Abstract
BACKGROUND AND OBJECTIVES: Low bone mineral density (BMD) and dementia commonly co-occur in older individuals, with bone loss accelerating in patients with dementia due to physical inactivity and poor nutrition. However, uncertainty persists over the extent to which bone loss already exists before onset of dementia. Therefore, we investigated how dementia risk was affected by BMD at various skeletal regions in community-dwelling older adults. METHODS: In a prospective population-based cohort study, BMD at the femoral neck, lumbar spine, and total body and the trabecular bone score (TBS) were obtained using dual-energy X-ray absorptiometry in 3,651 participants free from dementia between 2002 and 2005. Persons at risk of dementia were followed up until January 1, 2020. For analyses of the association between BMD at baseline and the risk of incident dementia, we used Cox proportional hazards regression analyses, adjusting for age, sex, educational attainment, physical activity, smoking status, body mass index, systolic and diastolic blood pressure, cholesterol level, high-density lipoprotein cholesterol, history of comorbidities (stroke and diabetes mellitus), and APOE genotype. RESULTS: Among the 3,651 participants (median age 72.3 ± 10.0 years, 57.9% women), 688 (18.8%) developed incident dementia during a median of 11.1 years, of whom 528 (76.7%) developed Alzheimer disease (AD). During the whole follow-up period, participants with lower BMD at the femoral neck (per SD decrease) were more likely to develop all-cause dementia (hazard ratio [HR] total follow-up 1.12, 95% CI 1.02-1.23) and AD (HRtotal follow-up 1.14, 95% CI 1.02-1.28). Within the first 10 years after baseline, the risk of dementia was greatest for groups with the lowest tertile of BMD (femoral neck BMD, HR0-10 years 2.03; 95% CI 1.39-2.96; total body BMD, HR0-10 years 1.42; 95% CI 1.01-2.02; and TBS, HR0-10 years 1.59; 95% CI 1.11-2.28). DISCUSSION: In conclusion, participants with low femoral neck and total body BMD and low TBS were more likely to develop dementia. Further studies should focus on the predictive ability of BMD for dementia.
| Original language | English |
|---|---|
| Pages (from-to) | e2125-e2133 |
| Journal | Neurology |
| Volume | 100 |
| Issue number | 20 |
| Early online date | 22 Mar 2023 |
| DOIs | |
| Publication status | Published - 16 May 2023 |
Bibliographical note
Funding Information:The Rotterdam Study is sponsored by the Erasmus Medical Center and Erasmus University Rotterdam, The Netherlands Organization for Scientific Research (I), The Netherlands Organization for Health Research and Development (ZonMW), the Research Institute for Diseases in the Elderly (RIDE), The Netherlands Genomics Initiative, the Ministry of Education, Culture and Science, the Ministry of Health, Welfare and Sports, the European Commission (DG XII), and the Municipality of Rotterdam. Further support was obtained from the Netherlands Consortium for Healthy Ageing. This study was partly performed as part of the Netherlands Consortium of Dementia Cohorts (NCDC), which also receives funding in the context of Deltaplan Dementie from ZonMW Memorabel (project number 73305095005) and Alzheimer Nederland. Further funding was obtained through the Stichting Erasmus Trustfonds (grant number 97030.2021.101.430/057/RB). Moreover, L. Oei is funded by an Erasmus MC fellowship grant.
Funding Information:
The Article Processing Charge was funded by UKB Waiver - Erasmus MC.
Funding Information:
The Rotterdam Study is sponsored by the Erasmus Medical Center and Erasmus University Rotterdam, The Netherlands Organization for Scientific Research (I), The Netherlands Organization for Health Research and Development (ZonMW), the Research Institute for Diseases in the Elderly (RIDE), The Netherlands Genomics Initiative, the Ministry of Education, Culture and Science, the Ministry of Health, Welfare and Sports, the European Commission (DG XII), and the Municipality of Rotterdam. Further support was obtained from the Netherlands Consortium for Healthy Ageing. This study was partly performed as part of the Netherlands Consortium of Dementia Cohorts (NCDC), which also receives funding in the context of Deltaplan Dementie from ZonMW Memorabel (project number 73305095005) and Alzheimer Nederland. Further funding was obtained through the Stichting Erasmus Trustfonds (grant number 97030.2021.101.430/057/RB). Moreover, L. Oei is funded by an Erasmus MC fellowship grant.
Publisher Copyright:
Copyright © 2023 The Author(s).
