Petry Clive J, Ong Ken K, Hughes Ieuan A, Acerini Carlo L, Dunger David B
Department of Paediatrics, Addenbrooke's Hospital, University of Cambridge, Hills Road, Box 116, Cambridge, CB2 0QQ, UK.
Medical Research Council Epidemiology Unit, University of Cambridge, Cambridge, CB2 0QQ, UK.
BMC Res Notes. 2018 Nov 19;11(1):821. doi: 10.1186/s13104-018-3933-1.
Previously we found that certain fetal imprinted genes represented as an allele score are associated with maternal pregnancy glucose concentrations. Recently it was reported that fetal polymorphisms with strong associations with birth weight tend to mediate these independently of increases in maternal pregnancy glucose concentrations. We therefore investigated whether potential associations between the fetal allele score and birth weight were related to maternal glucose concentrations in the Cambridge Baby Growth Study.
The fetal imprinted gene allele score was positively associated with birth weight (β = 63 (17-109) g/risk allele, β' = 0.113, p = 7.6 × 10, n = 405). This association was partially attenuated by adjusting for maternal glucose concentrations (β = 50 (4-95) g/risk allele, β' = 0.089, p = 0.03, n = 405). The allele score was also positively associated with risk of being large for gestational age at birth (odds ratio 1.60 (1.19-2.15) per risk allele, p = 2.1 × 10, n = 660) and negatively associated with risk of being small for gestational age at birth (odds ratio 0.65 (0.44-0.96) per risk allele, p = 0.03, n = 660). The large for gestational age at birth association was also partially attenuated by maternal glucose concentrations. These results suggest that associations between the fetal imprinted gene allele score and size at birth are mediated through both glucose-dependent and glucose-independent mechanisms.
此前我们发现,某些以等位基因评分表示的胎儿印记基因与孕妇孕期血糖浓度相关。最近有报道称,与出生体重密切相关的胎儿多态性往往独立于孕妇孕期血糖浓度升高而介导这些关联。因此,在剑桥婴儿生长研究中,我们调查了胎儿等位基因评分与出生体重之间的潜在关联是否与孕妇血糖浓度有关。
胎儿印记基因等位基因评分与出生体重呈正相关(β = 63(17 - 109)g/风险等位基因,β' = 0.113,p = 7.6×10⁻⁴,n = 405)。通过调整孕妇血糖浓度,这种关联部分减弱(β = 50(4 - 95)g/风险等位基因,β' = 0.089,p = 0.03,n = 405)。等位基因评分也与出生时大于胎龄的风险呈正相关(每个风险等位基因的优势比为1.60(1.19 - 2.15),p = 2.1×10⁻³,n = 660),与出生时小于胎龄的风险呈负相关(每个风险等位基因的优势比为0.65(0.44 - 0.96),p = 0.03,n = 660)。出生时大于胎龄的关联也因孕妇血糖浓度而部分减弱。这些结果表明,胎儿印记基因等位基因评分与出生时大小之间的关联是通过葡萄糖依赖和葡萄糖非依赖机制介导的。