Association between glutathione S-transferase T1 null genotype and risk of myelodysplastic syndromes: a comprehensive meta-analysis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-05-22

AUTHORS

Minghao Fang, Wen Zeng, Lifang Huang, Shuang Qin, Jianfeng Zhou, Hanying Sun, Fankai Meng

ABSTRACT

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematologic neoplasms, and the pathophysiology of these disorders is still unclear. Previous studies investigating the association between glutathione S-transferase Tl (GSTT1) null genotype and risk of MDS reported controversial results. We performed a comprehensive meta-analysis to clarify the effect of GSTT1 null genotype on risk of MDS. The strength of the association was measured by odds ratio (OR) with 95 % confidence interval (CI). Fifteen studies were finally included, involving a total of 1,796 cases and 2,502 controls. Subgroup analysis was performed by race. Meta-analysis of all 15 studies showed that the GSTT1 null genotype was significantly associated with an increased risk of MDS (OR = 1.47, 95 % CI 1.16–1.88, POR = 0.002; I2 = 54.4 %). Besides, an obvious association was also observed after adjusting the heterogeneity (OR = 1.32, 95 % CI 1.13–1.54, POR = 0.001; I2 = 9.0 %). Subgroup analysis by race suggested that this association existed in both Caucasians (OR = 1.40, 95 % CI 1.04–1.89, POR = 0.027) and Asians (OR = 1.68, 95 % CI 1.00–2.81, POR = 0.049). This meta-analysis suggests the GSTT1 null genotype is significantly associated with an increased risk of MDS in both Caucasians and Asians. More... »

PAGES

2747-2752

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13277-013-0828-6

DOI

http://dx.doi.org/10.1007/s13277-013-0828-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1038557039

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23696026


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