From Normal Cognition to Cognitive Impairment and Dementia: Impact of Orthostatic Hypotension

Author:

Xia Xin1ORCID,Wang Rui123,Vetrano Davide L.145,Grande Giulia1,Laukka Erika J.16ORCID,Ding Mozhu17ORCID,Fratiglioni Laura16,Qiu Chengxuan1ORCID

Affiliation:

1. Aging Research Center, Department of Neurobiology, Care Sciences and Society (NVS), Karolinska Institutet-Stockholm University, Sweden (X.X., R.W., D.L.V., G.G., E.J.L., M.D., L.F., C.Q.).

2. The Swedish School of Sport and Health Sciences, GIH, Stockholm, Sweden (R.W.).

3. Department of Medicine and Wisconsin Alzheimer’s Disease Research Center, University of Wisconsin School of Medicine and Public Health, Madison (R.W.).

4. Department of Geriatrics, Catholic University of Rome, Italy (D.L.V.).

5. Centro di Medicina dell’Invecchiamento, Fondazione Policlinico A. Gemelli, Rome, Italy (D.L.V.).

6. Stockholm Gerontology Research Center, Sweden (E.J.L., L.F.).

7. Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden (M.D.).

Abstract

The role of orthostatic hypotension (OH) in the continuum of cognitive aging remains to be clarified. We sought to investigate the associations of OH with dementia, cognitive impairment, no dementia (CIND), and CIND progression to dementia in older adults while considering orthostatic symptoms. This population-based cohort study included 2532 baseline (2001–2004) dementia-free participants (age ≥60 years; 62.6% women) in the SNAC-K (Swedish National Study on Aging and Care in Kungsholmen) who were regularly examined over 12 years. We further divided the participants into a baseline CIND-free cohort and a CIND cohort. OH was defined as a decrease by ≥20/10 mm Hg in systolic/diastolic blood pressure upon standing and further divided into asymptomatic and symptomatic OH. Dementia was diagnosed following the international criteria. CIND was defined as scoring ≥1.5 SDs below age group-specific means in ≥1 cognitive domain. Data were analyzed with flexible parametric survival models, controlling for confounding factors. Of the 2532 participants, 615 were defined with OH at baseline, and 322 were diagnosed with dementia during the entire follow-up period. OH was associated with an adjusted hazard ratio of 1.40 for dementia (95% CI, 1.10–1.76), 1.15 (0.94–1.40) for CIND, and 1.54 (1.05–2.25) for CIND progression to dementia. The associations of dementia and CIND progression to dementia with asymptomatic OH were similar to overall OH, whereas symptomatic OH was only associated with CIND progression to dementia. Our study suggests that OH, even asymptomatic OH, is associated with increased risk of dementia and accelerated progression from CIND to dementia in older adults.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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