The polymorphism of insulin-like growth factor-I (IGF-I) gene was exam
ined in Japanese postmenopausal women to analyze the genetic backgroun
d for osteoporosis. In this study, the dinucleotide (cytosine-adenine;
CA) repeat sequence lying upstream of the transcription initiation si
te of this gene was examined. We named the most frequent allele includ
ing (CA) 19 as J allele. There were 6 alleles (J-4 containing 17 CA re
peats: (CA)17, [J-2 (CA)18, J (CP;)19 J+2(CA)20, J+4(CA)21, J+6 (CA)22
]) in the Japanese population. The genotype distribution was different
from that of Caucasians. There was no different in bone mineral densi
ty (BMD) between the group with one or two alleles of each genotype an
d that without that genotype. When we separate the subjects into three
groups having two alleles, one allele, and no alleles, the three subj
ects who possess the allele 'J-2' in both strands had low BMD (Z score
of L2-4; -1.24 +/- 0.56, total body; -0.943 +/- 0.59, mean a SE). On
the other hand, sequence of IGF-I gene in this study was different fro
m reported sequence of IGF-I gene; that was 2 base pair (bp) deletion
following 3'end of CArepeat (-645adenine/-646guanine). The present stu
dy showed that there was no association between the microsatellite pol
ymorphism of IGF-I gene and BMD in Japanese postmenopausal women, but
some possibility remains that the microsatellite polymorphism of IGF-I
gene is useful to detect a kind of particular osteoporosis.