Abstract

BackgroundApolipoprotein E (ApoE) participates in lipoprotein metabolism and immune regulation. This study assessed association between ApoE polymorphisms with hyperuricemia and uric acid metabolism in Uygur men, Xinjiang, China.MethodsA total of 474 hyperuricemia patients and 518 healthy male controls were recruited from the Health Screening Center, Uygur region of Xinjiang, China and subjected to ApoE genotyping using a multiplex amplification refractory mutation system PCR.ResultsApolipoprotein E3/3 genotype was the predominant type with a frequency of 67.7%, while E2/2 was lower than E4/4 in Uygur males. The frequencies of ApoE2, E3, and E4 alleles were 8.5%, 80.1% and 11.4%, respectively. Distribution of ApoE genotypes was significantly different in hyperuricemia patients from the healthy controls (p < 0.001). Particularly, the frequency of ApoE E3/3 was 71.7%, E2/3 9.3%, E3/4 9.3%, E4/4 3.2%, E2/4 2.3%, and E2/2 0.2% in patients vs. 68.1%, 4.6%, 2.9%, 12%, 0.6%, and 4.6% in controls, respectively. Moreover, frequency of ApoE E2 allele was greater in the healthy controls than in patients (p < 0.001) and the highest level of uric acid occurred in those with ApoE2/4 and E3/4 genotypes, whereas the lowest uric acid level occurred in those with ApoE E2/2 genotype. In addition, the subjects with the ApoE2 allele had a lower uric acid and LDL-C level than those with the ApoE3 allele and ApoE4 allele (p < 0.05). The risk of developing hyperuricemia in subjects without the ApoE2 allele was 1.7 fold higher than those subjects with the ApoE2 allele.ConclusionsThis study revealed frequencies and distributions of ApoE alleles and genotypes in Uygur males, which are different from Han Chinese. ApoE E4 was associated with a slightly higher risk of primary hyperuricemia, whereas ApoE E2 was associated with reduced risk of primary hyperuricemia and LDL-C level.

Highlights

  • Apolipoprotein E (ApoE) participates in lipoprotein metabolism and immune regulation

  • Previous studies showed that in the pathogenesis of hyperuricemia, ApoE polymorphisms in patients with gout were reported to be associated with reduced renal excretion of urates [17,18]

  • Comparison of ApoE allele frequencies and genotype distribution in hyperuricemia with male Uygur controls The distribution of ApoE genotypes was consistent with the Hardy-Weinberg equilibrium

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Summary

Introduction

Apolipoprotein E (ApoE) participates in lipoprotein metabolism and immune regulation. This study assessed association between ApoE polymorphisms with hyperuricemia and uric acid metabolism in Uygur men, Xinjiang, China. Hyperuricemia refers to an abnormally high serum level of uric acid and commonly occurs in patients with lipoprotein metabolism disorders, metabolic syndrome and cardiovascular diseases [1]. Altered expression or genetic polymorphisms was considered as a risk factor for metabolic syndrome [7] and more recent studies have shown that ApoE participates in immunoregulation by suppression of T lymphocyte proliferation and regulation of macrophage function [8]. Previous studies showed that in the pathogenesis of hyperuricemia, ApoE polymorphisms in patients with gout were reported to be associated with reduced renal excretion of urates [17,18]

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