AUTHOR=Wen Min , Zhou Bo , Lin Xin , Chen Yunhua , Song Jialei , Li Yanmei , Zacksenhaus Eldad , Ben-David Yaacov , Hao Xiaojiang 

TITLE=Associations Between XPD Lys751Gln Polymorphism and Leukemia: A Meta-Analysis

JOURNAL=Frontiers in Genetics

VOLUME=9

YEAR=2018

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2018.00218

DOI=10.3389/fgene.2018.00218

ISSN=1664-8021

ABSTRACT=<p><bold>Objectives:</bold> The aim of the present study was to define the potential relationship of xeroderma pigmentosum group D (XPD) Lys751Gln polymorphisms and the risk of leukemia.</p><p><bold>Methods:</bold> Comprehensive electronic search in Pubmed, Web of Science, EBSCO, the Cochrane Library and China National Knowledge Infrastructure (CNKI) to find original articles about the association between XPD Lys751Gln polymorphisms and leukemia risk published before March 2017. Literature quality assessment was performed using the Newcastle-Ottawa Scale. Heterogeneity across studies was assessed by <italic>I</italic><sup>2</sup> statistics. Random- or fixed-effects models was used to calculate pooled odds ratios (ORs) in the presence or absence of heterogeneity, respectively. Sensitivity analysis was used to assess the influence of individual studies on the pooled estimate. Publication bias was investigated using funnel plots and Egger’s regression test. All data analyses were performed using Stata 14.0 and Revman 5.3.</p><p><bold>Results:</bold> Fourteen studies with a total of 7525 participants (2,757 patients; 4,768 controls) were included in this meta-analysis. We found that XPD Lys751Gln polymorphism significantly increased the risk of developing leukemia in both a dominant [Odds Ratio (OR)] = 1.21, 95%CI [1.10–1.35], <italic>P</italic> &lt; 0.001) and heterozygote (OR = 1.22, 95%CI [1.09–1.36], <italic>P</italic> &lt; 0.001) models. An allele model showed borderline significant increase in leukemia risk (OR = 1.13, 95%CI [1.00–1.27], <italic>P</italic> = 0.05). Subgroup analysis revealed a consistent association for some genetic models in Caucasian populations, adult or chronic groups, and in almost all models of childhood or acute groups.</p><p><bold>Conclusion:</bold> Our results overall indicate that XPD Lys751Gln polymorphism increases the risk of leukemia, especially in childhood and acute cases.</p>