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Variation of the fatty acid binding protein 2 gene is not associated with obesity and insulin resistance in Japanese subjects.
- Source :
-
Metabolism: clinical and experimental [Metabolism] 1999 May; Vol. 48 (5), pp. 655-7. - Publication Year :
- 1999
-
Abstract
- An alanine to threonine substitution at codon 54 of the fatty acid binding protein 2 (FABP2) gene has been associated with insulin resistance in Pima Indians and with obesity in aboriginal Canadians. We investigated whether this polymorphism contributes to obesity and insulin resistance in 258 Japanese subjects. Thirty-six subjects (13.9%) were homozygous for the Thr54 allele, 106 (41.1%) were heterozygous for the Ala54/Thr54 allele, and 116 (45.0%) were homozygous for the Ala54 allele. The frequency of the Thr54 allele was 0.34 and did not differ significantly between men and women. The incidence of non-insulin-dependent diabetes mellitus (NIDDM) was not different among the three genotypes. The variation at codon 54 of the FABP2 gene was not associated with obesity, hypertension, dyslipidemia, hyperuricemia, or hyperinsulinemia. These results suggest that the polymorphism at codon 54 of the FABP2 gene is not a major contributing factor to obesity and insulin resistance in Japanese subjects.
- Subjects :
- Adult
Aged
Alleles
Amino Acid Substitution genetics
Asian People genetics
Diabetes Mellitus, Type 2 genetics
Fatty Acid-Binding Protein 7
Fatty Acid-Binding Proteins
Female
Gene Frequency
Glucose Intolerance genetics
Heterozygote
Homozygote
Humans
Japan
Male
Middle Aged
Obesity ethnology
Reference Values
Carrier Proteins genetics
Genetic Variation physiology
Insulin Resistance genetics
Myelin P2 Protein genetics
Neoplasm Proteins
Obesity genetics
Tumor Suppressor Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 0026-0495
- Volume :
- 48
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Metabolism: clinical and experimental
- Publication Type :
- Academic Journal
- Accession number :
- 10337870
- Full Text :
- https://doi.org/10.1016/s0026-0495(99)90067-7