Evidence map›Paper›PMID 36091359›Full record

ArticleFrontiers in physiology2022

Peripheral chemoreflex modulation of renal hemodynamics and renal tissue PO2 in chronic heart failure with reduced ejection fraction.

Kiefer W Kious, Andrew Philipose, Luke J Smith, Jayson P Kemble, Stephanie C E Twohey, Kalie Savage, Hugo S Díaz, Rodrigo Del Rio, Noah J Marcus

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Kiefer W KiousDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Andrew PhiliposeDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Luke J SmithDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Jayson P KembleDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Stephanie C E TwoheyDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Kalie SavageDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Hugo S DíazLaboratory of Cardiorespiratory Control, Department of Physiology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Rodrigo Del RioLaboratory of Cardiorespiratory Control, Department of Physiology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Noah J MarcusDepartment of Physiology and Pharmacology, Des Moines University Medicine and Health Sciences, Des Moines, IA, United States.
Des Moines University · USPontificia Universidad Católica de Chile · CLSimpson College · US

Funding

The Role of the Carotid Body Chemoreflex in the Development of Renal Dysfunction in Chronic Heart FailureR15HL138600 · NHLBI · DES MOINES UNIV OSTEOPATHIC MEDICAL CTR · PI MARCUS, NOAH JUSTIN · 2017 to 2017
$380k
NHLBI NIH HHS R15 HL138600
6 · The paper itself

Abstract

Aberrant carotid body chemoreceptor (CBC) function contributes to increased sympathetic nerve activity (SNA) and reduced renal blood flow (RBF) in chronic heart failure (CHF). Intermittent asphyxia (IA) mimicking sleep apnea is associated with additional increases in SNA and may worsen reductions in RBF and renal PO2 (RPO2) in CHF. The combined effects of decreased RBF and RPO2 may contribute to biochemical changes precipitating renal injury. This study sought to determine the role of CBC activity on glomerular filtration rate (GFR), RBF and RPO2 in CHF, and to assess the additive effects of IA. Furthermore, we sought to identify changes in gene expression that might contribute to renal injury. We hypothesized that GFR, RBF, and RPO2 would be reduced in CHF, that decreases in RBF and RPO2 would be worsened by IA, and that these changes would be ameliorated by CBC ablation (CBD). Finally, we hypothesized that CHF would be associated with pro-oxidative pro-fibrotic changes in renal gene expression that would be ameliorated by CBD. CHF was induced in adult male Sprague Dawley rats using coronary artery ligation (CAL). Carotid body denervation was performed by cryogenic ablation. GFR was assessed in conscious animals at the beginning and end of the experimental period. At 8-weeks post-CAL, cardiac function was assessed via echocardiography, and GFR, baseline and IA RBF and RPO2 were measured. Renal gene expression was measured using qRT-PCR. GFR was lower in CHF compared to sham (

Indexed as

cardio renal syndrome (CRS)carotid body chemoreflexcarotid body denervation (CBD)heart failurerenal blood flow (RBF)renal oxygenation

Identifiers

PMID36091359
PMCPMC9459040
OpenAlexW4293199889

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.