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rs10830963 变异与孕前 BMI 相互作用,是妊娠期糖尿病起始产前胰岛素治疗的药物遗传学标志物。

The rs10830963 Variant in Interaction with Pre-Pregnancy BMI is a Pharmacogenetic Marker for the Initiation of Antenatal Insulin Therapy in Gestational Diabetes Mellitus.

机构信息

2nd Department of Internal Medicine, Semmelweis University, H-1088 Budapest, Hungary.

MTA-SE Molecular Medicine Research Group, Hungarian Academy of Sciences⁻Semmelweis University, H-1088 Budapest, Hungary.

出版信息

Int J Mol Sci. 2018 Nov 23;19(12):3734. doi: 10.3390/ijms19123734.

Abstract

The rs10830963 variant of the () gene is associated with the development of gestational diabetes mellitus (GDM). We hypothesized that carrying the rs10830963/ risk allele had effect on antenatal insulin therapy (AIT) initiation in GDM in a body mass index (BMI)-dependent manner. : In this post hoc analysis the rs10830963 genotype and the clinical data of 211 Caucasian GDM patients were assessed. As a first step, a pre-pregnancy BMI threshold was determined where the effect of rs10830963/ allele carrying on AIT initiation was the most significant using logistic regression. Maternal age adjusted real-life odds ratios (OR) values were calculated. The chi-square test was also used to calculate the p value and 10.000 bootstrap simulations were performed in each case to re-assess the statistical power and the OR. Carrying the rs10830963/ allele increased the odds of AIT initiation (OR = 5.2, = 0.02 [χ² test], statistical power = 0.53) in GDM patients with pre-pregnancy BMI ≥ 29 kg/m². The statistical power reached 0.77, when the pre-pregnancy BMI cutoff of 27 kg/m² was used and the genetic effect on AIT initiation was still significant, but only using the logistic regression model. Carrying the rs10830963/ risk allele-in interaction with pre-pregnancy BMI-is likely be considered as a candidate pharmacogenetic marker of antenatal insulin therapy initiation and should be further assessed in precision medicine trials in GDM.

摘要

基因的 rs10830963 变体与妊娠糖尿病(GDM)的发展有关。我们假设携带 rs10830963/风险等位基因会对 BMI 依赖的 GDM 患者产前胰岛素治疗(AIT)的起始产生影响。:在这项事后分析中,评估了 211 名高加索 GDM 患者的 rs10830963 基因型和临床数据。作为第一步,使用逻辑回归确定了一个孕前 BMI 阈值,在该阈值下,rs10830963/等位基因携带对 AIT 起始的影响最显著。计算了经母体年龄调整的真实比值比(OR)值。还使用卡方检验计算 p 值,并在每种情况下进行 10000 次 bootstrap 模拟,以重新评估统计效力和 OR。携带 rs10830963/等位基因增加了 AIT 起始的几率(OR=5.2,=0.02 [卡方检验],统计效力=0.53)在孕前 BMI≥29kg/m²的 GDM 患者中。当使用孕前 BMI 截止值为 27kg/m²时,统计效力达到 0.77,并且遗传效应对 AIT 起始仍有显著影响,但仅使用逻辑回归模型。携带 rs10830963/风险等位基因与孕前 BMI 相互作用,可能被认为是产前胰岛素治疗起始的候选药物遗传学标记,应在 GDM 的精准医学试验中进一步评估。

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