Association Between Four ABCA1 gene Polymorphisms and Risk of Non-Alcoholic Fatty Liver Disease in a Chinese Han Population

IF 0.6 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY Hepatitis Monthly Pub Date : 2018-05-22 DOI:10.5812/HEPATMON.66149
Cong Wang, Shousheng Liu, Linlin Lu, Songling Liao, Hai-Yan Yue, Q. Dong, Y. Xin, S. Xuan
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引用次数: 5

Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) as a severe health problem is the leading cause of morbidity and mortality from the chronic liver disease worldwide. NAFLD is tightly associated with dyslipidemia although the etiology is still unclear. ATP binding cassette subfamily A member 1 (ABCA1) is involved in cholesterol efflux, fatty acid oxidation, and inflammation. Although some reports show that the ABCA1 polymorphisms affect the lipids metabolism and severity of clinical liver diseases, the effects of ABCA1 polymorphisms on the development of NAFLD are unknown. Objectives: The current study was performed to investigate the association between the ABCA1 polymorphisms and the development of NAFLD and the effect of the four ABCA1 SNPs on the serum lipid levels. Methods: The ABCA1 polymorphisms (rs1800977, rs2066714, rs2066715, and rs2230808) were determined in 265 NAFLD patients and 126 healthy controls using the sequencing and polymerase chain reaction analysis. Serum lipid profiles and liver enzymes were examined using standard clinical laboratory methods. Results: There was a significant difference (P < 0.05) in the genotype of the ABCA1 rs1800977 G/A polymorphisms between NAFLD patients and healthy controls. No significant differences were found in genotypes and allele frequencies of the ABCA1 rs2066714T/C, rs2066715T/C, and rs2230808C/T between NAFLD patients and healthy controls. The ABCA1 rs1800977 A was independently associated with NAFLD after adjusting for the effects of age, gender, and BMI. Compared to the noncarriers in NAFLD patients, the carriers of ABCA1 rs2066714 C showed a significantly higher level of LDL (P = 0.045) and the carriers of ABCA1 rs2230808 T showed a significantly lower level of HDL (P = 0.039). Conclusions: We first demonstrated the association between the ABCA1 polymorphisms and the risk of NAFLD in a Chinese Han population. The ABCA1 rs1800977 may be a protective factor against the development of NAFLD. The ABCA1 rs2066714 C allele could increase the serum LDL cholesterol level, and the ABCA1 rs2230808 T allele could decrease the serum HDL cholesterol level in NAFLD patients.
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四种ABCA1基因多态性与中国汉族非酒精性脂肪性肝病风险的关系
背景:非酒精性脂肪性肝病(NAFLD)作为一种严重的健康问题,是世界范围内慢性肝病发病率和死亡率的主要原因。NAFLD与血脂异常密切相关,但病因尚不清楚。ATP结合盒亚家族A成员1 (ABCA1)参与胆固醇外排、脂肪酸氧化和炎症。虽然有报道表明ABCA1多态性影响脂质代谢和临床肝脏疾病的严重程度,但ABCA1多态性对NAFLD发展的影响尚不清楚。目的:本研究旨在探讨ABCA1多态性与NAFLD发生的关系,以及四个ABCA1 snp对血脂水平的影响。方法:采用测序和聚合酶链反应方法,对265例NAFLD患者和126例健康对照进行ABCA1多态性(rs1800977、rs2066714、rs2066715和rs2230808)检测。采用标准的临床实验室方法检测血脂和肝酶。结果:NAFLD患者与健康对照组ABCA1 rs1800977 G/ a多态性基因型差异有统计学意义(P < 0.05)。ABCA1 rs2066714T/C、rs2066715T/C和rs2230808C/T的基因型和等位基因频率在NAFLD患者和健康对照组之间无显著差异。在调整了年龄、性别和BMI的影响后,ABCA1 rs1800977 A与NAFLD独立相关。与非NAFLD患者相比,ABCA1 rs2066714 C携带者LDL水平显著升高(P = 0.045), ABCA1 rs2230808 T携带者HDL水平显著降低(P = 0.039)。结论:我们首次证明了ABCA1多态性与中国汉族人群NAFLD风险之间的关联。ABCA1 rs1800977可能是NAFLD发生的保护因子。ABCA1 rs2066714 C等位基因可升高NAFLD患者血清LDL胆固醇水平,ABCA1 rs2230808 T等位基因可降低NAFLD患者血清HDL胆固醇水平。
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来源期刊
Hepatitis Monthly
Hepatitis Monthly 医学-胃肠肝病学
CiteScore
1.50
自引率
0.00%
发文量
31
审稿时长
3 months
期刊介绍: Hepatitis Monthly is a clinical journal which is informative to all practitioners like gastroenterologists, hepatologists and infectious disease specialists and internists. This authoritative clinical journal was founded by Professor Seyed-Moayed Alavian in 2002. The Journal context is devoted to the particular compilation of the latest worldwide and interdisciplinary approach and findings including original manuscripts, meta-analyses and reviews, health economic papers, debates and consensus statements of the clinical relevance of hepatological field especially liver diseases. In addition, consensus evidential reports not only highlight the new observations, original research, and results accompanied by innovative treatments and all the other relevant topics but also include highlighting disease mechanisms or important clinical observations and letters on articles published in the journal.
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