Development and Validation of a Model for Prediction of End-Stage Liver Disease in People With HIV

被引:2
作者
Kim, H. Nina [1 ]
Nance, Robin M. [1 ]
Lo Re, Vincent, III [2 ]
Silverberg, Michael J. [3 ]
Franco, Ricardo [4 ]
Sterling, Timothy R. [5 ]
Cachay, Edward R. [6 ]
Horberg, Michael A. [7 ]
Althoff, Keri N. [8 ]
Justice, Amy C. [9 ,10 ]
Moore, Richard D. [8 ]
Klein, Marina [11 ]
Crane, Heidi M. [1 ]
Delaney, Joseph A. [1 ,12 ]
Kitahata, Mari M. [1 ]
机构
[1] Univ Washington, Dept Med, Seattle, WA 98104 USA
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Kaiser Permanente Northern Calif, Div Res, Oakland, CA USA
[4] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[6] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[7] Kaiser Permanente Midatlantic States, Res Inst, Rockville, MD USA
[8] Johns Hopkins Univ, Dept Med, Dept Epidemiol, Baltimore, MD USA
[9] Yale Univ Sch Med & Publ Hlth, Dept Med, New Haven, CT USA
[10] Vet Adm Connecticut Healthcare Syst, West Haven, CT USA
[11] McGill Univ, Dept Med, Hlth Ctr, Montreal, PQ, Canada
[12] Univ Manitoba, Coll Pharm, Winnipeg, MB, Canada
基金
美国医疗保健研究与质量局; 加拿大健康研究院; 美国国家卫生研究院;
关键词
end-stage liver disease; prediction; HEPATITIS-C VIRUS; SIMPLE NONINVASIVE INDEX; ALCOHOL-USE; SIGNIFICANT FIBROSIS; CIRRHOSIS; RISK; OUTCOMES; INFECTION; COHORT; PROGRESSION;
D O I
10.1097/QAI.0000000000002886
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: End-stage liver disease (ESLD) is a leading cause of non-AIDS-related death among people with HIV (PWH). Factors that increase the progression of liver disease include comorbidities and HIV-specific factors, but we currently lack a tool to apply this evidence into clinical practice. Methods: We developed and validated a risk prediction model for ESLD among PWH who received care in 12 cohorts of the North American AIDS Cohort Collaboration on Research and Design between 2000 and 2016 and had fibrosis-4 index > 1.45. The first occurrence of ascites, variceal bleed, spontaneous bacterial peritonitis, or hepatic encephalopathy was verified by standardized medical record review. The Bayesian model averaging was used to select predictors among biomarkers and diagnoses and the Harrell C statistic to assess model discrimination. Results: Among 13,787 PWH in the training set, 82% were men and 54% were Black with a mean age of 48 years. Three hundred ninety ESLD events occurred over a mean 5.4 years. Among the ESLD cases, 52% had hepatitis C virus, 15% hepatitis B virus, and 31% alcohol use disorder. Twelve factors together predicted ESLD risk moderately well (C statistic 0.79, 95% confidence interval: 0.76 to 0.81): age, sex, race/ethnicity, chronic hepatitis B or C, and routinely collected laboratory values reflecting hepatic impairment (serum albumin, aspartate aminotransferase, total bilirubin, and platelets) and lipid metabolism (triglycerides, high-density lipoprotein, and total cholesterol). Our model performed well in the test set (C statistic 0.81, 95% confidence interval: 0.76 to 0.86). Conclusion: This model of readily accessible clinical parameters predicted ESLD in a large diverse population of PWH.
引用
收藏
页码:396 / 404
页数:9
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