Affiliation:
1. Donetsk National Medical University
2. Central City Clinical Hospital No. 1
Abstract
Aim. A current overview of non-pharmacological and drug-based approaches to non-alcoholic fatty liver disease (NAFLD) combined with type 2 diabetes mellitus (T2D).Key points. NAFLD is associated with an increased cardiovascular risk (due to association with “metabolic syndrome”) and the risks of liver cirrhosis and hepatocellular carcinoma. Macro- and microvascular complications in T2D comorbidity entail a higher overall mortality. A conjunction of lifestyle change and rational medication strategies to reach the target levels of glycosylated haemoglobin, low-density lipoprotein cholesterol, systolic and diastolic blood pressure is key in management of such patients. A body weight loss by 5–7 % or more (through caloric restriction or a bariatric surgery) promotes a marked reduction in liver fat and even reversal of steatohepatitis. Metered exercise exerts this effect even at insignificant weight loss. Minimising alcohol consumption and smoking is critical. A hepatotropic drug therapy is most essential in moderate fibrotic NAFLD. It includes antidiabetic agents (metformin, thiazolidinediones, glucagon-like peptide-1 receptor agonists, sodium-glucose co-transporter-2 inhibitors), bile acid preparations (e.g., 24-nor-ursodeoxycholic acid), farnesoid X receptor agonists (obeticholic acid, tropifexor), statins, acetylsalicylic acid. Combinations are superior to individual-drug schemes.Conclusion. The management of combined NAFLD-T2D requires a close inter-specialty involvement from hepatology, gastroenterology, endocrinology and cardiology. This interdisciplinary problem can be tackled through persuasive lifestyle recommendations and choosing rational medication strategies with a proved hepatoprotective efficacy.
Publisher
Russian Gastroenterolgocial Society
Reference81 articles.
1. Zemlyanitsyna O.V., Dunaeva I.P., Savenkov V.I., Sinaiko V.M., Maltseva Yu.V., Kravchun N.A.Non-alcoholicfatty liver disease:prevalence, etiology and pathogenesis, directions of diagnosis and therapy (literature review and own data). Int Endocrinol J. 2018;14(7):684–93 (In Russ.). DOI: 10.22141/2224-0721.14.7.2018.148777
2. Kondratyuk E.A., Bodnar P.N., Lisyaniy N.I., Belskaya L.N., Lisyanaya T.A., Ponomareva I.G. Features of dysbiotic disorders in patients with type 2 diabetes mellitus and non-alcoholic fatty liver disease. Family medicine. 2015;3(59):181 (In Russ.).
3. Diehl A.M., Day C. Cause, pathogenesis, and treatment of nonalcoholic steatohepatitis. N Engl J Med. 2017;377:2063–72. DOI: 10.1056/NEJMra1503519
4. Steinacher D., Claudel T., Trauner M. Therapeutic mechanisms of bile acids and nor-ursodeoxycholic acid in non-alcoholic fatty liverdisease. DigDis. 2017;35:282–7. DOI: 10.1159/000454853
5. Zein C.O., Yerian L.M., Gogate P., Lopez R., Kirwan J.P., Feldstein A.E., et.al.Pentoxifyllineimproves nonalcoholic steatohepatitis: a randomized placebo-con-trolled trial.Hepatology. 2011;54:1610–9. DOI: 10.1002/hep.24544