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Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease

The protein Major Facilitator Superfamily Domain containing 2A (MFSD2a) was recently described as the primary carrier for docosahexaenoic acid (DHA) into the brain. Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by lower DHA levels in blood lipids. The aim of this...

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Autores principales: Sánchez-Campillo, María, Ruiz-Pastor, María José, Gázquez, Antonio, Marín-Muñoz, Juan, Noguera-Perea, Fuensanta, Ruiz-Alcaraz, Antonio J., Manzanares-Sánchez, Salvadora, Antúnez, Carmen, Larqué, Elvira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981746/
https://www.ncbi.nlm.nih.gov/pubmed/31861865
http://dx.doi.org/10.3390/ijms21010070
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author Sánchez-Campillo, María
Ruiz-Pastor, María José
Gázquez, Antonio
Marín-Muñoz, Juan
Noguera-Perea, Fuensanta
Ruiz-Alcaraz, Antonio J.
Manzanares-Sánchez, Salvadora
Antúnez, Carmen
Larqué, Elvira
author_facet Sánchez-Campillo, María
Ruiz-Pastor, María José
Gázquez, Antonio
Marín-Muñoz, Juan
Noguera-Perea, Fuensanta
Ruiz-Alcaraz, Antonio J.
Manzanares-Sánchez, Salvadora
Antúnez, Carmen
Larqué, Elvira
author_sort Sánchez-Campillo, María
collection PubMed
description The protein Major Facilitator Superfamily Domain containing 2A (MFSD2a) was recently described as the primary carrier for docosahexaenoic acid (DHA) into the brain. Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by lower DHA levels in blood lipids. The aim of this study was to investigate the expression of MFSD2a in the whole blood and brain as a potential biomarker of AD. Three groups were established: 38 healthy controls, 48 subjects with moderate AD (GDS4), and 47 with severe AD (GDS6). We analyzed postmortem brain samples from the hippocampus of 11 healthy controls and 11 severe AD patients. Fatty acid (FA) was determined in serum and brain by gas chromatography. Blood and brain MFSD2a protein expression was analyzed by Western blotting. We found a significant and progressive decline of MFSD2a levels in blood of AD patients (Control 0.83 ± 0.13, GDS4 0.72 ± 0.09, GDS6 0.48 ± 0.05*, p ˂ 0.01). We also corroborated a significant reduction of DHA and other n-3 long-chain polyunsaturated FA in serum of AD. No differences were found in MFSD2a expression or FA levels in brain of controls and AD subjects. MFSD2A carrier was analyzed in AD patients for the first time and the level of MFSD2a in the whole blood could be a potential biomarker of this disease.
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spelling pubmed-69817462020-02-07 Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease Sánchez-Campillo, María Ruiz-Pastor, María José Gázquez, Antonio Marín-Muñoz, Juan Noguera-Perea, Fuensanta Ruiz-Alcaraz, Antonio J. Manzanares-Sánchez, Salvadora Antúnez, Carmen Larqué, Elvira Int J Mol Sci Article The protein Major Facilitator Superfamily Domain containing 2A (MFSD2a) was recently described as the primary carrier for docosahexaenoic acid (DHA) into the brain. Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by lower DHA levels in blood lipids. The aim of this study was to investigate the expression of MFSD2a in the whole blood and brain as a potential biomarker of AD. Three groups were established: 38 healthy controls, 48 subjects with moderate AD (GDS4), and 47 with severe AD (GDS6). We analyzed postmortem brain samples from the hippocampus of 11 healthy controls and 11 severe AD patients. Fatty acid (FA) was determined in serum and brain by gas chromatography. Blood and brain MFSD2a protein expression was analyzed by Western blotting. We found a significant and progressive decline of MFSD2a levels in blood of AD patients (Control 0.83 ± 0.13, GDS4 0.72 ± 0.09, GDS6 0.48 ± 0.05*, p ˂ 0.01). We also corroborated a significant reduction of DHA and other n-3 long-chain polyunsaturated FA in serum of AD. No differences were found in MFSD2a expression or FA levels in brain of controls and AD subjects. MFSD2A carrier was analyzed in AD patients for the first time and the level of MFSD2a in the whole blood could be a potential biomarker of this disease. MDPI 2019-12-20 /pmc/articles/PMC6981746/ /pubmed/31861865 http://dx.doi.org/10.3390/ijms21010070 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sánchez-Campillo, María
Ruiz-Pastor, María José
Gázquez, Antonio
Marín-Muñoz, Juan
Noguera-Perea, Fuensanta
Ruiz-Alcaraz, Antonio J.
Manzanares-Sánchez, Salvadora
Antúnez, Carmen
Larqué, Elvira
Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title_full Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title_fullStr Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title_full_unstemmed Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title_short Decreased Blood Level of MFSD2a as a Potential Biomarker of Alzheimer’s Disease
title_sort decreased blood level of mfsd2a as a potential biomarker of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981746/
https://www.ncbi.nlm.nih.gov/pubmed/31861865
http://dx.doi.org/10.3390/ijms21010070
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