Intermittent Hypoxia induces premature adipose tissue senescence leading to cardiac remodeling and dysfunction – HYPOSEN
Obstructive sleep apnea is a growing worldwide health problem. The landmark feature of OSA is a chronic intermittent hypoxia (CIH) responsible for multiple organ damages including heart diseases. Under several pathophysiological conditions such as aging, vWAT senescence drives myocardial alterations through the release of profibrotic factors. Our lab has demonstrated that CIH profoundly alters both vWAT and heart structure and function, but little is known regarding their interactions in the context of CIH. Thus, our primary objective is to demonstrate that CIH induces a premature vWAT senescent phenotype, responsible for subsequent heart dysfunction. From this, we aim at i) bringing the proof-of-concept that strategies targeting CIH-induced vWAT senescence exert beneficial effects on cardiac alterations, and ii) identifying CIH-specific circulating biomarkers that may ultimately contribute to cardiac dysfunction.
Project coordination
Claire ARNAUD (HYPOXIE : PHYSIOPATHOLOGIE CARDIOVASCULAIRE ET RESPIRATOIRE)
The author of this summary is the project coordinator, who is responsible for the content of this summary. The ANR declines any responsibility as for its contents.
Partner
IMRB Institut Mondor de recherche biomédicale
HP2 HYPOXIE : PHYSIOPATHOLOGIE CARDIOVASCULAIRE ET RESPIRATOIRE
IAB Institut pour l'Avancée des Biosciences
Help of the ANR 484,748 euros
Beginning and duration of the scientific project:
December 2020
- 36 Months