Increased arterial stiffness was associated with cSVD, with an odds ratio of 1.24 per standard deviation increase (P < 0.01).
Are impaired cerebrovascular reactivity, cerebral autoregulation, and increased arterial stiffness associated with cerebral small vessel disease?
Participants from 142 studies (60 in meta-analysis) assessing radiological markers of cerebral small vessel disease (cSVD). The cerebrovascular reactivity (CVR) meta-analysis included 7 studies with 536 participants (32.9% women). The arterial stiffness (AS) meta-analysis included 37 studies with 27,952 participants (53.0% women).
Impaired cerebrovascular reactivity (CVR), impaired cerebral autoregulation, and increased arterial stiffness (AS)
Normal vascular function/stiffness or continuous comparison
Presence or progression of radiological markers of cerebral small vessel disease (cSVD) assessed by MRIsurrogate
Elevated arterial stiffness and impaired cerebrovascular reactivity are significantly associated with a higher burden of cerebral small vessel disease.
Absolute Event Rate: 0% vs 0%
Background Cerebral small vessel disease (cSVD) is a major contributing factor to ischemic stroke and dementia. However, the vascular pathologies of cSVD remain inconclusive. The aim of this systematic review and meta‐analysis was to characterize the associations between cSVD and cerebrovascular reactivity (CVR), cerebral autoregulation, and arterial stiffness (AS). Methods and Results MEDLINE, Web of Science, and Embase were searched from inception to September 2023 for studies reporting CVR, cerebral autoregulation, or AS in relation to radiological markers of cSVD. Data were extracted in predefined tables, reviewed, and meta‐analyses performed using inverse‐variance random effects models to determine pooled odds ratios (ORs). A total of 1611 studies were identified; 142 were included in the systematic review, of which 60 had data available for meta‐analyses. Systematic review revealed that CVR, cerebral autoregulation, and AS were consistently associated with cSVD (80.4%, 78.6%, and 85.4% of studies, respectively). Meta‐analysis in 7 studies (536 participants, 32.9% women) revealed a borderline association between impaired CVR and cSVD (OR, 2.26 95% CI, 0.99–5.14; P =0.05). In 37 studies (27 952 participants, 53.0% women) increased AS, per SD, was associated with cSVD (OR, 1.24 95% CI, 1.15–1.33; P <0.01). Meta‐regression adjusted for comorbidities accounted for one‐third of the AS model variance ( R 2 =29.4%, P moderators =0.02). Subgroup analysis of AS studies demonstrated an association with white matter hyperintensities (OR, 1.42 95% CI, 1.18–1.70; P <0.01). Conclusions The collective findings of the present systematic review and meta‐analyses suggest an association between cSVD and impaired CVR and elevated AS. However, longitudinal investigations into vascular stiffness and regulatory function as possible risk factors for cSVD remain warranted.
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Britton Scheuermann
Kansas State University
Shannon K. Parr
Kansas State University
Kiana M. Schulze
Kansas State University
Journal of the American Heart Association
St. Jude Children's Research Hospital
Cancer Research Center
Kansas State University
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Scheuermann et al. (Mon,) reported a other. Increased arterial stiffness was associated with cSVD, with an odds ratio of 1.24 per standard deviation increase (P < 0.01).
synapsesocial.com/papers/696857df6e935609b6785c41 — DOI: https://doi.org/10.1161/jaha.123.032616