Mediators of Inflammation

Mediators of Inflammation / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 4756295 |

Lei Mao, Xianghui Zhang, Yunhua Hu, Xinping Wang, Yanpeng Song, Jia He, Wenwen Yang, Jiaolong Ma, Yizhong Yan, Lati Mu, Jingyu Zhang, Kui Wang, Heng Guo, Rulin Ma, Shuxia Guo, "Nomogram Based on Cytokines for Cardiovascular Diseases in Xinjiang Kazakhs", Mediators of Inflammation, vol. 2019, Article ID 4756295, 8 pages, 2019.

Nomogram Based on Cytokines for Cardiovascular Diseases in Xinjiang Kazakhs

Academic Editor: Emmanuel Economou
Received29 Oct 2018
Accepted19 Feb 2019
Published05 May 2019


Background. This study involved the development of a predictive 5-year morbidity nomogram for cardiovascular diseases (CVD) in Xinjiang Kazakhs based on cytokine levels. Methods. The nomogram was based on a baseline survey of the town of Nalati in the Kazakh Autonomous Prefecture of Xinjiang from 2009 to 2013. By 2016, we had monitored 1508 people for a median time of 5.17 years and identified CVD events in the study population by collecting case information from local hospitals. The study population was divided into the training () and validation cohorts () in a 2 : 1 ratio. The area under the receiver operating characteristic curve (AUC) was used to verify the predictive accuracy of the nomogram. The result was assessed in a validation cohort. Results. At the end of the study, the incidence of CVD in Xinjiang Kazakhs was found to be 11.28%. We developed a new nomogram to predict the 5-year incidence of CVD based on age, interleukin-6 (IL-6), and adiponectin (APN) levels, diastolic blood pressure, and dyslipidemia. The AUC for the predictive accuracy of the nomogram was 0.836 (95% confidence interval: 0.802–0.869), which was higher than that for IL-6 and APN. These results were supported by validation studies. Conclusions. The nomogram model can more directly assess the risk of CVD in Kazakhs and can be used for CVD risk assessment.

1. Introduction

Cardiovascular diseases (CVD) are among the most common causes of death worldwide, and over three-quarters of CVD deaths occur in low- and middle-income countries [1]. CVD has become the leading cause of death in 27 provinces and cities in China, which is one of the most populous developing countries. The economic burden caused by CVD should not be underestimated [2]. The development of atherosclerosis is the pathophysiological basis of CVD. Free fatty acids (FFAs) [3], high-sensitivity C-reactive protein (hs-CRP) [4], adiponectin (APN) [5], insulin (INS) [6], and interleukin-6 (IL-6) [7] can induce atherosclerosis through arterial inflammation. Smoking, drinking, and other adverse lifestyle-related risk factors eventually lead to the development of CVD. Therefore, a complete understanding of the risk factors of CVD and the identification and control of risk factors in high-risk groups can help prevent the development of CVD and reduce the burden of disease.

The use of risk factors to construct a CVD risk assessment model for the estimation of the probability of CVD is effective. The classic Framingham study has predicted the risk of CVD in native white Americans over a decade; the risk prediction scale developed from this study is used to evaluate common clinical risk factors [8]. Chinese researchers have used this study as a reference for a prospective cohort study in 11 provinces and cities to investigate hypertension, hyperlipidemia, diabetes, and obesity, which are independent risk factors for CVD in the Han Chinese population [9]. The intermediate inflammatory and lipid factors in the CVD cascade can reflect premorbid status. The proximal or intermediate risk factors can be used to improve the predictive ability of a CVD model. In a multiethnic country, the prevalence of CVD varies among different ethnic groups and an established CVD risk prediction model cannot be uniformly applied to all groups. Therefore, based on the characteristics of different nationalities and population groups, a CVD model can be applied to a study population.

The population in our study included Kazakhs living in the remote rural areas of Western China. Kazakhs gather in mountainous pastures in Northern Xinjiang and have a mainly nomadic existence. Xinjiang has the second largest population of this local minority. Previous studies found that the CVD-related risk factors in the Kazakh population are hypertension, obesity, and metabolic syndrome (MetS), which have high prevalence rates [1012]. Their levels of FFAs, APN, INS, IL-6, and hs-CRP differed from those of other ethnic groups, and their risk of CVD is higher [1316]. In our study, cytokine levels combined with common risk factors for CVD were used to construct a nomogram for use in the Xinjiang Kazakh rural population and to evaluate the incidence and risk of CVD in these individuals. The data can be used for early screening of CVD in rural areas.

2. Materials and Methods

2.1. Study Population

The survey was conducted from 2009 to 2013 in Nalati town, Xinjiang Kazakh Autonomous Region, which is 4407 km (2739 miles) from Beijing. We successfully interviewed 1771 local Kazakh individuals aged 18 years or older who had resided in the village for at least 6 months. By the end of 2016, a total of 1508 Kazakh inhabitants with complete data were enrolled in the study and were followed up for a median of 5.17 years. We identified the CVD cases in this population using medical records from the People’s Hospital of Xinjiang Xinyuan County and Traditional Chinese Medicine Hospital of Xinjiang Xinyuan County. Each participant provided written informed consent and completed questionnaires. Evaluation included disease history, height, weight, waist circumference, hip circumference, and blood pressure. Blood pressure was measured three times in each subject using a mercury sphygmomanometer, and the average value was calculated. The study was approved by the Institutional Ethics Review Board of the First Affiliated Hospital of Shihezi University (IERB no. SHZ2010LL01).

Subjects with complete information were randomly assigned in a 2 : 1 ratio into the training cohort () to develop a nomogram and the internal validation cohort () to evaluate the predictive models.

2.2. Definitions

CVD was identified as follows: (1) hospitalizations for CVD at follow-up, coronary intervention (cardiac catheterization or coronary bypass), angina (or nitroglycerin after cohort study), and CVD death (ICD9: codes 390-495); (2) according to the hospital medical records, hospitalization was due to the following reasons: coronary artery atherosclerosis, coronary heart disease, unstable angina, myocardial infarction, heart failure, stroke, transient cerebral ischemia, and peripheral vascular disease (abdominal aortic aneurysm, peripheral vascular surgery, or carotid endarterectomy); and (3) the CVD events were recorded according to the hospitalization records and questionnaires. If two or more events of the same class of subjects occur, then the first occurrence was the outcome event.

Based on the diagnostic criteria recommended by the IDF, participants were considered to have MetS if they had abdominal obesity ( in women and ≥90 cm in men) and showed two or more of the following: (1) hypertriglyceridemia (≥150 g/dL); (2) low HDL-C (<50 mg/dL in women and <40 mg/dL in men); (3) high blood pressure (systolic blood or diastolic blood ); and (4) high fasting glucose (≥100 mg/dL).

Based on the China Adult Dyslipidemia Prevention Guide (2007) [15], dyslipidemia was defined as the presentation of any one or more of the following four items: (1) (200 mg/dL); (2) (40 mg/dL); (3) (160 mg/dL); and (4) (240 mg/dL).

2.3. Methods

Total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and fasting blood glucose were analyzed using an automatic biochemical analyzer (Olympus AU2700, Olympus Diagnostics, Hamburg, Germany) in the clinical laboratory.

FFA levels were determined by a colorimetric assay using kits purchased from Randox Laboratories Ltd. (Shanghai, China). ELISA kits for detecting the levels of INS, hs-CRP, IL-6, and APN were purchased from Elabscience Biotechnology (Wuhan, China).

2.4. Statistical Analysis

All statistical analyses were preformed using SPSS version 19.0, R (, The R Foundation), and EmpowerStats (, X&Y Solutions Inc., Boston, MA). Baseline comparisons between the two cohorts were performed using Student’s -test or the Mann-Whitney test for continuous variables where appropriate and chi-square tests for categorical variables. The hs-CRP, IL-6, and APN levels displayed a positively skewed distribution. After logarithmic (Lg10) transformation, the data were approximately normally distributed with a geometric mean () and corresponding 95% confidence intervals (95% CI) for hs-CRP, IL-6, and APN. Multivariable Cox proportional hazards regression analysis was used to identify independent risk factors through stepwise selection. A nomogram was established based on the results of multivariable analysis [17]. Discriminative ability was measured using an area under the receiver operating characteristic (ROC) curve (AUC) and a calibration curve by comparing the probability using the predictive nomogram to actually observe CVD probability. An ROC curve was drawn to determine the optimal threshold of the nomogram. A 2-sided value < 0.05 was considered statistically significant.

3. Results

3.1. The Baseline Characteristics of the Kazakhs

At the end of the study, 203 CVD events (CHD, myocardial infarction, stroke, etc.) were diagnosed, with a prevalence of 13.46%. In the training cohort, the average median age was 46.02 years old and 448 (44.6%) were male, of which 13.5% of the Kazakhs () were diagnosed CVD at the end of the follow-up. In the validation cohort, the average median age was 44.99 years old and 214 (42.5%) were male, of which 13.3% of the Kazakhs () were diagnosed CVD at the end of the follow-up. The baseline characteristics between the training cohort and the internal validation were not significantly different (Table 1).

VariablesTraining cohort (791)Validation cohort (264) value

Sex, male (%)338 (42.7)109 (41.3)0.681
Age (years)0.647
MetS (%)149 (18.8)56 (21.2)0.398
FFAs (mmol/L)0.483
INS (ng/mL)0.932
hs-CRP (pg/mL)0.747
IL-6 (ng/mL)34.52 (17.96-70.30)33.53 (18.69-76.01)0.655#
APN (ng/mL)0.400
CVD (%)94 (11.9)25 (9.5)0.283
Smoking (%)274 (34.6)86 (32.6)0.540
Alcohol drinking (%)96 (12.1)24 (9.1)0.177
Hypertension (%)275 (34.8)97 (36.7)0.561
Family history of hypertension (%)265 (33.5)103 (39.02)0.104
Diabetes (%)29 (3.7)16 (6.1)0.096
Dyslipidemia (%)309 (39.1)101 (38.3)0.816

#Mann-Whitney test.
3.2. Hazard Analysis in the Training Cohort

Univariate analysis showed that age, MetS, INS, Lg(hs-CRP), Lg(IL-6), FFAs, Lg(APN), SBP, DBP, body mass index (BMI), smoking, diabetes, family history of hypertension, and dyslipidemia were differed significantly between CVD and non-CVD cases. On Cox regression analysis, Lg(IL-6) (relative risk (HR) 1.252; 95% confidence interval (CI) 1.059–1.481), Lg(APN) (HR 0.075; 95% CI 0.588–0.845), DBP (HR 1.011; 95% CI 1.002–1.019), and dyslipidemia (HR 1.485; 95% CI 1.090–2.024) were independent risk factors for CVD patients in the Kazakh population. (Table 2).

Univariate analysisMultivariate analysis
valueβ valueHR95% CI

Sex, male n (%)53 (39.0)395 (45.5)0.157
Age (years)<0.001
MetS (%)46 (33.8)208 (23.9)0.014
INS (ng/mL)#14.22 (7.66-25.38)9.58 (5.42-20.67)0.001
Lg(hs-CRP) (pg/mL)<0.001
Lg(IL-6) (pg/mL)0.0210.2250.0091.2521.059-1.481
NEFA (mmol/L)#0.59 (0.40-1.10)0.48 (0.33-0.76)<0.001
Lg(ADP) (ng/mL)<0.001-0.350<0.0010.0750.588-0.845
SBP (mmHg)<0.001
DBP (mmHg)<0.0010.0110.0111.0111.002-1.019
Current smoker (%)61 (44.9)224 (28.1)<0.001
Alcohol drinking (%)20 (14.7)88 (10.1)0.109
Diabetes (%)8 (5.9)22 (2.5)0.033
Family history of hypertension (%)54 (39.7)237 (27.3)0.003
Dyslipidemia (%)46 (33.8)211 (24.3)0.0180.3590.0121.4851.090-2.024

Note: #Mann-Whitney test. MetS: metabolic syndrome; INS: insulin; hs-CRP: high-sensitivity C-reactive protein; IL-6: interleukin 6; NEFA: nonesterified fatty acids; ADP: adiponectin; SBP: systolic blood pressure; DBP: diastolic blood pressure; BMI: body mass index.
3.3. Usage of Nomogram

By taking a Kazakhs who is 50 years old as an example, drawing an upward vertical line from the age variable axis to the Point bar gets a point of 45. If the IL-6 of this Kazakh is 100 ng/mL, the point corresponding to the IL-6 variable is 7.5. If the APN of this Kazakh is 3.16 ng/mL, the point corresponding to the APN variable is 25. If the DBP of a Kazakh is 90 mmHg, the corresponding point is 27.5. And if he/she has dyslipidemia, the corresponding point is 10. The total points equal to 115 (). So, the risk of CVD is 30% when we draw a straight line from the total point axis to the risk of CVD axis (Figure 1).

3.4. Nomogram for CVD Prediction in Training Cohort

The prognosis for the independent risk factors of age, IL-6, ANP, DBP and dyslipidemia were incorporated into the nomogram. The AUC of the nomogram for CVD prediction was 0.836 (0.802-0.869), while the AUC was 0.576 (0.527-0.625) for Lg(IL-6) and 0.628 (0.582-0.675) for Lg(APN), respectively (Figure 2(a)). The difference was statistically significant between the nomogram and Lg(IL-6) () and between the nomogram and Lg(APN) (). In the training cohort, the Youden's index of nomogram was 0.514. ( and ) and an optimal cutoff of -2.293 (Table 3).

VariablesCutoffSen (%)Spe (%)Youden’s indexAUC (95% CI) value

Model 1Lg(IL-6)1.70347.7967.090.1490.576 (0.527-0.625)
Lg(APN)1.56176.4746.490.2300.628 (0.582-0.675)
Nomogram-2.29386.0365.360.5140.836 (0.802-0.869)

Model 2Lg(IL-6)1.49576.1251.830.2800.650 (0.582-0.719)
Lg(APN)1.47073.1353.900.2700.663 (0.593-0.733)
Nomogram-2.30788.0668.580.5670.812 (0.753-0.871)

Model 1, training cohort. Model 2, validation cohort. Sen: sensitivity; Spe: specificity.
3.5. Nomogram for CVD Prediction in Validation Cohort

Using CVD as the end point, the AUC was 0.812 (0.753-0.871) for the nomogram, 0.650 (0.582-0.719) for the Lg(IL-6), and 0.663 (0.593-0.733) for Lg(APN), respectively (Figure 2(b)). The difference was statistically significant between the nomogram and Lg(IL-6) () and between the nomogram and Lg(APN) (). In validation cohort, the nomogram had a Youden index value of 0.567 ( and ) and an optimal cutoff of -2.307 (Table 3).

4. Discussion

CVD is a life-threatening noncommunicable disease with high morbidity. In our study, the incidence of CVD was 13.46%; this was higher than in other reports [18, 19]. The prevalence of hypertension in the Xinjiang Kazakh population is high, and the potential population with CVD is large. Therefore, strengthening the primary prevention of CVD in this ethnic groups and reducing the risk and disease burden are necessary.

The prevalence of risk factors, including age, MetS, hypertension, obesity, smoking, diabetes, family history of hypertension, and dyslipidemia, was greater in Kazakh patients with CVD than in those without CVD. Many studies have reported that the prevalence of CVD is associated with age, hypertension, diabetes, smoking, and obesity [2024]. Insulin resistance, lipokine levels, and inflammation can also lead to adverse cardiovascular events [25]. Abnormal secretion of INS can lead to resistance, which plays a key role in atherosclerotic plaque formation [26]. Eddy et al. [27] suggested that the prevention of INS resistance in nondiabetic adults could prevent approximately 42% of myocardial infarctions and reduce the risk of CVD. Our study found that the levels of INS in the CVD group were significantly higher than those in the non-CVD group; moreover, INS resistance in the CVD group was more severe and the risk of CVD in Kazakhs was high. The decrease in INS sensitivity was related to the increase in serum FFA levels and the decrease in APN levels. This study also found that the FFA levels in the CVD group were higher than those in the non-CVD group, whereas the APN levels were lower than those in the non-CVD group. Elevated levels of FFAs can inhibit endogenous NO activity, affect vascular endothelial function, and aggravate the degree of atherosclerosis. However, APN is a hormone secreted by adipocytes, which can increase fatty acid oxidation, reduce FFA content, and improve lipid metabolism, thereby playing an antiatherosclerotic role. Therefore, the treatment of Kazakhs with elevated plasma FFA and decreased APN levels may be helpful for the prevention and treatment of CVD. hs-CRP and IL-6, as mediators and markers of atherosclerotic thrombosis, play an important role in the development of CVD [28]. The levels of hs-CRP and IL-6 in the CVD group were higher than those in the non-CVD group, consistent with the findings in previous studies [29, 30]. This suggested that the levels of hs-CRP and IL-6 were elevated, the population may be present in the pre-onset phase of CVD. Our study also found that the prevalence of MetS, diabetes, and dyslipidemia was greater in the population with CVD than in those without CVD. Multiple chronic diseases were clustered in some individuals, possibly because Kazakhs live in remote rural areas in Western China, lack health knowledge, have a unique high-fat and high-carbohydrate diet, and have chronic exposure to CVD risk factors. Thus, health education is needed for Kazakhs, in addition to the construction of a CVD predictive model, identification of high-risk groups, control of risk factors, and reduction in the incidence of chronic diseases, such as CVD.

Our CVD nomogram has 5 components: age, IL-6 and APN levels, DBP, and dyslipidemia, with a predictive ability higher than that of the Framingham study (AUC approximately 0.80) [31] and the simple model for a 10-year risk assessment program for ischemic cardiovascular disease in Chinese () [32]. All previous models included common CVD risk factors but lacked information on cytokines, such as IL-6 and APN. Changes in IL-6 and APN levels can reflect both the severity of atherosclerosis and thrombosis and the dynamic process of CVD. This study found that increased plasma IL-6 levels and decreased APN levels were risk factors for CVD in Kazakhs. The respective AUC values predictive of CVD were 0.576 and 0.628 and were significantly lower than those in the CVD nomogram. The plasma levels of IL-6 and APN can be used to predict CVD. The plasma levels of APN as a protective factor against atherosclerosis can also be used to predict the development of CVD [33]. However, IL-6 affected atherosclerosis through synergistic action with other inflammatory factors, subsequently leading to CVD [34]. Dyslipidemia is an independent risk factor for CVD, and its prevalence in Kazakhs is significantly higher than in the rest of China [35]. This study also found that the risk of CVD in Kazakh patients with dyslipidemia was 1.485 times higher than those without dyslipidemia, suggesting that the risk of CVD was increased by the presence of dyslipidemia. Although the indicators of dyslipidemia were included in most CVD predictive models, the weighting was different among models, suggesting the need to construct a targeted CVD risk model to maximize the usefulness of CVD risk factors.

Validation sampling is important for judging the applicability of a CVD model. By using a validation sample to evaluate predictive ability, we can accurately assess predictive efficacy and optimize predictive ability. Through the use of a validation sample for the CVD nomogram, the AUC was found to be 0.812 (95% CI: 0.753–0.871). This shows that the CVD nomogram can be applied locally to Kazakhs. Many studies have used models constructed by others to predict disease prevalence; these have “local advantages” and poor extrapolation ability [36]. This study constructed a CVD nomogram according to the characteristics of the Kazakh population. The model predicted the risk of CVD according to common and intermediate risk factors, including cytokine levels. This is a convenient and direct method for the determination of the risk of CVD.

This study has three advantages. First, based on the characteristics of local Kazakh disease prevalence, cytokines and common risk factors were used as predictors to construct a risk model for CVD in the Kazakh population. Second, we compared the aggregation characteristics of glucose and lipid (FFAs, INS, and APN) metabolism and inflammatory markers (IL-6 and hs-CRP) in patients with and without CVD in the Kazakh population. We discussed the risk factors for CVD and used these to construct a targeted CVD risk model. Finally, this study also verified the applicability of the model to a population group. Therefore, the CVD risk nomogram constructed in this study can be used for early screening in primary medical institutions to estimate the risk of CVD in local Kazakh populations and reduce its prevalence in rural areas of Xinjiang by controlling risk factors.

This study has some limitations. First, the included indicators do not fully cover all risk factors for CVD, thereby resulting in a limited predictive power of the model. Second, this study and CVD model were based on the characteristics of the Kazakh population. Whether the model can be applied to other ethnic groups requires further investigation. The small sample size of this study is mainly due to the nomadic lifestyle of Kazakhs, which prevented the follow-up of all subjects. Therefore, further research can supplement follow-up information, increase the sample size, and select more accurate indicators to reflect the risk of CVD, thereby improving the predictive ability of the model.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Shuxia Guo conceived and designed the study, oversaw the data analysis, and edited the manuscript. Lei Mao played a role in data analyses and wrote the manuscript. Lei Mao, Xianghui Zhang, and Wenwen Yang played a large role in data collection and data analysis. Yunhua Hu, Xinping Wang, Yanpeng Song, Jia He, Jiaolong Ma, Yizhong Yan, Lati Mu, Jingyu Zhang, Kui Wang, Heng Guo, and Rulin Ma helped collect the data. Lei Mao and Xianghui Zhang contributed equally to this work.


I want to thank the two most important women in my graduate career. Professor Shuxia Guo, thank you for your concern and trust. Miss Lijuan Ma, thank you for your support and understanding. You are the love of my life. We would also like to thank the clinical laboratory of the First Affiliated Hospital of Shihezi University School of Medicine for their test work. This research was supported by the National Natural Science Foundation of China (no. 81560551).


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