Bone mineral density and the risk of incident dementia: A meta‐analysis

Author:

Lary Christine W.12ORCID,Ghatan Samuel3,Gerety Meghan4ORCID,Hinton Alexandra2,Nagarajan Archana125,Rosen Clifford2,Ross Ryan D.6,Bennett David A.7,DeStefano Anita L.8,Ikram Mohammad A.3,Rivadeneira Fernando3,Kiel Douglas P.910,Seshadri Sudha1112,Beiser Alexa812

Affiliation:

1. Roux Institute at Northeastern University Portland Maine USA

2. MaineHealth Institute for Research Scarborough Maine USA

3. Erasmus Medical Center Rotterdam The Netherlands

4. University of Pennsylvania Philadelphia Pennsylvania USA

5. Tufts University Graduate School of Biomedical Sciences Boston Massachusetts USA

6. Department of Anatomy & Cell Biology Rush University Medical Center Chicago Illinois USA

7. Rush Alzheimer's Disease Center Rush University Medical Center Chicago Illinois USA

8. Boston University School of Public Health Boston Massachusetts USA

9. Hinda and Arthur Marcus Institute for Aging Research Hebrew SeniorLife Boston Massachusetts USA

10. Department of Medicine Beth Israel Deaconess Medical Center and Harvard Medical School Boston Massachusetts USA

11. Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, UT Health San Antonio Texas USA

12. Boston University School of Medicine Boston Massachusetts USA

Abstract

AbstractBackgroundIt is not known whether bone mineral density (BMD) measured at baseline or as the rate of decline prior to baseline (prior bone loss) is a stronger predictor of incident dementia or Alzheimer's disease (AD).MethodsWe performed a meta‐analysis of three longitudinal studies, the Framingham Heart Study (FHS), the Rotterdam Study (RS), and the Rush Memory and Aging Project (MAP), modeling the time to diagnosis of dementia as a function of BMD measures accounting for covariates. We included individuals with one or two BMD assessments, aged ≥60 years, and free of dementia at baseline with follow‐up available. BMD was measured at the hip femoral neck using dual‐energy X‐ray absorptiometry (DXA), or at the heel calcaneus using quantitative ultrasound to calculate estimated BMD (eBMD). BMD at study baseline (“baseline BMD”) and annualized percentage change in BMD prior to baseline (“prior bone loss”) were included as continuous measures. The primary outcome was incident dementia diagnosis within 10 years of baseline, and incident AD was a secondary outcome. Baseline covariates included age, sex, body mass index, ApoE4 genotype, and education.ResultsThe combined sample size across all three studies was 4431 with 606 incident dementia diagnoses, 498 of which were AD. A meta‐analysis of baseline BMD across three studies showed higher BMD to have a significant protective association with incident dementia with a hazard ratio of 0.47 (95% CI: 0.23–0.96; p = 0.038) per increase in g/cm2, or 0.91 (95% CI: 0.84–0.995) per standard deviation increase. We observed a significant association between prior bone loss and incident dementia with a hazard ratio of 1.30 (95% CI: 1.12–1.51; p < 0.001) per percent increase in prior bone loss only in the FHS cohort.ConclusionsBaseline BMD but not prior bone loss was associated with incident dementia in a meta‐analysis across three studies.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Geriatrics and Gerontology

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