Longitudinal Assessment of Bone Mineral Density in Women Living With and Without HIV Across Reproductive Phases

Author:

Swann Shayda A.12ORCID,King Elizabeth M.23,Prior Jerilynn C.245,Berger Claudie6,Mayer Ulrike2,Pick Neora27,Campbell Amber R.278,Côté Hélène C. F.128910,Murray Melanie C. M.12710ORCID,

Affiliation:

1. Experimental Medicine, University of British Columbia, Vancouver, Canada;

2. Women's Health Research Institute, Vancouver, Canada;

3. Faculty of Health Sciences, Simon Fraser University, Burnaby, Canada;

4. Centre for Menstrual Cycle and Ovulation Research (CeMCOR), Endocrinology and Metabolism, University of British Columbia, Vancouver, Canada;

5. School of Population and Public Health, University of British Columbia, Vancouver, Canada;

6. CaMosNational Coordinating Centre, McGill University, Montreal, Canada;

7. Oak Tree Clinic, BC Women's Hospital and Health Centre, Vancouver, Canada;

8. Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada;

9. Centre for Blood Research, University of British Columbia, Vancouver, Canada; and

10. Edwin S.H. Leong Healthy Aging Program, University of British Columbia, Vancouver, Canada.

Abstract

Background: Women living with HIV commonly experience low areal bone mineral density (BMD), but whether this is affected by low ovarian hormonal states (prolonged amenorrhea or menopause) is unknown. We compared rates of BMD loss between women living with HIV and HIV-negative control women and investigated its association with low ovarian hormonal states. Setting: Women living with HIV were enrolled from Vancouver Canada and controls from 9 Canadian sites. Methods: This longitudinal analysis included age-matched women living with HIV in the Children and Women: AntiRetrovirals and Markers of Aging cohort and controls in the population-based Canadian Multicentre Osteoporosis Study. Rate of change/year in BMD at the total hip and lumbar spine (L1–L4) between 3 and 5 years was compared between groups, adjusting for sociodemographic and clinical variables. Results: Ninety-two women living with HIV (median [interquartile range] age: 49.5 [41.6–54.1] years and body mass index: 24.1 [20.7–30.8] kg/m2) and 278 controls (age: 49.0 [43.0–55.0] years and body mass index: 25.8 [22.9–30.6] kg/m2) were included. Total hip BMD loss was associated with HIV (β: −0.003 [95% CI: −0.006 to −0.0001] g/cm2/yr), menopause (β: −0.007 [−0.01 to −0.005] g/cm2/yr), and smoking (β: −0.003 [−0.006 to −0.0002] g/cm2/yr); BMD gain was linked with higher body mass index (β: 0.0002 [0.0007–0.0004] g/cm2/yr). Menopause was associated with losing L1–L4 BMD (β: −0.01 [−0.01 to −0.006] g/cm2/yr). Amenorrhea was not associated with BMD loss. Conclusions: HIV and menopause negatively influenced total hip BMD. These data suggest women living with HIV require hip BMD monitoring as they age.

Funder

Canadian Institutes of Health Research

Canadian HIV Trials Network, Canadian Institutes of Health Research

Amgen Canada

Actavis

Dairy Farmers of Canada

Eli Lilly Canada

GE Lunar

Hologic

Merck Canada

Novartis Pharmaceuticals Corporation

P&G Pharmaceuticals Canada Inc.

Pfizer Canada

F. Hoffmann-La Roche

Sanofi-Aventis Canada Inc.

Servier Canada

The Arthritis Society

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Infectious Diseases

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