Capillary rarefaction from the kidney point of view

Author:

Afsar Baris1,Afsar Rengin E1,Dagel Tuncay2,Kaya Ege3,Erus Suat4,Ortiz Alberto5,Covic Adrian6,Kanbay Mehmet7

Affiliation:

1. Division of Nephrology, Department of Internal Medicine, Suleyman Demirel University School of Medicine, Isparta, Turkey

2. Department of Nephrology, Koc University Hospital, Istanbul, Turkey

3. Koc University School of Medicine, Istanbul, Turkey

4. Department of Thoracic Surgery, Koc University Hospital, Istanbul, Turkey

5. Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Fundación Renal Iñigo Alvarez de Toledo, Madrid, Spain

6. Department of Nephrology, Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania

7. Division of Nephrology, Department of Medicine, Koc University School of Medicine, Istanbul, Turkey

Abstract

ABSTRACT Capillary 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 -β1 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.

Funder

ISCIII

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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