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Association between brain amyloid deposition and longitudinal changes of white matter hyperintensities.
Cha, Woo-Jin; Yi, Dahyun; Ahn, Hyejin; Byun, Min Soo; Chang, Yoon Young; Choi, Jung-Min; Kim, Kyungtae; Choi, Hyeji; Jung, Gijung; Kang, Koung Mi; Sohn, Chul-Ho; Lee, Yun-Sang; Kim, Yu Kyeong; Lee, Dong Young.
Afiliação
  • Cha WJ; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
  • Yi D; Institute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea.
  • Ahn H; Interdisciplinary program of cognitive science, Seoul National University College of Humanities, Seoul, Republic of Korea.
  • Byun MS; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
  • Chang YY; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Choi JM; Department of Psychiatry, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea.
  • Kim K; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
  • Choi H; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
  • Jung G; Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
  • Kang KM; Institute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea.
  • Sohn CH; Department of Radiology, Seoul National University Hospital, Seoul, Republic of Korea.
  • Lee YS; Department of Radiology, Seoul National University Hospital, Seoul, Republic of Korea.
  • Kim YK; Department of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Lee DY; Department of Nuclear Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Alzheimers Res Ther ; 16(1): 50, 2024 03 07.
Article em En | MEDLINE | ID: mdl-38454444
ABSTRACT

BACKGROUND:

Growing evidence suggests that not only cerebrovascular disease but also Alzheimer's disease (AD) pathological process itself cause cerebral white matter degeneration, resulting in white matter hyperintensities (WMHs). Some preclinical evidence also indicates that white matter degeneration may precede or affect the development of AD pathology. This study aimed to clarify the direction of influence between in vivo AD pathologies, particularly beta-amyloid (Aß) and tau deposition, and WMHs through longitudinal approach.

METHODS:

Total 282 older adults including cognitively normal and cognitively impaired individuals were recruited from the Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's Disease (KBASE) cohort. The participants underwent comprehensive clinical and neuropsychological assessment, [11C] Pittsburgh Compound B PET for measuring Aß deposition, [18F] AV-1451 PET for measuring tau deposition, and MRI scans with fluid-attenuated inversion recovery image for measuring WMH volume. The relationships between Aß or tau deposition and WMH volume were examined using multiple linear regression analysis. In this analysis, baseline Aß or tau were used as independent variables, and change of WMH volume over 2 years was used as dependent variable to examine the effect of AD pathology on increase of WMH volume. Additionally, we set baseline WMH volume as independent variable and longitudinal change of Aß or tau deposition for 2 years as dependent variables to investigate whether WMH volume could precede AD pathologies.

RESULTS:

Baseline Aß deposition, but not tau deposition, had significant positive association with longitudinal change of WMH volume over 2 years. Baseline WMH volume was not related with any of longitudinal change of Aß or tau deposition for 2 years. We also found a significant interaction effect between baseline Aß deposition and sex on longitudinal change of WMH volume. Subsequent subgroup analyses showed that high baseline Aß deposition was associated with increase of WMH volume over 2 years in female, but not in male.

CONCLUSIONS:

Our findings suggest that Aß deposition accelerates cerebral WMHs, particularly in female, whereas white matter degeneration appears not influence on longitudinal Aß increase. The results also did not support any direction of influence between tau deposition and WMHs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva / Substância Branca Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva / Substância Branca Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article