1. Sex-Specific Metabolic Pathways Were Associated with Alzheimer’s Disease (AD) Endophenotypes in the European Medical Information Framework for AD Multimodal Biomarker Discovery Cohort
- Author
-
Kristel Sleegers, Frans R.J. Verhey, Giovanni B. Frisoni, Abdul Hye, Ellen Elisa De Roeck, Lorena Rami, José Luis Molinuevo, Cristina Legido-Quigley, Alison L. Baird, Pablo Martinez-Lage, Charlotte E. Teunissen, Lutz Frölich, Petronella Kettunen, Rebecca Green, Pieter Jelle Visser, Jill C. Richardson, Mara ten Kate, Petroula Proitsi, Stuart G. Snowden, Sarah Westwood, Henrik Zetterberg, Gwendoline Peyratout, Magda Tsolaki, Amera A. Ebshiana, Karen Meersmans, R. Vandenberghe, Alberto Lleó, Kaj Blennow, Isabelle Bos, Valerija Dobricic, Daniel Alcolea, Stephanie J.B. Vos, Julius Popp, Anders Wallin, Alejo J. Nevado-Holgado, Liu Shi, Philip Scheltens, Johannes Streffer, Peter Johannsen, Min Kim, Régis Bordet, Mikel Tainta, Sebastiaan Engelborghs, Simon Lovestone, Lars Bertram, Jodie Lord, Yvonne Freund-Levi, Olivier Blin, Jin Xu, Silvy Gabel, European Medical Information Framework Consortium, RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9), Clinical sciences, Neuroprotection & Neuromodulation, Neurology, Clinical chemistry, Amsterdam Neuroscience - Neurodegeneration, Amsterdam Neuroscience - Neuroinfection & -inflammation, and Radiology and nuclear medicine
- Subjects
Oncology ,medicine.medical_specialty ,QH301-705.5 ,tryptophan betaine ,Medicine (miscellaneous) ,Disease ,Kynurenate ,Article ,General Biochemistry, Genetics and Molecular Biology ,SERUM ,Metabolomics ,CEREBROSPINAL-FLUID ,MARKERS ,blood ,Dopamine ,Internal medicine ,KYNURENINE ,sex ,Medicine ,OLDER-PEOPLE ,Biology (General) ,BRAIN ,Biomarker discovery ,Biology ,METAANALYSIS ,business.industry ,neurology ,DEMENTIA ,Pharmacology. Therapy ,metabolic pathway ,vanillylmandelate ,Alzheimer's disease ,metabolomics ,Chemistry ,Endophenotype ,Cohort ,Human medicine ,Serotonin ,business ,Alzheimer’s disease ,medicine.drug - Abstract
Altres ajuts: Fundació Bancària Obra Social La Caixa, Fundació Catalana Síndrome de Down, Fundació La Marató de TV3, Fundación Española para el Fomento de la Investigación de la Esclerosis Lateral Amiotrófica, Fundación BBVA i Fundació Víctor Grífols i Lucas Background: physiological differences between males and females could contribute to the development of Alzheimer's Disease (AD). Here, we examined metabolic pathways that may lead to precision medicine initiatives. Methods: We explored whether sex modifies the association of 540 plasma metabolites with AD endophenotypes including diagnosis, cerebrospinal fluid (CSF) biomarkers, brain imaging, and cognition using regression analyses for 695 participants (377 females), followed by sex-specific pathway overrepresentation analyses, APOE ε4 stratification and assessment of metabolites' discriminatory performance in AD. Results: In females with AD, vanillylmandelate (tyrosine pathway) was increased and tryptophan betaine (tryptophan pathway) was decreased. The inclusion of these two metabolites (area under curve (AUC) = 0.83, standard error (SE) = 0.029) to a baseline model (covariates + CSF biomarkers, AUC = 0.92, SE = 0.019) resulted in a significantly higher AUC of 0.96 (SE = 0.012). Kynurenate was decreased in males with AD (AUC = 0.679, SE = 0.046). Conclusions: metabolic sex-specific differences were reported, covering neurotransmission and inflammation pathways with AD endophenotypes. Two metabolites, in pathways related to dopamine and serotonin, were associated to females, paving the way to personalised treatment.
- Published
- 2021
- Full Text
- View/download PDF