Sex difference in liver-related mortality and transplantation associated with dietary cholesterol in chronic hepatitis C virus infection
Yu L, Morishima C, Ioannou GN
The British journal of nutrition · 1 citation
Review labels
Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.
How it was studied
- Design
- Cohort study (indexed by PubMed)
- Studied in
- People
- Main outcome
- Clinical events such as disease or death
- Intake measured by
- Food frequency questionnaire
Who paid for it
- Funding
- Independent funding
- Government
- U.S. Department of Veterans Affairs
- Government
- Office of Research and Development
- Government
- National Institute of Diabetes and Digestive and Kidney Diseases
Based on 3 listed funder(s).
Publication
- Published
- 2015-11-06 · Br J Nutr · vol. 115 · issue 2 · pp. 193–201
- Publisher
- Cambridge University Press
- Cited
- 3 citations · more than 51% of similar papers · 0.1× the field average
- References
- 42 works
- Access
- Free to read
- Research areas
- Hepatitis C virus research · Liver Disease Diagnosis and Treatment · Liver Disease and Transplantation
- Keywords
- Liver transplantation, Cholesterol, Virus, Transplantation, Internal medicine, Medicine, Virology, Chronic hepatitis, Biology, Gastroenterology
- MeSH
- humans, hepatitis c, chronic, liver cirrhosis, cholesterol, dietary, antiviral agents, liver transplantation, risk factors, retrospective studies, cohort studies, sex factors, energy intake, middle aged, female, male
3 authors
From US
- Lei Yu · correspondingUniversity of Washington
- Chihiro MorishimaUniversity of Washington; University of Washington Applied Physics Laboratory
- George N. IoannouUniversity of Washington; VA Puget Sound Health Care System
Abstract
Dietary cholesterol induces hepatic inflammation and fibrosis in animals. We aimed to determine whether dietary cholesterol affects liver-related mortality in hepatitis C virus (HCV)-infected patients. We performed a retrospective cohort study using extended follow-up data from the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis Trial. The study included HCV patients with advanced fibrosis and compensated cirrhosis. The analysis included 657 patients who completed two FFQ. We assessed whether cholesterol intake, measured in mg/4184 kJ (mg/1000 kcal) of energy intake, was associated with liver-related death or transplantation. In 4·7 (sd 1·6) years, the incidence of liver-related death (n 46) or transplantation (n 52) was 31·8/1000 person-years. The relationship between cholesterol intake and liver-related death or transplantation was significantly different between men and women (test for interaction, P value=0·01). Each higher quartile of cholesterol intake was associated with an increased risk for liver-related death or transplantation in women (adjusted hazard ratio (AHR) 1·83; 95 % CI 1·12, 2·99; P trend=0·02), but not in men (AHR 0·96; 95 % CI 0·76, 1·22; P trend=0·73). Compared with women whose cholesterol intake was within the recommended guidelines (300 mg/d with a 8368 kJ (2000 kcal) diet), women who consumed more cholesterol had significantly increased risk for liver-related death or transplantation (AHR 4·04; 95 % CI 1·42, 11·5). High dietary cholesterol was associated with an increased risk for liver-related death and transplantation in HCV-infected women with advanced fibrosis or compensated cirrhosis. Future studies should assess whether reducing cholesterol intake, among women who consume an excessive amount, can decrease HCV-related mortality.
Abstract via Europe PMC. Copyright remains with the authors or publisher.
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