Insulin resistance and intestinal integrity in children with and without HIV infection in Uganda.


Journal

HIV medicine
ISSN: 1468-1293
Titre abrégé: HIV Med
Pays: England
ID NLM: 100897392

Informations de publication

Date de publication:
02 2020
Historique:
received: 06 06 2019
revised: 22 08 2019
accepted: 03 09 2019
pubmed: 24 10 2019
medline: 2 6 2021
entrez: 24 10 2019
Statut: ppublish

Résumé

The risk of cardiometabolic complications in children with perinatally acquired HIV infection (PHIVs) and in perinatally HIV-exposed but uninfected children (HEUs) and its relationship to systemic inflammation and markers of gut integrity are not well established. In this current study, we assed insulin resitance in PHIV compared to HEUs and HIV unexposed uninfected children and explored potential association with intestinal damage biomarkers. This was a cross-sectional study in PHIVs, HEUs and HIV-unexposed, uninfected children (HUUs) aged 2-10 years enrolled in Uganda. PHIVs were on stable antiretroviral therapy (ART) with HIV viral load  < 400 HIV-1 RNA copies/mL. Insulin resistance was estimated using the homeostasis model assessment of insulin resistance (HOMA-IR). We measured markers of systemic inflammation, monocyte activation and gut integrity. Kruskal-Wallis tests were used to compare markers by HIV status; Pearson correlation and multiple linear regressions were used to assess associations of the HOMA-IR index with biomarkers of intestinal damage and translocation. Overall, 172 participants were enrolled in the study (57 PHIVs, 59 HEUs and 56 HUUs). The median age was 7.8 [interquartile range (IQR) 6.39, 8.84] years, 55% were female and the median body mass index (BMI) was 15 (IQR 14.3, 15.8) kg/m Despite viral suppression, Ugandan PHIVs have disturbances in glucose metabolism. Higher BMI, and not immune activation or alteration of gut integrity, was associated with insulin resistance in this population.

Identifiants

pubmed: 31642582
doi: 10.1111/hiv.12808
pmc: PMC6980894
mid: NIHMS1051689
doi:

Substances chimiques

Cholesterol, HDL 0
Triglycerides 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-127

Subventions

Organisme : NICHD NIH HHS
ID : K23 HD088295
Pays : United States
Organisme : NIDDK NIH HHS
ID : R21 DK118757
Pays : United States
Organisme : Eunice Kennedy Shriver National Institute of Child Health and Human Development
ID : K23HD088295-01A1
Pays : International

Informations de copyright

© 2019 British HIV Association.

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Auteurs

S Dirajlal-Fargo (S)

University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
Case Western Reserve University, Cleveland, OH, USA.

L Shan (L)

Case Western Reserve University, Cleveland, OH, USA.

A Sattar (A)

Case Western Reserve University, Cleveland, OH, USA.

E Bowman (E)

Ohio State University School of Health and Rehabilitation Sciences, Columbus, OH, USA.

J Gabriel (J)

Ohio State University School of Health and Rehabilitation Sciences, Columbus, OH, USA.

M Kulkarni (M)

Ohio State University School of Health and Rehabilitation Sciences, Columbus, OH, USA.

N Funderburg (N)

Ohio State University School of Health and Rehabilitation Sciences, Columbus, OH, USA.

R Nazzinda (R)

Joint Clinical Research Centre, Makerere University, Kampala, Uganda.

V Musiime (V)

Joint Clinical Research Centre, Makerere University, Kampala, Uganda.

G A McComsey (GA)

University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Rainbow Babies and Children's Hospital, Cleveland, OH, USA.
Case Western Reserve University, Cleveland, OH, USA.

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Classifications MeSH