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Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria

Background. Human immunodeficiency virus (HIV) infection and the use of antiretroviral therapy (ART) may increase the risk of type 2 diabetes mellitus (T2DM). However, data from regions with a high burden of HIV/AIDS are limited. We determined the prevalence of T2DM at the time of presentation to a...

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Autores principales: Isa, Samson E., Oche, Agbaji O., Kang'ombe, Arthur R., Okopi, Joseph A., Idoko, John A., Cuevas, Luis E., Gill, Geoffrey V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996137/
https://www.ncbi.nlm.nih.gov/pubmed/27307508
http://dx.doi.org/10.1093/cid/ciw381
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author Isa, Samson E.
Oche, Agbaji O.
Kang'ombe, Arthur R.
Okopi, Joseph A.
Idoko, John A.
Cuevas, Luis E.
Gill, Geoffrey V.
author_facet Isa, Samson E.
Oche, Agbaji O.
Kang'ombe, Arthur R.
Okopi, Joseph A.
Idoko, John A.
Cuevas, Luis E.
Gill, Geoffrey V.
author_sort Isa, Samson E.
collection PubMed
description Background. Human immunodeficiency virus (HIV) infection and the use of antiretroviral therapy (ART) may increase the risk of type 2 diabetes mellitus (T2DM). However, data from regions with a high burden of HIV/AIDS are limited. We determined the prevalence of T2DM at the time of presentation to a large HIV clinic in Nigeria, as well as the incidence of diabetes 12 months following ART initiation. Methods. Data from patients enrolled for ART from 2011 to 2013 was analyzed, including 2632 patients on enrollment and 2452 reevaluated after 12 months of ART commencement. The presence of diabetes, and demographic, clinical, and biochemical data were retrieved from standardized databases. CD4(+), HIV RNA load, and hepatitis C virus status were noted. Bivariate and logistic regressions were used to identify risk factors for T2DM. Results. Baseline T2DM prevalence was 2.3% (95% confidence interval, 1.8%–2.9%); age, but not body mass index (BMI), was a risk factor for diabetes. After 12 months of ART, an additional 5.3% had developed T2DM. Newly developed diabetes was not associated with age, but was associated with BMI. There were no significant associations between prevalent or incident diabetes and CD4(+), viral load, or type of ART. Conclusions. Diabetes is not uncommon in HIV-infected individuals at the time of presentation to HIV services. Patients initiating ART have a high risk of developing diabetes in the first year of ART. Excessive weight gain should be avoided, as incident diabetes was associated with a BMI ≥25.0 kg/m(2).
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spelling pubmed-49961372016-08-25 Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria Isa, Samson E. Oche, Agbaji O. Kang'ombe, Arthur R. Okopi, Joseph A. Idoko, John A. Cuevas, Luis E. Gill, Geoffrey V. Clin Infect Dis HIV/AIDS Background. Human immunodeficiency virus (HIV) infection and the use of antiretroviral therapy (ART) may increase the risk of type 2 diabetes mellitus (T2DM). However, data from regions with a high burden of HIV/AIDS are limited. We determined the prevalence of T2DM at the time of presentation to a large HIV clinic in Nigeria, as well as the incidence of diabetes 12 months following ART initiation. Methods. Data from patients enrolled for ART from 2011 to 2013 was analyzed, including 2632 patients on enrollment and 2452 reevaluated after 12 months of ART commencement. The presence of diabetes, and demographic, clinical, and biochemical data were retrieved from standardized databases. CD4(+), HIV RNA load, and hepatitis C virus status were noted. Bivariate and logistic regressions were used to identify risk factors for T2DM. Results. Baseline T2DM prevalence was 2.3% (95% confidence interval, 1.8%–2.9%); age, but not body mass index (BMI), was a risk factor for diabetes. After 12 months of ART, an additional 5.3% had developed T2DM. Newly developed diabetes was not associated with age, but was associated with BMI. There were no significant associations between prevalent or incident diabetes and CD4(+), viral load, or type of ART. Conclusions. Diabetes is not uncommon in HIV-infected individuals at the time of presentation to HIV services. Patients initiating ART have a high risk of developing diabetes in the first year of ART. Excessive weight gain should be avoided, as incident diabetes was associated with a BMI ≥25.0 kg/m(2). Oxford University Press 2016-09-15 2016-06-15 /pmc/articles/PMC4996137/ /pubmed/27307508 http://dx.doi.org/10.1093/cid/ciw381 Text en © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, contact journals.permissions@oup.com.
spellingShingle HIV/AIDS
Isa, Samson E.
Oche, Agbaji O.
Kang'ombe, Arthur R.
Okopi, Joseph A.
Idoko, John A.
Cuevas, Luis E.
Gill, Geoffrey V.
Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title_full Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title_fullStr Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title_full_unstemmed Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title_short Human Immunodeficiency Virus and Risk of Type 2 Diabetes in a Large Adult Cohort in Jos, Nigeria
title_sort human immunodeficiency virus and risk of type 2 diabetes in a large adult cohort in jos, nigeria
topic HIV/AIDS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996137/
https://www.ncbi.nlm.nih.gov/pubmed/27307508
http://dx.doi.org/10.1093/cid/ciw381
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