Molecular Insights and Novel Approaches toward Individualized Arteriovenous Fistula Care.

Arteriovenus fistula maturation Biomarker Hemodialysis Kidney disease Omics

Journal

Blood purification
ISSN: 1421-9735
Titre abrégé: Blood Purif
Pays: Switzerland
ID NLM: 8402040

Informations de publication

Date de publication:
02 Aug 2022
Historique:
received: 14 03 2022
accepted: 27 06 2022
entrez: 2 8 2022
pubmed: 3 8 2022
medline: 3 8 2022
Statut: aheadofprint

Résumé

The aim of the paper is to summarize the current understanding of the molecular biology of arteriovenous fistula (AVF). It intends to encourage vascular access teams, care providers, and scientists, to explore new molecular tools for assessing the suitability of patients for AVF as vascular access for maintenance hemodialysis (HD). This review also highlights most recent discoveries and may serve as a guide to explore biomarkers and technologies for the assessment of kidney disease patients choosing to start kidney replacement therapy. Objective criteria for AVF eligibility are lacking partly because the underlying physiology of AVF maturation is poorly understood. Several molecular processes during a life cycle of an AVF, even before creation, can be characterized by measuring molecular fingerprints using newest "omics" technologies. In addition to hypothesis-driven strategies, untargeted approaches have the potential to reveal the interplay of hundreds of metabolites, transcripts, proteins, and genes underlying cardiovascular adaptation and vascular access-related adjustments at any given timepoint of a patient with kidney disease. As a result, regular monitoring of modifiable, molecular risk factors together with clinical assessment could help to reduce AVF failure rates, increase patency, and improve long-term outcomes. For the future, identification of vulnerable patients based on the assessment of biological markers of AVF maturation at different stages of the life cycle may aid in individualizing vascular access recommendations.

Identifiants

pubmed: 35917805
pii: 000525831
doi: 10.1159/000525831
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-10

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Xin Wang (X)

RRI Research Laboratory, Renal Research Institute, New York, New York, USA.

Leticia M Tapia Silva (LM)

Nephrology Service, Agustin O'Horan General Hospital Mérida, Mérida, Yucatán, Mexico.

Milind Nikam (M)

Clinical Affairs, Global Medical Office, Fresenius Medical Care, Singapore, Singapore.

Sandip Mitra (S)

Department of Renal Medicine, Manchester Academy of Health Sciences Centre, Manchester University Hospitals, Manchester, United Kingdom.

Syed Shaukat Abbas Zaidi (SSA)

Department of Renal Medicine, Manchester Academy of Health Sciences Centre, Manchester University Hospitals, Manchester, United Kingdom.

Nadja Grobe (N)

RRI Research Laboratory, Renal Research Institute, New York, New York, USA.

Classifications MeSH