Evidence map›Paper›PMID 37180798›Full record

ArticleFrontiers in cardiovascular medicine2023

Tale of two hearts: a TNNT2 hypertrophic cardiomyopathy case report.

Justin H Pham, John R Giudicessi, Marysia S Tweet, Lauren Boucher, D Brian Newman, Jeffrey B Geske

Abstract readCase Reports
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Justin H PhamMayo Clinic Alix School of Medicine, Mayo Clinic, Rochester, MN, United States.
John R GiudicessiDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester MN, United States.
Marysia S TweetDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester MN, United States.
Lauren BoucherDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester MN, United States.
D Brian NewmanDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester MN, United States.
Jeffrey B GeskeDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester MN, United States.

Funding

The Vascular, Autonomic, and Myocardial Phenotypes in Women with Myocardial Infarction due to Spontaneous Coronary Artery DissectionK23HL155506 · NHLBI · MAYO CLINIC ROCHESTER · PI Marysia S Tweet · 2021 to 2026
$808k
NHLBI NIH HHS K23 HL155506
6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is a heritable cardiomyopathy that is predominantly caused by pathogenic mutations in sarcomeric proteins. Here we report two individuals, a mother and her daughter, both heterozygous carriers of the same HCM-causing mutation in cardiac Troponin T (

Indexed as

cardiac troponin Tcase reportfamilial cardiomyopathyhypertrophic cardiomyopathyincomplete genetic penetranceTNNT2variable genetic expressivity

Identifiers

PMID37180798
PMCPMC10174446

What OpenQuestion holds

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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.