Abstract:
:Duchenne muscular dystrophy (DMD) is a common and severe X-linked myopathy, characterized by muscle degeneration due to altered or absent dystrophin. DMD has no effective cure, and the underlying molecular mechanisms remain incompletely understood. The aim of this study is to investigate the metabolic changes in DMD using mass spectrometry-based imaging. Nine human muscle biopsies from DMD patients and nine muscle biopsies from control individuals were subjected to untargeted MSI using matrix-assisted laser desorption/ionization Fourier-transform ion cyclotron resonance mass spectrometry. Both univariate and pattern recognition techniques have been used for data analysis. This study revealed significant changes in 34 keys metabolites. Seven metabolites were decreased in the Duchenne biopsies compared to control biopsies including adenosine triphosphate, and glycerophosphocholine. The other 27 metabolites were increased in the Duchenne biopsies, including sphingomyelin, phosphatidylcholines, phosphatidic acids and phosphatidylserines. Most of these dysregulated metabolites are tightly related to energy and phospholipid metabolism. This study revealed a deep metabolic remodelling in phospholipids and energy metabolism in DMD. This systems-based approach enabled exploring the metabolism in DMD in an unprecedented holistic and unbiased manner with hypothesis-free strategies.
journal_name
Sci Repjournal_title
Scientific reportsauthors
Dabaj I,Ferey J,Marguet F,Gilard V,Basset C,Bahri Y,Brehin AC,Vanhulle C,Leturcq F,Marret S,Laquerrière A,Schmitz-Afonso I,Afonso C,Bekri S,Tebani Adoi
10.1038/s41598-021-81090-1subject
Has Abstractpub_date
2021-01-21 00:00:00pages
1906issue
1issn
2045-2322pii
10.1038/s41598-021-81090-1journal_volume
11pub_type
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