» Articles » PMID: 29522570

Effect of Antiretroviral Therapy on Bone Turnover and Bone Mineral Density in Men with Primary HIV-1 Infection

Overview
Journal PLoS One
Date 2018 Mar 10
PMID 29522570
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Bone Disease in HIV: Need for Early Diagnosis and Prevention.

Schinas G, Schinas I, Ntampanlis G, Polyzou E, Gogos C, Akinosoglou K Life (Basel). 2024; 14(4).

PMID: 38672792 PMC: 11051575. DOI: 10.3390/life14040522.


Evaluation of bone mineral density, microarchitecture, and detection of fractures on young patients living with human immunodeficiency virus: when and how to screen?.

Gehrke B, Farias M, Wildemberg L, Ferraiuoli G, Ribeiro V, Bosgnoli R Endocrine. 2023; 83(1):214-226.

PMID: 37673836 DOI: 10.1007/s12020-023-03501-9.


Bone Mineral Content Estimation in People Living with HIV: Prediction and Validation of Sex-Specific Anthropometric Models.

Correia I, Navarro A, Cordeiro J, Gomide E, Mazzonetto L, Oliveira A Int J Environ Res Public Health. 2022; 19(19).

PMID: 36231634 PMC: 9566219. DOI: 10.3390/ijerph191912336.


Secondary Osteoporosis and Metabolic Bone Diseases.

Sobh M, Abdalbary M, Elnagar S, Nagy E, Elshabrawy N, Abdelsalam M J Clin Med. 2022; 11(9).

PMID: 35566509 PMC: 9102221. DOI: 10.3390/jcm11092382.


Contributory role of ART in the development of non-AIDS comorbidities in asymptomatic PLWHA.

Tasca K, Fagundes Vidal V, Manfio V, Barbosa A, de Souza L J Appl Biomed. 2021; 19(1):73-82.

PMID: 34907718 DOI: 10.32725/jab.2021.002.


References
1.
Grant P, Cotter A . Tenofovir and bone health. Curr Opin HIV AIDS. 2016; 11(3):326-32. PMC: 4844450. DOI: 10.1097/COH.0000000000000248. View

2.
Piso R, Rothen M, Rothen J, Stahl M . Markers of bone turnover are elevated in patients with antiretroviral treatment independent of the substance used. J Acquir Immune Defic Syndr. 2011; 56(4):320-4. DOI: 10.1097/QAI.0b013e31820cf010. View

3.
Brown T, Ross A, Storer N, Labbato D, McComsey G . Bone turnover, osteoprotegerin/RANKL and inflammation with antiretroviral initiation: tenofovir versus non-tenofovir regimens. Antivir Ther. 2011; 16(7):1063-72. PMC: 3915418. DOI: 10.3851/IMP1874. View

4.
Grant P, Kitch D, McComsey G, Collier A, Koletar S, Erlandson K . Long-term Bone Mineral Density Changes in Antiretroviral-Treated HIV-Infected Individuals. J Infect Dis. 2016; 214(4):607-11. PMC: 4957444. DOI: 10.1093/infdis/jiw204. View

5.
Grijsen M, Steingrover R, Wit F, Jurriaans S, Verbon A, Brinkman K . No treatment versus 24 or 60 weeks of antiretroviral treatment during primary HIV infection: the randomized Primo-SHM trial. PLoS Med. 2012; 9(3):e1001196. PMC: 3313945. DOI: 10.1371/journal.pmed.1001196. View