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Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers

AIM: The ε4 allele of apolipoprotein E gene (APOE) is a well‐known risk factor of late‐onset Alzheimer's disease. However, little is known why this variant confers a risk for Alzheimer's disease. The aim of this study was to examine the influence of the APOE genotype on cerebrospinal fluid...

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Autores principales: Sasayama, Daimei, Hattori, Kotaro, Yokota, Yuuki, Matsumura, Ryo, Teraishi, Toshiya, Yoshida, Sumiko, Kunugi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722685/
https://www.ncbi.nlm.nih.gov/pubmed/32426945
http://dx.doi.org/10.1002/npr2.12110
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author Sasayama, Daimei
Hattori, Kotaro
Yokota, Yuuki
Matsumura, Ryo
Teraishi, Toshiya
Yoshida, Sumiko
Kunugi, Hiroshi
author_facet Sasayama, Daimei
Hattori, Kotaro
Yokota, Yuuki
Matsumura, Ryo
Teraishi, Toshiya
Yoshida, Sumiko
Kunugi, Hiroshi
author_sort Sasayama, Daimei
collection PubMed
description AIM: The ε4 allele of apolipoprotein E gene (APOE) is a well‐known risk factor of late‐onset Alzheimer's disease. However, little is known why this variant confers a risk for Alzheimer's disease. The aim of this study was to examine the influence of the APOE genotype on cerebrospinal fluid (CSF) protein levels. METHODS: The present study performed a secondary analysis on our previously generated database to compare the CSF levels of 1128 proteins between APOE‐ε4 carriers (28 subjects) and noncarriers (104 subjects). All subjects were physically healthy Japanese individuals without dementia. RESULTS: CSF levels of apoE2, apoE3, and apoE4 were significantly higher (all nominal P < 10 × 10(−5), false discovery rate < 0.001) and those of tumor necrosis factor‐α (TNF‐α) were significantly lower (nominal P = 1.39 × 10(−6), false discovery rate < 0.001) in APOE‐ε4 carriers than in noncarriers. No significant correlation was observed between the CSF levels of TNF‐α and any of the apoE proteins. CONCLUSIONS: Our findings indicate the possible roles of apoE and TNF‐α in the pathogenesis of APOE‐ε4‐associated Alzheimer's disease.
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spelling pubmed-77226852020-12-08 Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers Sasayama, Daimei Hattori, Kotaro Yokota, Yuuki Matsumura, Ryo Teraishi, Toshiya Yoshida, Sumiko Kunugi, Hiroshi Neuropsychopharmacol Rep Micro Report AIM: The ε4 allele of apolipoprotein E gene (APOE) is a well‐known risk factor of late‐onset Alzheimer's disease. However, little is known why this variant confers a risk for Alzheimer's disease. The aim of this study was to examine the influence of the APOE genotype on cerebrospinal fluid (CSF) protein levels. METHODS: The present study performed a secondary analysis on our previously generated database to compare the CSF levels of 1128 proteins between APOE‐ε4 carriers (28 subjects) and noncarriers (104 subjects). All subjects were physically healthy Japanese individuals without dementia. RESULTS: CSF levels of apoE2, apoE3, and apoE4 were significantly higher (all nominal P < 10 × 10(−5), false discovery rate < 0.001) and those of tumor necrosis factor‐α (TNF‐α) were significantly lower (nominal P = 1.39 × 10(−6), false discovery rate < 0.001) in APOE‐ε4 carriers than in noncarriers. No significant correlation was observed between the CSF levels of TNF‐α and any of the apoE proteins. CONCLUSIONS: Our findings indicate the possible roles of apoE and TNF‐α in the pathogenesis of APOE‐ε4‐associated Alzheimer's disease. John Wiley and Sons Inc. 2020-05-19 /pmc/articles/PMC7722685/ /pubmed/32426945 http://dx.doi.org/10.1002/npr2.12110 Text en © 2020 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Society of NeuropsychoPharmacology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Micro Report
Sasayama, Daimei
Hattori, Kotaro
Yokota, Yuuki
Matsumura, Ryo
Teraishi, Toshiya
Yoshida, Sumiko
Kunugi, Hiroshi
Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title_full Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title_fullStr Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title_full_unstemmed Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title_short Increased apolipoprotein E and decreased TNF‐α in the cerebrospinal fluid of nondemented APOE‐ε4 carriers
title_sort increased apolipoprotein e and decreased tnf‐α in the cerebrospinal fluid of nondemented apoe‐ε4 carriers
topic Micro Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722685/
https://www.ncbi.nlm.nih.gov/pubmed/32426945
http://dx.doi.org/10.1002/npr2.12110
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