Nonalcoholic Fatty Liver Disease Risk Factors Affect Liver-Related Outcomes After Direct-Acting Antiviral Treatment for Hepatitis C
Liver Cancer
Male
Genotype
Clinical Sciences
Chronic Liver Disease and Cirrhosis
610
Clinical sciences
Hepacivirus
Direct-acting antivirals
Antiviral Agents
Hepatitis
Rare Diseases
Hepatitis - C
Non-alcoholic Fatty Liver Disease
Risk Factors
Fatty liver
616
Diabetes Mellitus
Humans
Obesity
Metabolic and endocrine
Nutrition
Cancer
Aged
Retrospective Studies
2. Zero hunger
Biomedical and Clinical Sciences
Gastroenterology & Hepatology
Liver Disease
Diabetes
Middle Aged
Hepatitis C
3. Good health
Infectious Diseases
Emerging Infectious Diseases
Good Health and Well Being
Female
Digestive Diseases
DOI:
10.1007/s10620-020-06457-2
Publication Date:
2020-07-11T06:02:33Z
AUTHORS (7)
ABSTRACT
Introduction: In hepatitis C (HCV) patients, obesity and/or diabetes may increase the risk of liver-related outcomes. We aimed to determine whether diabetes and/or obesity are associated with adverse outcomes in direct-acting antiviral (DAA)-treated HCV patients. Methods: We conducted a retrospective study of 33,003 HCV-infected, DAA-treated Veterans between 2013 and 2015. Body mass index was used to categorize patients into underweight (< 18.5 kg/m2), normal weight (18.5 to < 25 kg/m2), overweight (25 to < 30 kg/m2), obesity I (30 to < 35 kg/m2), and obesity II–III (> 35 kg/m2). Diabetes was defined by ICD-9/10 codes in association with hemoglobin A1c > 6.5% or medication prescriptions. Patients were followed from 180 days post-DAA initiation until 2/14/2019 to assess for development of cirrhosis, decompensations, hepatocellular carcinoma (HCC), and death. Multivariable Cox proportional hazards regression models were used to determine the association between diabetes and/or obesity and outcomes. Results: During a mean follow-up of 3 years, 10.1% patients died, 5.0% were newly diagnosed with cirrhosis, 4.7% had a decompensation and 4.0% developed HCC. Diabetes was associated with an increased risk of mortality (AHR = 1.25, 95% CI 1.10–1.42), cirrhosis (AHR = 1.31, 95% CI 1.16–1.48), decompensation (AHR = 1.74, 95% CI 1.31–2.31), and HCC (AHR = 1.32, 95% CI 1.01–1.72) among patients without baseline cirrhosis. Compared to normal-weight persons, obese persons had a higher risk of cirrhosis, but overweight and obese persons had lower risk of mortality and HCC. Conclusions: In this large DAA-treated Veterans cohort, pre-DAA diabetes increases mortality and liver-related events independent of SVR. Continued vigilance is warranted in patients with diabetes despite SVR. Elevated BMI categories appear to have improved outcomes, although further studies are needed to understand those associations.
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CITATIONS (27)
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