Identification of metabolites associated with preserved muscle volume after aneurysmal subarachnoid hemorrhage due to high protein supplementation and neuromuscular electrical stimulation

• Published in: Scientific reports Vol. 14; no. 1; pp. 15071 - 11
• Main Authors: Gusdon, Aaron M., Savarraj, Jude P. J., Feng, Diana, Starkman, Adam, Li, Guoyan, Bodanapally, Uttam, Zimmerman, William, Ryan, Alice S., Choi, Huimahn A., Badjatia, Neeraj
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.07.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 692/308/575; 692/53/2422; 692/617/375/534; Aged; Aneurysm; Aneurysmal subarachnoid hemorrhage; Atrophy; Correlation coefficient; Diet, High-Protein; Dietary Supplements; Electric Stimulation Therapy - methods; Electrical stimuli; Female; High protein diet; Humanities and Social Sciences; Humans; Male; Metabolites; Metabolome; Metabolomic; Metabolomics; Metabolomics - methods; Middle Aged; multidisciplinary; Muscle, Skeletal - metabolism; Muscle, Skeletal - pathology; Muscular Atrophy - etiology; N-acetylleucine; Neuromuscular electrical stimulation; Proteins; Quinolinate; Science; Science (multidisciplinary); Stroke; Subarachnoid hemorrhage; Subarachnoid Hemorrhage - complications; Subarachnoid Hemorrhage - therapy; Metabolomic; High protein diet; Quinolinate; Aneurysmal subarachnoid hemorrhage; Neuromuscular electrical stimulation; acetylleucine; N-acetylleucine
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-64666-5

The INSPIRE randomized clinical trial demonstrated that a high protein diet (HPRO) combined with neuromuscular electrical stimulation (NMES) attenuates muscle atrophy and may improve outcomes after aneurysmal subarachnoid hemorrhage We sought to identify specific metabolites mediating these effects. Blood samples were collected from subjects on admission prior to randomization to either standard of care (SOC; N = 12) or HPRO + NMES (N = 12) and at 7 days. Untargeted metabolomics were performed for each plasma sample. Sparse partial least squared discriminant analysis identified metabolites differentiating each group. Correlation coefficients were calculated between each metabolite and total protein per day and muscle volume. Multivariable models determined associations between metabolites and muscle volume. Unique metabolites (18) were identified differentiating SOC from HPRO + NMES. Of these, 9 had significant positive correlations with protein intake. In multivariable models, N -acetylleucine was significantly associated with preserved temporalis [OR 1.08 (95% CI 1.01, 1.16)] and quadricep [OR 1.08 (95% CI 1.02, 1.15)] muscle volume. Quinolinate was also significantly associated with preserved temporalis [OR 1.05 (95% CI 1.01, 1.09)] and quadricep [OR 1.04 (95% CI 1.00, 1.07)] muscle volume. N -acetylserine and β-hydroxyisovaleroylcarnitine were associated with preserved temporalis or quadricep volume. Metabolites defining HPRO + NMES had strong correlations with protein intake and were associated with preserved muscle volume.