Introduction: The close relationship existing between aging and thrombosis has growingly been studied in this last decade. The age-related development of a prothrombotic imbalance in the fibrinolysis homeostasis has been hypothesized as the basis of this increased cardiovascular and cerebrovascular risk. Fibrinolysis is the result of the interactions among multiple plasminogen activators and inhibitors constituting the enzymatic cascade, and ultimately leading to the degradation of fibrin. The plasminogen activator system plays a key role in a wide range of physiological and pathological processes. Methods: Narrative review. Results: Plasminogen activator inhibitor-1 (PAI-1) is a member of the superfamily of serine-protease inhibitors (or serpins), and the principal inhibitor of both the tissue-type and the urokinase-type plasminogen activator, the two plasminogen activators able to activate plasminogen. Current evidence describing the central role played by PAI-1 in a number of age-related subclinical (i.e., inflammation, atherosclerosis, insulin resistance) and clinical (i.e., obesity, comorbidities, Werner syndrome) conditions is presented. Conclusions: Despite some controversial and unclear issues, PAI-1 represents an extremely promising marker that may become a biological parameter to be progressively considered in the prognostic evaluation, in the disease monitoring, and as treatment target of age-related conditions in the future.

Plasminogen activator inhibitor-1 (PAI-1) : a key factor linking fibrinolysis and age-related subclinical and clinical conditions / M. Cesari, M. Pahor, R. Antonelli Incalzi. - In: CARDIOVASCULAR THERAPEUTICS. - ISSN 1755-5914. - 28:5(2010), pp. e72-e91. [10.1111/j.1755-5922.2010.00171.x]

Plasminogen activator inhibitor-1 (PAI-1) : a key factor linking fibrinolysis and age-related subclinical and clinical conditions

M. Cesari;
2010

Abstract

Introduction: The close relationship existing between aging and thrombosis has growingly been studied in this last decade. The age-related development of a prothrombotic imbalance in the fibrinolysis homeostasis has been hypothesized as the basis of this increased cardiovascular and cerebrovascular risk. Fibrinolysis is the result of the interactions among multiple plasminogen activators and inhibitors constituting the enzymatic cascade, and ultimately leading to the degradation of fibrin. The plasminogen activator system plays a key role in a wide range of physiological and pathological processes. Methods: Narrative review. Results: Plasminogen activator inhibitor-1 (PAI-1) is a member of the superfamily of serine-protease inhibitors (or serpins), and the principal inhibitor of both the tissue-type and the urokinase-type plasminogen activator, the two plasminogen activators able to activate plasminogen. Current evidence describing the central role played by PAI-1 in a number of age-related subclinical (i.e., inflammation, atherosclerosis, insulin resistance) and clinical (i.e., obesity, comorbidities, Werner syndrome) conditions is presented. Conclusions: Despite some controversial and unclear issues, PAI-1 represents an extremely promising marker that may become a biological parameter to be progressively considered in the prognostic evaluation, in the disease monitoring, and as treatment target of age-related conditions in the future.
Aging, Werner syndrome; Coagulation/ thrombosis; Ischemic heart disease; Lipids disorder/ atherosclerosis; Metabolic syndrome; Obesity; Vascular biology; Age Factors; Aging; Animals; Biomarkers; Cardiovascular Diseases; Evidence-Based Medicine; Humans; Plasminogen Activator Inhibitor 1; Risk Assessment; Risk Factors; Signal Transduction; Fibrinolysis; Pharmacology; Cardiology and Cardiovascular Medicine; Pharmacology (medical)
Settore MED/09 - Medicina Interna
2010
Article (author)
File in questo prodotto:
File Dimensione Formato  
Plasminogen Activator Inhibitor-1 (PAI-1)- A Key Factor Linking Fibrinolysis and Age-Related Subclinical and Clinical Conditions - Cesari et al. (2010).pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 222.2 kB
Formato Adobe PDF
222.2 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/550917
Citazioni
  • ???jsp.display-item.citation.pmc??? 180
  • Scopus 324
  • ???jsp.display-item.citation.isi??? 310
social impact