FTIR Spectroscopy and Blood-Derived Extracellular Vesicles Duo in Alzheimer’s Disease

Author:

Soares Martins Tânia1,Ferreira Maria1,Magalhães Sandra234,Leandro Kevin56,Almeida Luís P. de56,Vogelgsang Jonathan78,Breitling Benedict7,Hansen Niels7,Esselmann Hermann7,Wiltfang Jens179,da Cruz e Silva Odete A.B.1,Nunes Alexandra2,Henriques Ana Gabriela1

Affiliation:

1. Department of Medical Sciences, Neurosciences and Signaling Group, Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal

2. Department of Medical Sciences, Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal

3. Department of Chemistry, CICECO – Aveiro Institute of Materials, University of Aveiro, Aveiro, Portugal

4. Faculty of Medicine, UnIC@RISE – Cardiovascular Research and Development Center, University of Porto, Porto, Portugal

5. Faculty of Pharmacy, Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal

6. ViraVector–Viral Vector for Gene Transfer Core Facility, University of Coimbra, Coimbra, Portugal

7. Department of Psychiatry and Psychotherapy, University Medical Center Goettingen (UMG), Georg-August University, Goettingen, Germany

8. Translational Neuroscience Laboratory, McLean Hospital, Harvard Medical School, Belmont, MA, USA

9. German Center for Neurodegenerative Diseases (DZNE), Goettingen, Germany

Abstract

Background: Alzheimer’s disease (AD) diagnosis is difficult, and new accurate tools based on peripheral biofluids are urgently needed. Extracellular vesicles (EVs) emerged as a valuable source of biomarker profiles for AD, since their cargo is disease-specific and these can be easily isolated from easily accessible biofluids, as blood. Fourier Transform Infrared (FTIR) spectroscopy can be employed to analyze EVs and obtain the spectroscopic profiles from different regions of the spectra, simultaneously characterizing carbohydrates, nucleic acids, proteins, and lipids. Objective: The aim of this study was to identify blood-derived EVs (bdEVs) spectroscopic signatures with AD discriminatory potential. Methods: Herein, FTIR spectra of bdEVs from two biofluids (serum and plasma) and distinct sets of Controls and AD cases were acquired, and EVs’ spectra analyzed. Results: Analysis of bdEVs second derivative peaks area revealed differences between Controls and AD cases in distinct spectra regions, assigned to carbohydrates and nucleic acids, amides, and lipids. Conclusions: EVs’ spectroscopic profiles presented AD discriminatory value, supporting the use of bdEVs combined with FTIR as a screening or complementary tool for AD diagnosis.

Publisher

IOS Press

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