Anwardeen Najeha Rizwana, Naja Khaled, Elrayess Mohamed A
Biomedical Research Center, Qatar University, Doha, Qatar.
College of Medicine, QU Health, Qatar University, Doha, Qatar.
Front Pharmacol. 2024 Nov 28;15:1506767. doi: 10.3389/fphar.2024.1506767. eCollection 2024.
Metformin has become the frontline treatment in addressing the significant global health challenge of type 2 diabetes due to its proven effectiveness in lowering blood glucose levels. However, the reality is that many patients struggle to achieve their glycemic targets with the medication and the cause behind this variability has not been investigated thoroughly. While genetic factors account for only about a third of this response variability, the potential influence of metabolomics and the gut microbiome on drug efficacy opens new avenues for investigation. This review explores the different molecular signatures to uncover how the complex interplay between genetics, metabolic profiles, and gut microbiota can shape individual responses to metformin. By highlighting the insights from recent studies and identifying knowledge gaps regarding metformin-microbiota interplay, we aim to highlight the path toward more personalized and effective diabetes management strategies and moving beyond the one-size-fits-all approach.
由于二甲双胍在降低血糖水平方面已被证实有效,它已成为应对2型糖尿病这一重大全球健康挑战的一线治疗药物。然而,现实情况是,许多患者在使用该药物时难以实现血糖目标,而这种变异性背后的原因尚未得到充分研究。虽然遗传因素仅占这种反应变异性的约三分之一,但代谢组学和肠道微生物群对药物疗效的潜在影响为研究开辟了新途径。本综述探讨了不同的分子特征,以揭示遗传学、代谢谱和肠道微生物群之间复杂的相互作用如何塑造个体对二甲双胍的反应。通过强调近期研究的见解并确定关于二甲双胍与微生物群相互作用的知识空白,我们旨在突出通往更个性化和有效糖尿病管理策略的道路,并超越一刀切的方法。