Zhang Yan, Tong Sheng-Chun, Guan Li-Hua, Na Fei, Zhao Wei, Wei Li
Department of Gynecology, Fourth Affiliated Hospital, China Medical University, Shenyang, 110032, China.
Tumour Biol. 2013 Dec;34(6):3317-21. doi: 10.1007/s13277-013-0900-2. Epub 2013 Jun 20.
The role of vitamin D receptor (VDR) BsmI polymorphism in ovarian cancer development has been studied in various populations, but those results are discordant controversial and ambiguous. Thus, we performed a meta-analysis to assess the association between VDR BsmI polymorphism and susceptibility to ovarian cancer more precisely. Odds ratio (OR) and its 95% confidence interval (95% CI) were used for statistical analysis. Nine individual studies with a total 2,331 cases and 3,301 controls were included into this meta-analysis. There was no heterogeneity among those nine studies. Meta-analysis of total nine studies suggested that there was no association between VDR BsmI polymorphism and susceptibility to ovarian cancer (B vs. b, OR = 1.02, 95% CI = 0.94-1.10, P = 0.616, I(2) = 0%; BB vs. bb, OR = 1.02, 95 % CI = 0.87-1.20, P = 0.810, I(2) = 0 %; BB/Bb vs. bb, OR = 1.05, 95% CI = 0.94-1.18, P = 0.391, I(2) = 0 %; BB vs. bb/Bb, OR = 0.99, 95% CI = 0.85-1.14, P = 0.853, I(2) = 0 %). Meta-analysis of seven studies from Caucasians also showed that there was no association between VDR BsmI polymorphism and susceptibility to ovarian cancer. This meta-analysis suggests that there is no association between VDR BsmI polymorphism and susceptibility to ovarian cancer in Caucasians. Future studies from Asians or Africans are needed to further assess the above association.
维生素D受体(VDR)BsmI基因多态性在卵巢癌发生发展中的作用已在不同人群中进行了研究,但这些结果存在不一致、有争议且不明确的情况。因此,我们进行了一项荟萃分析,以更精确地评估VDR BsmI基因多态性与卵巢癌易感性之间的关联。采用比值比(OR)及其95%置信区间(95%CI)进行统计分析。本荟萃分析纳入了9项个体研究,共2331例病例和3301例对照。这9项研究之间不存在异质性。对全部9项研究的荟萃分析表明,VDR BsmI基因多态性与卵巢癌易感性之间无关联(B与b相比,OR = 1.02,95%CI = 0.94 - 1.10,P = 0.616,I² = 0%;BB与bb相比,OR = 1.02,95%CI = 0.87 - 1.20,P = 0.810,I² = 0%;BB/Bb与bb相比,OR = 1.05,95%CI = 0.94 - 1.18,P = 0.391,I² = 0%;BB与bb/Bb相比,OR = 0.99,95%CI = 0.85 - 1.14,P = 0.853,I² = 0%)。对7项来自白种人的研究进行的荟萃分析也表明,VDR BsmI基因多态性与卵巢癌易感性之间无关联。这项荟萃分析表明,在白种人中,VDR BsmI基因多态性与卵巢癌易感性之间无关联。需要来自亚洲或非洲人群的进一步研究来进一步评估上述关联。