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Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity

BACKGROUND: Co-existence of diabetes in the HIV infected reportedly further complicates the attendant impairment of immunity and increases susceptibility to opportunistic infections. OBJECTIVE: This study aimed to evaluate some immune and inflammatory parameters in HIV and type 2 diabetes (T2D) co-m...

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Autores principales: Chukwuanukwu, Rebecca Chinyelu, Nwosu, Ngozi Bernice, Ifeanyichukwu, Martin Ositadinma, Nsonwu-Anyanwu, Augusta Chinyere, Manafa, Patrick Onochie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Makerere Medical School 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398510/
https://www.ncbi.nlm.nih.gov/pubmed/37545969
http://dx.doi.org/10.4314/ahs.v23i1.14
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author Chukwuanukwu, Rebecca Chinyelu
Nwosu, Ngozi Bernice
Ifeanyichukwu, Martin Ositadinma
Nsonwu-Anyanwu, Augusta Chinyere
Manafa, Patrick Onochie
author_facet Chukwuanukwu, Rebecca Chinyelu
Nwosu, Ngozi Bernice
Ifeanyichukwu, Martin Ositadinma
Nsonwu-Anyanwu, Augusta Chinyere
Manafa, Patrick Onochie
author_sort Chukwuanukwu, Rebecca Chinyelu
collection PubMed
description BACKGROUND: Co-existence of diabetes in the HIV infected reportedly further complicates the attendant impairment of immunity and increases susceptibility to opportunistic infections. OBJECTIVE: This study aimed to evaluate some immune and inflammatory parameters in HIV and type 2 diabetes (T2D) co-morbidity: Immunoglobulin M and G (IgM and IgG), Interleukin-6, CD4+ T-cells and C-reactive protein. METHOD: The study involved 200 subjects grouped according to their HIV and diabetes status: Group 1 ‘Diabetic HIV seropositive’ (n=40), Group 2 ‘Non diabetic HIV seropositive’(n=60), Group 3 ‘Diabetic HIV seronegative’(n=50), and Group 4 'Control non diabetic HIV seronegative'(n=50). Blood samples were collected for testing. RESULTS: CRP levels were significantly elevated in diabetes and HIV co-morbidity compared to other groups. IL–6 levels were significantly higher in diabetics with or without HIV infection. In addition, IL-6 was significantly elevated in individuals with poor glycemic control (HbA1c > 9.0%) compared to those with good glycemic control. IgG and IgM levels in diabetic HIV seropositive subjects were highest compared with other groups. CONCLUSION: The increased IL-6, CRP, IgG, IgM and decreased CD4+ T cell counts observed in co-morbidity suggest that HIV and T2D co-morbidity exacerbate the immune and inflammatory impairment observed in either disease entity.
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spelling pubmed-103985102023-08-04 Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity Chukwuanukwu, Rebecca Chinyelu Nwosu, Ngozi Bernice Ifeanyichukwu, Martin Ositadinma Nsonwu-Anyanwu, Augusta Chinyere Manafa, Patrick Onochie Afr Health Sci Articles BACKGROUND: Co-existence of diabetes in the HIV infected reportedly further complicates the attendant impairment of immunity and increases susceptibility to opportunistic infections. OBJECTIVE: This study aimed to evaluate some immune and inflammatory parameters in HIV and type 2 diabetes (T2D) co-morbidity: Immunoglobulin M and G (IgM and IgG), Interleukin-6, CD4+ T-cells and C-reactive protein. METHOD: The study involved 200 subjects grouped according to their HIV and diabetes status: Group 1 ‘Diabetic HIV seropositive’ (n=40), Group 2 ‘Non diabetic HIV seropositive’(n=60), Group 3 ‘Diabetic HIV seronegative’(n=50), and Group 4 'Control non diabetic HIV seronegative'(n=50). Blood samples were collected for testing. RESULTS: CRP levels were significantly elevated in diabetes and HIV co-morbidity compared to other groups. IL–6 levels were significantly higher in diabetics with or without HIV infection. In addition, IL-6 was significantly elevated in individuals with poor glycemic control (HbA1c > 9.0%) compared to those with good glycemic control. IgG and IgM levels in diabetic HIV seropositive subjects were highest compared with other groups. CONCLUSION: The increased IL-6, CRP, IgG, IgM and decreased CD4+ T cell counts observed in co-morbidity suggest that HIV and T2D co-morbidity exacerbate the immune and inflammatory impairment observed in either disease entity. Makerere Medical School 2023-03 /pmc/articles/PMC10398510/ /pubmed/37545969 http://dx.doi.org/10.4314/ahs.v23i1.14 Text en © 2023 Chukwuanukwu RC et al. https://creativecommons.org/licenses/by/4.0/Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Chukwuanukwu, Rebecca Chinyelu
Nwosu, Ngozi Bernice
Ifeanyichukwu, Martin Ositadinma
Nsonwu-Anyanwu, Augusta Chinyere
Manafa, Patrick Onochie
Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title_full Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title_fullStr Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title_full_unstemmed Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title_short Evaluation of some immune and inflammatory responses in diabetes and HIV co-morbidity
title_sort evaluation of some immune and inflammatory responses in diabetes and hiv co-morbidity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398510/
https://www.ncbi.nlm.nih.gov/pubmed/37545969
http://dx.doi.org/10.4314/ahs.v23i1.14
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