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. 2017 Jan;51(1):70-76.
doi: 10.1097/MCG.0000000000000566.

Diabetes Mellitus is Associated With Higher Risk of Developing Decompensated Cirrhosis in Chronic Hepatitis C Patients

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Diabetes Mellitus is Associated With Higher Risk of Developing Decompensated Cirrhosis in Chronic Hepatitis C Patients

Mohammed J Saeed et al. J Clin Gastroenterol. 2017 Jan.

Abstract

Goals: To investigate the association of diabetes with risk of decompensated cirrhosis in patients with chronic hepatitis C (CHC).

Background: Direct-acting antivirals are highly effective in treating CHC but very expensive. CHC patients at high risk of progression to symptomatic liver disease may benefit most from early treatment.

Study: We conducted a retrospective cohort study using the 2006 to 2013 Truven Health Analytics MarketScan Commercial Claims and Encounters database including inpatient, outpatient, and pharmacy claims from private insurers. CHC and cirrhosis were identified using ICD-9-CM diagnosis codes; baseline diabetes was identified by diagnosis codes or antidiabetic medications. CHC patients were followed to identify decompensated cirrhosis. Multivariable Cox proportional hazards regression was used to model the risk of decompensated cirrhosis by baseline cirrhosis.

Results: There were 75,805 CHC patients with median 1.9 years follow-up. A total of 10,317 (13.6%) of the CHC population had diabetes. The rates of decompensated cirrhosis per 1000 person-years were: 185.5 for persons with baseline cirrhosis and diabetes, 119.8 for persons with cirrhosis and no diabetes, 35.3 for persons with no cirrhosis and diabetes, and 17.1 for persons with no cirrhosis and no diabetes. Diabetes was associated with increased risk of decompensated cirrhosis in persons with baseline cirrhosis (adjusted hazard ratio=1.4; 95% confidence interval, 1.3-1.6) and in persons without baseline cirrhosis (adjusted hazard ratio=1.9; 95% confidence interval, 1.7-2.1).

Conclusions: In a privately insured US population with CHC, the adjusted risk of decompensated cirrhosis was higher in diabetic compared with nondiabetic patients. Diabetes status should be included in prioritization of antiviral treatment.

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Conflict of interest statement

MJS declares no conflict of interest. MAO has done consulting work for Merck, Pfizer and Sanofi-Pasteur. WGP has done consulting work for Merck and Abbvie. RMP declares no conflict of interest.

Figures

Figure 1
Figure 1
Illustration of Study Design Chronic hepatitis C was defined by ICD-9-CM diagnosis codes: having ≥1 inpatient facility code for chronic hepatitis, or having ≥1 hepatitis C code (acute or chronic) followed by a chronic hepatitis C code >30 and ≤180 days apart on outpatient or provider claims. Decompensated cirrhosis included any of: bleeding esophageal varices, ascites, hepatic encephalopathy, hepatocellular carcinoma, spontaneous bacterial peritonitis or hepatorenal syndrome.
Figure 2
Figure 2
Algorithm with Inclusion/Exclusion Criteria to Identify Patients with Chronic Hepatitis C from Health Insurer Claims Data *The baseline period was defined as the first 6 months beginning on the date when chronic hepatitis C definition was met
Figure 3
Figure 3
Kaplan-Meier Curves of Decompensated Cirrhosis-free Survival Stratified by Cirrhosis and Diabetes at Baseline Decompensated cirrhosis included any of: bleeding esophageal varices, ascites, hepatic encephalopathy, hepatocellular carcinoma, spontaneous bacterial peritonitis or hepatorenal syndrome. Neither= neither cirrhosis nor diabetes, both= both cirrhosis and diabetes

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References

    1. Armstrong GL, Wasley A, Simard EP, et al. The prevalence of hepatitis C virus infection in the United States, 1999 through 2002. Ann Intern Med. 2006;144:705–714. - PubMed
    1. Shakil AO, Conry-Cantilena C, Alter HJ, et al. Volunteer blood donors with antibody to hepatitis C virus: clinical biochemical, virologic, histologic features. The Hepatitis C Study Group. Ann Intern Med. 1995;123:330–337. - PubMed
    1. Alter MJ, Margolis HS, Krawczynski K, et al. The natural history of community-acquired hepatitis C in the United States. The Sentinel Counties Chronic non-A, non-B Hepatitis Study Team. N Engl J Med. 1992;327:1899–1905. - PubMed
    1. Esteban JI, Lopez-Talavera JC, Genesca J, et al. High rate of infectivity and liver disease in blood donors with antibodies to hepatitis C virus. Ann Intern Med. 1991;115:443–449. - PubMed
    1. Seeff LB, Buskell-Bales Z, Wright EC, et al. Long-term mortality after transfusion-associated non-A, non-B hepatitis. The National Heart, Lung, and Blood Institute Study Group. N Engl J Med. 1992;327:1906–1911. - PubMed

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