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. 2014 Jan 28;28(3):345-53.
doi: 10.1097/QAD.0000000000000070.

Lower peak bone mass and abnormal trabecular and cortical microarchitecture in young men infected with HIV early in life

Affiliations

Lower peak bone mass and abnormal trabecular and cortical microarchitecture in young men infected with HIV early in life

Michael T Yin et al. AIDS. .

Abstract

Introduction: HIV infection and antiretroviral therapy (ART) early in life may interfere with acquisition of peak bone mass, thereby increasing fracture risk in adulthood.

Methods: We conducted a cross-sectional study of dual-energy X-ray absorptiometry (DXA) and high-resolution peripheral quantitative computed tomography (HR-pQCT) in 30 HIV-infected African-American or Hispanic Tanner stage 5 men aged 20-25 on ART (15 perinatally infected and 15 infected during adolescence) and 15 HIV-uninfected controls.

Results: HIV-infected men were similar in age and BMI, but were more likely to be African-American (P = 0.01) than uninfected men. DXA-derived areal bone mineral density (aBMD) Z-scores were 0.4-1.2 lower in HIV-infected men at the spine, hip, and radius (all P < 0.05). At the radius and tibia, total and trabecular volumetric BMD (vBMD), and cortical and trabecular thickness were between 6 and 19% lower in HIV-infected than uninfected men (P <0.05). HIV-infected men had dramatic deficiencies in plate-related parameters by individual trabeculae segmentation (ITS) analyses and 14-17% lower bone stiffness by finite element analysis. Differences in most HR-pQCT parameters remained significant after adjustment for race/ethnicity. No DXA or HR-pQCT parameters differed between men infected perinatally or during adolescence.

Conclusion: At an age by which young men have typically acquired peak bone mass, HIV-infected men on ART have lower BMD, markedly abnormal trabecular plate and cortical microarchitecture, and decreased whole bone stiffness, whether infected perinatally or during adolescence. Reduced bone strength in young adults infected with HIV early in life may place them at higher risk for fractures as they age.

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Figures

Fig. 1
Fig. 1. Representative high-resolution peripheral quantitative computed tomography (HR-pQCT) images from 24-year-old HIV-infected (left) and HIV-uninfected (right) African–American men at the radius (top) and tibia (bottom)
HR-pQCT, high-resolution peripheral quantitative computed tomography.
Fig. 2
Fig. 2. Percentage difference in high-resolution peripheral quantitative computed tomography measures between HIV-infected and HIV-uninfected men at the radius and tibia
Ct.Th, cortical thickness; HR-pQCT, high-resolution peripheral quantitative computed tomography; Tb.N, trabecular number; Tb.Sp (SD), trabecular separation standard deviation; Tb.SP, trabecular separation; vBMD, volumetric bone mineral density. *P < 0.05 after adjustment for race/ethnicity.
Fig. 3
Fig. 3. Percentage difference in individual trabeculae segmentation and micro finite element analysis measures between HIV-infected and HIV-uninfected men at the radius and tibia
μFEA, micro finite element analysis; ITS, individual trabeculae segmentation; pBV/TV and rBV/TV, plate and rod bone volume fraction; P–P, P–R, and R–R Junc.D, plate–plate, plate–rod, and rod–rod junction density; pTb.N and rTb.N, plate and rod number; P–R ratio, plate-to-rod ratio; pTb.Th and rTb.Th, plate and rod thickness; pTb.S, plate surface area; rTb.ℓ, mm, rod length. *P < 0.05 after adjustment for race/ethnicity.

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