98%
921
2 minutes
20
Background/aim: 5-methyltetrahydrofolate-homocysteine methyltransferase reductase (MTRR) is responsible for folate metabolism, and we aimed to investigate its genetic role in colorectal cancer (CRC) among Taiwanese.
Materials And Methods: A total of 362 cases and 362 controls were recruited and their MTRR rs1801394 (A66G) and rs1532268 (C524T) genotypes were examined. The behavioral factors and clinicalpathological factors were also analyzed.
Results: MTRR rs1801394 genotypes were associated with CRC risk (p for trend=0.0087). In detail, G/G genotype was associated with lower risk (p=0.0049, OR=0.39, 95%CI=0.20-0.76). As for allelic frequency analysis, G allele was also associated with decreased CRC risk (p=0.0026, OR=0.68, 95%CI=0.53-0.88). There was no significant association as for MTRR rs1532268. Among non-smokers and non-alcohol drinkers, those with G/G genotype were at 0.38- and 0.46-fold odds of having CRC. There were no significant protective effects among smokers or alcohol drinkers.
Conclusion: MTRR rs1801394 GG genotype can be a protective marker for CRC risk in Taiwan.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.21873/anticanres.15716 | DOI Listing |
Circ Genom Precis Med
August 2025
Department of Medical Genetics, Hallym University College of Medicine, Chuncheon, Republic of Korea.
Background: Congenital heart disease (CHD) is the most common heterogeneous birth defect, with prevalence varying across populations. A comprehensive meta-analysis could refine the genetic risk estimates and enhance our understanding of CHD susceptibility.
Methods: We conducted a meta-analysis of 175 case-control studies investigating 107 genetic variants across 72 gene regions.
Discov Oncol
August 2025
Center of Clinical Laboratory, First Affiliated Hospital of Soochow University, 188 Shizi Road, Suzhou, 215006, Jiangsu, People's Republic of China.
Purpose: Previous research on the correlation between methionine synthase (MTR) and methionine synthase reductase (MTRR) gene polymorphisms and the susceptibility to glioma has yielded varied results. This study aims to elucidate the potential impact of MTR and MTRR polymorphisms as contributing factors in the development of glioma.
Patients And Methods: A comprehensive review of the relevant literature was conducted across several major databases, encompassing records from their inception through April 2025.
Matern Fetal Med
April 2025
Human Cytogenetics and Genomics Laboratory, Faculty of Allied Health Sciences, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, Tamilnadu 603103, India.
Toxicol Rep
June 2025
Department of Human Genetics and Molecular Medicine, Central University of Punjab, Bathinda 151001, India.
Many studies have been performed to explore the role of xenobiotic metabolizing gene variants and male infertility risk. However, the results remain inconclusive and contradictory. Therefore, the objective of the present study was to investigate the association among 16 genes and its 24 variants ( rs1001179, rs7943316, rs4880 rs1050450 rs1048943, rs4646903 rs1695 rs1801133, rs1801131, rs2274976, rs2066472, rs2236225 rs1801394 rs3892097 rs854560, rs662 rs7493 rs1799930 rs6721961 rs2066853, rs1476080, rs6960165, null ) involved in xenobiotic metabolism and their correlation with male infertility.
View Article and Find Full Text PDFZh Nevrol Psikhiatr Im S S Korsakova
May 2025
Altai State Medical University, Barnaul, Russia.
Objective: To assess the role of genetic polymorphisms in folate metabolism enzyme genes in the manifestation of migraine in children.
Material And Methods: The study included 54 children aged 7 to 18 years with clinical manifestations of migraine. The control group consisted of 115 children without neurological disorders.