Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment

Abstract Background Sarcopenia is a loss of muscle mass and strength causing disability, morbidity, and mortality in older adults, which is characterized by alterations of the neuromuscular junctions (NMJs). SNAP-25 is essential for the maintenance of NMJ integrity, and the expression of this protei...

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Main Authors: Simone Agostini, Roberta Mancuso, Andrea Saul Costa, Franca Rosa Guerini, Fabio Trecate, Rossella Miglioli, Elisabetta Menna, Beatrice Arosio, Mario Clerici, the SA. M. B. A. project
Format: Article
Language:English
Published: BMC 2021-07-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-021-02989-x
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spelling doaj-5e81dcd7cc4d40f696dea2c2d6fa25ec2021-07-25T11:07:01ZengBMCJournal of Translational Medicine1479-58762021-07-0119111110.1186/s12967-021-02989-xSarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatmentSimone Agostini0Roberta Mancuso1Andrea Saul Costa2Franca Rosa Guerini3Fabio Trecate4Rossella Miglioli5Elisabetta Menna6Beatrice Arosio7Mario Clerici8the SA. M. B. A. projectIRCCS Fondazione Don Carlo Gnocchi ONLUSIRCCS Fondazione Don Carlo Gnocchi ONLUSIRCCS Fondazione Don Carlo Gnocchi ONLUSIRCCS Fondazione Don Carlo Gnocchi ONLUSIRCCS Fondazione Don Carlo Gnocchi ONLUSIRCCS Fondazione Don Carlo Gnocchi ONLUSCNR-Institute of NeuroscienceGeriatric Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore PoliclinicoIRCCS Fondazione Don Carlo Gnocchi ONLUSAbstract Background Sarcopenia is a loss of muscle mass and strength causing disability, morbidity, and mortality in older adults, which is characterized by alterations of the neuromuscular junctions (NMJs). SNAP-25 is essential for the maintenance of NMJ integrity, and the expression of this protein was shown to be modulated by the SNAP-25 rs363050 polymorphism and by a number of miRNAs. Methods We analysed these parameters in a cohort of sarcopenic patients undergoing structured rehabilitation. The rs363050 genotype frequency distribution was analyzed in 177 sarcopenic patients and 181 healthy controls (HC). The concentration of seven miRNAs (miR-451a, miR-425-5p, miR155-5p, miR-421-3p, miR-495-3p, miR-744-5p and miR-93-5p), identified by mouse brain miRNome analysis to be differentially expressed in wild type compared to SNAP-25 ± heterozygous mice, was analyzed as well by droplet digital PCR (ddPCR) in a subgroup of severe sarcopenic patients undergoing rehabilitation. Results The SNAP-25 rs363050 AA genotype was significantly more common in sarcopenic patients compared to HC (pc = 0.01); miR-451a was significantly up-regulated in these patients before rehabilitation. Rehabilitation modified miRNAs expression, as miR-155-5p, miR-421-3p, miR-451a, miR-425-5p, miR-744-5p and miR-93-5p expression was significantly up-regulated (p < 0.01), whereas that of miR-495-3p was significantly down-regulated (p < 0.001) by rehabilitation. Notably, rehabilitation-associated improvement of the muscle-skeletal SPPB score was significantly associated with the reduction of miR-451a expression. Conclusion These results support the hypothesis of a role for SNAP-25 in sarcopenia and suggest SNAP-25-associated miRNAs as circulatory biomarkers of rehabilitative outcome for sarcopenia.https://doi.org/10.1186/s12967-021-02989-xSarcopeniaRehabilitationSNAP-25miRNAsBiomarkers
collection DOAJ
language English
format Article
sources DOAJ
author Simone Agostini
Roberta Mancuso
Andrea Saul Costa
Franca Rosa Guerini
Fabio Trecate
Rossella Miglioli
Elisabetta Menna
Beatrice Arosio
Mario Clerici
the SA. M. B. A. project
spellingShingle Simone Agostini
Roberta Mancuso
Andrea Saul Costa
Franca Rosa Guerini
Fabio Trecate
Rossella Miglioli
Elisabetta Menna
Beatrice Arosio
Mario Clerici
the SA. M. B. A. project
Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
Journal of Translational Medicine
Sarcopenia
Rehabilitation
SNAP-25
miRNAs
Biomarkers
author_facet Simone Agostini
Roberta Mancuso
Andrea Saul Costa
Franca Rosa Guerini
Fabio Trecate
Rossella Miglioli
Elisabetta Menna
Beatrice Arosio
Mario Clerici
the SA. M. B. A. project
author_sort Simone Agostini
title Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
title_short Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
title_full Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
title_fullStr Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
title_full_unstemmed Sarcopenia associates with SNAP-25 SNPs and a miRNAs profile which is modulated by structured rehabilitation treatment
title_sort sarcopenia associates with snap-25 snps and a mirnas profile which is modulated by structured rehabilitation treatment
publisher BMC
series Journal of Translational Medicine
issn 1479-5876
publishDate 2021-07-01
description Abstract Background Sarcopenia is a loss of muscle mass and strength causing disability, morbidity, and mortality in older adults, which is characterized by alterations of the neuromuscular junctions (NMJs). SNAP-25 is essential for the maintenance of NMJ integrity, and the expression of this protein was shown to be modulated by the SNAP-25 rs363050 polymorphism and by a number of miRNAs. Methods We analysed these parameters in a cohort of sarcopenic patients undergoing structured rehabilitation. The rs363050 genotype frequency distribution was analyzed in 177 sarcopenic patients and 181 healthy controls (HC). The concentration of seven miRNAs (miR-451a, miR-425-5p, miR155-5p, miR-421-3p, miR-495-3p, miR-744-5p and miR-93-5p), identified by mouse brain miRNome analysis to be differentially expressed in wild type compared to SNAP-25 ± heterozygous mice, was analyzed as well by droplet digital PCR (ddPCR) in a subgroup of severe sarcopenic patients undergoing rehabilitation. Results The SNAP-25 rs363050 AA genotype was significantly more common in sarcopenic patients compared to HC (pc = 0.01); miR-451a was significantly up-regulated in these patients before rehabilitation. Rehabilitation modified miRNAs expression, as miR-155-5p, miR-421-3p, miR-451a, miR-425-5p, miR-744-5p and miR-93-5p expression was significantly up-regulated (p < 0.01), whereas that of miR-495-3p was significantly down-regulated (p < 0.001) by rehabilitation. Notably, rehabilitation-associated improvement of the muscle-skeletal SPPB score was significantly associated with the reduction of miR-451a expression. Conclusion These results support the hypothesis of a role for SNAP-25 in sarcopenia and suggest SNAP-25-associated miRNAs as circulatory biomarkers of rehabilitative outcome for sarcopenia.
topic Sarcopenia
Rehabilitation
SNAP-25
miRNAs
Biomarkers
url https://doi.org/10.1186/s12967-021-02989-x
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