| Literature DB >> 12646233 |
Makoto Daimon1, Guijin Ji, Tamotsu Saitoh, Toshihide Oizumi, Makoto Tominaga, Takahiro Nakamura, Keisuke Ishii, Tadashi Matsuura, Kiyoshi Inageda, Hiroto Matsumine, Takashi Kido, Lwin Htay, Naoyuki Kamatani, Masaaki Muramatsu, Takeo Kato.
Abstract
The etiology of type 2 diabetes (DM) is polygenic. We investigated here genes and polymorphisms that associate with DM in the Japanese population. Single-nucleotide polymorphisms (SNPs) of 398 derived from 120 candidate genes were examined for association with DM in a population-based case-control study. The study group consisted of 148 cases and 227 controls recruited from Funagata, Japan. No evident subpopulation structure was detected for the tested population. The association tests were conducted with standard allele positivity tables (chi(2) tests) between SNP genotype frequency and case-control status. The independent association of the SNPs from serum triglyceride levels and body mass index was examined by multiple logistic regression analysis. A value of P<0.01 was accepted as statistically significant. Six genes (met proto-oncogene, ATP-binding cassette transporter A1, fatty acid binding protein 2, LDL receptor defect C complementing, aldolase B, and sulfonylurea receptor) were shown to be associated with DM.Entities:
Mesh:
Substances:
Year: 2003 PMID: 12646233 DOI: 10.1016/s0006-291x(03)00248-1
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575