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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7722685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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