Arterial stiffness and progression of white matter hyperintensities of presumed vascular origin in community-dwelling older adults of Amerindian ancestry: The Atahualpa Project Cohort

Oscar H. Del Brutto, Robertino M. Mera, Aldo F. Costa, Bettsy Y. Recalde, Denisse A. Rumbea, Mark J. Sedler

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6 Citas (Scopus)

Resumen

Objective: Arterial stiffness – as measured by the aortic pulse wave velocity (aPWV) – has been associated with biomarkers of cerebral small vessel disease (cSVD), in particular with white matter hyperintensities (WMH) of presumed vascular origin. Most studies have been conducted in White and Asian populations, and information on this relationship in other ethnic groups is limited. We designed a longitudinal prospective study to assess the impact of aPWV on WMH progression in individuals of Amerindian ancestry. Patients and methods: Participants of the Atahualpa Project Cohort were assessed at baseline with aPWV determinations, clinical interviews and brain MRIs. At the end of the study, brain MRIs were repeated in order to ascertain WMH progression. Poisson regression models adjusted for demographics and cardiovascular risk factors were fitted to assess WMH progression incidence rate by baseline levels of aPWV. Results: The study included 260 individuals aged ≥60 years (mean age: 65.6 ± 6.1 years; 57 % women). The mean aPWV was 9.9 ± 1.5 m/s. Follow-up MRIs revealed WMH progression in 102 (39 %) individuals after a mean follow-up of 6.5 ± 1.4 years. Unadjusted analysis showed a higher baseline aPWV among subjects that developed WMH progression compared with those who did not (p < 0.001). Multivariate Poisson regression models showed an increased WMH progression rate among individuals in the second (IRR: 2.06; 95 % C.I.: 1.09–3.88) and third (IRR: 2.75; 95 % C.I.: 1.29–5.87) tertiles of aPWV compared with those in the first tertile. Conclusions: aPWV is associated with WMH progression, suggesting a link between atherosclerosis and cSVD in the study population.

Idioma originalInglés
Número de artículo107411
PublicaciónClinical Neurology and Neurosurgery
Volumen221
DOI
EstadoPublicada - oct. 2022

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