University of Colorado Anschutz Medical Campus, Department of Obstetrics and Gynecology, Division of Family Planning, 12631 E 17th Ave, B198-2, Aurora, CO 80045, USA.
University of Colorado Anschutz Medical Campus, Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, 12850 E Montview Blvd, Aurora, CO 80045, USA.
Contraception. 2020 Sep;102(3):180-185. doi: 10.1016/j.contraception.2020.05.002. Epub 2020 May 12.
To identify genetic variants associated with weight gain related to etonogestrel contraceptive implant use.
We conducted a retrospective analysis from a parent pharmacogenomic study of healthy, reproductive-aged women using etonogestrel implants. We reviewed medical records to calculate objective weight changes from implant insertion to study enrollment and asked participants about subjective weight gain (yes/no) during contraceptive implant use. We used genotyping data (99 genetic variants) from the parent study to conduct backward-stepwise generalized linear modeling to identify genetic variants associated with objective weight changes.
Among 276 ethnically diverse participants, median body-mass index (BMI) was 25.8 kg/m (range 18.5-48.1). We found a median weight change of +3.2 kg (range -27.6 to +26.5) from implant insertion to study enrollment. Report of subjective weight gain had minimal agreement with measured weight gain during implant use (Cohen's kappa = 0.21). Our final generalized linear model contained two variables associated with objective weight change that met conservative statistical significance (p < 5.0 × 10). Participants with two copies (homozygous) of the ESR1 rs9340799 variant on average gained 14.1 kg more than all other participants (p = 1.4 × 10). Higher enrollment BMI was also associated with objective weight gain (β = 0.54, p = 9.4 × 10).
Genetic variants in the estrogen receptor 1 (ESR1) do not have known associations with obesity or metabolic syndrome, but there is physiologic plausibility for a progestin-mediated genetic association between ESR1 and weight gain. Additional genetic research is needed to substantiate our findings and elucidate further advances in individualized counseling on the risk of weight gain with exogenous steroid hormones.
Genetic variation in the estrogen receptor 1 gene may account for variability in weight gain among etonogestrel contraceptive implant users. If these findings can be replicated with other progestin-containing medications, we may be able to better individualize contraceptive counseling.
鉴定与依托孕烯植入避孕相关的体重增加相关的遗传变异。
我们对使用依托孕烯植入物的健康育龄妇女进行了一项回顾性分析,这是一项母体药物基因组学研究。我们查阅了病历,计算了从植入物插入到研究入组时的客观体重变化,并询问了参与者在使用避孕植入物期间的主观体重增加(是/否)。我们使用来自母体研究的基因分型数据(99 个遗传变异)进行逐步后退广义线性建模,以鉴定与客观体重变化相关的遗传变异。
在 276 名种族多样化的参与者中,中位数体重指数(BMI)为 25.8kg/m(范围 18.5-48.1)。我们发现从植入物插入到研究入组时的平均体重变化为+3.2kg(范围-27.6 至+26.5)。在使用植入物期间报告的主观体重增加与测量的体重增加之间的一致性很小(科恩氏κ=0.21)。我们的最终广义线性模型包含两个与客观体重变化相关的变量,这些变量达到了保守的统计学意义(p<5.0×10)。与所有其他参与者相比,携带两个 ESR1 rs9340799 变体副本(纯合子)的参与者平均体重增加了 14.1kg(p=1.4×10)。较高的入组 BMI 也与客观体重增加相关(β=0.54,p=9.4×10)。
雌激素受体 1(ESR1)中的遗传变异与肥胖或代谢综合征没有已知的关联,但孕激素介导的 ESR1 与体重增加之间的遗传关联具有生理学上的合理性。需要进一步的遗传研究来证实我们的发现,并阐明对外源性甾体激素体重增加风险的个体化咨询的进一步进展。
雌激素受体 1 基因的遗传变异可能解释了依托孕烯避孕植入物使用者体重增加的变异性。如果这些发现可以用其他含有孕激素的药物复制,我们可能能够更好地对避孕咨询进行个体化。