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1. Introduction
IR is the collective physiological and pathological bases of metabolic diseases, such as abdominal obesity, hypertension, diabetes, and dyslipidemia, and it is considered the central link of the development of such diseases [1, 2]. Moreover, IR and insufficient insulin secretion are the main factors associated with the development of type 2 diabetes mellitus (T2DM) and are regarded as the important clinical markers for the early diagnosis and late follow-up of such condition [3]. And quite a few studies have shown that dyslipidemia was an early manifestation of IR [4], and some scholars believed that hypertriglyceridemia was indeed a representation of IR [5]. Simultaneously, TG and HDL-C levels were found to be negatively and positively, respectively, correlated to insulin sensitivity index [6, 7]. Consequently, the focus of studies has gradually shifted from the initial view that glycometabolism disorder was the primary manifestation of IR and T2DM to the notion that abnormal blood lipid was the first manifestation and core link to their onset [8, 9].
To date, IR has been identified as a potential mechanism of numerous chronic diseases. However, its role in predicting the risk of a disease and establishing effective treatment strategies has been limited due to the lack of practical quantitative and universal diagnostic methods. Previously, the hyperinsulinemic clamp technique was used as a golden index for the evaluation of IR [10]. However, it was challenging to use in patients due to its complex nature and high cost. At present, the homeostasis model assessment as an index of insulin resistance (HOMA-IR) is the recognized diagnostic criterion [11]; however, this tool requires the identification of fasting insulin in the serum (FINS), and standardized methods for it in laboratories are limited. In addition, FINS is susceptible to the influence of islet β cell function and hypoglycemic drugs. All the disadvantages will make the implementation of clinical and epidemiological research challenging, and IR will be more difficult to be identified in natural population. Instead, BLIs can be easily identified in regular physical examinations and epidemiological surveys, and their close correlation to IR also provided opportunities and possibilities for the early detection and screening of IR. A superior predictive value has been attributed to lipoprotein ratios, such as TC/HDL-C and LDL-C/HDL-C ratios [7]. In particular, the TG/HDL-C ratio has emerged as a marker of IR [12] in nondiabetic individuals as well as a good predictor of metabolic syndrome (MS) and cardiovascular disease (CVD) [13].
In addition, numerous studies have presented the importance of ethnic characteristics on adequate cut-off points for the identification of individuals at the risk of IR. China is a multiethnic country, and a high number of studies have reported about the Han population in central China [14, 15]; only few have assessed the Uygur, Kazakh, and Han people living in the remote rural areas of China. At the same time, we know that common metabolic diseases are significantly correlated to ethnic customs, living environment, and lifestyle habits. Analyzing the relationship between BLIs and IR in different populations and corresponding diagnostic thresholds is of great importance for effective and targeted disease control and improvement of the health of the nation. Moreover, simple and inexpensive means, such as screening for IR using BLIs, were more in demand in areas with relatively backward economic and medical conditions, which include areas in Xinjiang, China. In the present study, the Uygur, Kazakh, and Han populations in the Xinjiang region of China were included, and the relationship between BLIs and IR was analyzed, the ROC curve was obtained, and the threshold of IR screening for each ethnic group was identified, which provided the basis for the establishment and improvement of IR screening and diagnostic strategies in Xinjiang.
2. Participants and Methods
2.1. Subjects
Our survey was conducted from 2009 to 2013 in the five regions of Xinjiang, including Ili Kazak Autonomous Prefecture, Kashgar Prefecture, Shihezi, Tarbagatay Prefecture, and Changji Hui Autonomous Prefecture. This survey collected information about chronic disease (including metabolic syndrome, hypertension, diabetes mellitus, dyslipidemia, and cardiovascular disease) from residents (≥18 years old and having lived locally for more than 10 years). On this basis, we randomly selected subjects for experimental detection of this study. The formula for estimating the sample size is as follows:
In the formula,
2.2. Gold Standard of IR
The homeostasis model assessment was applied to assess the status of IR (HOMA-IR) and was defined as follows:
2.3. Laboratory Tests
TC, TG, LDL-C, HDL-C, and fasting glucose levels were assessed by a biochemical autoanalyzer (Olympus AU 2700, Olympus Diagnostics, Hamburg, Germany) in a clinical laboratory. FINS was determined by radioimmunoassay with a kit purchased from Beijing Atomic Tech Co. Ltd. (Beijing, China).
2.4. Statistical Analysis
All of the analyses were performed with SPSS (version 25.0) and statistical software packages R (https://www.r-project.org/, The R Foundation) and Empower Stats (http://www.empowerstats.com, X & Y Solutions, Inc., Boston, MA). Comparisons of the general clinical data between the two groups (IR and non-IR groups) were performed using Student’s
3. Results
3.1. Description of the Basic Information
A total of 969 participants were included in the study, of which 418 (43.1%) were Uygurs, 331 (34.2%) were Kazakhs, and 220 (22.7%) were Hans. First, we compared the IR and BLIs among the three nationalities, and results showed that such indicators significantly differed in terms of race (
Table 1
Comparison of BLIs among three nationalities.
Nation | Uygurs ( |
Kazakhs ( |
Hans ( |
||
---|---|---|---|---|---|
HOMA-IR | 10.733 | 0.000 | |||
TG (mmol/L) | 11.939 | 0.000 | |||
TC (mmol/L) | 5.385 | 0.005 | |||
HDL-C (mmol/L) | 53.270 | 0.000 | |||
LDL-C (mmol/L) | 26.699 | 0.000 | |||
TG/HDL-C | 5.065 | 0.006 | |||
TC/HDL-C | 36.071 | 0.000 | |||
LDL-C/HDL-C | 34.987 | 0.000 | |||
1/HDL-C (1/mmol/L) | 51.615 | 0.000 |
Notes: HOMA-IR = homeostasis model assessment of insulin resistance; TG = triglyceride; TC = total cholesterol; HDL-C = high-density lipoprotein cholesterol; LDL-C = low-density lipoprotein cholesterol.
Table 2
Comparison of general clinical data.
Index | Uygurs ( |
Kazakhs ( |
Hans ( | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Non-IR | IR | Non-IR | IR | Non-IR | IR | |||||||
Sex (males/females) | 144/170 | 54/50 | 1.152 | 0.283 | 104/144 | 42/41 | 1.895 | 0.169 | 79/86 | 19/36 | 2.969 | 0.085 |
Age (year) | 0.144 | 0.885 | 0.363 | 0.716 | -0.411 | 0.682 | ||||||
Weight (kg) | -1.924 | 0.055 | -0.660 | 0.510 | -1.305 | 0.193 | ||||||
Height (cm) | -0.511 | 0.609 | -1.088 | 0.277 | 0.174 | 0.862 | ||||||
Waistline (cm) | -1.439 | 0.151 | -1.289 | 0.198 | -2.058 | 0.041 | ||||||
Hipline (cm) | -0.625 | 0.533 | -0.375 | 0.708 | -1.287 | 0.199 | ||||||
SBP (mmHg) | -0.883 | 0.378 | -0.218 | 0.828 | -0.501 | 0.617 | ||||||
DBP (mmHg) | -0.430 | 0.668 | 0.407 | 0.684 | 0.132 | 0.895 | ||||||
WHR | -1.672 | 0.095 | -1.590 | 0.113 | -1.770 | 0.078 | ||||||
BMI (kg/m2) | -2.105 | 0.036 | -0.817 | 0.414 | -1.684 | 0.094 | ||||||
TG (mmol/L) | -1.272 | 0.041 | -2.747 | 0.007 | -2.683 | 0.009 | ||||||
TC (mmol/L) | -1.007 | 0.314 | -0.470 | 0.639 | -0.658 | 0.512 | ||||||
HDL-C (mmol/L) | 0.661 | 0.509 | 2.326 | 0.019 | 1.933 | 0.045 | ||||||
LDL-C (mmol/L) | -0.544 | 0.587 | -0.750 | 0.454 | -1.216 | 0.225 | ||||||
TG/HDL-C | -1.162 | 0.034 | -2.642 | 0.010 | -2.582 | 0.012 | ||||||
TC/HDL-C | -1.173 | 0.028 | -2.952 | 0.003 | -2.273 | 0.026 | ||||||
LDL-C/HDL-C | -1.005 | 0.315 | -2.214 | 0.027 | -2.378 | 0.020 | ||||||
1/HDL-C (1/mmol/L) | -1.032 | 0.303 | -2.491 | 0.013 | -2.093 | 0.040 |
Notes: SBP = systolic blood pressure; DBP = diastolic blood pressure; WHR = waist-to-hip ratio; BMI = body mass index; TG = triglyceride; TC = total cholesterol; HDL-C = high-density lipoprotein cholesterol; LDL-C = low-density lipoprotein cholesterol.
3.2. Multivariate Logistic Regression Analysis
To eliminate the confounding effects of other factors on the relationship between BLIs and IR, we used multivariate logistic regression analysis to adjust such factors. Results showed that the BMI, TG level, TG/HDL-C ratio, and TC/HDL-C ratio of the Uygurs were included using the regression equation, and the TG level, HDL-C level, TG/HDL-C ratio, TC/HDL-C ratio, LDL-C/HDL-C ratio, and 1/HDL-C level of the Kazakh still differed significantly after adjusting for other factors. The findings observed in Hans were similar to those in Kazakhs (Table 3).
Table 3
Multivariate logistic regression analysis.
Variables | Uygurs | Kazakhs | Hans | ||||||
---|---|---|---|---|---|---|---|---|---|
OR | 95% CI for OR | OR | 95% CI for OR | OR | 95% CI for OR | ||||
Waistline (cm) | — | — | — | — | — | — | 2.259 | (0.807, 4.962) | 0.028 |
BMI (kg/m2) | 2.025 | (0.967, 4.087) | 0.019 | — | — | — | — | — | — |
TG (mmol/L) | 3.698 | (1.265, 6.279) | 0.000 | 2.215 | (0.968, 5.525) | 0.033 | 1.543 | (1.180, 2.018) | 0.002 |
HDL-C (mmol/L) | — | — | — | 1.876 | (0.879, 2.416) | 0.029 | 2.189 | (1.023, 7.567) | 0.032 |
TG/HDL-C | 4.645 | (1.225, 9.208) | 0.000 | 5.007 | (0.935, 11.086) | 0.000 | 4.529 | (1.161, 9.012) | 0.000 |
TC/HDL-C | 2.357 | (1.027, 6.107) | 0.008 | 4.954 | (1.345, 9.948) | 0.000 | 5.412 | (0.879, 10.246) | 0.000 |
LDL-C/HDL-C | — | — | — | 2.987 | (0.919, 6.059) | 0.011 | 1.854 | (1.161, 2.862) | 0.010 |
1/HDL-C (1/mmol/L) | — | — | — | 1.957 | (0.739, 4.238) | 0.036 | 7.354 | (1.360, 19.775) | 0.021 |
Notes: BMI = body mass index; TG = triglyceride; TC = total cholesterol; HDL-C = high-density lipoprotein cholesterol; LDL-C = low-density lipoprotein cholesterol.
3.3. Use of the Nomogram
For example, in Uygurs, if the TG level was 4 mmol/L, an upward vertical line can be drawn from the TG axis to the point bar to obtain the point of 25. Other indicators can also be manipulated such as this, and we assumed that the TG/HDL-C ratio of 6 had a score of 10 points, the HDL-C level of 1 mmol/L had 10 points, the LDL-C/HDL-C ratio of 4 had 5 points, the 1/HDL-C level of 0.8 had 6 points, and the TC/HDL-C ratio of 6 had 15 points. Then, the total score was 71 (
[figures omitted; refer to PDF]
3.4. Screening Value and Cut-off Point Analysis
In Uygurs, the AUC of the nomogram for the prediction of IR prediction was 0.571, and the optimal cut-off value was -1.123. Among the single indicators, the TG level had the largest AUC at 0.570, and the optimal cut-off value was 1.515. The AUC of the nomogram for Kazakhs was 0.661, and the optimal cut-off value was -1.321. Moreover, among the single indicators, the TG/HDL-C ratio had the largest AUC at 0.629, and the optimal cut-off was 1.230. For Hans, the AUC of the nomogram was 0.625, and the optimal cut-off value was -1.074. The TG/HDL-C ratio had the largest AUC at 0.617 among the single indicators, and the optimal cut-off value was 1.495 (Table 4, Figure 2).
Table 4
Analysis of diagnostic tests and ROC curve.
Variables | AUC | 95% CI for AUC | Cut-off | Spe | Sen | |
---|---|---|---|---|---|---|
Uygurs | TG (mmol/L) | 0.570 | (0.505, 0.635) | 1.515 | 0.720 | 0.462 |
TG/HDL-C | 0.563 | (0.497, 0.629) | 1.005 | 0.567 | 0.606 | |
TC/HDL-C | 0.504 | (0.441, 0.567) | 3.175 | 0.306 | 0.769 | |
Nomogram | 0.571 | (0.506, 0.635) | -1.123 | 0.650 | 0.539 | |
Kazakhs | TG (mmol/L) | 0.607 | (0.533, 0.681) | 1.425 | 0.790 | 0.422 |
HDL-C (mmol/L) | 0.585 | (0.514, 0.657) | 1.435 | 0.436 | 0.735 | |
TG/HDL-C | 0.629 | (0.558, 0.701) | 1.230 | 0.835 | 0.398 | |
TC/HDL-C | 0.538 | (0.468, 0.609) | 2.885 | 0.706 | 0.410 | |
LDL-C/HDL-C | 0.593 | (0.522, 0.664) | 1.905 | 0.694 | 0.518 | |
1/HDL-C (1/mmol/L) | 0.585 | (0.514, 0.657) | 0.695 | 0.436 | 0.735 | |
Nomogram | 0.661 | (0.595, 0.728) | -1.321 | 0.488 | 0.771 | |
Hans | TG (mmol/L) | 0.615 | (0.520, 0.710) | 1.585 | 0.636 | 0.636 |
TG/HDL-C | 0.617 | (0.526, 0.709) | 1.495 | 0.752 | 0.473 | |
TC/HDL-C | 0.533 | (0.436, 0.630) | 4.095 | 0.824 | 0.364 | |
LDL-C/HDL-C | 0.599 | (0.509, 0.689) | 2.595 | 0.867 | 0.327 | |
1/HDL-C (1/mmol/L) | 0.575 | (0.483, 0.667) | 0.775 | 0.673 | 0.509 | |
HDL-C (mmol/L) | 0.575 | (0.483, 0.667) | 1.285 | 0.685 | 0.509 | |
Nomogram | 0.625 | (0.537, 0.713) | -1.074 | 0.727 | 0.582 |
Notes: TG = triglyceride; TC = total cholesterol; HDL-C = high-density lipoprotein cholesterol; LDL-C = low-density lipoprotein cholesterol; Sen = sensitivity; Spe = specificity.
[figures omitted; refer to PDF]
4. Discussion
In view of the global epidemic of metabolic diseases in recent years, including DM, MS, or CVD, it was of great clinical and preventive significance to develop a simple and inexpensive screening tool to help clinicians quickly identify individuals who are at risk. The pathogenesis of these diseases has been linked to IR, which was found to be associated with dyslipidemia, including low HDL-C level, high TG level, and postprandial lipid level [17–19], and all these atherosclerotic lipid abnormalities preceded other symptoms of diabetes, such as elevated blood sugar level, and another obvious advantage was that they were easy to detect. The current research systematically analyzed the relationship between various BLIs and IR among three major ethnic groups in remote areas of China. In relation to this, exploratory analysis was made on the predictive and diagnostic value of these indices for IR and the appropriate cut-off points, which will lay a foundation for the screening and diagnosis of metabolic diseases, such as IR and diabetes.
Significant racial differences were observed in terms of IR and various related indicators of blood lipid. In this study, the homeostasis model assessment method was used to calculate the HOMA-IR [16]. Results showed significant differences in IR levels among the Uygurs, Kazakhs, and Hans, and the Kazakhs had the highest IR level at 5.27 mmol/L. Previous studies have found that the prevalence of dyslipidemia, DM, and MS in Kazakhs was higher than that in Uygurs and Hans [20], indicating that the state of IR and metabolic diseases was accordant among the three races, and this result coincided with the view that IR was the pathological basis of metabolic diseases. In addition, the levels of BLIs were also distinct, and all these phenomena indicated that indexes and criteria should be selected and formulated according to different crowds, which was conducive in improving the sensitivity and specificity of the screening tool [15, 21].
To scientifically and accurately select the screening tools for IR, correlation analysis was carried out in our study. First, according to the HOMA-IR, the participants of all nationalities were divided into the IR and non-IR groups for univariate analysis. We found that the relevance between IR and BLIs among the different nationalities was different, but the TG level and TG/HDL-C ratio were correlated to IR in all three races, which was consistent with the conclusion of other studies showing that the TG/HDL-C ratio can be used as an alternative index to diagnose IR [7, 22]. Second, multivariate logistic regression analysis was used to determine the independence of each index. After adjusting for confounding factors, the TG level and TG/HDL-C ratio of the three multitudes were still correlated to IR, and these independent indexes may be significant for the diagnosis of IR [23].
The screening value of each lipid index and the optimal cut-off point varied in different races. According to the AUC of the ROC curve, the index with an
This study had several limitations. First, this study included three main ethnic groups in the remote northwest of China. Although the sample was abundant, the sample size of each ethnic group was relatively small. This may lead to the exclusion of some key indicators in the diagnostic tests. For example, in Uygurs, only three indicators were eventually included. Second, although more variables have been included when we analyzed the confounding factors, some sociological factors have not been considered, which may have an impact on the judgment of the independence of the relevant indicators. Therefore, the screening value of the BLIs for IR must be further analyzed after expanding the samples and variables to obtain more scientific and accurate diagnostic indicators and the best cut-off point.
In summary, a series of metabolic diseases have become a major public health problem, and early detection, diagnosis, and treatment are the primary tasks that prevent and treat these diseases. This study is aimed at analyzing the screening value of BLIs for IR to obtain the best index and cut-off point with national suitability. After a multiangle analysis, it was concluded that the screening value after union of BLIs for IR was the highest. In terms of independent BLIs, TG had the most prominent screening value for IR in Uygurs, while the value of TG/HDL-C ratio was the highest for both Kazakhs and Hans; at the same time, racial differences also showed up at the best cut-off point. This kind of research was important for governments to establish and carry out simple, inexpensive, efficient, and feasible screening tools. In the future, we can further evaluate the diagnostic value of BLIs for IR, T2DM, MS, and CVD in wider remote rural areas to improve the survival rate and quality of life of patients.
Disclosure
Shu-Xia Guo and Shu-gang Li are co-corresponding author.
Acknowledgments
This work was supported by the grants from the School-Level Project sponsored independently by Shihezi University (no. KX018205) and the National Innovation and Entrepreneurship Training Program for College Students in 2019 of Shihezi University (no. 201910759026) and the National Science and Technology Support Projects for the “Eleventh Five-Years Plan” of China (no. 2009 BAI82B04). We would like to thank Rulin Ma, Yusong Ding, and Lijuan Ma who have contributed to this study. At the same time, we sincerely thank those who participated in this paper. We would also like to thank the clinical laboratory of the First Affiliated Hospital of Shihezi University School of Medicine for their test work.
Glossary
Abbreviations
AUC:Area under the curve
BLIs:Blood lipid indicators
CI:Confidence interval
CVD:Cardiovascular disease
DBP:Diastolic blood pressure
FINS:Fasting insulin
HDL-C:High-density lipoprotein cholesterol
HOMA-IR:Homeostasis model assessment of insulin resistance
IR:Insulin resistance
LDL-C:Low-density lipoprotein cholesterol
MS:Metabolic syndrome
OR:Odds ratio
ROC:Receiver operating characteristic
SBP:Systolic blood pressure
TC:Total cholesterol
TG:Triglyceride
T2DM:Type 2 diabetes mellitus
WC:Waist circumference.
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Abstract
Objective. This study is aimed at evaluating the diagnostic value of blood lipid indicators (BLIs) for insulin resistance (IR) among major ethnic groups in Xinjiang, China, to identify the most valuable indicators and appropriate cut-off points for each ethnic group and to lay the foundation for the early detection, diagnosis, and treatment of metabolic diseases in remote rural areas. Methods. Overall, 418 Uygurs, 331 Kazakhs, and 220 Hans were randomly included in our study. The homeostasis model assessment was the gold standard for identifying IR. The receiver operating characteristic (ROC) curve was used to evaluate the diagnostic value, and the nomogram was utilized to analyze the predictive value. The size of the area under the curve (AUC) reflected the accuracy of screening and prediction. Results. Differences in races were observed in terms of IR and BLIs, and the Kazakhs had the highest IR level at 5.27 mmol/L. The correlation between IR and BLIs differed among the three races. For the Kazakhs and Hans, all BLIs, except total cholesterol (TC), were correlated to IR. However, for the Uygurs, only the triglyceride (TG) level, TG/high-density lipoprotein cholesterol (HDL-C) ratio, and TC/HDL-C ratio were associated with IR. After further adjustment of confounding factors, these indicators were still correlated to IR. BLIs that independently correlated to IR in the three nationalities had a certain diagnostic value for IR. In terms of the AUC size, the TG level was the highest in Uygurs, the TG/HDL-C ratio was the highest for Kazakhs and Hans, and the corresponding best cut-off points for IR were 1.515, 1.230, and 1.495 mmol/L, respectively. In addition, for each race, when the indicators with a certain diagnostic value were combined, the diagnostic value for IR was higher. Conclusion. BLIs had a certain diagnostic value for IR and could be used as a screening tool for IR among Uygurs, Kazakhs, and Hans in Xinjiang. These findings are extremely important for the prevention and treatment of IR and metabolic diseases in remote rural areas.
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1 Department of Public Health, Shihezi University School of Medicine, Shihezi Xinjiang 832002, China
2 Department of Public Health, Shihezi University School of Medicine, Shihezi Xinjiang 832002, China; Department of Pathology and Key Laboratory of Xinjiang Endemic and Ethnic Diseases (Ministry of Education), Shihezi University School of Medicine, Shihezi Xinjiang 832002, China