Bonnet Fabrice, Scheen André
Department of Endocrinology, Diabetes and Nutrition, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Department of Endocrinology, Diabetes and Nutrition, Division of Clinical Pharmacology, Center for Interdisciplinary Research on Medicines (CIRM), University of Liège, CHU, Liège, Belgium.
Diabetes Obes Metab. 2017 Apr;19(4):473-481. doi: 10.1111/dom.12854. Epub 2017 Feb 22.
Metformin is the most widely prescribed drug for patients with type 2 diabetes mellitus and the first-line pharmacological option as supported by multiple international guidelines, yet a rather large proportion of patients cannot tolerate metformin in adequate amounts because of its associated gastrointestinal (GI) adverse events (AEs). GI AEs typically encountered with metformin therapy include diarrhoea, nausea, flatulence, indigestion, vomiting and abdominal discomfort, with diarrhoea and nausea being the most common. Although starting at a low dose and titrating slowly may help prevent some GI AEs associated with metformin, some patients are unable to tolerate metformin at all and it may also be difficult to convince patients to start metformin again after a bout of GI AEs. Despite this clinical importance, the underlying mechanisms of the GI intolerance associated with metformin are poorly known. In the present review, we discuss: the epidemiology of metformin-associated GI intolerance and its underlying mechanisms; genotype variability and associated factors affecting metformin GI intolerance, such as comorbidities, co-medications and bariatric surgery; clinical consequences and therapeutic strategies to overcome metformin GI intolerance. These strategies include appropriate titration of immediate-release metformin, use of extended-release metformin, the promise of delayed-release metformin and gut microbiome modulators, as well as alternative pharmacological therapies when metformin cannot be tolerated at all. Given the available data, all efforts should be made to maintain metformin before considering a shift to another drug therapy.
二甲双胍是2型糖尿病患者中处方最广泛的药物,也是多项国际指南支持的一线药物选择,但相当大比例的患者因二甲双胍相关的胃肠道(GI)不良事件(AE)而无法耐受足够剂量的二甲双胍。二甲双胍治疗中常见的胃肠道不良事件包括腹泻、恶心、肠胃胀气、消化不良、呕吐和腹部不适,其中腹泻和恶心最为常见。虽然从低剂量开始并缓慢滴定可能有助于预防一些与二甲双胍相关的胃肠道不良事件,但一些患者根本无法耐受二甲双胍,而且在经历一轮胃肠道不良事件后,也可能难以说服患者再次开始服用二甲双胍。尽管这一临床问题很重要,但与二甲双胍相关的胃肠道不耐受的潜在机制却鲜为人知。在本综述中,我们讨论:二甲双胍相关胃肠道不耐受的流行病学及其潜在机制;影响二甲双胍胃肠道不耐受的基因变异和相关因素,如合并症、联合用药和减肥手术;克服二甲双胍胃肠道不耐受的临床后果和治疗策略。这些策略包括适当滴定速释二甲双胍、使用缓释二甲双胍、延迟释放二甲双胍和肠道微生物群调节剂的前景,以及在完全无法耐受二甲双胍时的替代药物治疗。鉴于现有数据,在考虑改用其他药物治疗之前,应尽一切努力维持二甲双胍的使用。