Novel metabolic and lipidomic biomarkers of sarcopenia

• Published in: Journal of cachexia, sarcopenia and muscle Vol. 15; no. 5; pp. 2175 - 2186
• Main Authors: Hsu, Wei‐Hsiang, Wang, San‐Yuan, Chao, Yen‐Ming, Chang, Ke‐Vin, Han, Der‐Sheng, Lin, Yun‐Lian
• Format: Journal Article
• Language: English
• Published: Germany John Wiley & Sons, Inc 01.10.2024; John Wiley and Sons Inc; Wiley
• Subjects: Aged; Amino acids; Biomarker; Biomarkers; Biomarkers - blood; Body composition; Clinical trials; Cytokines; Exercise; Female; Gait; Hospitals; Humans; Intervention; Lipidome; Lipidomics - methods; Lipids; Male; Metabolism; Metabolites; Metabolome; Metabolomics - methods; Middle Aged; Muscle function; Musculoskeletal system; Nutrition; Older people; Original; Physical fitness; Plasma; Resistance training; Sarcopenia; Sarcopenia - blood; Sarcopenia - diagnosis; Sarcopenia - metabolism; Strength training; United States > US; Metabolome; Sarcopenia; Biomarker; Lipidome; Nutrition; Resistance training
• ISSN: 2190-5991; 2190-6009; 2190-6009
• DOI: 10.1002/jcsm.13567

Background The pathophysiology of sarcopenia is complex and multifactorial and has not been fully elucidated. The impact of resistance training and nutritional support (RTNS) on metabolomics and lipodomics in older adults with sarcopenia remains uncertain. This study aimed to explore potential biomarkers of sarcopenia and clinical indicators of RTNS in older sarcopenic adults. Methods Older individuals diagnosed with sarcopenia through routine health checkups at a community hospital were recruited for a 12‐week randomized controlled trial focusing on RTNS. Plasma metabolomic and lipidomic profiles of 45 patients with sarcopenia and 47 matched controls were analysed using 1H‐nuclear magnetic resonance (1H‐NMR) and liquid chromatography‐mass spectrometer (LC–MS). Results At baseline, the patient and control groups had similar age, sex, and height distribution. The patient group had significantly lower weight, BMI, grip strength, gait speed, skeletal muscle index, lean mass of both the upper and lower limbs, and lower limb bone mass. There was a significant difference in 12 metabolites between the control and patient groups. They are isoleucine (patient/control fold change [FC] = 0.86 ± 0.04, P = 0.0005), carnitine (FC = 1.05 ± 0.01, P = 0.0110), 1‐methylhistamine/3‐methylhistamine (FC = 1.24 ± 0.14, P = 0.0039), creatinine (FC = 0.71 ± 0.04, P < 0.0001), carnosine (FC = 0.71 ± 0.04, P = 0.0007), ureidopropionic acid (FC = 0.61 ± 0.10, P = 0.0107), uric acid (FC = 0.88 ± 0.03, P = 0.0083), PC (18:2/20:0) (FC = 0.69 ± 0.03, P = 0.0010), PC (20:2/18:0) (FC = 0.70 ± 0.06, P = 0.0014), PC (18:1/20:1) (FC = 0.74 ± 0.05, P = 0.0015), PI 32:1 (FC = 4.72 ± 0.17, P = 0.0006), and PI 34:3 (FC = 1.88 ± 0.13, P = 0.0003). Among them, carnitine, 1‐methylhistamine/3‐methylhistamine, creatinine, ureidopropionic acid, uric acid, PI 32:1, and PI 34:3 were first identified. Notably, PI 32:1 had highest diagnostic accuracy (0.938) for sarcopenia. 1‐Methylhistamine/3‐methylhistamine, carnosine, PC (18:2/20:0), PI 32:1, and PI 34:3 levels were not different from the control group after RTNS. These metabolites are involved in amino acid metabolism, lipid metabolism, and the PI3K‐AKT/mTOR signalling pathway through the ingenuity pathway analysis. Conclusions These findings provide information on metabolic changes, lipid perturbations, and the role of RTNS in patients with sarcopenia. They reveal new insights into its pathological mechanisms and potential therapies.