Iron Deficiency in Pulmonary Arterial Hypertension: A Deep Dive into the Mechanisms.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
23 02 2021
Historique:
received: 13 01 2021
revised: 13 02 2021
accepted: 18 02 2021
entrez: 6 3 2021
pubmed: 7 3 2021
medline: 27 8 2021
Statut: epublish

Résumé

Pulmonary arterial hypertension (PAH) is a severe cardiovascular disease that is caused by the progressive occlusion of the distal pulmonary arteries, eventually leading to right heart failure and death. Almost 40% of patients with PAH are iron deficient. Although widely studied, the mechanisms linking between PAH and iron deficiency remain unclear. Here we review the mechanisms regulating iron homeostasis and the preclinical and clinical data available on iron deficiency in PAH. Then we discuss the potential implications of iron deficiency on the development and management of PAH.

Identifiants

pubmed: 33672218
pii: cells10020477
doi: 10.3390/cells10020477
pmc: PMC7926484
pii:
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Marceau Quatredeniers (M)

INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique, Hôpital Marie Lannelongue, F-92350 Le Plessis-Robinson, France.
Faculté de Médecine, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

Pedro Mendes-Ferreira (P)

Cardiovascular R&D Center, Faculty of Medicine of the University of Porto, 4200-450 Porto, Portugal.
Paris-Porto Pulmonary Hypertension Collaborative Laboratory (3PH), UMR_S 999, INSERM, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

Diana Santos-Ribeiro (D)

Institute of Experimental and Clinical Research (IREC), Pneumology, ENT and Dermatology, Université catholique de Louvain (UCL), 1060 Brussels, Belgium.

Morad K Nakhleh (MK)

INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique, Hôpital Marie Lannelongue, F-92350 Le Plessis-Robinson, France.
Faculté de Médecine, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

Maria-Rosa Ghigna (MR)

INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique, Hôpital Marie Lannelongue, F-92350 Le Plessis-Robinson, France.
Faculté de Médecine, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

Sylvia Cohen-Kaminsky (S)

INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique, Hôpital Marie Lannelongue, F-92350 Le Plessis-Robinson, France.
Faculté de Médecine, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

Frédéric Perros (F)

INSERM UMR_S 999, Hypertension Pulmonaire: Physiopathologie et Innovation Thérapeutique, Hôpital Marie Lannelongue, F-92350 Le Plessis-Robinson, France.
Faculté de Médecine, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.
Paris-Porto Pulmonary Hypertension Collaborative Laboratory (3PH), UMR_S 999, INSERM, Université Paris-Saclay, F-94270 Le Kremlin-Bicêtre, France.

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