Cerebrospinal fluid soluble insulin receptor levels in Alzheimer's disease.

IF 4 Q1 CLINICAL NEUROLOGY Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring Pub Date : 2024-05-25 eCollection Date: 2024-04-01 DOI:10.1002/dad2.12603
Peter Thomas, Manon Leclerc, Kira Evitts, Caitlin Brown, Wyatt Miller, Angela J Hanson, William A Banks, Laura Gibbons, Kimiko Domoto-Reilly, Suman Jayadev, Ge Li, Elaine Peskind, Jessica E Young, Frederic Calon, Elizabeth M Rhea
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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 (Aβ)42 and Aβ40 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 (Aβ)42 and Aβ40.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 Aβ42 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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阿尔茨海默病的脑脊液可溶性胰岛素受体水平。
简介脑胰岛素抵抗和缺乏是阿尔茨海默病(AD)的一贯特征。胰岛素抵抗可由胰岛素受体(IR)的表面表达介导。胰岛素受体裂解会产生可溶性胰岛素受体(sIR):我们测量了两个队列中AD诊断谱系个体脑脊液(CSF)中的sIR水平:西雅图(n = 58)和魁北克阿尔茨海默病早期识别联合会(CIMA-Q;n = 61)。我们利用人类细胞系进一步研究了脑细胞对sIR的贡献:结果:AD 患者的 CSF sIR 水平没有统计学差异。在CIMA-Q队列中,CSF sIR与淀粉样蛋白β(Aβ)42和Aβ40水平显著相关,CSF sIR与认知能力也显著相关。表达淀粉样前体蛋白 "瑞典 "突变的人类神经元能产生明显更多的sIR,人类星形胶质细胞也能在炎症和胰岛素刺激下释放sIR:讨论:这些数据支持进一步研究sIR在AD中的产生和作用:脑脊液(CSF)可溶性胰岛素受体(sIR)水平与淀粉样β(Aβ)42和Aβ40呈正相关。人类星形胶质细胞也可产生 sIR,肿瘤坏死因子 α 和胰岛素可刺激其产生。
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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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