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Proteomic analyses reveal plasma EFEMP1 and CXCL12 as biomarkers and determinants of neurodegeneration

by Clinical Neuropsychologist | Monday, August 12, 2024 | Dementia

Abstract INTRODUCTION Plasma proteomic analyses of unique brain atrophy patterns may illuminate peripheral drivers of neurodegeneration and identify novel biomarkers for predicting clinically relevant outcomes. METHODS We identified proteomic signatures associated...

The MIND diet, brain transcriptomic alterations, and dementia

by Clinical Neuropsychologist | Monday, August 12, 2024 | Dementia

Abstract INTRODUCTION Dietary patterns are associated with dementia risk, but the underlying molecular mechanisms are largely unknown. METHODS We used RNA sequencing data from post mortem prefrontal cortex tissue and annual cognitive evaluations from 1204 participants...

APOE ε4–associated downregulation of the IL‐7/IL‐7R pathway in effector memory T cells: Implications for Alzheimer’s disease

by Clinical Neuropsychologist | Monday, August 12, 2024 | Dementia

Abstract INTRODUCTION The apolipoprotein E (APOE) ε4 allele exerts a significant influence on peripheral inflammation and neuroinflammation, yet the underlying mechanisms remain elusive. METHODS The present study enrolled 54 patients diagnosed with late-onset...

Association of cortical morphology, white matter hyperintensity, and glymphatic function in frontotemporal dementia variants

by Clinical Neuropsychologist | Monday, August 12, 2024 | Dementia

Abstract INTRODUCTION Frontotemporal dementia (FTD) can be phenotypically divided into behavioral variant FTD (bvFTD), nonfluent variant primary progressive aphasia (nfvPPA), and semantic variant PPA (svPPA). However, the neural underpinnings of this phenotypic...

Whole exome sequencing analyses identified novel genes for Alzheimer’s disease and related dementia

by Clinical Neuropsychologist | Monday, August 12, 2024 | Dementia

Abstract INTRODUCTION The heritability of Alzheimer’s disease (AD) is estimated to be 58%–79%. However, known genes can only partially explain the heritability. METHODS Here, we conducted gene-based exome-wide association study (ExWAS) of rare variants and...
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