Department of Internal Medicine, Minia University, Minia, Egypt.
Therap Adv Gastroenterol. 2011 Nov;4(6):419-31. doi: 10.1177/1756283X11405251.
The prevalence of type 2 diabetes mellitus and insulin resistance are higher among people chronically infected with hepatitis C (CHC) when compared with the general population and people with other causes of chronic liver disease. Both insulin resistance and diabetes are associated with adverse outcomes across all stages of CHC, including the liver transplant population. CHC is also associated with the development of hepatic steatosis, a common histological feature present in approximately 55% (32-81%) of cases. There is a complex interrelationship between insulin resistance and hepatic steatosis and both are postulated to aggravate each other. The peroxisome proliferator-activated receptors (PPARs) are nuclear factors involved in the regulation of glucose, lipid homeostasis, inflammatory response, cell differentiation, and cell cycle. The relationship between hepatitis C virus replication and PPARs has been the focus of recent study. Given the availability of potent agonists, PPARs may represent a novel pharmacological target in the treatment of CHC.
与普通人群和其他原因导致的慢性肝病患者相比,慢性丙型肝炎(CHC)患者的 2 型糖尿病和胰岛素抵抗的患病率更高。胰岛素抵抗和糖尿病均与 CHC 的各个阶段(包括肝移植人群)的不良结局相关。CHC 还与肝脂肪变性的发生相关,这是一种常见的组织学特征,在约 55%(32-81%)的病例中存在。胰岛素抵抗和肝脂肪变性之间存在复杂的相互关系,两者相互加重。过氧化物酶体增殖物激活受体(PPARs)是参与调节葡萄糖、脂质稳态、炎症反应、细胞分化和细胞周期的核因子。丙型肝炎病毒复制与 PPARs 之间的关系一直是近期研究的重点。鉴于有效的激动剂的存在,PPARs 可能成为 CHC 治疗的新的药理学靶点。