Amino Acid Profiles in Older Adults with Frailty: Secondary Analysis from MetaboFrail and BIOSPHERE Studies

Author:

Calvani Riccardo12ORCID,Picca Anna13ORCID,Rodriguez-Mañas Leocadio45ORCID,Tosato Matteo1ORCID,Coelho-Júnior Hélio José2,Biancolillo Alessandra6ORCID,Laosa Olga37,Gervasoni Jacopo1ORCID,Primiano Aniello1,Santucci Lavinia1ORCID,Giampaoli Ottavia8ORCID,Bourdel-Marchasson Isabelle910,Regueme Sophie C.11,Sinclair Alan J.12,Urbani Andrea12,Landi Francesco12,Gambassi Giovanni12,Marini Federico8ORCID,Marzetti Emanuele12ORCID

Affiliation:

1. Fondazione Policlinico Universitario “Agostino Gemelli” IRCCS, 00168 Rome, Italy

2. Department of Geriatrics and Orthopedics, Università Cattolica del Sacro Cuore, 00168 Rome, Italy

3. Department of Medicine and Surgery, LUM University, 70010 Casamassima, Italy

4. Servicio de Geriatría, Hospital Universitario de Getafe, 28905 Getafe, Spain

5. Centro de Investigación Biomédica en Red “Fragilidad y Envejecimiento Saludable” (CIBERFES), Instituto de Salud Carlos III, 28029 Madrid, Spain

6. Department of Physical and Chemical Sciences, Università degli Studi dell’Aquila, 67100 L’Aquila, Italy

7. Geriatric Research Group, Biomedical Research Foundation at Getafe University Hospital, 28905 Getafe, Spain

8. Department of Chemistry, Sapienza Università di Roma, 00185 Rome, Italy

9. Clinical Gerontology Department, Bordeaux University Hospital, 33000 Bordeaux, France

10. CRMSB, CNRS UMR 5536, Université de Bordeaux, 33000 Bordeaux, France

11. CHU Bordeaux, Pole Gérontologie Clinique, 33000 Bordeaux, France

12. Foundation for Diabetes Research in Older People (fDROP), King’s College, London WC2R 2LS, UK

Abstract

An altered amino acid metabolism has been described in frail older adults which may contribute to muscle loss and functional decline associated with frailty. In the present investigation, we compared circulating amino acid profiles of older adults with physical frailty and sarcopenia (PF&S, n = 94), frail/pre-frail older adults with type 2 diabetes mellitus (F-T2DM, n = 66), and robust non-diabetic controls (n = 40). Partial least squares discriminant analysis (PLS–DA) models were built to define the amino acid signatures associated with the different frailty phenotypes. PLS–DA allowed correct classification of participants with 78.2 ± 1.9% accuracy. Older adults with F-T2DM showed an amino acid profile characterized by higher levels of 3-methylhistidine, alanine, arginine, ethanolamine, and glutamic acid. PF&S and control participants were discriminated based on serum concentrations of aminoadipic acid, aspartate, citrulline, cystine, taurine, and tryptophan. These findings suggest that different types of frailty may be characterized by distinct metabolic perturbations. Amino acid profiling may therefore serve as a valuable tool for frailty biomarker discovery.

Funder

European Commission—EU 7th Framework Programme

Fondazione Roma

Università Cattolica del Sacro Cuore

European Union—Next Generation EU

Italian Ministry of Health

non-profit research foundation “Centro Studi Achille e Linda Lorenzon”

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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