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Estimated Pulse-Wave Velocity and Magnetic Resonance Imaging Markers of Cerebral Small-Vessel Disease in the NOMAS.
Ariko, Taylor A; Aimagambetova, Botagoz; Gardener, Hannah; Gutierrez, Jose; Elkind, Mitchell S V; Wright, Clinton B; Zhao, Weizhao; Rundek, Tatjana.
Afiliação
  • Ariko TA; Evelyn F. McKnight Brain Institute, University of Miami Miami FL.
  • Aimagambetova B; Department of Biomedical Engineering University of Miami Miami FL.
  • Gardener H; Evelyn F. McKnight Brain Institute, University of Miami Miami FL.
  • Gutierrez J; Department of Neurology University of Miami Miller School of Medicine Miami FL.
  • Elkind MSV; Evelyn F. McKnight Brain Institute, University of Miami Miami FL.
  • Wright CB; Department of Neurology University of Miami Miller School of Medicine Miami FL.
  • Zhao W; Department of Neurology, Vagelos College of Physicians and Surgeons Columbia University New York NY.
  • Rundek T; Department of Neurology, Vagelos College of Physicians and Surgeons Columbia University New York NY.
J Am Heart Assoc ; 13(15): e035691, 2024 Aug 06.
Article em En | MEDLINE | ID: mdl-39023069
ABSTRACT

BACKGROUND:

Pulse-wave velocity is a measure of arterial stiffness and a risk factor for cardiovascular disease. Recently, an estimated pulse-wave velocity (ePWV) was introduced that was predictive of increased risk of cardiovascular disease. Our objective was to determine whether ePWV was associated with cerebral small-vessel disease on magnetic resonance imaging. METHODS AND

RESULTS:

We included 1257 participants from the NOMAS (Northern Manhattan Study). The ePWV values were calculated using a nonlinear function of age and mean arterial blood pressure. The association between ePWV and white matter hyperintensity volume was assessed. Modification by race and ethnicity was evaluated. Associations between ePWV and other cerebral small-vessel disease markers, covert brain infarcts, cerebral microbleeds, and enlarged perivascular spaces, were explored as secondary outcomes. Mean±SD age of the cohort was 64±8 years; 61% were women; 18% self-identified as non-Hispanic Black, 67% as Hispanic, and 15% as non-Hispanic White individuals. Mean±SD ePWV was 11±2 m/s in the total NOMAS population and was similar across race and ethnic groups. The ePWV was significantly associated with white matter hyperintensity volume (ß=0.23 [95% CI, 0.20-0.26]) after adjustment. Race and ethnicity modified the association between ePWV and white matter hyperintensity volume, with stronger associations in Hispanic and non-Hispanic Black individuals. Significant associations were found between ePWV and covert brain infarcts, cerebral microbleeds, and perivascular spaces after adjustment.

CONCLUSIONS:

The ePWV function may provide a vascular mechanism for deleterious cerebrovascular outcomes in individuals with cerebral small-vessel disease and is particularly apparent in the racial and ethnic minorities represented in the NOMAS cohort.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Doenças de Pequenos Vasos Cerebrais / Rigidez Vascular / Análise de Onda de Pulso Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Doenças de Pequenos Vasos Cerebrais / Rigidez Vascular / Análise de Onda de Pulso Limite: Aged / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article