Discrimination and Calibration of the Veterans Aging Cohort Study Index 2.0 for Predicting Mortality Among People With Human Immunodeficiency Virus in North America

被引:18
|
作者
McGinnis, Kathleen A. [1 ]
Justice, Amy C. [1 ,2 ,3 ]
Moore, Richard D. [4 ]
Silverberg, Michael J. [5 ]
Althoff, Keri N. [4 ]
Karris, Maile [6 ]
Lima, Viviane D. [7 ]
Crane, Heidi M. [8 ]
Horberg, Michael A. [9 ]
Klein, Marina B. [10 ]
Gange, Stephen J. [4 ]
Gebo, Kelly A. [4 ]
Mayor, Angel [11 ]
Tate, Janet P. [1 ,2 ]
机构
[1] Vet Affairs Connecticut Healthcare Syst, 950 Campbell Ave, West Haven, CT 06516 USA
[2] Yale Sch Med, New Haven, CT USA
[3] Yale Sch Publ Hlth, New Haven, CT USA
[4] Johns Hopkins Univ, Baltimore, MD USA
[5] Kaiser Permanente Northern Calif, Oakland, CA USA
[6] Univ Calif San Diego, San Diego, CA 92103 USA
[7] Univ British Columbia, Vancouver, BC, Canada
[8] Univ Washington, Seattle, WA 98195 USA
[9] Kaiser Permanente Midatlantic Permanente Res Inst, Rockville, MD USA
[10] McGill Univ, Montreal, PQ, Canada
[11] Univ Cent Caribe, Bayamon, PR USA
基金
美国国家卫生研究院; 加拿大健康研究院; 美国医疗保健研究与质量局;
关键词
VACS Index 2.0; calibration; mortality; HIV; MYOCARDIAL-INFARCTION; RISK; THERAPY;
D O I
10.1093/cid/ciab883
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. The updated Veterans Aging Cohort Study (VACS) Index 2.0 combines general and human immunodeficiency virus (HIV)-specific biomarkers to generate a continuous score that accurately discriminates risk of mortality in diverse cohorts of persons with HIV (PWH), but a score alone is difficult to interpret. Using data from the North American AIDS Cohort Collaboration (NA-ACCORD), we translate VACS Index 2.0 scores into validated probability estimates of mortality. Methods. Because complete mortality ascertainment is essential for accurate calibration, we restricted analyses to cohorts with mortality from the National Death Index or equivalent sources. VACS Index 2.0 components were ascertained from October 1999 to April 2018. Mortality was observed up to March 2019. Calibration curves compared predicted (estimated by fitting a gamma model to the score) to observed mortality overall and within subgroups: cohort (VACS/NA-ACCORD subset), sex, age <50 or >= 50 years, race/ethnicity, HIV-1 RNA <= 500 or >500 copies/mL, CD4 count <350 or >= 350 cells/mu L, and years 1999-2009 or 2010-2018. Because mortality rates have decreased over time, the final model was limited to 2010-2018. Results. Among 37 230 PWH in VACS and 8061 PWH in the NA-ACCORD subset, median age was 53 and 44 years; 3% and 19% were women; and 48% and 39% were black. Discrimination in NA-ACCORD (C-statistic = 0.842 [95% confidence interval {CI},.830-.854]) was better than in VACS (C-statistic = 0.813 [95% CI,.809-.817]). Predicted and observed mortality largely overlapped in VACS and the NA-ACCORD subset, overall and within subgroups. Conclusions. Based on this validation, VACS Index 2.0 can reliably estimate probability of all-cause mortality, at various follow-up times, among PWH in North America.
引用
收藏
页码:297 / 304
页数:8
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