| Literature DB >> 25883419 |
Jagdish Kaur Chahil1, Khamsigan Munretnam1, Nurulhafizah Samsudin1, Say Hean Lye1, Nikman Adli Nor Hashim1, Nurul Hanis Ramzi1, Sharmila Velapasamy1, Ler Lian Wee1, Livy Alex1.
Abstract
Genome-wide association studies have discovered multiple single nucleotide polymorphisms (SNPs) associated with the risk of common diseases. The objective of this study was to demonstrate the replication of previously published SNPs that showed statistical significance for breast cancer in the Malaysian population. In this case-control study, 80 subjects for each group were recruited from various hospitals in Malaysia. A total of 768 SNPs were genotyped and analyzed to distinguish risk and protective alleles. A total of three SNPs were found to be associated with increased risk of breast cancer while six SNPs showed protective effect. All nine were statistically significant SNPs (p ≤ 0.01), five SNPs from previous studies were successfully replicated in our study. Significant modifiable (diet) and non-modifiable (family history of breast cancer in first degree relative) risk factors were also observed. We identified nine SNPs from this study to be either conferring susceptibility or protection to breast cancer which may serve as potential markers in risk prediction.Entities:
Keywords: Association; Breast cancer; Case–control study; Risk prediction model; SNP
Year: 2014 PMID: 25883419 PMCID: PMC4393382 DOI: 10.1007/s12291-013-0414-0
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915