University of Rochester School of Nursing, Rochester, NY, USA; Department of Public Health Sciences, University of Rochester, Rochester, NY, USA.
Department of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, USA.
Nutrition. 2018 Apr;48:61-66. doi: 10.1016/j.nut.2017.11.008. Epub 2017 Dec 2.
To examine the associations of two obesity-associated genes, FTO (rs9939609) and GNB3 (rs5443) single nucleotide polymorphisms (SNPs), with early pregnancy body mass index, gestational weight gain, and postpartum weight retention.
Secondary data analysis of self-identified white (n = 580) and black (n = 194) women who participated in a randomized controlled trial (2009-2014) and provided a saliva sample of DNA. Bivariate relationships were assessed using analysis of variance. Multiple regression models assessed the relationship between outcomes and gene SNPs, controlling for income, parity, and smoking status.
FTO and GNB3 gene associations with pregnancy weight were different by racial group and early pregnancy body mass index. Obese black women homozygote for the FTO risk allele (AA) had a higher gestational weight gain compared with non-risk homozygotes (TT) (P = 0.006). GNB3 non-risk CC homozygotes tended to have a lower gestational weight gain compared with heterozygotes (P = 0.05). White GNB3 C carriers tended to be heavier in early pregnancy (P <0.1) and GNB3 homozygote (TT) overweight women tended to have lower postpartum weight retention than C carriers.
The FTO gene and possibly the GNB3 gene are associated with high gestational weight gain in obese black women. Obese carriers of the FTO risk allele gained 4.1 kg (AT) and 7.6 kg (TT) more than those without risk alleles. Overweight GNB3 heterozygotes (CT) gained 6.6 kg less than homozygotes (CC). Overweight or obese black women who have either risk variant are at risk for high gestational weight gain.
探讨两个肥胖相关基因 FTO(rs9939609)和 GNB3(rs5443)单核苷酸多态性(SNP)与早孕体重指数、妊娠期体重增加和产后体重滞留的关系。
对参加 2009-2014 年随机对照试验并提供唾液 DNA 样本的自报白人和黑人(n=580 和 194)女性进行二次数据分析。采用方差分析评估两变量关系。多元回归模型评估了基因 SNP 与结局之间的关系,控制了收入、产次和吸烟状况。
FTO 和 GNB3 基因与妊娠体重的关联因种族和早孕体重指数而异。肥胖的黑人女性 FTO 风险等位基因(AA)纯合子的妊娠期体重增加高于非风险纯合子(TT)(P=0.006)。GNB3 非风险 CC 纯合子的妊娠期体重增加倾向于低于杂合子(P=0.05)。携带 GNB3 C 的白人女性在早孕时体重往往更重(P<0.1),GNB3 纯合子(TT)超重女性的产后体重滞留率低于 C 携带者。
FTO 基因和可能的 GNB3 基因与肥胖黑人女性的高妊娠期体重增加有关。携带 FTO 风险等位基因的肥胖者比不携带风险等位基因者多增加 4.1kg(AT)和 7.6kg(TT)。超重 GNB3 杂合子(CT)比纯合子(CC)少增加 6.6kg。超重或肥胖的黑人女性,如果携带任一风险变体,都有发生高妊娠期体重增加的风险。