Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/124656
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Type: Journal article
Title: The association between blood pressure variability and cerebral small-vessel disease: a systematic review and meta-analysis
Author: Tully, P.J.
Yano, Y.
Launer, L.
Kario, K.
Nagai, M.
Mooijaart, S.P.
Claassen, J.A.H.R.
Simona Lattanzi, S.
Vincent, A.
Tzourio, C.
Citation: Journal of the American Heart Association, 2020; 9(1):e013841-1-e013841-16
Publisher: Wiley
Issue Date: 2020
ISSN: 2047-9980
2047-9980
Statement of
Responsibility: 
Phillip J. Tully, Yuichiro Yano, Lenore J. Launer, Kazuomi Kario, Michiaki Nagai, Simon P. Mooijaart, Jurgen A.H.R. Claassen, Simona Lattanzi, Andrew D. Vincent, Christophe Tzourio, on behalf of the Variability in Blood Pressure and Brain Health Consortium
Abstract: Background: Research links blood pressure variability (BPV) with stroke; however, the association with cerebral small‐vessel disease (CSVD) remains unclear. As BPV and mean blood pressure are interrelated, it remains uncertain whether BPV adds additional information to understanding cerebrovascular morphological characteristics. Methods and Results: A systematic review was performed from inception until March 3, 2019. Eligibility criteria included population, adults without stroke (<4 weeks); exposure, BPV quantified by any metric over any duration; comparison, (1) low versus high or mean BPV and (2) people with versus without CSVD; and outcomes, (1) CSVD as subcortical infarct, lacunae, white matter hyperintensities, cerebral microbleeds, or enlarged perivascular spaces; and (2) standardized mean difference in BPV. A total of 27 articles were meta‐analyzed, comprising 12 309 unique brain scans. A total of 31 odds ratios (ORs) were pooled, indicating that higher systolic BPV was associated with higher odds for CSVD (OR, 1.27; 95% CI, 1.14–1.42; I2=85%) independent of mean systolic pressure. Likewise, higher diastolic BPV was associated with higher odds for CSVD (OR, 1.30; 95% CI, 1.14–1.48; I2=53%) independent of mean diastolic pressure. There was no evidence of a pairwise interaction between systolic/diastolic and BPV/mean ORs (P=0.47), nor a difference between BPV versus mean pressure ORs (P=0.58). Fifty‐four standardized mean differences were pooled and provided similar results for pairwise interaction (P=0.38) and difference between standardized mean differences (P=0.70). Conclusions: On the basis of the available studies, BPV was associated with CSVD independent of mean blood pressure. However, more high‐quality longitudinal data are required to elucidate whether BPV contributes unique variance to CSVD morphological characteristics.
Keywords: Blood pressure measurement/monitoring; blood pressure variability; high blood pressure; meta-analysis; systematic review; white matter disease
Description: Includes 46 pages of Supplemental Material
Rights: © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
DOI: 10.1161/JAHA.119.013841
Grant ID: http://purl.org/au-research/grants/nhmrc/1053578
Published version: https://www.ahajournals.org/doi/full/10.1161/JAHA.119.013841?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed
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