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HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation
BACKGROUND: Increased incidence of cardiovascular diseases (CVD) in both HIV infection and type 2 diabetes (T2D) compared to the general population has been described. Little is known about the combined effect of HIV infection and T2D on inflammation and endothelial function, both of which may contr...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372333/ https://www.ncbi.nlm.nih.gov/pubmed/28356058 http://dx.doi.org/10.1186/s12879-017-2334-8 |
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author | Hove-Skovsgaard, Malene Gaardbo, Julie Christine Kolte, Lilian Winding, Kamilla Seljeflot, Ingebjørg Svardal, Asbjørn Berge, Rolf Kristian Gerstoft, Jan Ullum, Henrik Trøseid, Marius Nielsen, Susanne Dam |
author_facet | Hove-Skovsgaard, Malene Gaardbo, Julie Christine Kolte, Lilian Winding, Kamilla Seljeflot, Ingebjørg Svardal, Asbjørn Berge, Rolf Kristian Gerstoft, Jan Ullum, Henrik Trøseid, Marius Nielsen, Susanne Dam |
author_sort | Hove-Skovsgaard, Malene |
collection | PubMed |
description | BACKGROUND: Increased incidence of cardiovascular diseases (CVD) in both HIV infection and type 2 diabetes (T2D) compared to the general population has been described. Little is known about the combined effect of HIV infection and T2D on inflammation and endothelial function, both of which may contribute to elevated risk of CVD. METHODS: Cross-sectional study including 50 HIV-infected persons on combination anti-retroviral therapy (cART), with HIV RNA <200 copies/mL (n = 25 with T2D (HIV + T2D+), n = 25 without T2D (HIV + T2D-)) and 50 uninfected persons (n = 22 with T2D (HIV-T2D+) and n = 28 without T2D (HIV-T2D-)). Groups were matched on age and sex. High sensitive C-reactive protein (hsCRP) was used to determine inflammation (cut-off 3 mg/L). The marker of endothelial dysfunction asymmetric dimethylarginine (ADMA) was measured using high performance liquid chromatography. Trimethylamine-N-oxide (TMAO), a microbiota-dependent, pro-atherogenic marker was measured using stable isotope dilution LC/MS/MS. RESULTS: The percentage of HIV + T2D+, HIV + T2D-, HIV-T2D+, and HIV-T2D- with hsCRP above cut-off was 50%, 19%, 47%, and 11%, respectively. HIV + T2D+ had elevated ADMA (0.67 μM (0.63-0.72) compared to HIV + T2D- (0.60 μM (0.57-0.64) p = 0.017), HIV-T2D+ (0.57 μM (0.51-63) p = 0.008), and HIV-T2D- (0.55 μM (0.52-0.58) p < 0.001). No differences in TMAO between groups were found. However, a positive correlation between ADMA and TMAO was found in the total population (r(s) = 0.32, p = 0.001), which was mainly driven by a close correlation in HIV + T2D+ (r(s) = 0.63, p = 0.001). CONCLUSION: Elevated inflammation and evidence of endothelial dysfunction was found in HIV-infected persons with T2D. The effect on inflammation was mainly driven by T2D, while both HIV infection and T2D may contribute to endothelial dysfunction. Whether gut microbiota is a contributing factor to this remains to be determined. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2334-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5372333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53723332017-03-31 HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation Hove-Skovsgaard, Malene Gaardbo, Julie Christine Kolte, Lilian Winding, Kamilla Seljeflot, Ingebjørg Svardal, Asbjørn Berge, Rolf Kristian Gerstoft, Jan Ullum, Henrik Trøseid, Marius Nielsen, Susanne Dam BMC Infect Dis Research Article BACKGROUND: Increased incidence of cardiovascular diseases (CVD) in both HIV infection and type 2 diabetes (T2D) compared to the general population has been described. Little is known about the combined effect of HIV infection and T2D on inflammation and endothelial function, both of which may contribute to elevated risk of CVD. METHODS: Cross-sectional study including 50 HIV-infected persons on combination anti-retroviral therapy (cART), with HIV RNA <200 copies/mL (n = 25 with T2D (HIV + T2D+), n = 25 without T2D (HIV + T2D-)) and 50 uninfected persons (n = 22 with T2D (HIV-T2D+) and n = 28 without T2D (HIV-T2D-)). Groups were matched on age and sex. High sensitive C-reactive protein (hsCRP) was used to determine inflammation (cut-off 3 mg/L). The marker of endothelial dysfunction asymmetric dimethylarginine (ADMA) was measured using high performance liquid chromatography. Trimethylamine-N-oxide (TMAO), a microbiota-dependent, pro-atherogenic marker was measured using stable isotope dilution LC/MS/MS. RESULTS: The percentage of HIV + T2D+, HIV + T2D-, HIV-T2D+, and HIV-T2D- with hsCRP above cut-off was 50%, 19%, 47%, and 11%, respectively. HIV + T2D+ had elevated ADMA (0.67 μM (0.63-0.72) compared to HIV + T2D- (0.60 μM (0.57-0.64) p = 0.017), HIV-T2D+ (0.57 μM (0.51-63) p = 0.008), and HIV-T2D- (0.55 μM (0.52-0.58) p < 0.001). No differences in TMAO between groups were found. However, a positive correlation between ADMA and TMAO was found in the total population (r(s) = 0.32, p = 0.001), which was mainly driven by a close correlation in HIV + T2D+ (r(s) = 0.63, p = 0.001). CONCLUSION: Elevated inflammation and evidence of endothelial dysfunction was found in HIV-infected persons with T2D. The effect on inflammation was mainly driven by T2D, while both HIV infection and T2D may contribute to endothelial dysfunction. Whether gut microbiota is a contributing factor to this remains to be determined. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2334-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-29 /pmc/articles/PMC5372333/ /pubmed/28356058 http://dx.doi.org/10.1186/s12879-017-2334-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hove-Skovsgaard, Malene Gaardbo, Julie Christine Kolte, Lilian Winding, Kamilla Seljeflot, Ingebjørg Svardal, Asbjørn Berge, Rolf Kristian Gerstoft, Jan Ullum, Henrik Trøseid, Marius Nielsen, Susanne Dam HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title | HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title_full | HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title_fullStr | HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title_full_unstemmed | HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title_short | HIV-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
title_sort | hiv-infected persons with type 2 diabetes show evidence of endothelial dysfunction and increased inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372333/ https://www.ncbi.nlm.nih.gov/pubmed/28356058 http://dx.doi.org/10.1186/s12879-017-2334-8 |
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