Publication:
Capillary rarefaction from the kidney point of view

dc.contributor.coauthorAfsar, Baris
dc.contributor.coauthorAfsar, Rengin E.
dc.contributor.coauthorOrtiz, Alberto
dc.contributor.coauthorCovic, Adrian
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorDağel, Tuncay
dc.contributor.kuauthorErus, Suat
dc.contributor.kuauthorKanbay, Mehmet
dc.contributor.kuauthorKaya, Ege
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T22:45:28Z
dc.date.issued2018
dc.description.abstractCapillary rarefaction is broadly defined as a reduction in vascular density. Capillary rarefaction in the kidneys is thought to promote hypoxia, impair hemodynamic responses and predispose to chronic kidney disease (CKD) progression and hypertension development. Various mechanisms have been suggested to play a role in the development of capillary rarefaction, including inflammation, an altered endothelial-tubular epithelial cell crosstalk, a relative deficiency in angiogenic growth factors, loss of pericytes, increased activity of Transforming growth factor -beta 1 and thrombospondin-1, vitamin D deficiency, a link to lymphatic neoangiogenesis and INK4a/ARF (Cylin-dependent kinase inhibitor 2a; CDKN2A). In this review, we summarize the tools available to monitor capillary rarefaction noninvasively in the clinic, the contribution of capillary rarefaction to CKD and hypertension, the known mechanisms of capillary rarefaction, and potential future strategies to attenuate capillary rarefaction and reduce its negative impact. Therapeutic strategies to be explored in more detail include optimization of antihypertensive therapy, vitamin D receptor activators, sirtuin 1 activators, Hypoxia inducible factor prolyl hydroxylase inhibitors and stem cell therapy.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipIntensificacion ISCIII
dc.description.sponsorshipRETIC REDINREN [RD 016/0009] A.O. was supported by Intensificacion ISCIII and RETIC REDINREN RD 016/0009 FEDER funds.
dc.description.volume11
dc.identifier.doi10.1093/ckj/sfx133
dc.identifier.eissn2048-8513
dc.identifier.issn2048-8505
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85050679168
dc.identifier.urihttps://doi.org/10.1093/ckj/sfx133
dc.identifier.urihttps://hdl.handle.net/20.500.14288/6089
dc.identifier.wos449486200001
dc.keywordsCapillary
dc.keywordsChronic kidney disease
dc.keywordsHypertension
dc.keywordsHypoxia-inducible factor
dc.keywordsPericyte
dc.keywordsRarefaction
dc.keywordsEndothelial growth-factor
dc.keywordsHypoxia-inducible factor
dc.keywordsMesenchymal transition
dc.keywordsTubulointerstitial fibrosis
dc.keywordsMicrovascular rarefaction
dc.keywordsEssential-hypertension
dc.keywordsInterstitial fibrosis
dc.keywordsVascular rarefaction
dc.keywordsProgenitor cells
dc.keywordsRenal fibrosis
dc.language.isoeng
dc.publisherOxford University Press (OUP)
dc.relation.ispartofClinical Kidney Journal
dc.subjectUrology
dc.subjectNephrology
dc.titleCapillary rarefaction from the kidney point of view
dc.typeReview
dspace.entity.typePublication
local.contributor.kuauthorKanbay, Mehmet
local.contributor.kuauthorDağel, Tuncay
local.contributor.kuauthorErus, Suat
local.contributor.kuauthorKaya, Ege
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1KUH (KOÇ UNIVERSITY HOSPITAL)
local.publication.orgunit2KUH (Koç University Hospital)
local.publication.orgunit2School of Medicine
person.familyNameDağel
person.familyNameErus
person.familyNameKanbay
person.familyNameKaya
person.givenNameTuncay
person.givenNameSuat
person.givenNameMehmet
person.givenNameEge
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