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The association between apolipoprotein e and gallstone disease: An updated meta-analysis

  • Lizhuo Li
  • , Xin Qiao
  • , Xia Wang
  • , Di Liu
  • , Qingmu Xue
  • , Lu Han
  • , Fei Dai
  • , Guomin Ma
  • , Zhipeng Yang
  • , Tao Zhang
  • , Shuo Yang
  • , Shikang Cai
  • , Mingyue Gao
  • , Jingyun Yang
  • Capital Medical University
  • Hainan Medical University
  • Shenyang Medical College
  • The Second Affiliated Hospital of Xi'an Jiaotong University
  • Liaoning Provincial People's Hospital
  • Ministry of the Public Security
  • Shanghai University
  • Rush University
  • Rush University Medical Center

科研成果: 期刊稿件文章同行评审

7 引用 (Scopus)

摘要

Background: Gallstone disease (GSD) is a common biliary tract disease worldwide. Previous studies have investigated the association of apolipoprotein E (APOE) E4 with GSD and reported inconsistent results. Methods: In this paper, we conducted meta-analyses to examine whether APOE E4 is associated with the risk of GSD. A systematic literature search was performed in PubMed, Cochrane Library, EMBASE, and Google Scholar using the following inclusion criteria: 1) Studies on human subjects; 2) subjects in the control group must undergo ultrasound GSD screening, and presence of GSD in the experiment group can be clearly determined, e.g., diagnosis of GSD through ultrasound screening or a previous history of cholecystectomy or cholelithiasis; 3) the studies reported APOE genotype data (APOE E4+ vs. E4-) for subjects with and without GSD. In all the meta-analyses, we used random-effects models to calculate the odds ratios (ORs) as a measure of association as well as the corresponding confidence intervals (CIs). Results: Our literature search found 13 publications with 14 studies, including a total of 1632 GSD patients and 5001 controls, that met the eligibility criteria and were included in the meta-analyses. We did not find a significant association between APOE E4 and risk of GSD (OR = 1.23, 95% CI: 0.89-1.68; p = 0.205). No significant associations were observed in subgroup analyses by gender and mean age. We obtained similar insignificant findings if an additive model was used, if subjects who had E2E4 genotype were excluded, or if low-quality studies were excluded. Conclusion: Our meta-analysis found insufficient evidence for the effect of APOE E4 on GSD risk. Future studies with large sample sizes that control for important confounding/risk factors are needed to validate our findings and to explore other genetic loci that might affect GSD risk.

源语言英语
文章编号109
期刊BMC Medical Genetics
20
1
DOI
出版状态已出版 - 14 6月 2019
已对外发布

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