Subclinical Myocardial Fibrosis in South African Youth With HIV: Results From the CTAAC-Heart Study.

antiretroviral myocardial fibrosis myocardial magnetic resonance imaging perinatally acquired HIV youth with HIV

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 21 08 2024
accepted: 25 09 2024
medline: 17 10 2024
pubmed: 17 10 2024
entrez: 17 10 2024
Statut: epublish

Résumé

Few data exist on myocardial fibrosis and inflammation in youth with HIV. We performed cardiovascular magnetic resonance (CMR) on a cross section of South African youth: youth with perinatally acquired HIV (YPHIV) undergoing antiretroviral therapy (ART), youth with nonperinatally acquired HIV (YNPHIV) receiving ART, and youth without HIV. Quantile regression models were fit to assess the association between HIV status and CMR outcomes: subclinical fibrosis (late gadolinium enhancement [LGE] mass and fraction, native T1, extracellular volume) and inflammation (native T1, T2 mapping). Of 464 youth, 287 were YPHIV, 87 were YNPHIV, and 90 were HIV seronegative. The median age was 16 years (range, 11-24). LGE mass was higher in YPHIV and YNPHIV than in youth who were HIV seronegative (1.85 vs 2.00 vs 1.41 g, respectively), as was fraction (5.8% vs 6.4% vs 4.5%); native T1 was highest in YNPHIV. In adjusted analyses, when compared with youth with HIV seronegativity, YPHIV and YNPHIV exhibited higher LGE mass (β = 0.468, Despite ART use, YPHIV and YNPHIV appear to have higher subclinical myocardial fibrosis than youth who are HIV seronegative and healthy adults in South Africa and may benefit from early screening/monitoring for cardiovascular disease.

Sections du résumé

Background UNASSIGNED
Few data exist on myocardial fibrosis and inflammation in youth with HIV.
Methods UNASSIGNED
We performed cardiovascular magnetic resonance (CMR) on a cross section of South African youth: youth with perinatally acquired HIV (YPHIV) undergoing antiretroviral therapy (ART), youth with nonperinatally acquired HIV (YNPHIV) receiving ART, and youth without HIV. Quantile regression models were fit to assess the association between HIV status and CMR outcomes: subclinical fibrosis (late gadolinium enhancement [LGE] mass and fraction, native T1, extracellular volume) and inflammation (native T1, T2 mapping).
Results UNASSIGNED
Of 464 youth, 287 were YPHIV, 87 were YNPHIV, and 90 were HIV seronegative. The median age was 16 years (range, 11-24). LGE mass was higher in YPHIV and YNPHIV than in youth who were HIV seronegative (1.85 vs 2.00 vs 1.41 g, respectively), as was fraction (5.8% vs 6.4% vs 4.5%); native T1 was highest in YNPHIV. In adjusted analyses, when compared with youth with HIV seronegativity, YPHIV and YNPHIV exhibited higher LGE mass (β = 0.468,
Conclusions UNASSIGNED
Despite ART use, YPHIV and YNPHIV appear to have higher subclinical myocardial fibrosis than youth who are HIV seronegative and healthy adults in South Africa and may benefit from early screening/monitoring for cardiovascular disease.

Identifiants

pubmed: 39416995
doi: 10.1093/ofid/ofae555
pii: ofae555
pmc: PMC11482013
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofae555

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. All authors: No reported conflicts.

Auteurs

Jennifer Jao (J)

Division of Pediatric Infectious Diseases, Division of Adult Infectious Diseases, Department of Pediatrics, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

Heather J Zar (HJ)

Department of Pediatrics and Child Health and SA-MRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.

Morné Kahts (M)

Division of Cardiology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
University of Cape Town/South African Medical Research Council Extramural Unit on Intersection of Noncommunicable Diseases With Infectious Diseases.

Stephen Jermy (S)

University of Cape Town/South African Medical Research Council Extramural Unit on Intersection of Noncommunicable Diseases With Infectious Diseases.
Division of Biomedical Engineering, Department of Human Biology, University of Cape Town, Cape Town, South Africa.

Daniel Egan (D)

Division of Cardiology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
University of Cape Town/South African Medical Research Council Extramural Unit on Intersection of Noncommunicable Diseases With Infectious Diseases.

Mothabisi N Nyathi (MN)

Division of Epidemiology and Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.

Nana Akua Asafu-Agyei (NA)

Department of Pediatrics and Child Health and SA-MRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.

Justine Legbedze (J)

Division of Pediatric Infectious Diseases, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.

Emma Carkeek (E)

Department of Pediatrics and Child Health and SA-MRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.

Nomawethu Jele (N)

Department of Pediatrics and Child Health and SA-MRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.

Tafadzwa Mautsa (T)

Department of Pediatrics and Child Health and SA-MRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.

Lauren Balmert Bonner (LB)

Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

Grace A McComsey (GA)

Department of Medicine, Department of Pediatrics, Case Western Reserve University, Cleveland, Ohio, USA.

Matthew Feinstein (M)

Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Division of Adult Cardiology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

Irwin J Kurland (IJ)

Division of Adult Endocrinology, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA.

Landon Myer (L)

Division of Epidemiology and Biostatistics, School of Public Health, University of Cape Town, Cape Town, South Africa.

Ntobeko A B Ntusi (NAB)

Division of Cardiology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
University of Cape Town/South African Medical Research Council Extramural Unit on Intersection of Noncommunicable Diseases With Infectious Diseases.
African Research Universities Alliance/The Guild of European Research-Intensive Universities Cluster of Research Excellence on Noncommunicable Diseases and Associated Multimorbidity.

Classifications MeSH