Genetic polymorphisms of ALDH2 and ADH2 are not associated with risk of hepatocellular carcinoma among East Asians

The aldehyde dehydrogenase 2 ( ALDH2 ) and alcohol dehydrogenase 2 ( ADH2 ) genes have been implicated in the development of hepatocellular carcinoma (HCC). However, the results have been inconsistent. In this study, we performed a meta-analysis to clarify the associations between polymorphisms of A...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Tumor biology 2012-06, Vol.33 (3), p.841-846
Hauptverfasser: Zhou, Daming, Xiao, Li, Zhang, Yun, Xian, Jianchun, Jiang, Jijun, Zong, Wenhong, Huang, Zuxuan, Yang, Yongfeng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The aldehyde dehydrogenase 2 ( ALDH2 ) and alcohol dehydrogenase 2 ( ADH2 ) genes have been implicated in the development of hepatocellular carcinoma (HCC). However, the results have been inconsistent. In this study, we performed a meta-analysis to clarify the associations between polymorphisms of ALDH2 and ADH2 genes and HCC. Published literatures from PubMed and Embase were retrieved. Pooled odds ratio (OR) with 95% confidence interval (CI) was calculated using fixed- or random-effects model. Ten studies including 1,231 HCC cases and 1,849 controls were included in the meta-analysis of the association between ALDH2 polymorphism and HCC risk. The results indicated that ALDH2 polymorphism was not significantly associated with risk of HCC (homogeneous co-dominant model: OR = 0.99, 95% CI 0.72–1.34; heterogeneous co-dominant model: OR = 0.90, 95% CI 0.75–1.08; dominant model: OR = 0.91, 95% CI 0.70–1.18; recessive model: OR = 1.11, 95% CI 0.66–1.87). In addition, four studies including 518 cases and 607 controls were included in the meta-analysis of the association between ADH2 polymorphism and HCC risk. There was no association between ADH2 polymorphism and HCC risk (homogeneous co-dominant model: OR = 0.93, 95% CI 0.58–1.51; heterogeneous co-dominant model: OR = 1.39, 95% CI 0.87–2.23; dominant model: OR = 1.19, 95% CI 0.76–1.88; recessive model: OR = 0.91, 95% CI 0.54–1.54). Further analysis suggested that the ALDH2 polymorphism–alcohol interaction was marginally associated with HCC risk under the dominant model (OR = 2.05, 95% CI 1.01–4.17). However, the result was not robust by sensitivity analysis. The results from the present meta-analysis indicated that there was no significant association between ALDH2 polymorphism, ADH2 polymorphism, or ALDH2 polymorphism–alcohol intake interaction and HCC risk in the East Asians.
ISSN:1010-4283
1423-0380
DOI:10.1007/s13277-011-0309-8