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      Acarbose Use and Liver Injury in Diabetic Patients With Severe Renal Insufficiency and Hepatic Diseases: A Propensity Score-Matched Cohort Study

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          Abstract

          Background: Acarbose has been deemed contraindicated in diabetic patients with chronic kidney disease (CKD) or end-stage renal disease (ESRD), but such use is not uncommon. We tested whether this concept hold true in this population with different background hepatic diseases.

          Methods: All incident diabetic patients ( n = 2,036,531) with stage 5 CKD/ESRD were enrolled from Taiwan between 2017 and 2013 and divided into those without chronic liver disease (CLD), with CLD but without cirrhosis, and those with cirrhosis. Among each group, acarbose users, defined as cumulative use >30 days within the preceding year, were propensity-score matched 1:2 to non-users. Our main outcome was the development of liver injury events during follow-up.

          Results: Acarbose users did not exhibit an increased incidence of liver injury during follow-up compared to non-users (hazard ratio and 95% confidence interval, 1.04 [0.88–1.25], 0.97 [0.61–1.56], and 0.71 [0.33–1.54] among those without CLD, with CLD but without cirrhosis, and those with cirrhosis, respectively), after adjusting for demographic profiles, comorbidities, potentially hepatotoxic medication use, and diabetic severity.

          Conclusions: The incidence of liver injury did not increase significantly among diabetic acarbose users with severe renal insufficiency than non-users, regardless of the presence or absence of chronic liver disease. Our findings support the renaissance of acarbose as a useful adjunct in diabetic patients with stage 5 and 5D chronic kidney disease.

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          Most cited references36

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          Global guideline for type 2 diabetes.

          (2014)
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            Spectrum of liver disease in type 2 diabetes and management of patients with diabetes and liver disease.

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              Prevalence of chronic liver disease and cirrhosis by underlying cause in understudied ethnic groups: The multiethnic cohort.

              Chronic liver disease (CLD) and cirrhosis are major sources of morbidity and mortality in the United States. Little is known about the epidemiology of these two diseases in ethnic minority populations in the United States. We examined the prevalence of CLD and cirrhosis by underlying etiologies among African Americans, Native Hawaiians, Japanese Americans, Latinos, and whites in the Multiethnic Cohort. CLD and cirrhosis cases were identified using Medicare claims between 1999 and 2012 among the fee-for-service participants (n = 106,458). We used International Classification of Diseases Ninth Revision codes, body mass index, history of diabetes mellitus, and alcohol consumption from questionnaires to identify underlying etiologies. A total of 5,783 CLD (3,575 CLD without cirrhosis and 2,208 cirrhosis) cases were identified. The prevalence of CLD ranged from 3.9% in African Americans and Native Hawaiians to 4.1% in whites, 6.7% in Latinos, and 6.9% in Japanese. Nonalcoholic fatty liver disease (NAFLD) was the most common cause of CLD in all ethnic groups combined (52%), followed by alcoholic liver disease (21%). NAFLD was the most common cause of cirrhosis in the entire cohort. By ethnicity, NAFLD was the most common cause of cirrhosis in Japanese Americans, Native Hawaiians, and Latinos, accounting for 32% of cases. Alcoholic liver disease was the most common cause of cirrhosis in whites (38.2%), while hepatitis C virus was the most common cause in African Americans (29.8%).
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                07 August 2018
                2018
                : 9
                : 860
                Affiliations
                [1] 1Department of Medicine, National Taiwan University Hospital BeiHu Branch , Taipei, Taiwan
                [2] 2Nephrology Division, Department of Internal Medicine, National Taiwan University Hospital , Taipei, Taiwan
                [3] 3Geriatric and Community Medicine Research Center, National Taiwan University Hospital BeiHu Branch , Taipei, Taiwan
                [4] 4College of Public Health, Institute of Epidemiology and Preventive Medicine, National Taiwan University , Taipei, Taiwan
                Author notes

                Edited by: Raffaele Capasso, Università degli Studi di Napoli Federico II, Italy

                Reviewed by: M. Isabel Lucena, Universidad de Málaga, Spain; Francois Verrey, Universität Zürich, Switzerland

                *Correspondence: Kuo-Liong Chien klchien@ 123456ntu.edu.tw

                This article was submitted to Gastrointestinal and Hepatic Pharmacology, a section of the journal Frontiers in Pharmacology

                Article
                10.3389/fphar.2018.00860
                6090209
                30131698
                55def549-b74a-453d-a4ad-71932233ba2c
                Copyright © 2018 Chao, Wang, Huang and Chien.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 May 2018
                : 16 July 2018
                Page count
                Figures: 2, Tables: 9, Equations: 0, References: 46, Pages: 15, Words: 8765
                Categories
                Pharmacology
                Original Research

                Pharmacology & Pharmaceutical medicine
                acarbose,chronic kidney disease,diabetes mellitus,drug-induced liver injury,end-stage renal disease,hepatotoxicity

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