The Regulation and Characterization of Mitochondrial-Derived Methylmalonic Acid in Mitochondrial Dysfunction and Oxidative Stress: From Basic Research to Clinical Practice.
Journal
Oxidative medicine and cellular longevity
ISSN: 1942-0994
Titre abrégé: Oxid Med Cell Longev
Pays: United States
ID NLM: 101479826
Informations de publication
Date de publication:
2022
2022
Historique:
received:
07
04
2021
revised:
16
04
2022
accepted:
23
04
2022
entrez:
3
6
2022
pubmed:
4
6
2022
medline:
7
6
2022
Statut:
epublish
Résumé
Methylmalonic acid (MMA) can act as a diagnosis of hereditary methylmalonic acidemia and assess the status of vitamin B12. Moreover, as a new potential biomarker, it has been widely reported to be associated with the progression and prognosis of chronic diseases such as cardiovascular events, renal insufficiency, cognitive impairment, and cancer. MMA accumulation may cause oxidative stress and impair mitochondrial function, disrupt cellular energy metabolism, and trigger cell death. This review primarily focuses on the mechanisms and epidemiology or progression in the clinical study on MMA.
Identifiants
pubmed: 35656023
doi: 10.1155/2022/7043883
pmc: PMC9155905
doi:
Substances chimiques
Methylmalonic Acid
8LL8S712J7
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
7043883Informations de copyright
Copyright © 2022 Yige Liu et al.
Déclaration de conflit d'intérêts
There are no conflicts of interest to declare.
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