The MTHFR C677T Polymorphism and Risk of Acute Lymphoblastic Leukemia: an Updated Meta-analysis Based on 37 Case-control Studies

التفاصيل البيبلوغرافية
العنوان: The MTHFR C677T Polymorphism and Risk of Acute Lymphoblastic Leukemia: an Updated Meta-analysis Based on 37 Case-control Studies
المؤلفون: Shu-Ting Jia, Jihong Zhang, Ying Luo, Qiang Zhang, Wen-Ru Tang, Jing Hou, Bo-Yuan Wang, Yuan Jiang
المصدر: Asian Pacific Journal of Cancer Prevention. 14:6357-6362
بيانات النشر: Asian Pacific Organization for Cancer Prevention, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Risk, Cancer Research, medicine.medical_specialty, Genotype, Epidemiology, Bioinformatics, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Methylenetetrahydrofolate Reductase (NADPH2), Polymorphism, Genetic, biology, business.industry, Public Health, Environmental and Occupational Health, Case-control study, Publication bias, Odds ratio, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Confidence interval, Genotype frequency, Oncology, Case-Control Studies, Meta-analysis, Methylenetetrahydrofolate reductase, biology.protein, business
الوصف: Background: The C677T polymorphism of the methylenetetrahydrofolate reductase (MTHFR) has been associated with acute lymphoblastic leukemia (ALL). However, results were conflicting. The aim of this study was to quantitatively summarize the evidence for the MTHFRC677T polymorphism and ALL risk. Methods: Electronic searches of PubMed and the Chinese Biomedicine database were conducted to select case-control studies containing available genotype frequencies of C677T and the odds ratio (OR) with 95% confidence interval (CI) was used to assess the strength of any association. Results: Case-control studies including 6,371 cases and 10,850 controls were identified. The meta-analysis stratified by ethnicity showed that individuals with the homozygous TT genotype had decreased risk of ALL (OR= 0.776, 95% CI: 0.687~0.877, p< 0.001) in Caucasians (OR= 0.715, 95% CI: 0.655~0.781, p= 0.000). However, results among Asians (OR=0.711, 95% CI: 0.591~1.005, p= 0.055) and others (OR=0.913, 95% CI: 0.656~1.271, p= 0. 590) did not suggest an association. A symmetric funnel plot, the Egger’s test (P=0.093), and the Begg- test (P=0.072) were all suggestive of the lack of publication bias. Conclusion: This meta-analysis supports the idea that the MTHFR C677T genotype is associated with risk of ALL in Caucasians. To draw comprehensive and true conclusions, further prospective studies with larger numbers of participants worldwide are needed to examine associations between the MTHFRC677T polymorphism and ALL.
تدمد: 1513-7368
DOI: 10.7314/apjcp.2013.14.11.6357
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d72fba9396b8d44e54fc9ffba1edc9c
https://doi.org/10.7314/apjcp.2013.14.11.6357
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....5d72fba9396b8d44e54fc9ffba1edc9c
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15137368
DOI:10.7314/apjcp.2013.14.11.6357