Peristenotic Collateral Circulation in Atherosclerotic Renovascular Disease: Association With Kidney Function and Response to Treatment.
Aged
Atherosclerosis
/ diagnostic imaging
Blood Pressure
/ physiology
Collateral Circulation
/ physiology
Female
Glomerular Filtration Rate
/ physiology
Humans
Kidney
/ diagnostic imaging
Kidney Diseases
/ diagnostic imaging
Magnetic Resonance Imaging
Male
Middle Aged
Multidetector Computed Tomography
Renal Artery Obstruction
/ diagnostic imaging
Renal Circulation
/ physiology
atrophy
hypoxia
inflammation
renal artery
renin
Journal
Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
pubmed:
9
6
2020
medline:
17
4
2021
entrez:
9
6
2020
Statut:
ppublish
Résumé
The significance of peristenotic collateral circulation (PCC) development around a stenotic renal artery is unknown. We tested the hypothesis that PCC is linked to loss of kidney function and recovery potential in patients with atherosclerotic renovascular disease (ARVD). Thirty-four patients with ARVD were assigned to medical-therapy with or without revascularization based on clinical indications. The PCC was visualized using multidetector computed tomography and defined relative to segmental arteries in patients with essential hypertension. PCC number before and 3 months after treatment was correlated with various renal parameters. Thirty-four stenotic kidneys from 30 patients were analyzed. PCC number correlated inversely with kidney volume. ARVD-stenotic kidneys with baseline PCC (collateral ARVD [C-ARVD], n=13) associated with elevated 24-hour urine protein and stenotic kidney vein level of tumor necrosis factor-α, lower single-kidney volume and blood flow, and greater hypoxia than in stenotic kidneys with no PCC (no collateral ARVD [NC-ARVD], n=17). Revascularization (but not medical-therapy alone) improved stenotic kidney function and reduced inflammation in both NC-ARVD and C-ARVD. In C-ARVD, revascularization also increased stenotic kidney volume, blood flow, and oxygenation to levels comparable to NC-ARVD, and induced PCC regression. However, revascularization improved systolic blood pressure, plasma renin activity, and filtration fraction only in NC-ARVD. Therefore, patients with C-ARVD have greater kidney dysfunction, atrophy, hypoxia, and inflammation compared with patients with NC-ARVD, suggesting that PCC does not effectively protect the stenotic kidney in ARVD. Renal artery revascularization improved in C-ARVD stenotic kidney function, but not hypertension or renin-angiotensin system activation. These observations may help direct management of patients with ARVD.
Identifiants
pubmed: 32507040
doi: 10.1161/HYPERTENSIONAHA.120.15057
pmc: PMC7347430
mid: NIHMS1593971
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
497-505Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK122734
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK100081
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK104273
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK102325
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK120292
Pays : United States
Références
J Am Heart Assoc. 2019 Mar 5;8(5):e011220
pubmed: 30819021
Am J Kidney Dis. 1997 Nov;30(5):646-52
pubmed: 9370179
Kidney Int. 2014 Mar;85(3):677-85
pubmed: 24067437
Clin J Am Soc Nephrol. 2016 Jul 7;11(7):1180-8
pubmed: 27225988
Hypertension. 1991 Jun;17(6 Pt 2):982-8
pubmed: 2045180
Ann Surg. 1973 Aug;178(2):138-42
pubmed: 4723421
N Engl J Med. 2014 Jan 2;370(1):13-22
pubmed: 24245566
Ann Intern Med. 2009 Jun 16;150(12):840-8, W150-1
pubmed: 19414832
Hypertension. 2015 May;65(5):976-82
pubmed: 25712725
Curr Opin Nephrol Hypertens. 2016 Mar;25(2):144-51
pubmed: 26741885
Eur Radiol. 2018 Feb;28(2):727-735
pubmed: 28894898
Microcirculation. 2020 Feb;27(2):e12591
pubmed: 31520431
Stroke. 2019 Sep;50(9):2604-2611
pubmed: 31337296
Radiology. 2013 Sep;268(3):770-8
pubmed: 23788716
Radiology. 2015 Aug;276(2):490-8
pubmed: 25848903
Nephrol Dial Transplant. 2016 Nov;31(11):1855-1863
pubmed: 27474749
Circ Cardiovasc Interv. 2012 Oct;5(5):720-8
pubmed: 23048054
Clin J Am Soc Nephrol. 2013 Apr;8(4):546-53
pubmed: 23258796
N Engl J Med. 2009 Nov 12;361(20):1953-62
pubmed: 19907042
Kidney Int. 2019 Apr;95(4):948-957
pubmed: 30904069
JACC Cardiovasc Interv. 2017 May 8;10(9):906-914
pubmed: 28473112
Int J Hypertens. 2019 Jan 30;2019:3872065
pubmed: 30838132
J Vasc Interv Radiol. 2005 Oct;16(10):1295-300
pubmed: 16221898
Medicine (Baltimore). 2018 Apr;97(17):e0417
pubmed: 29702990
Acta Physiol (Oxf). 2019 Sep;227(1):e13292
pubmed: 31046189
Acad Radiol. 2019 Nov;26(11):1488-1494
pubmed: 30655055
Kidney Int. 2003 Jan;63(1):276-82
pubmed: 12472793
Circ Res. 1979 Nov;45(5):579-82
pubmed: 487519
Nephrol Dial Transplant. 2012 Nov;27(11):4153-61
pubmed: 22923545
Am J Hypertens. 2013 Feb;26(2):209-17
pubmed: 23382405
J Am Heart Assoc. 2019 Jun 4;8(11):e012584
pubmed: 31433703
Am J Hypertens. 2018 Nov 13;31(12):1307-1316
pubmed: 30107490
Hypertension. 2010 Apr;55(4):961-6
pubmed: 20194303
J Hypertens. 2018 Jan;36(1):126-135
pubmed: 28786860
J Cardiovasc Comput Tomogr. 2018 Mar - Apr;12(2):149-152
pubmed: 29339048
Hypertension. 2018 Nov;72(5):1023-1030
pubmed: 30354824
World J Nephrol. 2018 Nov 24;7(7):143-147
pubmed: 30510913
J Am Soc Nephrol. 2017 Sep;28(9):2777-2785
pubmed: 28461553
Circulation. 2003 Dec 9;108(23):2877-82
pubmed: 14623811
Stroke. 2015 Nov;46(11):3302-9
pubmed: 26451027
PLoS One. 2019 Jul 10;14(7):e0219605
pubmed: 31291361
Hypertension. 2016 Aug;68(2):401-10
pubmed: 27324229