Lambert Assoumou1, Christine Katlama, Jean-Paul Viard, Michelle Bentata, Anne Simon, Christian Roux, Sami Kolta, Dominique Costagliola, Sylvie Rozenberg. 1. aINSERM bUPMC Univ Paris 06, UMRS 943 cAP-HP, Hôpital Pitié-Salpêtrière, Service de Maladies Infectieuses et Tropicales dAP-HP, Centre de Diagnostic et de Thérapeutique, Hôtel-Dieu, Paris eAP-HP, Hôpital Avicenne, Service de maladies infectieuses, Bobigny fAP-HP, Hôpital Pitié-Salpêtrière, Service de médecines internes gRheumatology Department, Cochin Hospital, Paris-Descartes University hAP-HP, Hôpital Pitié-Salpêtrière, Service de Rhumatologie and UPMC Univ Paris 06, Paris, France.
Abstract
OBJECTIVE: Although osteopenia is common in HIV-infected patients, there is by now limited data on the evolution of bone mineral density in this population. We aimed to evaluate the course of osteopenia over a 2-year period in HIV-1-infected men, and to identify risk factors for abnormal bone mineral density (BMD) decline. METHODS: HIV-1-infected men on combined antiretroviral therapy (cART) screened in the ANRS 120 Fosivir trial, diagnosed with low BMD (-2.5 ≤T-score <-1), not receiving antiosteoporotic agents, with sequential dual-energy-X ray-absorptiometry (DXA) available at baseline were eligible for this study and had a second DXA performed between months 24 and 36. RESULTS: We enrolled 94 men with a median age of 46 years [interquartile range (IQR), 41-53], BMI 22 kg/m² (21-25) and a CD4 cell nadir of 164/μl (69-261). They were receiving cART for a median of 7.5 years (5.8-9.5). Over a median interval of 2.6 years (2.3-2.9) between the two DXA tests, the mean change in BMD was -0.5 ± 1.7% per year (P = 0.010) at the lumbar spine and -0.4 ± 1.8% per year (P = 0.033) at the hip. BMD fell by more than the smallest detectable difference (SDD) in, respectively, 25.5 and 27.7% of patients at the lumbar spine and hip. Tenofovir (TDF) exposure was independently associated with a larger decline in BMD at both sites [lumbar spine, OR = 2.4 (1.2-4.9); hip, OR = 2.8 (1.3-5.9)]. CONCLUSION: Although osteopenia overall modestly changes over 2 years in long-term cART-treated patients, a quarter of patients experienced a significant loss (>1 SDD) associated with TDF exposure.
OBJECTIVE: Although osteopenia is common in HIV-infectedpatients, there is by now limited data on the evolution of bone mineral density in this population. We aimed to evaluate the course of osteopenia over a 2-year period in HIV-1-infectedmen, and to identify risk factors for abnormal bone mineral density (BMD) decline. METHODS:HIV-1-infectedmen on combined antiretroviral therapy (cART) screened in the ANRS 120 Fosivir trial, diagnosed with low BMD (-2.5 ≤T-score <-1), not receiving antiosteoporotic agents, with sequential dual-energy-X ray-absorptiometry (DXA) available at baseline were eligible for this study and had a second DXA performed between months 24 and 36. RESULTS: We enrolled 94 men with a median age of 46 years [interquartile range (IQR), 41-53], BMI 22 kg/m² (21-25) and a CD4 cell nadir of 164/μl (69-261). They were receiving cART for a median of 7.5 years (5.8-9.5). Over a median interval of 2.6 years (2.3-2.9) between the two DXA tests, the mean change in BMD was -0.5 ± 1.7% per year (P = 0.010) at the lumbar spine and -0.4 ± 1.8% per year (P = 0.033) at the hip. BMD fell by more than the smallest detectable difference (SDD) in, respectively, 25.5 and 27.7% of patients at the lumbar spine and hip. Tenofovir (TDF) exposure was independently associated with a larger decline in BMD at both sites [lumbar spine, OR = 2.4 (1.2-4.9); hip, OR = 2.8 (1.3-5.9)]. CONCLUSION: Although osteopenia overall modestly changes over 2 years in long-term cART-treated patients, a quarter of patients experienced a significant loss (>1 SDD) associated with TDF exposure.
Authors: Pablo Tebas; Princy Kumar; Charles Hicks; Catherine Granier; Brian Wynne; Sherene Min; Keith Pappa Journal: AIDS Date: 2015-11-28 Impact factor: 4.177
Authors: Tara McGinty; Aoife G Cotter; Caroline A Sabin; Alan Macken; Eoin Kavanagh; Juliet Compston; Gerard Sheehan; John Lambert; Patrick W G Mallon Journal: PLoS One Date: 2019-03-21 Impact factor: 3.240