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

María Sánchez-Campillo(Universidad de Murcia), María José Ruiz-Pastor(Universidad de Murcia), Antonio Gázquez(Universidad de Murcia), Juan Marín-Muñoz(Hospital Universitario Virgen de la Arrixaca), Fuensanta Noguera-Perea(Hospital Universitario Virgen de la Arrixaca), Antonio J. Ruiz‐Alcaraz(Universidad de Murcia), Salvadora Manzanares(Hospital Universitario Virgen de la Arrixaca), Carmen Antúnez(Hospital Universitario Virgen de la Arrixaca), Elvira Larqué(Universidad de Murcia)
International Journal of Molecular Sciences
December 20, 2019
Cited by 27Open Access
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Abstract

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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