Evidence map›Paper›PMID 32829663›Full record

ArticleHypertension (Dallas, Tex. : 1979)2020

Quantification of Renal Sympathetic Vasomotion as a Novel End Point for Renal Denervation.

Peter Ricci Pellegrino, Irving H Zucker, Yiannis S Chatzizisis, Han-Jun Wang, Alicia M Schiller

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06480786 (Spinal Cord Stimulation for Patients With Painful Diabetic Neuropathy and Peripheral Arterial Disease), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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.

NCT06480786 narecruitingnot on this mapstarted 2024, after this paper: background citation

Spinal Cord Stimulation for Patients With Painful Diabetic Neuropathy and Peripheral Arterial Disease: Mechanistic Insights From a Single-center, Randomized, Blinded, Sham-controlled Cross-over Proof-of-concept Trial

TypeinterventionalSponsorUniversity of NebraskaRan2024 to 2027Enrolled15ConditionsPeripheral Arterial Disease, Painful Diabetic Neuropathy, Diabetes Mellitus, Type 2, Chronic PainArmsSpinal cord stimulation, Sham stimulation
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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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

5 authors at 1 institution in 1 country.

Peter Ricci PellegrinoFrom the Department of Anesthesiology (P.R.P., H.-J.W., A.M.S.), University of Nebraska Medical Center, Omaha.
Irving H ZuckerDepartment of Cellular and Integrative Physiology (I.H.Z., A.M.S., H-J.W.), University of Nebraska Medical Center, Omaha.
Yiannis S ChatzizisisDivision of Cardiovascular Medicine (Y.S.C.), University of Nebraska Medical Center, Omaha.
Han-Jun WangDivision of Cardiovascular Medicine (Y.S.C.), University of Nebraska Medical Center, Omaha.
Alicia M SchillerFrom the Department of Anesthesiology (P.R.P., H.-J.W., A.M.S.), University of Nebraska Medical Center, Omaha.
University of Nebraska Medical Center · US

Funding

The Role of Excitatory Input into the PVN on Increased Sympathetic Drive in HeartP01HL062222 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CORNISH, KURTIS G · 1999 to 2019
$32.2M
Central Rho-Kinase Inhibition and Ang II-induced Sympatho-excitationF30HL118974 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PELLEGRINO, PETER RICCI · 2014 to 2016
$118k
NHLBI NIH HHS F30 HL118974NHLBI NIH HHS P01 HL062222
6 · The paper itself

Abstract

Renal sympathetic denervation, a potentially revolutionary interventional treatment for hypertension, faces an existential problem due to the inability to confirm successful ablation of the targeted renal sympathetic nerves. Based on the observation that renal sympathetic nerve activity exerts rhythmic, baroreflex-driven, and vasoconstrictive control of the renal vasculature, we developed a novel technique for identifying rhythmic sympathetic vascular control using a time-varying, 2-component Windkessel model of the renal circulation. This technology was tested in 2 different animal models of renal denervation; 10 rabbits underwent chronic, surgical renal denervation, and 9 pigs underwent acute, functional renal denervation via intrathecal administration of ropivacaine. Both methods of renal denervation reduced negative admittance gain, negative phase shift renal vascular control at known sympathetic vasomotor frequencies, consistent with a reduction in vasoconstrictive, baroreflex-driven renal sympathetic vasomotion. Classic measures like mean renal blood flow and mean renal vascular resistance were not significantly affected in either model of renal denervation. Renal sympathetic vasomotion monitoring could provide intraprocedural feedback for interventionists performing renal denervation and serve more broadly as a platform technology for the evaluation and treatment of diseases affecting the sympathetic nervous system.

Indexed as

AnimalsBaroreflexDenervationDisease Models, AnimalHeart RateHypertensionKidneyRabbitsSwineSympathectomySympathetic Nervous Systembaroreflexheart failurehomeostasisrenal denervationsympathetic nervous systemvascular resistance

Identifiers

PMID32829663
PMCPMC7673653
OpenAlexW3080606295

What OpenQuestion holds

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Registered trials

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.