Evidence map›Paper›PMID 30511897›Full record

ArticleJournal of the American Heart Association2018

Pulmonary Vein Ganglia Are Remodeled in the Diabetic Heart.

Guillaume Bassil, Mengmeng Chang, Audrys Pauza, Jesus Diaz Vera, Athanasios Tsalatsanis, Bruce G Lindsey, Sami F Noujaim

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Glia of the heart's nervous system.Nature reviews. Neuroscience · 2025
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Pulmonary Vein Ganglia Are Remodeled in the Diabetic Heart.Journal of the American Heart Association · 2018
    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

7 authors at 3 institutions in 2 countries.

Guillaume Bassil1 Department of Internal Medicine Weill Cornell Medical College New York NY.
Mengmeng Chang2 Department of Molecular Pharmacology and Physiology Morsani College of Medicine University of South Florida Tampa FL.
Audrys Pauza3 Laboratories for Integrative Neuroscience and Endocrinology University of Bristol United Kingdom.
Jesus Diaz Vera2 Department of Molecular Pharmacology and Physiology Morsani College of Medicine University of South Florida Tampa FL.
Athanasios Tsalatsanis4 Research Methodology and Biostatistics Morsani College of Medicine University of South Florida Tampa FL.
Bruce G Lindsey2 Department of Molecular Pharmacology and Physiology Morsani College of Medicine University of South Florida Tampa FL.
Sami F Noujaim2 Department of Molecular Pharmacology and Physiology Morsani College of Medicine University of South Florida Tampa FL.
University of South Florida · USCornell University · USUniversity of Bristol · GB

Funding

Molecular Mechanisms for Atrial Fibrillation in AgingR01HL129136 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI NOUJAIM, SAMI FOUAD · 2015 to 2019
$2.0M
NHLBI NIH HHS R01 HL129136
6 · The paper itself

Abstract

Background Cardiac autonomic neuropathy is thought to cause adverse cardiovascular effects in diabetes mellitus. Pulmonary vein ganglia ( PVG ), which have been implicated in normal and abnormal heart rhythm regulation, have not been fully investigated in type 1 diabetes mellitus (T1D). We examined the functional and anatomical effects of T1D on PVG and studied the details of T1D-induced remodeling on the PVG structure and function. Methods and Results We used a mouse model of T1D (Akita mouse), immunofluorescence, isolated Langendorff-perfused hearts, and mathematical simulations to explore the effects of T1D on PVG . Whole-mount atrial immunofluorescence of choline acetyltransferase and tyrosine hydroxylase labeling showed that sympathetic and parasympathetic somas of the PVG neurons were significantly hypotrophied in T1D hearts versus wild type. Stimulation of PVG in isolated Langendorff-perfused hearts caused more pronounced P-P interval prolongation in wild type compared with Akita hearts. Propranolol resulted in a comparable P-P prolongation in both phenotypes, and atropine led to more pronounced P-P interval shortening in wild type compared with Akita hearts. Numerical modeling using network simulations revealed that a decrease in the sympathetic and parasympathetic activities of PVG in T1D could explain the experimental results. Conclusions T1D leads to PVG remodeling with hypotrophy of sympathetic and parasympathetic cell bodies and a concomitant decrease in the PVG sympathetic and parasympathetic activities.

Indexed as

Neuronal PlasticityAnimalsDiabetes Mellitus, Type 1Diabetic CardiomyopathiesDiabetic NephropathiesDisease Models, AnimalElectrocardiographyFluorescent Antibody TechniqueGangliaHeartMiceMice, Mutant StrainsMicroscopy, ConfocalPulmonary Veinsautonomic nervous systemdiabetes mellituspulmonary vein

Identifiers

PMID30511897
PMCPMC6405566
OpenAlexW2901744265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.