Validity of hemoglobin A1c for diagnosing diabetes among people with and without HIV in Uganda.


Journal

International journal of STD & AIDS
ISSN: 1758-1052
Titre abrégé: Int J STD AIDS
Pays: England
ID NLM: 9007917

Informations de publication

Date de publication:
04 2019
Historique:
pubmed: 5 2 2019
medline: 23 10 2019
entrez: 5 2 2019
Statut: ppublish

Résumé

Sub-Saharan Africa (SSA) is facing a growing co-epidemic of chronic HIV infection and diabetes. Hemoglobin A1c (A1c) may underestimate glycemia among people living with HIV (PLWH). We estimated the validity of A1c to diagnose diabetes among PLWH and HIV-uninfected persons in rural Uganda. Data were derived from a cohort of PLWH and age- and gender-matched HIV-uninfected comparators. We compared A1c to fasting blood glucose (FBG) using Pearson correlations, regression models, and estimated the sensitivity and specificity of A1c for detecting diabetes with FBG ≥126 mg/dL as reference standard. Approximately half (48%) of the 212 participants were female, mean age of 51.7 years (SD = 7.0) at enrollment. All PLWH (n = 118) were on antiretroviral therapy for a median of 7.5 years with mean CD4 cell count of 442 cells/µL. Mean FBG (89.7 mg/dL) and A1c (5.6%) were not different between PLWH and HIV-uninfected ( P > 0.50) groups, but the HIV-uninfected group had a higher prevalence of A1c >5.7% (33% vs. 20%, P = 0.024). We found a relatively strong correlation between A1c and FBG (r = 0.67). An A1c ≥6.5% had a poor sensitivity (46%, 95% CI 26-67%) but high specificity (98%, 95% CI 96-99%) for detecting diabetes. More work is needed to define an optimal A1c for screening diabetes in SSA.

Identifiants

pubmed: 30714875
doi: 10.1177/0956462418823406
pmc: PMC6719298
mid: NIHMS1047820
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
hemoglobin A1c protein, human 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

479-485

Subventions

Organisme : NIA NIH HHS
ID : R24 AG044325
Pays : United States
Organisme : NIMH NIH HHS
ID : K23 MH099916
Pays : United States
Organisme : FIC NIH HHS
ID : K43 TW010715
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG024409
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH113494
Pays : United States
Organisme : NHLBI NIH HHS
ID : R21 HL124712
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI060354
Pays : United States

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Auteurs

James Muchira (J)

1 University of Massachusetts Boston, College of Nursing and Health Sciences, Boston, MA, USA.

Eileen Stuart-Shor (E)

2 Beth Israel Deaconess Medical Center, Boston, MA, USA.

Jen Manne-Goehler (J)

3 Harvard T.H. Chan School of Public Health, Boston, MA, USA.
4 Massachusetts General Hospital, Boston, MA, USA.

Janet Lo (J)

4 Massachusetts General Hospital, Boston, MA, USA.
5 Harvard Medical School, Boston, MA, USA.

Alexander C Tsai (AC)

4 Massachusetts General Hospital, Boston, MA, USA.
5 Harvard Medical School, Boston, MA, USA.
6 Mbarara University of Science and Technology, Mbarara, Uganda.

Bernard Kakukire (B)

6 Mbarara University of Science and Technology, Mbarara, Uganda.

Samson Okello (S)

3 Harvard T.H. Chan School of Public Health, Boston, MA, USA.
6 Mbarara University of Science and Technology, Mbarara, Uganda.

Mark J Siedner (MJ)

4 Massachusetts General Hospital, Boston, MA, USA.
5 Harvard Medical School, Boston, MA, USA.
6 Mbarara University of Science and Technology, Mbarara, Uganda.

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