4.4 Article

Serious clinical events in HIV-positive persons with chronic kidney disease

期刊

AIDS
卷 33, 期 14, 页码 2173-2188

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0000000000002331

关键词

chronic kidney disease; chronic kidney disease; HIV; modifiable risk factors; prognosis; renal; serious clinical events

资金

  1. Highly Active Antiretroviral Therapy Oversight Committee (HAART-OC)
  2. Danish National Research Foundation (CHIP) [DNRF126]
  3. Dutch Ministry of Health, Welfare and Sport through the Center for Infectious Disease Control of the National Institute for Public Health and the Environment
  4. Agence nationale de recherches sur le sida et les hepatites virales (ANRS) [7]
  5. Asia Pacific HIV Observational Database, a program of The Foundation for AIDS Research, amfAR
  6. U.S. National Institutes of Health's National Institute of Allergy and Infectious Diseases (NIAID) [U01-AI069907]
  7. Merck Sharp Dohme
  8. Gilead Sciences
  9. Bristol-Myers Squibb
  10. Boehringer Ingelheim
  11. Janssen-Cilag
  12. ViiV Healthcare
  13. Australian Government Department of Health and Ageing
  14. Faculty of Medicine, The University of New South Wales
  15. Fondo de Investigacion Sanitaria [FIS 99/0887]
  16. Fundacion para la Investigacion y la Prevencion del SIDA en Espana [FIPSE 3171/00]
  17. National Institute of Allergy and Infectious Diseases, National Institutes of Health [5U01AI042170-10, 5U01AI046362-03]
  18. European Union's Seventh Framework Programme for research, technological development and demonstration under EuroCoord grant [260694]
  19. Janssen RD
  20. Merck and Co. Inc.
  21. Pfizer Inc.
  22. GlaxoSmithKline LLC [Swiss National Science Foundation] [108787]
  23. AbbVie
  24. GlaxoSmithKline
  25. Pfizer
  26. Janssen Pharmaceuticals
  27. Swiss National Science Foundation [148522]
  28. Danish National Research Foundation (PERSIMUNE) [DNRF126]

向作者/读者索取更多资源

Objectives: Predictors of chronic kidney disease (CKD) amongst HIV-positive persons are well established, but insights into the prognosis after CKD including the role of modifiable risk factors are limited. Design: Prospective cohort study. Methods: D:A:D participants developing CKD (confirmed, >3 months apart, eGFR <= 60 ml/min per 1.73 m 2 or 25% eGFR decrease when eGFR <= 60 ml/min per 1.73 m(2)) were followed to incident serious clinical events (SCE); end stage renal and liver disease (ESRL and ESLD), cardiovascular disease (CVD), AIDS-defining and non-AI DS-defining malignancies (NADM), other AIDS or death, 6 months after last visit or 1 February 2016. Poisson regression models considered associations between SCE and modifiable risk factors. Results: During 2.7 (IQR 1.1-5.1) years median follow-up 595 persons with CKD (24.1%) developed a SCE [incidence rate 68.9/1000 PYFU (95% confidence interval 63.4-74.4)] with 8.3% (6.9-9.0) estimated to experience any SCE at 1 year. The most common SCE was death (12.7%), followed by NADM (5.8%), CVD (5.6%), other AIDS (5.0%) and ESRD (2.9%). Crude SCE ratios were significantly higher in those with vs. without CKD, strongest for ESRD [65.9 (43.8-100.9)] and death [4.8 (4.3-5.3)]. Smoking was consistently associated with all CKD-related SCE. Diabetes predicted CVD, NADM and death, whereas dyslipidaemia was only significantly associated with CVD. Poor HIV-status predicted other AIDS and death, eGFR less than 30 ml/min per 1.73 m(2) predicted CVD and death and low BMI predicted other AIDS and death. Conclusion: In an era where many HIV-positive persons require less monitoring because of efficient antiretroviral treatment, persons with CKD carry a high burden of SCE. Several potentially modifiable risk factors play a central role for CKD-related morbidity and mortality. Copyright (C) 2019 Wolters Kluwer Health, Inc. All rights reserved.

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