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Premature Spinal Bone Loss in Women Living with HIV is Associated with Shorter Leukocyte Telomere Length

Bibliographic Data

ID15512650
AuthorsShirin Kalyan (0000-0002-7332-2225, University of British Columbia), Neora Pick (0000-0003-4123-3698, University of British Columbia, corresponding author), Alice Mai (University of British Columbia), Melanie C M Murray (0000-0001-9538-2758, University of British Columbia), Kristen M Kidson (University of British Columbia), Jackson Chu (University of British Columbia), Arianne Albert (0000-0002-3050-0888, Women's Health Research Institute), Hélène C F Côté (0000-0002-0399-5141, University of British Columbia), Evelyn J Maan (0000-0001-5930-3514, B.C. Women's Hospital & Health Centre), Azita Goshtasebi (University of British Columbia), Deborah Money (0000-0003-4411-7473, University of British Columbia), Jerilynn C Prior (0000-0003-3232-0597, University of British Columbia)
Year2018
Volume15
Issue5
Pages1018-1018
Publication date2018-05-18
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph15051018
PMID29783641
OpenAlexW2803449397
LanguageEN

With advances in combination antiretroviral therapy (cART), people living with HIV are now surviving to experience aging. Evidence suggests that individuals living with HIV are at greater risk for low bone mineral density (BMD), osteoporosis, and fractures. Better understanding of the pathophysiology of bone health in women living with HIV (WLWH) is important for treatment strategies. The goal of this study was to explore new biological factors linked to low BMD in WLWH. Standardized BMD measures of WLWH were compared to reference values from an unselected population of women from the same geographical region of the same age range. Linear regression analysis was used to assess relationships among health-related characteristics, cellular aging (measured by leukocyte telomere length; LTL), cART, and BMD of WLWH. WLWH ( n = 73; mean age 43 ± 9 years) had lower BMD Z -scores at the lumbar spine (LS) (mean difference = -0.39, p p = 0.012) relative to controls ( n = 290). WLWH between 50 and 60 years ( n = 17) had lower Z -scores at the LS ( p = 0.008) and TH ( p = 0.027) compared to controls ( n = 167). Among WLWH, LS BMD was significantly associated with LTL (R2 = 0.09, p = 0.009) and BMI (R2 = 0.06, p = 0.042). Spinal BMD was adversely affected in WLWH. Reduction of LTL was strongly associated with lower BMD and may relate to its pathophysiology and premature aging in WLWH

Bone density · Bone mineral · Osteoporosis · Population · Bone and Joint Diseases · Cytomegalovirus and herpesvirus research · HIV-related health complications and treatments · Medicine · Internal Medicine · Physiology

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