glucose tolerance, and diabetes (2.7% to 4.5%) increased. ose with diabetes had a BMI of 26.3 ± 3.4, higher than those with prediabetes (25.4 ± 3.3) and those without diabetes (23.3 ± 3.3) ( Table 1) .

is study analyzed the effects of age, gender, BMI, alcohol consumption, smoking, and some biochemical indicators on prediabetes and diabetes in the Chinese population. We found that women have much lower rates of prediabetes and diabetes than men. Compared to men, women had a 44 percent lower risk of prediabetes, with an effect value (HR) of 0.58 percent and a 95 percent confidence interval (95% CI) for (0.56, 0.61). e effect HR and 95% confidence interval for diabetes in women were 0.44 and (0.4, 0.49), respectively. Compared with participants without a family history of diabetes, participants with a family history of diabetes had a higher incidence, with effect 

is study drew a smoothing fitting curve to analyze the relationship between TG/HDL ratio and prediabetes and diabetes mellitus in the Chinese population (Figures 2 and 3) . e results showed that TG/HDL had a saturation effect on both prediabetes and diabetes mellitus (Tables 3 and 4) , and the inflection points were 1.04 and 1.33, respectively. Prediabetes: Table 3 ). In this study, it was found that when TG/HDL ≥ 1.04, the risk of prediabetes was much higher than that when TG/HDL < 1.04 (Figure 4) , and when TG/ HDL ≥ 1.33, the risk of diabetes was much higher than that when TG/HDL < 1.33 ( Figure 5 ). Table 5 shows the association between the TG/HDL ratio and the probability of prediabetes after adjusting for potential confounders. We have built four regression models to analyze the results, while model 1 was adjusted according to age, gender, and BMI. In model 2, family history of diabetes, smoking, drinking, and hypertension were added on the basis of model 1, and in model 3, ALT, AST, BUN, LDL, FPG, and TC were added on the basis of model 2. e results showed that the ratio of TG/HDL was related to the occurrence of prediabetes in all models. In the population with TG/HDL < 1.04, the effect value HR and 95% confidence interval of the unadjusted model were 7.71 and (7.05, 8.43 ). e effect value HR and 95% confidence interval adjusted for model 1 were 2.37 and (2.15, 2.62), P < 0.001, and the difference was statistically significant. e effect value HR and 95% confidence interval adjusted for model 2 were 2.29 and (2.07, 2.53), P < 0.001, and the difference was statistically significant. e effect value HR and 95% confidence interval adjusted according to model 3 were 1.57 and (1.42, 1.73), P < 0.001, and the difference was statistically significant. In the population with TG/HDL ≥ 1.04, the effect HR and 95% confidence interval adjusted according to the complete model were 1.00 and (0.98, 1.02), P � 0.9558. e effect value had no clinical value, and the difference was not statistically significant. Table 6 shows the relationship between the TG/HDL ratio and the probability of developing diabetes after adjusting for potential confounders. e results showed that adjusted model 3, model 2, and model 1 suggested that the ratio of TG/HDL was related to the occurrence of diabetes. In the population with TG/ HDL < 1.33, the effect value HR and 95% confidence interval of the unadjusted model were 6.60 and (5.86, 7.43), respectively. e effect value HR and 95% confidence interval adjusted for model 1 were 2.46 and (2.16, 2.81), respectively, P < 0.001, and the difference was statistically significant. e effect value HR and 95% confidence interval adjusted for model 2 were 1.14 and (1.11, 1.16), respectively, P < 0.001, and the difference was statistically significant. e effect value HR and 95% confidence interval adjusted according to model 3 were 2.28 and (1.99, 2.61), respectively, P < 0.001, and the difference was statistically significant. In the population with TG/HDL ≥ 1.33, the unadjusted model effect value (HR) and 95% confidence interval (95% CI) were 1.23 and (1.21, 1.25), respectively. e effect value HR and 95% confidence interval adjusted for model 1 were 1.13 and (1.10, 1.16), respectively, P < 0.001, and the difference was statistically significant. e effect value HR and 95% confidence interval adjusted for model 2 were 1.14 and (1.11, 1.16), respectively, P < 0.001, and the difference was statistically Figure 6 shows that the relationship between the ratio of TG/HDL and the incidence of prediabetes remained stable in all subgroups. Figure 7 shows that the relationship between the ratio of TG/HDL and the 

Our results showed that, after adjusting for potential confounding factors, the ratio of TG/HDL was positively correlated with the occurrence of prediabetes and diabetes mellitus, with saturation effect, and the inflection points were 1.04 and 1.33, respectively. Prediabetes: the effect value and 95% confidence interval before and after the inflection point were 1. e association between TG/HDL and prediabetes reached the maximum when BMI was 18.5-24; that is, the effect value of TG/HDL was more significant in the younger population and was more significant in the population with a BMI of 18.5-24, which accounted for the majority of the study, but had a low proportion of diabetes. erefore, it was more meaningful to pay attention to this group of people.

In previous studies, TG/HDL was often used to evaluate insulin resistance [34] [35] [36] [37] [38] . Recent studies have found a correlation between TG/HDL and the incidence of diabetes [39] [40] [41] [42] . However, these studies did not include patients with prediabetes. When participants develop insulin resistance, it does not lead directly to the onset of diabetes in the patient. However, it gradually leads to impaired glucose tolerance, and in most cases, these individuals will develop diabetes [9] . In contrast, on the basis of diabetes, our study further included participants with abnormal glucose metabolism and clinically elevated fasting blood glucose into the analysis and found that TG/ HDL is not only associated with diabetes but also related to impaired glucose tolerance. Our findings are helpful for the early detection of diabetes and timely measures.

Compared with another study based on the same database, TG/HDL and diabetes effect size was slightly different from the previous study [43] . First of all, Chen et al.'s study suggested that TG/HDL had no interaction in all age groups (P -interaction � 0.3871), which was contrary to our results, which suggested that TG/HDL had interaction in all age groups (P -interaction <0.001), and the effect of TG/HDL on diabetes gradually decreased with the increase of age. In addition, they found an inflection point of 1.186, and the HR and 95% CI of the first and second paragraphs were anterior: 1.718 (1.433, 2.060), posterior: 1.409 (0.981, 1.120). is and our results are different. is may differ from the way lost data Hazard ratio (95% CI) International Journal of Endocrinology Research shows that when the TG/HDL ratio increases, free fatty acid in the body will increase, leading to liver triglyceride and low-density lipoprotein. High TG levels are more likely to lead to insulin resistance [45] . When at high TG/HDL level, too much TG binds to insulin receptors, preventing insulin receptors from functioning properly, reduce insulin sensitivity, lead to insulin resistance, and eventually lead to impaired glucose tolerance and diabetes.

Due to the particularity of the data and composition, we cannot guarantee the results of other groups or non-Chinese races nor can we represent specific groups' applicability (pregnant women, children, etc.). At the same time, due to the particularity of the data, diet, exercise, and others can affect the result of residual confusion. Second, we define impaired glucose tolerance as diabetic patients whose fasting blood glucose is greater than or higher than 6.0 mmol/L or self-reported rather than based on the OGTT test or the determination of glycosylated hemoglobin levels, which may be insufficient. In the future, more detailed methods will be needed for more comprehensive follow-up studies.

Although there are some disadvantages, our study has some merits: (1) compared with previous similar studies, our study has a larger sample size and, for the first time, increases the relationship between prediabetes incidence and TG/HDL. (2) Compared with previous studies, our statistical method is more accurate, which solves the nonlinear problem and further analyzes the relationship between TG/HDL and impaired glucose tolerance at different levels. (3) In this study, we analyzed the independent variables from the perspective of both continuous variables and classified variables, which further reduced the contingency in the analysis and increased the results' reliability.

In conclusion, our study results showed that the increased TG/ HDL-C ratio was positively correlated with the risk of prediabetes and diabetes. An elevated TG/HDL-C ratio increases the risk of impaired glucose tolerance in the future, leading to an increased incidence of diabetes. is highlights that lowering the TG/HDL-C ratio may not only reduce the effect on the cardiovascular disease but also contribute to the reduction of the risk of abnormal glucose metabolism. erefore, monitoring the TG/HDL-C ratio can effectively identify the prediabetic and high-risk diabetic population in the Chinese population, thus helping to warn and control the number of diabetic populations.

BMI: Body mass index FPG: Fasting blood glucose HDL: High-density lipoprotein LDL: Low-density lipoprotein ALT: Alanine aminotransferase AST: Aspartate transaminase CCR: Creatinine clearance rate BUN: Blood urea nitrogen.

e data used to support the findings of this study can be downloaded from the 'DATADRYAD' database (http:// www.Datadryad.org).

In previous studies, Chen et al. [46] and others have made it clear that the study strictly complies with the Helsinki Declaration.

All participants obtained informed consent.

Yuanyuan Liu and Gang Luo are the co-first authors.

e authors declare that they have no conflicts of interest.

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anks are due to Yuanyuan Liu for assistance with the experiments and to Gang Luo for valuable discussion. 

Rongpeng Gong and Xiaoxing Wei conceived the idea. Rongpeng Gong, Yuanyuan Liu, and Gang Luo wrote the manuscript. Zixin Xu, Gang Luo, and Rongpeng Gong collected and read the literature and revised the article. Xiaoxing Wei and Lixin Yang read through and corrected the manuscript. All authors read and approved the final manuscript. Rongpeng Gong is the first author. Xiaoxing Wei and Lixin Yang are the corresponding authors of this paper.