Abstract

Low bone mineral density (BMD) and fragility fractures are common in individuals infected with HIV, who are undergoing antiretroviral therapy (ART). In high-income countries, dual energy X-ray absorptiometrry is typically used to evaluate osteopenia or osteoporosis in HIV infected individuals. However, this technology is unavailable in low andmiddle income countries, so a different approach is needed. The aim of this study was to use X-ray scans of the spine to determine the prevalence of and associated risk factors for vertebral fractures in HIVinfected patients in a tertiary-care hospital in Mexico. We conducted a cross-sectional study of outpatients who were >40 years old and receiving ART at the Hospital de Infectología, La Raza National Medical Center in Mexico City, Mexico. We used semi-quantitative morphometric analysis of centrally digitized X-ray images to assess vertebral deformities in the spine. Anterior, middle and posterior vertebral heights were measured, and height ratios were calculated. For each vertebral body, fractures were graded on the basis of height ratio reductions, and a spine deformity index’ (SDI) value was calculated by summing the grades of the vertebral deformities: An SDI>1 was indicative of a vertebral fracture. We included 104 patients, 87% of whom were men. The median age was 49 years [interquartile range (IQR) 42-52]. The most common stage of HIV infection, as defined by the Centers for Disease Control, was B2 in 40 (39%) of patients. Forty seven (45%) patients were on ART regimens that included protease inhibitors (PIs) and 100 (96%) being treated with tenofovir. The median time of ART was 6.5 years (IQR 1.6-9.0). Of the 104 patients in our study, 83 (80%) had undetectable viral load, as assessed by HIV-1 RNA levels, 32 (31%) showed evidence of a previous fracture, 4 (4%) were co-infected with hepatitis C virus, and 57 (55%) had a history of corticosteroid treatment. The prevalence of vertebral fractures was 25%, 95% confidence interval 17-34%. We assessed whether gender, HCV co-infection, previous corticosteroid use, AIDS, total HIV viral load, and current and previous use of PIs were associated with fractures in our study group, but we did not observe a significant association between any of these factors and vertebral fractures. The prevalence of vertebral fractures was high among HIV-infected patients. We propose that screening for bone disease should be performed in HIV individuals who are at risk of fragility fractures. Furthermore, we suggest that X-ray based assessment of the spine should be considered in patients who are at increased risk of fragility fractures, irrespective of BMD levels, particularly in elderly patients in low and middle income countries.

Highlights

  • Individuals with osteoporosis, a skeletal disorder characterized by compromised bone strength, have an increased risk of fracture.[1]

  • Low bone mineral density (BMD), including that seen in individuals with premature osteopenia and osteoporosis, is more common in persons who are infected with human immunodeficiency virus (HIV)[2] than in uninfected persons, and there is evidence showing that antiretroviral therapy (ART) could increase bone loss

  • Low BMD is more prevalent in HIV infected subjects, and antiretroviral therapy (ART) can increase bone loss;[3] this treatment is associated with a 2-6% decrease in BMD over the first 2 years, which is similar in magnitude to that observed during the first 2 years of menopause.[4]

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Summary

Introduction

Individuals with osteoporosis, a skeletal disorder characterized by compromised bone strength, have an increased risk of fracture.[1] Low bone mineral density (BMD), including that seen in individuals with premature osteopenia and osteoporosis, is more common in persons who are infected with human immunodeficiency virus (HIV)[2] than in uninfected persons, and there is evidence showing that antiretroviral therapy (ART) could increase bone loss. Low BMD is more prevalent in HIV infected subjects, and antiretroviral therapy (ART) can increase bone loss;[3] this treatment is associated with a 2-6% decrease in BMD over the first 2 years, which is similar in magnitude to that observed during the first 2 years of menopause.[4] Chronic hepatitis C co-infection are associated with higher incidences of fractures whereas older age, female gender, an acquired immune deficiency syndrome (AIDS) diagnosis, baseline plasma HIV RNA viral load, and low body mass index (BMI) are related with low BMD.[5].

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