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Cerebrospinal fluid soluble insulin receptor levels in Alzheimer's disease.
Thomas, Peter; Leclerc, Manon; Evitts, Kira; Brown, Caitlin; Miller, Wyatt; Hanson, Angela J; Banks, William A; Gibbons, Laura; Domoto-Reilly, Kimiko; Jayadev, Suman; Li, Ge; Peskind, Elaine; Young, Jessica E; Calon, Frederic; Rhea, Elizabeth M.
Afiliação
  • Thomas P; Geriatric Research Education and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA.
  • Leclerc M; Faculty of Pharmacy Laval University Quebec Quebec Canada.
  • Evitts K; Neuroscience Axis CHU de Québec Research Center - Laval University Quebec Quebec Canada.
  • Brown C; Department of Bioengineering University of Washington Seattle Washington USA.
  • Miller W; Institute for Stem Cells and Regenerative Medicine University of Washington Seattle Washington USA.
  • Hanson AJ; Geriatric Research Education and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA.
  • Banks WA; Geriatric Research Education and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA.
  • Gibbons L; Department of Medicine, Division of Gerontology and Geriatric Medicine University of Washington School of Medicine Seattle Washington USA.
  • Domoto-Reilly K; Geriatric Research Education and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA.
  • Jayadev S; Department of Medicine, Division of Gerontology and Geriatric Medicine University of Washington School of Medicine Seattle Washington USA.
  • Li G; Department of Medicine University of Washington Seattle Washington USA.
  • Peskind E; Department of Neurology University of Washington Seattle Washington USA.
  • Young JE; Department of Neurology University of Washington Seattle Washington USA.
  • Calon F; Veterans Affairs Northwest Mental Illness Research, Education, and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA.
  • Rhea EM; Department of Psychiatry and Behavioral Sciences University of Washington School of Medicine Seattle Washington USA.
Alzheimers Dement (Amst) ; 16(2): e12603, 2024.
Article em En | MEDLINE | ID: mdl-38800123
ABSTRACT

INTRODUCTION:

Brain insulin resistance and deficiency is a consistent feature of Alzheimer's disease (AD). Insulin resistance can be mediated by the surface expression of the insulin receptor (IR). Cleavage of the IR generates the soluble IR (sIR).

METHODS:

We measured the levels of sIR present in cerebrospinal fluid (CSF) from individuals along the AD diagnostic spectrum from two cohorts Seattle (n = 58) and the Consortium for the Early Identification of Alzheimer's Disease-Quebec (CIMA-Q; n = 61). We further investigated the brain cellular contribution for sIR using human cell lines.

RESULTS:

CSF sIR levels were not statistically different in AD. CSF sIR and amyloid beta (Aß)42 and Aß40 levels significantly correlated as well as CSF sIR and cognition in the CIMA-Q cohort. Human neurons expressing the amyloid precursor protein "Swedish" mutation generated significantly greater sIR and human astrocytes were also able to release sIR in response to both an inflammatory and insulin stimulus.

DISCUSSION:

These data support further investigation into the generation and role of sIR in AD. Highlights Cerebrospinal fluid (CSF) soluble insulin receptor (sIR) levels positively correlate with amyloid beta (Aß)42 and Aß40.CSF sIR levels negatively correlate with cognitive performance (Montreal Cognitive Assessment score).CSF sIR levels in humans remain similar across Alzheimer's disease diagnostic groups.Neurons derived from humans with the "Swedish" mutation in which Aß42 is increased generate increased levels of sIR.Human astrocytes can also produce sIR and generation is stimulated by tumor necrosis factor α and insulin.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article