Association Between Blood Pressure Variability With Dementia and Cognitive Impairment: A Systematic Review and Meta-Analysis

Author:

de Heus Rianne A.A.1,Tzourio Christophe2ORCID,Lee Emily Jo Lynn3ORCID,Opozda Melissa34,Vincent Andrew D.3,Anstey Kaarin J.56,Hofman Albert7,Kario Kazuomi8ORCID,Lattanzi Simona9ORCID,Launer Lenore J.10ORCID,Ma Yuan7ORCID,Mahajan RajivORCID,Mooijaart Simon P.1112ORCID,Nagai Michiaki13,Peters Ruth1415ORCID,Turnbull Deborah16,Yano Yuichiro1718ORCID,Claassen Jurgen A.H.R.1,Tully Phillip J.3ORCID,

Affiliation:

1. Radboud University Medical Center, Department of Geriatric Medicine, Radboudumc Alzheimer Center, Donders Institute for Brain, Cognition, and Behaviour, Nijmegen, the Netherlands (R.A.A.d.H., J.A.H.R.C.).

2. Bordeaux Population Health, Univeristy of Bordeaux, Inserm, Team Healthy, UMR 1219, CHU Bordeaux, France (C.T.).

3. Adelaide Medical School (E.J.L.L., M.O., A.D.V., P.J.T.), Freemasons Centre for Male Health and Wellbeing, The University of Adelaide, Australia.

4. Centre for Nutrition and Gastrointestinal Research (M.O.), South Australian Health and Medical Research Institute, Australia.

5. School of Psychology (K.J.A.), University of New South Wales, Sydney, Australia.

6. Neuroscience Research Australia (K.J.A.), University of New South Wales, Sydney, Australia.

7. Department of Epidemiology, Harvard T H Chan School of Public Health, Boston, MA (A.H., Y.M.).

8. Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan (K.K.).

9. Neurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy (S.L.).

10. Intramural Research Program, National Institute on Aging, National Institutes of Health, Bethesda, MD (L.J.L.).

11. University of Adelaide, Lyell McEwin Hospital (R.M.), South Australian Health and Medical Research Institute, Australia.

12. Department of Gerontology and Geriatrics, Leiden University Medical Center, Institute for Evidence-Based Medicine in Old Age, the Netherlands (S.P.M.).

13. Department of Cardiology, Hiroshima City Asa Hospital, Japan (M.N.).

14. Neuroscience Research Australia (R.P.), University of New South Wales, Sydney, Australia.

15. Imperial College London, United Kingdom (R.P.).

16. School of Psychology (D.T.), Freemasons Centre for Male Health and Wellbeing, The University of Adelaide, Australia.

17. Yokohama City University Center for Novel and Exploratory Clinical Trials, Yokohama City University Hospital, Japan (Y.Y.).

18. The Department of Family Medicine and Community Health, Duke University, Durham, NC (Y.Y.).

Abstract

Research links high blood pressure variability (BPV) with stroke and cerebrovascular disease, however, its association with cognition remains unclear. Moreover, it remains uncertain which BP-derived parameter (ie, variability or mean) holds more significance in understanding vascular contributions to cognitive impairment. We searched PubMed, Embase, PsycINFO, and Scopus and performed a meta-analysis of studies that quantified the association between resting BPV with dementia or cognitive impairment in adults. Two authors independently reviewed all titles, abstracts, and full-texts and extracted data, following Preferred Reporting Items for Systematic Reviews and Meta-Analyses and Meta-Analysis of Observational Studies in Epidemiology guidelines. Study quality was assessed using the (modified) Newcastle-Ottawa Scale. A multilevel meta-analysis was used, which included effect sizes for both BPV and mean BP, with a combined end point of dementia or cognitive impairment as primary outcome. In the primary analysis, 54 effect sizes were extracted from 20 studies, with a total analytical sample of n=7 899 697. Higher systolic BPV (odds ratio [OR], 1.25 [95% CI, 1.16–1.35]), mean systolic pressure (OR, 1.12 [95% CI, 1.02–1.29]), diastolic BPV (OR, 1.20 [95% CI, 1.12–1.29]), and mean diastolic pressure (OR, 1.16 [95% CI, 1.04–1.29]) were associated with dementia and cognitive impairment. A direct comparison showed that mean BP effect sizes were less strong than BPV effect sizes (OR, 0.92 [95% CI, 0.87–0.97], P <0.01), indicating that the relative contribution of BPV exceeded that of mean BP. Methodological and statistical heterogeneity was high. Secondary analyses were less consistent as to whether BPV and mean BP were differentially associated with dementia subtypes and cognitive domains. Future studies are required to investigate BPV as a target for dementia prevention.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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