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Switch from tenofovir to raltegravir increases low bone mineral density and decreases markers of bone turnover over 48 weeks
Author(s) -
Bloch M,
Tong WWY,
Hoy J,
Baker D,
Lee FJ,
Richardson R,
Carr A
Publication year - 2014
Publication title -
hiv medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.53
H-Index - 79
eISSN - 1468-1293
pISSN - 1464-2662
DOI - 10.1111/hiv.12123
Subject(s) - raltegravir , medicine , bone remodeling , bone mineral , darunavir , osteocalcin , ritonavir , confidence interval , adverse effect , tenofovir , frax , endocrinology , viral load , urology , gastroenterology , osteoporosis , human immunodeficiency virus (hiv) , antiretroviral therapy , alkaline phosphatase , immunology , biochemistry , chemistry , osteoporotic fracture , enzyme
Background Tenofovir, particularly when given with a ritonavir‐boosted protease inhibitor ( rPI ), reduces bone mineral density ( BMD ) and increases bone turnover markers ( BTMs ), both of which are associated with increased fracture risk. Raltegravir has not been associated with bone loss. Methods In an open‐label, nonrandomized, pilot study, tenofovir was switched to raltegravir in adults also receiving a rPI for at least 6 months with a spine or hip T ‐score ≤ −1.0 and plasma HIV RNA < 50 HIV ‐1 RNA copies/mL for at least 3 months. The primary endpoint was BMD change by dual‐energy X ‐ray absorptiometry. Student's paired t ‐test was used to compare continuous variables. Factors associated with BMD increase were assessed using linear regression. Results Thirty‐seven patients were enrolled in the study: 97% were male, the mean age was 49 years, the mean T‐scores were −1.4 (spine) and −1.3 (total left hip), and the mean tenofovir treatment duration was 3.1 years. BMD increases were significant at weeks 24 and 48. At week 48, spine BMD increased by 3.0% [95% confidence interval ( CI ) 1.9, 4.0%; P < 0.0001] and left total hip BMD increased by 2.5% (95% CI 1.6, 3.3%; P < 0.0001). BTMs ( N ‐telopeptide, osteocalcin and bone alkaline phosphatase) all decreased significantly at week 24 (P ≤ 0.0017). There were no raltegravir‐related serious or grade 3−4 adverse events. HIV viral load remained <50 copies/mL plasma on raltegravir/ rPI therapy. Conclusions Switching virologically suppressed HIV ‐infected adults with low BMD taking an rPI from tenofovir to raltegravir was safe and significantly improved hip and spine BMD and reduced markers of bone turnover over 48 weeks.