TY - JOUR
T1 - Current Medical Therapy and Revascularization in Peripheral Artery Disease of the Lower Limbs: Impacts on Subclinical Chronic Inflammation
AU - Cecchini, Andrea Leonardo
AU - Biscetti, Federico
AU - Manzato, Matteo
AU - Lo Sasso, Lorenzo
AU - Rando, Maria Margherita
AU - Nicolazzi, Maria Anna
AU - Rossini, Enrica
AU - Eraso, Luis H
AU - Dimuzio, Paul J
AU - Massetti, Massimo
AU - Gasbarrini, Antonio
AU - Flex, Andrea
PY - 2023
Y1 - 2023
N2 - Peripheral artery disease (PAD), coronary artery disease (CAD), and cerebrovascular disease (CeVD) are characterized by atherosclerosis and inflammation as their underlying mechanisms. This paper aims to conduct a literature review on pharmacotherapy for PAD, specifically focusing on how different drug classes target pro-inflammatory pathways. The goal is to enhance the choice of therapeutic plans by considering their impact on the chronic subclinical inflammation that is associated with PAD development and progression. We conducted a comprehensive review of currently published original articles, narratives, systematic reviews, and meta-analyses. The aim was to explore the relationship between PAD and inflammation and evaluate the influence of current pharmacological and nonpharmacological interventions on the underlying chronic subclinical inflammation. Our findings indicate that the existing treatments have added anti-inflammatory properties that can potentially delay or prevent PAD progression and improve outcomes, independent of their effects on traditional risk factors. Although inflammation-targeted therapy in PAD shows promising potential, its benefits have not been definitively proven yet. However, it is crucial not to overlook the pleiotropic properties of the currently available treatments, as they may provide valuable insights for therapeutic strategies. Further studies focusing on the anti-inflammatory and immunomodulatory effects of these treatments could enhance our understanding of the mechanisms contributing to the residual risk in PAD and pave the way for the development of novel therapies.
AB - Peripheral artery disease (PAD), coronary artery disease (CAD), and cerebrovascular disease (CeVD) are characterized by atherosclerosis and inflammation as their underlying mechanisms. This paper aims to conduct a literature review on pharmacotherapy for PAD, specifically focusing on how different drug classes target pro-inflammatory pathways. The goal is to enhance the choice of therapeutic plans by considering their impact on the chronic subclinical inflammation that is associated with PAD development and progression. We conducted a comprehensive review of currently published original articles, narratives, systematic reviews, and meta-analyses. The aim was to explore the relationship between PAD and inflammation and evaluate the influence of current pharmacological and nonpharmacological interventions on the underlying chronic subclinical inflammation. Our findings indicate that the existing treatments have added anti-inflammatory properties that can potentially delay or prevent PAD progression and improve outcomes, independent of their effects on traditional risk factors. Although inflammation-targeted therapy in PAD shows promising potential, its benefits have not been definitively proven yet. However, it is crucial not to overlook the pleiotropic properties of the currently available treatments, as they may provide valuable insights for therapeutic strategies. Further studies focusing on the anti-inflammatory and immunomodulatory effects of these treatments could enhance our understanding of the mechanisms contributing to the residual risk in PAD and pave the way for the development of novel therapies.
KW - atherosclerosis
KW - inflammation
KW - lower extremity arterial disease
KW - peripheral artery disease
KW - residual risk
KW - atherosclerosis
KW - inflammation
KW - lower extremity arterial disease
KW - peripheral artery disease
KW - residual risk
UR - https://publicatt.unicatt.it/handle/10807/263556
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85177744761&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85177744761&origin=inward
U2 - 10.3390/ijms242216099
DO - 10.3390/ijms242216099
M3 - Article
SN - 1422-0067
VL - 24
SP - 104
EP - 132
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 22
ER -