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首页> 外文期刊>DMW: Deutsche Medizinische Wochenschrift >Secondary causes of fatty liver disease - an update on pathogenesis, diagnosis and treatment strategies
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Secondary causes of fatty liver disease - an update on pathogenesis, diagnosis and treatment strategies

机译:脂肪肝病的二次成因 - 发病机制,诊断和治疗策略的更新

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摘要

Secondary causes of fatty liver disease are important to recognize since specific therapy options are available for some of these causes. Common causes of secondary fatty liver disease comprise hepatitis C virus infection (HCV), endocrinological diseases, nutritional and intestinal diseases as well as genetic liver and metabolic diseases. Certain drugs may also predispose to the development of fatty liver disease. Primary fatty liver disease, also known as non-alcoholic fatty liver disease (NAFLD) is defined by the presence of steatosis hepatis without relevant alcohol consumption or other causes of secondary fatty liver disease. NAFLD occurs more frequently in patients with metabolic syndrome and thus can be seen as the hepatic manifestation of the metabolic syndrome. Therefore, presence of features of the metabolic syndrome should be assessed in all patients with fatty liver disease. Furthermore, alcohol consumption should be determined to rule out alcoholic liver disease (ASH). Further diagnostic work up for secondary causes of fatty liver disease should include screening for HCV infection, for hypothyroidism and for drugs associated with steatosis development. In a next step screening for Wilson's disease, hemochromatosis, celiac disease and lipid metabolism disorders should be performed. An extended endocrinological workup and a liver biopsy should be considered if the etiology of fatty liver disease remains unclear. Common genetic polymorphisms have been identified in several genes, such as PNPLA3, TM6SF2 and MBOAT7, which may promote the development and the progression of fatty liver disease irrespective of the underlying etiology (e. g. metabolic syndrome, ASH or HCV). The risk variants in these genes have additive effects on steatosis development and diseases progression towards fibrosis and cirrhosis. The diagnosis of secondary causes of fatty liver disease may allow for therapeutic intervention and prevent disease progression. Accordingly, secondary causes of fatty liver disease should be considered during the diagnostic workup of NAFLD patients.
机译:脂肪肝疾病的二次原因对于识别,因为某些原因可用特异性治疗方案。继发性肝病的常见原因包括丙型肝炎病毒感染(HCV),内分泌疾病,营养和肠疾病以及遗传肝癌和代谢疾病。某些药物也可能易于发展脂肪肝病。原发性脂肪肝病,也称为非酒精脂肪肝疾病(NAFLD)由脂肪变性的存在而没有相关的酒精消耗或其他原因的继发性脂肪肝病。 NAFLD在代谢综合征患者中更频繁地发生,因此可以被视为代谢综合征的肝脏表现。因此,应在所有脂肪肝病的患者中评估代谢综合征的特征的存在。此外,应确定醇消耗以排除酒精性肝病(灰)。进一步诊断脂肪肝疾病的二次原因的诊断综合应包括筛查HCV感染,用于甲状腺功能减退症和与脂肪变性发展相关的药物。在下一步筛选威尔逊疾病的筛查中,应进行血细胞瘤,乳糜泻和脂质代谢障碍。如果脂肪肝疾病的病因仍然尚不清楚,则应考虑延长的内分泌后处理和肝脏活组织检查。已经在几种基因中鉴定了常见的遗传多态性,例如Pnpla3,TM6SF2和MBoAT7,其可以促进脂肪肝疾病的发育和进展,而不管潜在的病因如何(例如代谢综合征,灰分或HCV)。这些基因的风险变体对脂肪变性发育和疾病朝纤维化和肝硬化的进展具有添加剂影响。脂肪肝疾病的二次原因的诊断可能允许治疗干预和预防疾病进展。因此,在NAFLD患者的诊断后,应考虑脂肪肝疾病的继发性原因。

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