Serum total bilirubin levels are negatively correlated with metabolic syndrome in aged Chinese women: a community-based study.

We evaluated serum total bilirubin levels as a predictor for metabolic syndrome (MetS) and investigated the relationship between serum total bilirubin levels and MetS prevalence. This cross-sectional study included 1728 participants over 65 years of age from Eastern China. Anthropometric data, lifestyle information, and previous medical history were collected. We then measured serum levels of fasting blood-glucose, total cholesterol, triglycerides, and total bilirubin, as well as alanine aminotransferase activity. The prevalence of MetS and each of its individual component were calculated per quartile of total bilirubin level. Logistic regression was used to assess the correlation between serum total bilirubin levels and MetS. Total bilirubin level in the women who did not have MetS was significantly higher than in those who had MetS (P<0.001). Serum total bilirubin quartiles were linearly and negatively correlated with MetS prevalence and hypertriglyceridemia (HTG) in females (P<0.005). Logistic regression showed that serum total bilirubin was an independent predictor of MetS for females (OR: 0.910, 95%CI: 0.863-0.960; P=0.001). The present study suggests that physiological levels of serum total bilirubin might be an independent risk factor for aged Chinese women, and the prevalence of MetS and HTG are negatively correlated to serum total bilirubin levels.

Introduction

Metabolic syndrome (MetS) is a group of common, complex disorders including insulin resistance, hypertension, dyslipidemia, and obesity (especially abdominal obesity) (1). It is also strongly associated with cardiovascular disease. The overall prevalence of MetS in adult populations is about 20–30%, depending on age, ethnicity, gender, and diagnostic criteria (2,3). The incidence of MetS has been shown to increase with age (2), and aged populations are therefore at high risk for MetS.

The exact pathophysiological characteristics of MetS are still unclear. However, studies show that systemic inflammation, insulin resistance, altered adipokine levels and oxidative stress play important roles in MetS development (4,5). Meanwhile, bilirubin has been characterized as a potent antioxidant (6 –8) and has been demonstrated to be negatively associated with oxidative stress (9,10). Several studies have also shown that bilirubin levels are negatively related to hypertension, diabetes (11,12), MetS, and insulin resistance (13). A retrospective study in 6205 male Koreans showed that bilirubin levels are negatively correlated with the incidence of MetS (14), and could be used as a predictor for MetS. Other studies have also shown that the serum bilirubin level can be used as an early biomarker for the progression to MetS in asymptomatic patients (15). Together, these findings suggest that bilirubin plays a role in the development of MetS.

All studies to date investigating the association between bilirubin and MetS focus on young people (16), a wide range of ages, or postmenopausal women. Importantly, the association has not been examined in aged people. In the present cross-sectional study, people of 65 years of age or older from 11 communities in Eastern China were included. We evaluated serum total bilirubin levels as a predictor for MetS, and further analyzed the potential relationship between serum total bilirubin levels and MetS prevalence.

Subjects and Methods

Subjects

Participants in this cross-sectional study were males or females ≥65 years of age that lived in any of the 11 communities in Pudong New Area, Shanghai, for at least 5 years. Enrollment took place between January–March 2012. Exclusion criteria were clinical or laboratory evidence of severe systemic diseases (such as cancer, renal failure, or heart failure), goiter, liver dysfunction (activities of alanine aminotransferase higher than 3-fold the upper limit of the normal range (120 U/L); or total bilirubin level higher than 17.1 μmol/L), or HIV-AIDS. In addition, athletes (including professional and amateur athletes) and participants who regularly exercised were also excluded.

General information was obtained, including date of birth, physical activity, and history of smoking and drinking. Previous medical history was obtained with a standardized questionnaire. Participants who smoked every day or every few days, and had smoked more than 100 cigarettes during their lifetime were considered smokers. Daily alcohol consumption was converted into grams of alcohol consumed per day. Male participants consuming more than 20–30 g of alcohol per day or female participants consuming more than 10–20 g of alcohol per day were considered drinkers. Participants with a known history of using oral antidiabetic agents or insulin were considered diabetic. Participants with a history of acute myocardial infarction, or coronary angiogram showing stenosis of the coronary artery ≥50% were considered to have a history of coronary heart disease. Participants with systolic blood pressure ≥140 mmHg, diastolic blood pressure ≥90 mmHg, or with a history of using oral anti-hypertensive drugs were considered to have a history of hypertension.

This study was approved by the Institutional Review Board of the Third People's Hospital, Shanghai Jiaotong University School of Medicine, and performed according to the Helsinki Declaration. All participants signed informed consents.

Anthropometric data

Participant anthropometric data were collected by trained medical staff following standard procedures. Blood pressure was measured twice after 10 min of rest, and the mean was calculated for analyses. Body mass index (BMI) was calculated as weight/height2 (kg/m2).

Biochemical data

Participants were asked to fast for at least 8 h. Blood was collected and placed in room temperature for 1-3 h and was then centrifuged at 1704 g for 15 min to separate the serum. Levels of fasting blood-glucose (FBG), total cholesterol (TC), triglycerides (TG), and total bilirubin (TBIL), as well as alanine aminotransferase (ALT) activity were measured in an automatic biochemical analyzer (Hitachi 7600-020, Japan) using enzyme colorimetric method with reagent from Roche company (Switzerland).

Definition of MetS

MetS was diagnosed according to the Chinese Diabetes Society criteria (2004) (17). Participants with three or more of the following items were diagnosed with MetS: 1) hypertension: blood pressure ≥140/90 mmHg, or use of anti-hypertensive medication; 2) hypertriglycerides: fasting plasma triglycerides ≥1.7 mmol/L, or low high-density lipoprotein level (HDL; <1 mmol/L for males and <1.3 mmol/L for females); 3) hyperglycemia: FBG ≥6.1 mmol/L, or use of anti-diabetic agents; and 4) overweight or obesity: BMI ≥25 kg/m2.

Statistical analyses

SPSS v.13.0 software (USA) was used for statistical analyses. Quantitative data with normal distributions are reported as means and standard deviations (SD). Quantitative data with skewed distributions are reported as quartiles, and qualitative data are reported as rates. Analysis of variance was used for comparing quantitative data between three or more groups, while non-parametric tests were used for comparisons of qualitative data. Participants were divided into quartiles according to total bilirubin levels as follows: Q1, <10.1 μmol/L for males and <8.8 μmol/L for females; Q2, 10.1–12.15 μmol/L for males and 8.8–10.7 μmol/L for females; Q3, 12.15–14.4 μmol/L for males and 10.7–12.7 μmol/L for females, and Q4, ≥14.4 μmol/L for males and ≥12.7 μmol/L for females. The prevalence of MetS and of each component was then estimated. Logistic regression was used to assess the independent predictors of MetS in males and females. P<0.05 was considered to be statistically significant.

Results

Baseline characteristics

Baseline characteristics of participants are summarized in Table 1. A total of 1728 eligible participants including 744 males (43.1%) and 984 females (56.9%) were enrolled in the present study. The mean age of the participants was 72.68±6.33 and 73.49±6.87 years for males and females, respectively. This difference was statistically significant (P=0.011). The prevalence of MetS was 25.3 and 30.1% in the male and female subjects, respectively, and the difference was statistically significant (P<0.001). Similarly, the proportions of diabetes, coronary heart disease, and hypertension in the male and female subjects were significantly different. BMI and FBG were not significantly different between the two genders. However, weight, height, blood pressure, TG, TC, ALT and TBIL were significantly different between the two genders (P<0.05).

Characteristics of female participants

The prevalence of MetS in female subjects was 30.1%. The clinical and biochemical characteristics of the females are shown in Table 2. The levels of some components of the MetS (including the FBG, blood pressure, TG, and BMI) were significantly higher, while the total bilirubin level was significantly lower in females with MetS than in those without MetS (P=0.002).

Associations between total bilirubin level and the risk of MetS

The prevalence of MetS and its components in the sample are summarized in Table 3. The number of males in each quartile of total bilirubin level was as follows: Q1: 187, Q2: 185, Q3: 189, and Q4: 183, and the mean ages were 72.57±6.14, 72.72±6.39, 72.68±6.47, and 72.75±6.37 years, respectively. For females, the number of participants in each quartile was as follows: Q1: 258, Q2: 240, Q3: 249, and Q4: 237, and the mean ages were 74.46±7.01, 72.65±6.38, 73.28±7.21, and 74.49±6.72 years, respectively. The prevalence of MetS and hypertriglyceridemia (HTG) decreased with increased levels of total bilirubin, and a linear correlation was found between the quartiles of total bilirubin levels and the prevalence of MetS and HTG.

Independent predictors of MetS

Logistic regression was performed with MetS prevalence as the dependent variable. Independent variables were age, gender, physical activity, smoking, drinking, total bilirubin, total cholesterol and ALT. We found that total bilirubin (OR: 0.952, 95%CI: 0.915–0.990; P=0.014) and ALT (OR: 1.048, 95%CI: 1.038–1.058; P<0.001) were independent predictors of MetS. Results of the stratified analyses by gender are shown in Table 4. These findings suggest that every 1 μmol/L increase in total bilirubin level reduces the risk of female MetS by 9.0% (OR: 0.910, 95%CI: 0.863–0.960; P=0.001).

Discussion

In the present cross-sectional study in aged patients from Eastern China, we found that serum total bilirubin may be an independent risk factor for MetS in females. We also found that the prevalence of MetS and HTG were negatively related to the serum levels of total bilirubin.

Association between serum total bilirubin levels and MetS risk is still under debate. In another study performed in Shanghai that included participants over 40 years of age, Wu et al. (18) showed that serum total bilirubin levels were negatively associated with MetS risk in both females and males. In contrast, a Japanese study found that serum total bilirubin levels were negatively associated with the risk of MetS in males but not in females (19). However, the participants included in the Japanese study were over 20 years of age, which may explain this discrepancy. Another study in the USA found that serum total bilirubin levels were negatively associated with MetS, as well as with central obesity and low HDL levels, in participants between the ages of 12 and 17 years. However, no comparison between males and females was performed (16). Bilirubin levels may be affected by several factors including diet and smoking (20). However, this hypothesis could not be verified since no detailed information was available in the present study. Future studies should be performed to investigate whether the correlation between the total bilirubin level and MetS is associated with the status of smoking, drinking, and diet.

The molecular mechanisms involved in the protective effects of bilirubin on MetS are still unclear. Recent studies show that oxidative stress plays an important role in insulin resistance and the development of MetS (5). In vitro and in vivo evidence demonstrate that bilirubin is an endogenous antioxidant, which may inhibit the oxidation of lipid and lipoprotein under physiological conditions (6,21). It is estimated that bilirubin accounts for approximately 10% of all antioxidant effects in healthy adults, and the level of bilirubin is negatively associated with serum levels of oxidative biomarkers (22,23). Increased levels of bilirubin may therefore result in higher antioxidant effects, which in turn reduce the risk of developing MetS.

We also show that total serum bilirubin levels are negatively correlated with HTG and high FGB in aged females. These findings agree with other studies showing that total bilirubin serum levels are closely linked to triglyceride levels, hypertension, diabetes, and insulin resistance, which are risk factors for MetS (14,24). Another study shows that physiological levels of serum total bilirubin were negatively associated with MetS in a Korean sample without distinct metabolic or cardiovascular disorders. The study further revealed a negative relationship between total bilirubin and abdominal obesity as well as with HTG (25). Other reports have shown that bilirubin may function as an endogenous lipid-reducing agent, thereby affecting lipid metabolism (26). This pathological mechanism underlies Gilbert syndrome, in which an increase in indirect bilirubin levels enhance cholesterol excretion and decrease its production, thereby disrupting lipid balance (26). However, in the present study, only total bilirubin was measured. Thus, association between total serum bilirubin levels and MetS risk could not be further assessed to differentiate the effects of indirect and direct bilirubin.

Our findings should be considered in light of a few limitations. First, as a cross-sectional study, we could not conclusively show a causal relationship between the serum total bilirubin levels and MetS in females. Second, the effects from other underlying diseases, as well as drugs for diabetes, coronary heart disease, hypertension, and hyperlipidemia could not be clearly elucidated. Total bilirubin level and ALT activity were measured only once for each patient, yet they may have transient fluctuations; therefore, not all the underlying liver diseases could be clearly diagnosed by the data collected. Third, the data about smoking and drinking may not be very correct, as these data were self-reported. Fourth, we only measured total bilirubin level, while the direct and indirect bilirubin levels were not measured.

In summary, this large community-based study suggests that a physiological level of serum total bilirubin is an independent risk factor for aged Chinese women. Furthermore, we found that the prevalence of MetS and HTG was negatively related to physiological levels of serum total bilirubin.