Noninfectious Comorbidity in the African Cohort Study
Author:
Ake Julie A1, Polyak Christina S12, Crowell Trevor A12, Kiweewa Francis3, Semwogerere Michael3, Maganga Lucas4, Bahemana Emmanuel4, Maswai Jonah25, Langat Rither25, Owuoth John25, Otieno Solomon25, Keshinro Babajide6, Esber Allahna L12, Liu Michelle12, Eller Leigh Anne12, Ganesan Kavitha12, Parikh Ajay P12, Hamm Tiffany E12, Robb Merlin L12, Hickey Patrick W1, Valcour Victor G7, Michael Nelson L1, Falodun O, Song K, Milazzo M, Zhang C, Deshano R, Thompson C, Smith G, Mebrahtu T, Coakley P, Lombardi K, Imbach M, Peel S, Malia J, Kroidl A, Kroidl I, Geldmacher C, Kafeero C, Nambuya A, Tegamanyi J, Birungi H, Mugagga O, Nassali G, Wangiri P, Nantabo M, Nambulondo P, Atwijuka B, Asiimwe A, Nabanoba C T, Semwogerere M, Mwesigwa R, Jjuuko S, Namagembe R, Bagyendagye E, Tindikahwa A, Rwomushana I, Ssentongo F, Kibuuka H, Millard M, Kapkiai J, Wangare S, Mangesoi R, Chepkwony P, Bor L, Maera E, Kasembeli A, Rotich J, Kipkoech C, Chepkemoi W, Rono A, Kesi Z, Ngeno J, Langat E, Labosso K, Langat K, Kirui R, Rotich L, Mabwai M, Chelangat E, Agutu J, Tonui C, Changwony E, Bii M, Chumba E, Korir J, Sugut J, Gitonga D, Ngetich R, Kiprotich S, Rehema W, Ogari C, Ouma I, Adimo O, Ogai S, Okwaro C, Maranga E, Ochola J, Obambo K, Sing’oei V, Otieno L, Nyapiedho O, Sande N, Odemba E, Wanjiru F, Khamadi S, Chiweka E, Lwilla A, Mkondoo D, Somi N, Kiliba P, Mwaipopo M, Mwaisanga G, Muhumuza J, Mkingule N, Mwasulama O, Sanagare A, Kishimbo P, David G, Mbwayu F, Mwamwaja J, Likiliwike J, Muhumuza J, Mcharo R, Mkingule N, Mwasulama O, Mtafya B, Lueer C, Kisinda A, Mbena T, Mfumbulwa H, Mwandumbya L, Edwin P, Olomi W, Adamu Y, Akintunde A, Tiamiyu A B, Afoke K, Shehu M, Harrison N E, Agbaim U C, Adegbite O A, Eluwa R M, Adelakun G A, Ikegbunam A U, Mbibi J C, Oni F O, Ndbuisi R O, Elemere J, Azuakola N, Williams T T, Ayogu M, Enameguono O, Odo A F, Ukaegbu I C, Ugwuezumba O, Odeyemi S O, Okeke N C, Umeji L, Rose A, Daniel H, Nwando H, Nicholas E I, Iyanda T, Okolo C, Mene V Y, Dogonyaro B, Olabulo O, Akinseli O, Onukun F, Knopp G,
Affiliation:
1. US Military Human Immunodeficiency Virus (HIV) Research Program, Walter Reed Army Institute of Research, Silver Spring, Bethesda, Maryland 2. Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland 3. Makerere University Walter Reed Project, Kampala, Uganda 4. Mbeya Medical Research Program, Tanzania 5. Henry M. Jackson Foundation Medical Research International, Nairobi, Kenya 6. US Military HIV Research Program, Walter Reed Army Institute of Research, Abuja, Nigeria 7. University of California San Francisco School of Medicine
Abstract
Abstract
Background
Noninfectious comorbid diseases (NCDs) contribute to morbidity and mortality in human immunodeficiency virus (HIV)–infected populations in resource-rich countries. With antiretroviral therapy (ART) scale-up in Africa, understanding burden NCD informs public health strategy.
Methods
At enrollment, participants at 11 HIV clinics in Kenya, Uganda, Tanzania, and Nigeria underwent medical history, physical, laboratory, and neuropsychological assessments to identify elevated blood pressure, hypercholesterolemia, dysglycemia, renal insufficiency, and cognitive impairment. Poisson regression models estimated adjusted relative risks (ARRs) and 95% confidence intervals (CIs) for the number of NCDs associated with factors of interest. Logistic regression was used to evaluate each NCD separately among HIV-infected participants.
Results
Among 2720 participants with complete NCD data, 2159 (79.4%) were HIV-infected. Of those, 1426 (66.0%) were taking ART and 813 (37.7%) had at least 1 NCD. HIV infection was associated with more NCDs, especially with ART (ARR, 1.42; 95% CI, 1.22–1.66). In addition to age, body mass index, and program site, ART usage was associated with more NCDs (ARR, 1.50; 95% CI, 1.27–1.78 for virologically suppressed and ARR, 1.38; 95% CI, 1.13–1.68 for viremic) among HIV-infected participants. In participants taking ART, CD4 nadir below 200 cells/mm3 was associated with more NCDs (ARR, 1.43; 95% CI, 1.06–1.93). ART use was independently associated with hypercholesterolemia and dysglycemia. Program site was significantly associated with all comorbidities except renal insufficiency.
Conclusions
HIV infection was a risk for NCDs, which were common in HIV-infected participants, geographically variable, and largely consistent with metabolic complications of first-line ART.
Funder
Military Infectious Disease Research Program National Institute of Mental Health
Publisher
Oxford University Press (OUP)
Subject
Infectious Diseases,Microbiology (medical)
Cited by
49 articles.
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