Mazzotti Arianna, Caletti Maria Turchese, Marchignoli Francesca, Forlani Giulia, Marchesini Giulio
Department of Medical & Surgical Sciences, Alma Mater University, Bologna, Italy.
Department of Medical & Surgical Sciences, Alma Mater University, Bologna, Italy.
Dig Liver Dis. 2017 Mar;49(3):235-240. doi: 10.1016/j.dld.2016.12.028. Epub 2016 Dec 30.
Type 2 diabetes (T2DM) and nonalcoholic fatty liver disease (NAFLD) are highly prevalent in the community, and share common pathogenic mechanisms. There is also evidence that T2DM may be favored by hepatic fat accumulation; in turn the presence of T2DM is a risk factor for liver disease progression. The treatment of T2DM has considerably changed in the past few years; new drug classes, promoting glucose-lowering through mechanisms different from classical insulin-sensitizing or insulin-secreting action, have been added to continuing lifestyle intervention. Metformin and pioglitazone may be safely used in the presence of liver fat, whereas sulfonylureas and insulin itself have been associated with NAFLD progression and adverse outcome. Drugs acting on the incretin axis and on Na-glucose co-transport at renal tubular level offer new hopes for a tailored treatment able to reduce the burden of hepatic triglyceride accumulation and liver disease progression.
2型糖尿病(T2DM)和非酒精性脂肪性肝病(NAFLD)在社区中非常普遍,并且具有共同的致病机制。也有证据表明,肝脏脂肪堆积可能有利于T2DM的发生;反过来,T2DM的存在是肝病进展的一个危险因素。在过去几年中,T2DM的治疗发生了很大变化;除了持续的生活方式干预外,还增加了新的药物类别,这些药物通过不同于经典的胰岛素增敏或胰岛素分泌作用的机制促进血糖降低。在存在肝脏脂肪的情况下,可以安全使用二甲双胍和吡格列酮,而磺脲类药物和胰岛素本身与NAFLD进展及不良结局有关。作用于肠促胰岛素轴和肾小管水平的钠-葡萄糖共转运的药物为能够减轻肝脏甘油三酯堆积负担和肝病进展的个性化治疗带来了新希望。