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Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection

INTRODUCTION: Previous studies indicate that human immunodeficiency virus (HIV)-infection and combination antiretroviral therapy (cART) can affect bone turnover. Furthermore, HIV-infected patients have lower bone mineral density (BMD) compared to a healthy reference population. OBJECTIVE: To evaluat...

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Autores principales: Vlot, Mariska C., Grijsen, Marlous L., Prins, Jan M., de Jongh, Renate T., de Jonge, Robert, den Heijer, Martin, Heijboer, Annemieke C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844537/
https://www.ncbi.nlm.nih.gov/pubmed/29522570
http://dx.doi.org/10.1371/journal.pone.0193679
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author Vlot, Mariska C.
Grijsen, Marlous L.
Prins, Jan M.
de Jongh, Renate T.
de Jonge, Robert
den Heijer, Martin
Heijboer, Annemieke C.
author_facet Vlot, Mariska C.
Grijsen, Marlous L.
Prins, Jan M.
de Jongh, Renate T.
de Jonge, Robert
den Heijer, Martin
Heijboer, Annemieke C.
author_sort Vlot, Mariska C.
collection PubMed
description INTRODUCTION: Previous studies indicate that human immunodeficiency virus (HIV)-infection and combination antiretroviral therapy (cART) can affect bone turnover. Furthermore, HIV-infected patients have lower bone mineral density (BMD) compared to a healthy reference population. OBJECTIVE: To evaluate the longitudinal effect of HIV-infection and cART on bone turnover markers (BTMs) and BMD in men with primary HIV-infection (PHI). DESIGN, METHODS: Thirty-five PHI-men were divided into two groups, those that received cART for the first time (n = 26) versus no-cART (n = 9). Dual-energy X-ray absorptiometry (DXA) was performed on femoral neck (FN), total hip (TH) and lumbar spine (LS) and BTMs (P1NP, alkaline phosphatase, osteocalcin, ICTP and CTX) were measured at baseline and follow-up. RESULTS: At baseline, the median CD4+ T-cell count was 455 cells/mm3 (IQR 320–620) and plasma viral load 5.4 log10 copies/mL (IQR 4.7–6.0) in the cART treated group, compared to 630 (IQR 590–910) and 4.8 (IQR 4.2–5.1) in the untreated group. The median follow-up time was 60.7 weeks (IQR 24.7–96.0). All BTMs, except ICTP, showed a significant increase during cART versus no changes of BTMs in the untreated group. FN and TH BMD showed a significant decrease in both groups. LS BMD did not change in both groups. CONCLUSION: Bone turnover increased in PHI-men treated with cART which was accompanied by a decrease in FN and TH BMD. No increase of bone turnover was seen in untreated PHI-men. Our study suggests that cART results in increased bone turnover and decreased BMD of the hip in PHI-men.
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spelling pubmed-58445372018-03-23 Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection Vlot, Mariska C. Grijsen, Marlous L. Prins, Jan M. de Jongh, Renate T. de Jonge, Robert den Heijer, Martin Heijboer, Annemieke C. PLoS One Research Article INTRODUCTION: Previous studies indicate that human immunodeficiency virus (HIV)-infection and combination antiretroviral therapy (cART) can affect bone turnover. Furthermore, HIV-infected patients have lower bone mineral density (BMD) compared to a healthy reference population. OBJECTIVE: To evaluate the longitudinal effect of HIV-infection and cART on bone turnover markers (BTMs) and BMD in men with primary HIV-infection (PHI). DESIGN, METHODS: Thirty-five PHI-men were divided into two groups, those that received cART for the first time (n = 26) versus no-cART (n = 9). Dual-energy X-ray absorptiometry (DXA) was performed on femoral neck (FN), total hip (TH) and lumbar spine (LS) and BTMs (P1NP, alkaline phosphatase, osteocalcin, ICTP and CTX) were measured at baseline and follow-up. RESULTS: At baseline, the median CD4+ T-cell count was 455 cells/mm3 (IQR 320–620) and plasma viral load 5.4 log10 copies/mL (IQR 4.7–6.0) in the cART treated group, compared to 630 (IQR 590–910) and 4.8 (IQR 4.2–5.1) in the untreated group. The median follow-up time was 60.7 weeks (IQR 24.7–96.0). All BTMs, except ICTP, showed a significant increase during cART versus no changes of BTMs in the untreated group. FN and TH BMD showed a significant decrease in both groups. LS BMD did not change in both groups. CONCLUSION: Bone turnover increased in PHI-men treated with cART which was accompanied by a decrease in FN and TH BMD. No increase of bone turnover was seen in untreated PHI-men. Our study suggests that cART results in increased bone turnover and decreased BMD of the hip in PHI-men. Public Library of Science 2018-03-09 /pmc/articles/PMC5844537/ /pubmed/29522570 http://dx.doi.org/10.1371/journal.pone.0193679 Text en © 2018 Vlot et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Vlot, Mariska C.
Grijsen, Marlous L.
Prins, Jan M.
de Jongh, Renate T.
de Jonge, Robert
den Heijer, Martin
Heijboer, Annemieke C.
Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title_full Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title_fullStr Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title_full_unstemmed Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title_short Effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary HIV-1 infection
title_sort effect of antiretroviral therapy on bone turnover and bone mineral density in men with primary hiv-1 infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844537/
https://www.ncbi.nlm.nih.gov/pubmed/29522570
http://dx.doi.org/10.1371/journal.pone.0193679
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