Irisin and Secondary Osteoporosis in Humans.

Cushing’s disease Prader–Willi syndrome growth hormone hyperparathyroidism inflammatory bowel disease irisin osteoporosis

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
08 Jan 2022
Historique:
received: 30 11 2021
revised: 31 12 2021
accepted: 05 01 2022
entrez: 21 1 2022
pubmed: 22 1 2022
medline: 23 2 2022
Statut: epublish

Résumé

Irisin is a peptide secreted by skeletal muscle following exercise that plays an important role in bone metabolism. Numerous experiments in vitro and in mouse models have shown that the administration of recombinant irisin promotes osteogenesis, protects osteocytes from dexamethasone-induced apoptosis, prevents disuse-induced loss of bone and muscle mass, and accelerates fracture healing. Although some aspects still need to be elucidated, such as the dose- and frequency-dependent effects of irisin in cell cultures and mouse models, ample clinical evidence is emerging to support its physiological relevance on bone in humans. A reduction in serum irisin levels, associated with an increased risk of osteoporosis and bone fractures, was observed in postmenopausal women and in both men and women during aging, Recently, cohort studies of subjects with secondary osteoporosis showed that these patients have lower circulating levels of irisin, suggesting that this myokine could be a novel marker to monitor bone quality in this disease. Although there are still few studies, this review discusses the emerging data that are highlighting the involvement of irisin in some diseases that cause secondary osteoporosis.

Identifiants

pubmed: 35054874
pii: ijms23020690
doi: 10.3390/ijms23020690
pmc: PMC8775753
pii:
doi:

Substances chimiques

FNDC5 protein, human 0
Fibronectins 0
Recombinant Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Tecnopolo per la Medicina di Precisione
ID : B84I18000540002

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Auteurs

Roberta Zerlotin (R)

Department of Emergency and Organ Transplantation, University of Bari, 70124 Bari, Italy.

Angela Oranger (A)

Department of Emergency and Organ Transplantation, University of Bari, 70124 Bari, Italy.

Patrizia Pignataro (P)

Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari, 70124 Bari, Italy.

Manuela Dicarlo (M)

Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari, 70124 Bari, Italy.

Filippo Maselli (F)

Department of Neurology, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, 16132 Genoa, Italy.

Giorgio Mori (G)

Department of Clinical and Experimental Medicine, University of Foggia, 71100 Foggia, Italy.

Silvia Concetta Colucci (SC)

Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari, 70124 Bari, Italy.

Maria Grano (M)

Department of Emergency and Organ Transplantation, University of Bari, 70124 Bari, Italy.

Graziana Colaianni (G)

Department of Emergency and Organ Transplantation, University of Bari, 70124 Bari, Italy.

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