Bradykinin B


Journal

BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793

Informations de publication

Date de publication:
11 05 2023
Historique:
received: 17 05 2022
accepted: 30 04 2023
medline: 15 5 2023
pubmed: 12 5 2023
entrez: 11 5 2023
Statut: epublish

Résumé

Intradialytic hypotension (IDH) is a common clinical complication and is associated with increased morbidity and mortality in patients undergoing maintenance hemodialysis (MHD). The pathogenesis of IDH has been attributed to the rapid reduction of plasma volume during hemodialysis and the inadequate compensatory mechanisms in response to hypovolemia, such as the lack of vasoconstriction. This may be due to the increased production of vasodilators, such as bradykinin. In this study we test the hypothesis that bradykinin B We performed a post-hoc analysis of a double-blind, placebo-controlled, randomized, 2 × 2 crossover clinical trial comparing the continuous infusion of icatibant, a bradykinin B Seven of the patients had IDH, defined as a reduction of systolic blood pressure equal to or greater than 20 mmHg during hemodialysis. Stratified analysis, based on the presence of IDH, revealed that icatibant prevented the decrease in blood pressure compared to placebo in patients with IDH [blood pressure at average nadir (2.5 h after hemodialysis): Placebo,114.3 ± 8.9 vs. icatibant, 125.6 ± 9.1 mmHg, mean ± S.E.M]. Icatibant did not affect blood pressure in the group of patients without IDH. Bradykinin B2 receptor blocker may prevent the occurrence of IDH. Further studies should evaluate the hemodynamic effects of icatibant during hemodialysis and the symptomatology associated with IDH.

Identifiants

pubmed: 37170244
doi: 10.1186/s12882-023-03192-4
pii: 10.1186/s12882-023-03192-4
pmc: PMC10176680
doi:

Substances chimiques

Receptors, Bradykinin 0
Bradykinin S8TIM42R2W

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

134

Subventions

Organisme : NIDDK NIH HHS
ID : K23DK100533
Pays : United States
Organisme : NCRR NIH HHS
ID : 1UL-1RR024975
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Jorge L Gamboa (JL)

Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, 2222 Pierce Avenue 561B-PRB, Nashville, TN, 37232-6602, USA. jorge.gamboa@vanderbilt.edu.

Cindy A Mambungu (CA)

Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.
Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.

Adrienne R Clagett (AR)

Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.
Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.

Hui Nian (H)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.

Chang Yu (C)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.

T Alp Ikizler (TA)

Veterans Administration Tennessee Valley Healthcare System, Nashville, TN, USA.
Department of Medicine, Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.

Nancy J Brown (NJ)

Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, 2222 Pierce Avenue 561B-PRB, Nashville, TN, 37232-6602, USA.

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Classifications MeSH