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RESEARCH PRODUCT
Fatty Acid Profiles in Demented Patients: Identification of Hexacosanoic Acid (C26:0) as a Blood Lipid Biomarker of Dementia
Meryam DebbabiSamia Hadj AhmedWafa ChaabaneSofiene Ben AmmouMahbouba FrihAmira ZarroukAmira ZarroukOlivier RouaudJean-marc RiedingerGérard LizardMohamed HammamiSonia Hammamisubject
Malemedicine.medical_specialtyPathologyChromatography GasErythrocytesBlood lipidsNeuropsychological TestsBiologyMass Spectrometrychemistry.chemical_compoundInternal medicinemedicineHumansDementiaVascular dementiaAgedAged 80 and overchemistry.chemical_classificationFatty acid metabolismGeneral NeuroscienceFatty AcidsFatty acidLipid metabolismGeneral MedicineMiddle AgedPeroxisomemedicine.diseasePsychiatry and Mental healthClinical PsychologyEndocrinologyROC CurvechemistryBiomarker (medicine)DementiaFemaleGeriatrics and GerontologyMental Status Scheduledescription
Background: Several lipid metabolism alterations have been described in the brain and plasma of Alzheimer’s disease (AD) patients, suggesting a relation between lipid metabolism alteration and dementia. 15 16 Objective: We attempted to identify blood fatty acids as biomarkers of dementia. 17 Methods: Fatty acid profiles were established using gas chromatography with or without mass spectrometry on matched plasma and red blood cells (RBCs) of demented patients diagnosed with AD, vascular dementia, or other dementia, and compared with a control group of elderly individuals. The severity of dementia was evaluated with the Mini-Mental State Examination test. 18 19 20 Results: Fatty acid analysis showed significant variations of fatty acid levels in demented patients including AD patients. The highest plasma and RBC accumulation was found with hexacosanoic acid (C26:0). These data suggest that alterations of desaturase and elongase activity may contribute to cognitive dysfunction. 21 22 23 Conclusion: The variations of fatty acid levels and the accumulation of C26:0 in the plasma and RBCs highlight an alteration of fatty acid metabolism in demented patients and point toward possible peroxisomal dysfunction. It is suggested that C26:0 may constitute a convenient blood biomarker of dementia that could be useful in routine medical practice. 24 25 26
year | journal | country | edition | language |
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2014-11-28 | Journal of Alzheimer's Disease |