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Patterns of progression of cerebral small vessel disease markers in older adults of Amerindian ancestry: a population-based, longitudinal prospective cohort study.
Del Brutto, Oscar H; Mera, Robertino M; Costa, Aldo F; Rumbea, Denisse A; Recalde, Bettsy Y; Del Brutto, Victor J.
Affiliation
  • Del Brutto OH; School of Medicine and Research Center, Universidad Espíritu Santo-Ecuador, Urbanización Toscana, Apt 3H, Km 4.5 vía Puntilla-Samborondón, 092301, Samborondón, Ecuador. oscardelbrutto@hotmail.com.
  • Mera RM; Biostatistics/Epidemiology, Freenome, Inc., South San Francisco, CA, USA.
  • Costa AF; Department of Neurology, Hospital Universitario Reina Sofía, Córdoba, Spain.
  • Rumbea DA; School of Medicine and Research Center, Universidad Espíritu Santo-Ecuador, Urbanización Toscana, Apt 3H, Km 4.5 vía Puntilla-Samborondón, 092301, Samborondón, Ecuador.
  • Recalde BY; School of Medicine and Research Center, Universidad Espíritu Santo-Ecuador, Urbanización Toscana, Apt 3H, Km 4.5 vía Puntilla-Samborondón, 092301, Samborondón, Ecuador.
  • Del Brutto VJ; Department of Neurology, University of Miami Miller School of Medicine, Miami, FL, USA.
Aging Clin Exp Res ; 34(11): 2751-2759, 2022 Nov.
Article in En | MEDLINE | ID: mdl-35999426
BACKGROUND: Progression of cerebral small vessel disease (cSVD) markers has been studied in different races/ethnic groups. However, information from individuals of Amerindian ancestry is lacking. We sought to evaluate progression patterns of cSVD markers in community-dwelling older adults of Amerindian ancestry. METHODS: Following a longitudinal prospective study design, participants of the Atahualpa Project Cohort aged ≥ 60 years received a baseline brain MRI and clinical interviews. Those who also received a brain MRI at the end of the study were included. Poisson regression models were fitted to assess cSVD markers progression according to their baseline load after a median follow-up of 6.5 ± 1.4 years. Logistic regression models were fitted to assess interrelations in the progression of the different cSVD markers at the end of the study. RESULTS: The study included 263 individuals (mean age: 65.7 ± 6.2 years). Progression of white matter hyperintensities (WMH) was noticed in 103 (39%) subjects, cerebral microbleeds in 25 (12%), lacunes in 12 (5%), and enlarged basal ganglia-perivascular spaces (BG-PVS) in 56 (21%). Bivariate Poisson regression models showed significant associations between WMH severity at baseline and progression of WMH and enlarged BG-PVS. These associations became non-significant in multivariate models adjusted for clinical covariates. Logistic regression models showed interrelated progressions of WMH, cerebral microbleeds and enlarged BG-PVS. The progression of lacunes was independent. CONCLUSIONS: Patterns of cSVD marker progression in this population of Amerindians are different than those reported in other races/ethnic groups. The independent progression of lacunes suggests different pathogenic mechanisms with other cSVD markers.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Small Vessel Diseases Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans Language: En Journal: Aging Clin Exp Res Journal subject: GERIATRIA Year: 2022 Type: Article Affiliation country: Ecuador

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Small Vessel Diseases Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans Language: En Journal: Aging Clin Exp Res Journal subject: GERIATRIA Year: 2022 Type: Article Affiliation country: Ecuador