PMID- 25265230 OWN - NLM STAT- MEDLINE DCOM- 20150601 LR - 20211021 IS - 1473-5571 (Electronic) IS - 0269-9370 (Print) IS - 0269-9370 (Linking) VI - 28 IP - 16 DP - 2014 Oct 23 TI - Opportunistic infections and AIDS malignancies early after initiating combination antiretroviral therapy in high-income countries. PG - 2461-73 LID - 10.1097/QAD.0000000000000456 [doi] AB - BACKGROUND: There is little information on the incidence of AIDS-defining events which have been reported in the literature to be associated with immune reconstitution inflammatory syndrome (IRIS) after combined antiretroviral therapy (cART) initiation. These events include tuberculosis, mycobacterium avium complex (MAC), cytomegalovirus (CMV) retinitis, progressive multifocal leukoencephalopathy (PML), herpes simplex virus (HSV), Kaposi sarcoma, non-Hodgkin lymphoma (NHL), cryptococcosis and candidiasis. METHODS: We identified individuals in the HIV-CAUSAL Collaboration, which includes data from six European countries and the US, who were HIV-positive between 1996 and 2013, antiretroviral therapy naive, aged at least 18 years, had CD4 cell count and HIV-RNA measurements and had been AIDS-free for at least 1 month between those measurements and the start of follow-up. For each AIDS-defining event, we estimated the hazard ratio for no cART versus less than 3 and at least 3 months since cART initiation, adjusting for time-varying CD4 cell count and HIV-RNA via inverse probability weighting. RESULTS: Out of 96 562 eligible individuals (78% men) with median (interquantile range) follow-up of 31 [13,65] months, 55 144 initiated cART. The number of cases varied between 898 for tuberculosis and 113 for PML. Compared with non-cART initiation, the hazard ratio (95% confidence intervals) up to 3 months after cART initiation were 1.21 (0.90-1.63) for tuberculosis, 2.61 (1.05-6.49) for MAC, 1.17 (0.34-4.08) for CMV retinitis, 1.18 (0.62-2.26) for PML, 1.21 (0.83-1.75) for HSV, 1.18 (0.87-1.58) for Kaposi sarcoma, 1.56 (0.82-2.95) for NHL, 1.11 (0.56-2.18) for cryptococcosis and 0.77 (0.40-1.49) for candidiasis. CONCLUSION: With the potential exception of mycobacterial infections, unmasking IRIS does not appear to be a common complication of cART initiation in high-income countries. CI - 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins CN - The HIV-CAUSAL Collaboration FAU - Lodi, Sara AU - Lodi S AD - Centro Nacional de Epidemiologia, Instituto de Salud Carlos III, Madrid, Spain AD - Harvard School of Public Health, Boston, Massachusetts, US FAU - del Amo, Julia AU - del Amo J AD - Centro Nacional de Epidemiologia, Instituto de Salud Carlos III, Madrid, Spain AD - CIBERESP, Instituto de Salud Carlos III, Madrid, Spain FAU - Moreno, Santiago AU - Moreno S AD - Ramon y Cajal Hospital, Madrid, Spain AD - University of Alcala de Henares, Madrid, Spain FAU - Bucher, Heiner C AU - Bucher HC AD - Basel Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, Switzerland FAU - Furrer, Hansjakob AU - Furrer H AD - Department of Infectious Diseases, Bern University Hospital and University of Bern, Switzerland FAU - Logan, Roger AU - Logan R AD - Harvard School of Public Health, Boston, Massachusetts, US FAU - Sterne, Jonathan AU - Sterne J AD - Bristol University, United Kingdom FAU - Perez-Hoyos, Santiago AU - Perez-Hoyos S AD - CIBERESP, Instituto de Salud Carlos III, Madrid, Spain AD - Vall d'Hebron Research Institute, Barcelona, Spain FAU - Jarrin, Inma AU - Jarrin I AD - Centro Nacional de Epidemiologia, Instituto de Salud Carlos III, Madrid, Spain AD - CIBERESP, Instituto de Salud Carlos III, Madrid, Spain FAU - Phillips, Andrew AU - Phillips A AD - University College London, United Kingdom FAU - Olson, Ashley AU - Olson A AD - Medical Research Council, Clinical Trials Unit in University College of London, London, United Kingdom FAU - van Sighem, Ard AU - van Sighem A AD - Stichting HIV Monitoring, Amsterdam, the Netherlands FAU - Reiss, Peter AU - Reiss P AD - Stichting HIV Monitoring, Amsterdam, the Netherlands FAU - Sabin, Caroline AU - Sabin C AD - University College London, United Kingdom FAU - Jose, Sophie AU - Jose S AD - University College London, United Kingdom FAU - Justice, Amy AU - Justice A AD - Yale University School of Medicine, New Haven, Connecticut AD - VA Connecticut Healthcare System, West Haven FAU - Goulet, Joseph AU - Goulet J AD - VA Connecticut Healthcare System, West Haven FAU - Miro, Jose M AU - Miro JM AD - Hospital Clinic - IDIBAPS, University of Barcelona, Barcelona, Spain FAU - Ferrer, Elena AU - Ferrer E AD - Bellvitge-IDIBELL Hospital, University of Barcelona, L'Hospitalet de Llobregat, Spain FAU - Meyer, Laurence AU - Meyer L AD - Univ Paris Sud, UMR 1018, le Kremlin Bicetre, France AD - Inserm, UMR 1018, le Kremlin Bicetre, France AD - AP-HP, Hopital de Bicetre, Service de Sante Publique, le Kremlin Bicetre, France FAU - Seng, Remonie AU - Seng R AD - Inserm, UMR 1018, le Kremlin Bicetre, France AD - AP-HP, Hopital de Bicetre, Service de Sante Publique, le Kremlin Bicetre, France FAU - Vourli, Georgia AU - Vourli G AD - Athens University Medical School, Athens, Greece FAU - Antoniadou, Anastasia AU - Antoniadou A AD - Athens University Medical School, Attikon Hospital, Athens, Greece FAU - Dabis, Francois AU - Dabis F AD - Universite Victor Segalen Bordeaux 2, Bordeaux, France FAU - Vandenhede, Mari-Anne AU - Vandenhede MA AD - Universite Victor Segalen Bordeaux 2, Bordeaux, France FAU - Costagliola, Dominique AU - Costagliola D AD - Sorbonne Universites, UPMC Univ Paris 06, UMR_S 1136, Institut Pierre Louis d'Epidemiologie et de Sante Publique, F-75013, Paris, France AD - INSERM, UMR_S 1136, Institut Pierre Louis d'Epidemiologie et de Sante Publique, F-75013, Paris, France FAU - Abgrall, Sophie AU - Abgrall S AD - Sorbonne Universites, UPMC Univ Paris 06, UMR_S 1136, Institut Pierre Louis d'Epidemiologie et de Sante Publique, F-75013, Paris, France AD - INSERM, UMR_S 1136, Institut Pierre Louis d'Epidemiologie et de Sante Publique, F-75013, Paris, France AD - AP-HP, Hopital Avicenne, Service des maladies infectieuses et tropicales, Bobigny, France FAU - Hernan, Miguel A AU - Hernan MA AD - Harvard School of Public Health, Boston, Massachusetts, US AD - Harvard-MIT Division of Health Sciences and Technology, Boston, US LA - eng GR - R01 AI102634/AI/NIAID NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - England TA - AIDS JT - AIDS (London, England) JID - 8710219 RN - 0 (Anti-Retroviral Agents) SB - IM MH - AIDS-Related Opportunistic Infections/*epidemiology MH - Adolescent MH - Adult MH - Aged MH - Anti-Retroviral Agents/*therapeutic use MH - Antiretroviral Therapy, Highly Active/*methods MH - Developed Countries MH - Europe MH - Female MH - HIV Infections/*drug therapy MH - Humans MH - Incidence MH - Male MH - Middle Aged MH - Neoplasms/*epidemiology MH - United States MH - Young Adult PMC - PMC4495885 MID - NIHMS697193 EDAT- 2014/09/30 06:00 MHDA- 2015/06/02 06:00 PMCR- 2015/10/23 CRDT- 2014/09/30 06:00 PHST- 2014/09/30 06:00 [entrez] PHST- 2014/09/30 06:00 [pubmed] PHST- 2015/06/02 06:00 [medline] PHST- 2015/10/23 00:00 [pmc-release] AID - 00002030-201410230-00014 [pii] AID - 10.1097/QAD.0000000000000456 [doi] PST - ppublish SO - AIDS. 2014 Oct 23;28(16):2461-73. doi: 10.1097/QAD.0000000000000456.