Benido Silva Vânia, Fonseca Liliana, Pereira Maria Teresa, Vilaverde Joana, Pinto Clara, Pichel Fernando, Almeida Maria do Céu, Dores Jorge
Department of Endocrinology, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Department of Obstetrics, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Endocr Connect. 2022 May 10;11(5):e210540. doi: 10.1530/EC-21-0540.
Metformin has emerged as a safe and effective pharmacological alternative to insulin in gestational diabetes mellitus (GDM), being associated with lower maternal weight gain and hypoglycemia risk. Nevertheless, glycemic control is unaccomplished in a considerable proportion of women only treated with metformin. We aim to determine the metformin monotherapy failure rate in GDM and to identify predictors of its occurrence.
This was a retrospective multicenter study including pregnant women with GDM patients who started metformin as a first-line pharmacological treatment (n = 2891). A comparative analysis of clinical and analytical data between the group of women treated with metformin monotherapy and those needing combined therapy with insulin was performed.
In 685 (23.7%) women with GDM, combined therapy to achieve adequate glycemic control was required. Higher pregestational BMI (OR 1.039; CI 95% 1.008-1.071; P-value = 0.013), higher fasting plasma glucose (PG) levels in oral glucose tolerance test (OGTT) (OR 1.047; CI 95% 1.028-1.066; P-value <0.001) and an earlier gestational age (GA) at metformin introduction (0.839; CI 95% 0.796-0.885, P-value < 0.001) were independent predictive factors for metformin monotherapy failure. The best predictive cutoff values were a fasting PG in OGTT ≥87 mg/dL and GA at metformin introduction ≤29 weeks.
In 685 (23.7%) women, combined therapy with insulin to reach glycemic control was required. Higher pre-gestational BMI, fasting PG levels in OGTT ≥87 mg/dL and introduction of metformin ≤29 weeks of GA were independent predictive factors for metformin monotherapy failure. The early recognition of these characteristics can contribute to the establishment of individualized therapeutic strategies and attain better metabolic control during pregnancy.
二甲双胍已成为妊娠期糖尿病(GDM)中胰岛素的一种安全有效的药理学替代药物,与较低的母体体重增加和低血糖风险相关。然而,仅接受二甲双胍治疗的相当一部分女性血糖控制未达标。我们旨在确定GDM中二甲双胍单药治疗失败率,并确定其发生的预测因素。
这是一项回顾性多中心研究,纳入了开始将二甲双胍作为一线药物治疗的GDM孕妇(n = 2891)。对接受二甲双胍单药治疗的女性组与需要胰岛素联合治疗的女性组之间的临床和分析数据进行了比较分析。
在685名(23.7%)GDM女性中,需要联合治疗以实现充分的血糖控制。孕前BMI较高(OR 1.039;95%CI 1.008 - 1.071;P值 = 0.013)、口服葡萄糖耐量试验(OGTT)中空腹血糖(PG)水平较高(OR 1.047;95%CI 1.028 - 1.066;P值 < 0.001)以及开始使用二甲双胍时的孕周较早(0.839;95%CI 0.796 - 0.885,P值 < 0.001)是二甲双胍单药治疗失败的独立预测因素。最佳预测临界值为OGTT中的空腹PG≥87 mg/dL以及开始使用二甲双胍时的孕周≤29周。
在685名(23.7%)女性中,需要胰岛素联合治疗以实现血糖控制。孕前BMI较高、OGTT中空腹PG水平≥87 mg/dL以及开始使用二甲双胍时孕周≤29周是二甲双胍单药治疗失败的独立预测因素。早期识别这些特征有助于制定个体化治疗策略,并在孕期实现更好的代谢控制。