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载脂蛋白 B-100 基因多态性与胆石症和胆囊癌风险的关系:一项荟萃分析。

Roles of ApoB-100 gene polymorphisms and the risks of gallstones and gallbladder cancer: a meta-analysis.

机构信息

Institute of Hepatopancreatobiliary Surgery, Southwest Hospital, Third Military Medical University, Chongqing City, PR China.

出版信息

PLoS One. 2013 Apr 18;8(4):e61456. doi: 10.1371/journal.pone.0061456. Print 2013.

Abstract

BACKGROUND

Gallstones (GS) is the major manifestation of gallbladder disease, and is the most common risk factor for gallbladder cancer (GBC). Previous studies investigating the association between ApoB-100 gene polymorphisms and the risks of GS and GBC have yielded conflicting results. Therefore, we performed a meta-analysis to clarify the effects of ApoB-100 gene polymorphisms on the risks of GS and GBC.

METHODS

A computerized literature search was conducted to identify the relevant studies from PubMed and Embase. Fixed or random effects model was selected based on heterogeneity test. Publication bias was estimated using Begg's funnel plots and Egger's regression test.

RESULTS

A total of 10, 3, and 3 studies were included in the analyses of the association between ApoB-100 XbaI, EcoRI, or insertion/deletion (ID) polymorphisms and the GS risks, respectively, while 3 studies were included in the analysis for the association between XbaI polymorphism and GBC risk. The combined results showed a significant association in Chinese (X+ vs. X-, OR = 2.37, 95%CI 1.52-3.70; X+X+/X+X- vs. X+X+, OR = 2.47, 95%CI 1.55-3.92), but not in Indians or Caucasians. Null association was observed between EcoRI or ID polymorphisms and GS risks. With regard to the association between XbaI polymorphism and GBC risk, a significant association was detected when GBC patients were compared with healthy persons and when GBC patients were compared with GS patients. A significant association was still detected when GBC patients (with GS) were compared with the GS patients (X+X+ vs. X-X-, OR = 0.33, 95%CI 0.12-0.90).

CONCLUSION

The results of this meta-analysis suggest that the ApoB-100 X+ allele might be associated with increased risk of GS in Chinese but not in other populations, while the ApoB-100 X+X+ genotype might be associated with reduced risk of GBC. Further studies with larger sample sizes are needed to confirm these results.

摘要

背景

胆石症(GS)是胆囊疾病的主要表现,也是胆囊癌(GBC)的最常见危险因素。既往研究调查了载脂蛋白 B-100 基因多态性与 GS 和 GBC 风险之间的关系,结果存在矛盾。因此,我们进行了荟萃分析以阐明载脂蛋白 B-100 基因多态性对 GS 和 GBC 风险的影响。

方法

计算机检索 PubMed 和 Embase 中相关研究。根据异质性检验,选择固定或随机效应模型。使用 Begg 漏斗图和 Egger 回归检验评估发表偏倚。

结果

分别纳入 10 项、3 项和 3 项研究分析载脂蛋白 B-100 XbaI、EcoRI 或插入/缺失(ID)多态性与 GS 风险的关系,纳入 3 项研究分析 XbaI 多态性与 GBC 风险的关系。合并结果显示,在中国人群中 X+等位基因与 GS 风险相关(X+ vs. X-,OR=2.37,95%CI 1.52-3.70;X+X+/X+X- vs. X+X+,OR=2.47,95%CI 1.55-3.92),但在印度人群和高加索人群中未见相关性。EcoRI 或 ID 多态性与 GS 风险无关。XbaI 多态性与 GBC 风险的关系研究中,与健康人群相比,与 GS 患者相比,均有显著相关性。与 GS 患者(X+X+ vs. X-X-,OR=0.33,95%CI 0.12-0.90)相比,GS 合并 GBC 患者(X+X+ vs. X-X-,OR=0.33,95%CI 0.12-0.90)也有显著相关性。

结论

本荟萃分析结果提示载脂蛋白 B-100 X+等位基因可能与中国人 GS 风险增加相关,但与其他人群无关,而载脂蛋白 B-100 X+X+基因型可能与 GBC 风险降低相关。需要更大样本量的进一步研究来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c3d/3630192/a84bfdfba66e/pone.0061456.g001.jpg

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