Prospective International Study of Incidence and Predictors of Immune Reconstitution Inflammatory Syndrome and Death in People Living With Human Immunodeficiency Virus and Severe Lymphopenia.
AIDS
HIV
biomarkers
death
immune reconstitution inflammatory syndrome (IRIS)
Journal
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213
Informations de publication
Date de publication:
27 07 2020
27 07 2020
Historique:
received:
03
05
2019
accepted:
03
09
2019
pubmed:
11
9
2019
medline:
28
4
2021
entrez:
11
9
2019
Statut:
ppublish
Résumé
Patients living with human immunodeficiency virus (PLWH) with low CD4 counts are at high risk for immune reconstitution inflammatory syndrome (IRIS) and death at antiretroviral therapy (ART) initiation. We investigated the clinical impact of IRIS in PLWH and CD4 counts <100 cells/μL starting ART in an international, prospective study in the United States, Thailand, and Kenya. An independent review committee adjudicated IRIS events. We assessed associations between baseline biomarkers, IRIS, immune recovery at week 48, and death by week 48 with Cox models. We enrolled 506 participants (39.3% were women). Median age was 37 years, and CD4 count was 29 cells/μL. Within 6 months of ART, 97 (19.2%) participants developed IRIS and 31 (6.5%) died. Participants with lower hemoglobin at baseline were at higher IRIS risk (hazard ratio [HR], 1.2; P = .004). IRIS was independently associated with increased risk of death after adjustment for known risk factors (HR, 3.2; P = .031). Being female (P = .004) and having a lower body mass index (BMI; P = .003), higher white blood cell count (P = .005), and higher D-dimer levels (P = .044) were also significantly associated with increased risk of death. Decision-tree analysis identified hemoglobin <8.5 g/dL as predictive of IRIS and C-reactive protein (CRP) >106 μg/mL and BMI <15.6 kg/m2 as predictive of death. For PLWH with severe immunosuppression initiating ART, baseline low BMI and hemoglobin and high CRP and D-dimer levels may be clinically useful predictors of IRIS and death risk.
Sections du résumé
BACKGROUND
Patients living with human immunodeficiency virus (PLWH) with low CD4 counts are at high risk for immune reconstitution inflammatory syndrome (IRIS) and death at antiretroviral therapy (ART) initiation.
METHODS
We investigated the clinical impact of IRIS in PLWH and CD4 counts <100 cells/μL starting ART in an international, prospective study in the United States, Thailand, and Kenya. An independent review committee adjudicated IRIS events. We assessed associations between baseline biomarkers, IRIS, immune recovery at week 48, and death by week 48 with Cox models.
RESULTS
We enrolled 506 participants (39.3% were women). Median age was 37 years, and CD4 count was 29 cells/μL. Within 6 months of ART, 97 (19.2%) participants developed IRIS and 31 (6.5%) died. Participants with lower hemoglobin at baseline were at higher IRIS risk (hazard ratio [HR], 1.2; P = .004). IRIS was independently associated with increased risk of death after adjustment for known risk factors (HR, 3.2; P = .031). Being female (P = .004) and having a lower body mass index (BMI; P = .003), higher white blood cell count (P = .005), and higher D-dimer levels (P = .044) were also significantly associated with increased risk of death. Decision-tree analysis identified hemoglobin <8.5 g/dL as predictive of IRIS and C-reactive protein (CRP) >106 μg/mL and BMI <15.6 kg/m2 as predictive of death.
CONCLUSIONS
For PLWH with severe immunosuppression initiating ART, baseline low BMI and hemoglobin and high CRP and D-dimer levels may be clinically useful predictors of IRIS and death risk.
Identifiants
pubmed: 31504347
pii: 5560189
doi: 10.1093/cid/ciz877
pmc: PMC7384325
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
652-660Subventions
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States
Informations de copyright
Published by Oxford University Press for the Infectious Diseases Society of America 2019.
Références
PLoS Med. 2013;10(9):e1001510
pubmed: 24137103
Nat Rev Microbiol. 2012 Jan 09;10(2):150-6
pubmed: 22230950
N Engl J Med. 2015 Aug 27;373(9):795-807
pubmed: 26192873
N Engl J Med. 2017 Jul 20;377(3):233-245
pubmed: 28723333
Clin Infect Dis. 2018 Mar 4;66(suppl_2):S132-S139
pubmed: 29514234
Clin Infect Dis. 2011 Jun;52(11):1374-83
pubmed: 21596680
AIDS Res Ther. 2017 May 30;14(1):30
pubmed: 28558783
Clin Infect Dis. 2012 Feb 1;54(3):424-33
pubmed: 22095568
Biometrics. 2011 Mar;67(1):39-49
pubmed: 20377575
J Infect Dis. 2013 Dec 1;208(11):1784-93
pubmed: 23908475
N Engl J Med. 2014 Jun 26;370(26):2487-98
pubmed: 24963568
PLoS Med. 2008 Oct 21;5(10):e203
pubmed: 18942885
Cochrane Database Syst Rev. 2018 Jul 24;7:CD009012
pubmed: 30039850
Open Forum Infect Dis. 2016 Apr 06;3(2):ofw073
pubmed: 27191006
EBioMedicine. 2016 Jan 14;4:115-23
pubmed: 26981576
Stat Med. 2017 Nov 30;36(27):4391-4400
pubmed: 28913837
AIDS. 2017 Oct 23;31(16):2217-2225
pubmed: 28742529
AIDS. 2018 Nov 13;32(17):2525-2531
pubmed: 30289810
Clin Infect Dis. 2015 Apr 1;60(7):1120-7
pubmed: 25516189
Clin Infect Dis. 2016 Jun 15;62(12):1571-1577
pubmed: 27025828
N Engl J Med. 2011 Oct 20;365(16):1482-91
pubmed: 22010914
Lancet Infect Dis. 2010 Apr;10(4):251-61
pubmed: 20334848
N Engl J Med. 2018 Nov 15;379(20):1915-1925
pubmed: 30428290
J Infect Dis. 2018 Aug 14;218(6):922-926
pubmed: 29718342
AIDS. 2019 Apr 1;33(5):895-902
pubmed: 30649057
Curr Opin HIV AIDS. 2016 Mar;11(2):191-200
pubmed: 26720550
Lancet Public Health. 2017 Jan;2(1):e35-e46
pubmed: 29249478
Curr HIV/AIDS Rep. 2014 Sep;11(3):223-32
pubmed: 24950732
PLoS One. 2018 Jan 31;13(1):e0192030
pubmed: 29385208
Lancet. 2006 Mar 11;367(9513):817-24
pubmed: 16530575
Clin Infect Dis. 2018 Mar 5;66(6):893-903
pubmed: 29373672
N Engl J Med. 2015 Aug 27;373(9):808-22
pubmed: 26193126
PLoS One. 2018 Apr 20;13(4):e0195985
pubmed: 29677205
PLoS One. 2013 May 17;8(5):e63541
pubmed: 23691062
J Infect Dis. 2011 Jun 1;203(11):1637-46
pubmed: 21592994
PLoS Med. 2014 Sep 09;11(9):e1001718
pubmed: 25203931
Lancet HIV. 2016 Oct;3(10):e490-8
pubmed: 27658875