Alanine to threonine substitution at codon 54 of the fatty acid-binding protein 2 (FABP2) gene was recently shown to be associated
with insulin resistance in Pima Indians. It has been hypothesized that the mutation may result in enhanced intestinal uptake
of fatty acids, and thereby an impairment of insulin action. We analysed the association of the Ala54Thr substitution with
insulin sensitivity and abdominal fat thickness in 395 Japanese men aged 50.5 ± 8.8 years (mean ± SD) with a body mass index
of 24.4 ± 3.0 kg/m
2. The frequency of the Thr54 allele was 0.34. Although the polymorphism was not significantly associated with diabetes or
impaired glucose tolerance, subjects homozygous for the Thr54 allele had higher basal insulin levels. Analysis by homeostasis
model assessment showed an association between the amino acid substitution and greater insulin resistance, and slightly higher
beta-cell function. Oral glucose tolerance tests performed in 392 subjects without fasting hyperglycaemia showed higher 2-h
insulin concentrations in individuals homozygous for the Thr54 allele when compared with heterozygotes or homozygotes for
the Ala54 allele. No significant association was obtained between the polymorphism of the FABP2 gene and body mass index.
However, ultrasound measurements of abdominal fat thickness revealed a greater accumulation of intra-abdominal fat in subjects
homozygous for the Thr54 allele, whereas subcutaneous fat thickness was not associated with the polymorphism. These observations
suggest that the Ala54Thr substitution in the FABP2 gene is associated with insulin resistance in Japanese men, and that visceral
fat accumulation might be involved in the impaired insulin action associated with the substitution. [Diabetologia (1997) 40:
706–710]
Keywords Fatty acid-binding protein 2 - intestinal fatty acid binding protein - insulin resistance - visceral fat.
Received: 30 December 1996 and in revised form: 10 March 1997