Evidence map›Paper›PMID 37821712›Full record

ArticleThe international journal of cardiovascular imaging2024

Clinical and genetic predictors of cardiac dysfunction assessed by echocardiography in patients with hereditary hemochromatosis.

Pedro Cortés, Abdelhadi A Elsayed, Fernando F Stancampiano, Fernanda M Barusco, Brian P Shapiro, Yan Bi, Michael G Heckman, Zhongwei Peng, Prakash Kempaiah, William C Palmer

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In one paragraph

Article in The international journal of cardiovascular imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Iron overload cardiomyopathy.Heart failure reviews · 2026
    Review
  2. Review
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

10 authors at 4 institutions in 1 country.

Pedro CortésDivision of Community Internal Medicine, Mayo Clinic, Jacksonville, FL, 32224, USA.ORCID http://orcid.org/0000-0002-2505-2283
Abdelhadi A ElsayedClinical Research Unit, Mayo Clinic, Jacksonville, FL, 32224, USA.
Fernando F StancampianoDivision of Community Internal Medicine, Mayo Clinic, Jacksonville, FL, 32224, USA.ORCID http://orcid.org/0000-0002-9162-1632
Fernanda M BaruscoUniversity of Central Florida, Orlando, FL, 32816, USA.
Brian P ShapiroDivision of Cardiovascular Medicine, Mayo Clinic, Jacksonville, FL, 32224, USA.
Yan BiDivision of Gastroenterology and Hepatology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.
Michael G HeckmanDivision of Clinical Trials and Biostatistics, Mayo Clinic, Jacksonville, FL, 32224, USA.
Zhongwei PengDivision of Clinical Trials and Biostatistics, Mayo Clinic, Jacksonville, FL, 32224, USA.
Prakash KempaiahDivision of Infectious Diseases, Mayo Clinic, Jacksonville, FL, 32224, USA.
William C PalmerDivision of Gastroenterology and Hepatology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA. palmer.william@mayo.edu.
Mayo Clinic in Florida · USJacksonville College · USUniversity of Central Florida · USWinnMed · US

Funding

Division of Community Internal Medicine, Mayo Clinic Florida NA
6 · The paper itself

Abstract

purposeHereditary hemochromatosis (HH) may cause iron deposition in cardiac tissue. We aimed to describe the echocardiographic findings in patients with HH and identify risk factors for cardiac dysfunction.

methodsIn this retrospective study, we included patients with HH who underwent transthoracic echocardiography at our tertiary care center between August 2000 and July 2022. We defined three primary outcomes for cardiac dysfunction: 1) left ventricular ejection fraction (LVEF) < 55%, 2) ratio between early mitral inflow velocity and mitral annular early diastolic velocity (E/e') > 15, and 3) global longitudinal strain (GLS) < 18. Multivariable logistic regression was utilized to identify predictors of cardiac dysfunction.

results582 patients (median age 57 years, 61.2% male) were included. The frequency of LVEF < 55%, E/e

conclusionWe found the traditional risk factors of male sex, and history of myocardial infarction or heart failure, were associated with a reduced LVEF, irrespective of the underlying HFE genetic mutation. Patients with a C282Y/H63D genetic mutation had a higher frequency of myocardial infarction, yet this mutation was associated with reduced odds of diastolic dysfunction compared to other genetic mutations in patients with a normal LVEF.

Indexed as

HemochromatosisMyocardial InfarctionEchocardiographyFemaleHumansMaleMiddle AgedMitral ValvePredictive Value of TestsRetrospective StudiesStroke VolumeVentricular Function, LeftCardiac dysfunctionEchocardiogramHereditary hemochromatosisHFE gene

Identifiers

PMID37821712
OpenAlexW4387542081

What OpenQuestion holds

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Registered trials

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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.