Raoufi Atefeh, Rahimi Kelarijani Behdad, Ahadi Hamid Reza, Hassani Derakhshandeh Bahareh, Nooroollahzadeh Zahra, Hajifathali Abbas
Hematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Biology, Central Tehran Branch, Islamic Azad University, Tehran, Iran.
Iran J Public Health. 2021 Jan;50(1):83-92. doi: 10.18502/ijph.v50i1.5074.
The relation between methylenetetrahydrofolate reductase)MTHFR(polymorphisms and the risk of developing Chronic lymphocytic leukemia (CLL) is not still clear, while there are reports about the association of C677T and A1298C polymorphisms with developing CLL, there are other reports that rolled out the association of MTHFR polymorphisms with developing CLL. Therefore herein we carried out this meta-analysis to clear the association of polymorphisms with the risk of CLL.
A comprehensive search was performed through PubMed, Scopus and Embase from inception to Aug 2020. Odds ratios (OR) with their corresponding 95% confidence intervals (CI) for five possible genetic models were calculated. Heterogeneity was evaluated using the Cochran Q test and the I2 statistic.
Totals of 1290 cases and 1887 controls for the C677T polymorphism and 1117 cases and 1256 controls for the A1298C polymorphism were included in our analysis. Analyzing the C677T and A1298C polymorphisms genotypes showed an association between polymorphism at A1298C under Allelic model and the risk of CLL (OR = 1.12, 95% CI = 1.01-1.25), however there was no association between polymorphism at C677T and risk of CLL.
The risk of developing CLL might be associated with polymorphism at A1298C under allelic model and not associated with polymorphisms at C677T, However, further studies considering other factors such as age, gender, ethnicity, gene-gene interaction and environmental condition are needed to clear the true association of polymorphisms with CLL.
亚甲基四氢叶酸还原酶(MTHFR)基因多态性与慢性淋巴细胞白血病(CLL)发病风险之间的关系尚不清楚。虽然有报道称C677T和A1298C多态性与CLL发病有关,但也有其他报道排除了MTHFR多态性与CLL发病的关联。因此,我们进行了这项荟萃分析,以明确多态性与CLL风险的关联。
从创刊至2020年8月,通过PubMed、Scopus和Embase进行了全面检索。计算了五种可能遗传模型的比值比(OR)及其相应的95%置信区间(CI)。使用Cochran Q检验和I2统计量评估异质性。
我们的分析纳入了1290例C677T多态性病例和1887例对照,以及1117例A1298C多态性病例和1256例对照。对C677T和A1298C多态性基因型的分析显示,在等位基因模型下,A1298C多态性与CLL风险之间存在关联(OR = 1.12,95% CI = 1.01 - 1.25),然而C677T多态性与CLL风险之间没有关联。
在等位基因模型下,CLL发病风险可能与A1298C多态性有关,而与C677T多态性无关。然而,需要进一步研究考虑年龄、性别、种族、基因-基因相互作用和环境条件等其他因素,以明确多态性与CLL的真正关联。