Paternal Allele of IGF2 Gene Haplotype CTG Is Associated With Fetal and Placental Growth in Japanese
著者
長屋, 建
(Nagaya, Ken)
Makita, Y
Taketazu, G
Okamoto, T
Nakamura, E
Hayashi, T
Fujieda, K
上位タイトル
Pediatric Research
Vol.66,
No.2
(2009.
8)
,p.135-
139
識別番号
ISSN
0031-3998
DOI
10.1203/PDR.0b013e3181a9e818
抄録
IGF-II associates with feto-placental growth in rodent and human. determined three tag-single nucleotide polymorphisms (SNPs) to investigate haplotype frequency of IGF2 relative to size at birth in 134 healthy Japanese infants. In addition, a total of 276 healthy infants were investigated to determine whether common genetic variation of IGF2 might contribute to feto-placental growth Using haplotype analysis. Further, quantitative methylation analysis of the IGF2/HI9 wits performed using the MassARRAY Compact system. In the initial study,. the frequency of haplotype CTG front the paternal allele in small for date (SFD) infants was significantly higher than that in non-SFD infants (p = 0.03). In second Study, the CTG haplotype infants exhibited significantly lower birth length, weight. and placental weight Compared with non-CTG infants. Further, the number of infants less than - 1,5 SD (SD) birth weight in CTG haplotype was higher than those if non-CTG infants. There was no significant difference in the methylation status of HI9/IGF2 in the two haplotypes. In conclusion, inheriting the IGF2 CTG haplotype front I paternal allele results ill reduced feto-placental growth. but it is not associated with the methylation Status of IGF2/HI9. (Pediatr Res 66: 135-139, 2009)
