Orthostatic hypotension and its association with cerebral small vessel disease in a memory clinic population

Author:

Wiersinga Julia H.I.12,Rhodius-Meester Hanneke F.M.134,Wolters Frank J.56,Trappenburg Marijke C.178,Lemstra Afina W.3,Barkhof Frederik3910,Peters Mike J.L.11,van der Flier Wiesje M.31012,Muller Majon12

Affiliation:

1. Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Internal Medicine section Geriatrics

2. Amsterdam Cardiovascular Sciences, Atherosclerosis & Ischemic Syndromes

3. Amsterdam UMC location Vrije Universiteit Amsterdam, Alzheimer Center Amsterdam & Department of Neurology, Amsterdam, The Netherlands

4. Oslo University Hospital, Department of Geriatric Medicine, Ullevål, Oslo, Norway

5. Erasmus Medical Center, Department of Epidemiology, Rotterdam

6. Erasmus Medical Center, Departments of Radiology & Nuclear Medicine and Alzheimer Center Erasmus MC, Rotterdam, The Netherlands

7. Amstelland Hospital, Department of Internal Medicine section Geriatrics, Amstelveen

8. Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Radiology, Amsterdam, The Netherlands

9. Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK

10. Amsterdam Neuroscience, Neurodegeneration, Brain Imaging, Amsterdam

11. UMC Utrecht, University of Utrecht, Department of Internal Medicine section Geriatrics, Utrecht

12. Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Epidemiology and Biostatistics, Amsterdam

Abstract

Background: Orthostatic hypotension (OH), an impaired blood pressure (BP) response to postural change, has been associated with cognitive decline and dementia, possibly through cerebral small vessel disease (CSVD). We hypothesized that longer duration of BP drop and a larger BP drop is associated with increased risk of CSVD. Methods: This cross-sectional study included 3971 memory clinic patients (mean age 68 years, 45% female, 42% subjective cognitive complaints, 17% mild cognitive impairment, 41% dementia) from the Amsterdam Ageing Cohort and Amsterdam Dementia Cohort. Early OH (EOH) was defined as a drop in BP of ±20 mmHg systolic and/or 10 mmHg diastolic only at 1 min after standing, and delayed/prolonged OH (DPOH) at 1 and/or 3 min after standing. Presence of CSVD [white matter hyperintensities (WMH), lacunes, microbleeds] was assessed with MRI (n = 3584) or CT brain (n = 389). Results: The prevalence of early OH was 9% and of delayed/prolonged OH 18%. Age- and sex-adjusted logistic regression analyses showed that delayed/prolonged OH, but not early OH, was significantly associated with a higher burden of WMH (OR, 95%CI: 1.21, 1.00–1.46) and lacunes (OR, 95%CI 1.34, 1.06–1.69), but not microbleeds (OR, 95%CI 1.22, 0.89–1.67). When adjusting for supine SBP, these associations attenuated (ORs, 95%CI for WMH 1.04, 0.85–1.27; for lacunes 1.21, 0.91–1.62; for microbleeds 0.95, 0.68–1.31). A larger drop in SBP was associated with increased risk of WMH and microbleeds, however, when adjusted for supine SBP, this effect diminished. Conclusions: Among memory clinic patients, DPOH is more common than EOH. While longer duration and larger magnitude of BP drop coincided with a higher burden of CSVD, these associations were largely explained by high supine BP.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology,Internal Medicine

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