Evidence map›Paper›PMID 33283202›Full record

ArticleJACC. CardioOncology2020

Plasma Hepatocyte Growth Factor for Diagnosis and Prognosis in Light Chain and Transthyretin Cardiac Amyloidosis.

Kathleen W Zhang, Jennifer Miao, Joshua D Mitchell, Jose Alvarez-Cardona, Kelsey Tomasek, Yan Ru Su, Mary Gordon, R Frank Cornell, Daniel J Lenihan

Abstract read
In one paragraph

Article in JACC. CardioOncology, 2020. 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
–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

9 citing papers in PubMed.

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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

9 authors.

Kathleen W ZhangCardio-Oncology Center of Excellence, Division of Cardiology, Washington University School of Medicine, St. Louis, MO.
Jennifer MiaoDepartment of Internal Medicine, Vanderbilt University Medical Center, Nashville, TN.
Joshua D MitchellCardio-Oncology Center of Excellence, Division of Cardiology, Washington University School of Medicine, St. Louis, MO.
Jose Alvarez-CardonaCardio-Oncology Center of Excellence, Division of Cardiology, Washington University School of Medicine, St. Louis, MO.
Kelsey TomasekDepartment of Internal Medicine, Vanderbilt University Medical Center, Nashville, TN.
Yan Ru SuDepartment of Internal Medicine, Vanderbilt University Medical Center, Nashville, TN.
Mary GordonDepartment of Internal Medicine, Vanderbilt University Medical Center, Nashville, TN.
R Frank CornellDivision of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN.
Daniel J LenihanCardio-Oncology Center of Excellence, Division of Cardiology, Washington University School of Medicine, St. Louis, MO.

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
NCATS NIH HHS UL1 TR002345
6 · The paper itself

Abstract

backgroundDelays in diagnosis of cardiac amyloidosis are common, usually resulting from nonspecific findings on clinical examination and testing. A discriminatory plasma biomarker could result in earlier diagnosis and improve prognosis assessment.

objectivesTo determine the diagnostic and prognostic utility of hepatocyte growth factor (HGF) in light chain and transthyretin cardiac amyloidosis.

methods188 patients with cardiac amyloidosis, amyloidosis without cardiac involvement, or symptomatic heart failure with left ventricular hypertrophy (LVH) or reduced ejection fraction (HFrEF) were enrolled prospectively. Serum biomarkers were measured at study enrollment, and all patients with amyloidosis were followed for all-cause mortality, cardiac transplant, or left ventricular assist device implant. Multinomial logistic regression and Kaplan-Meier survival estimates tested the association of biomarker levels with cardiac amyloidosis and clinical outcomes, respectively. Harrell's C-statistic and the likelihood ratio test compared the prognostic accuracy of plasma biomarkers.

resultsHGF was significantly higher in patients with cardiac amyloidosis (p<0.001). An HGF level of 205 pg/mL discriminated cardiac amyloidosis from LVH and HFrEF with 86% sensitivity, 84% specificity, and an area under the curve of 0.88 (95% CI 0.83-0.94). In patients with amyloidosis, elevated HGF levels were associated with worse event-free survival over a median follow-up period of 2.6 years (p<0.001) with incremental prognostic accuracy over NT-proBNP and troponin-T (p<0.001).

conclusionsHGF discriminates light chain and transthyretin cardiac amyloidosis from patients with symptomatic HF with LVH or HFrEF, and is associated with worse cardiac outcomes. Confirmation of these findings in a larger, multi-center study enrolling confirmed and suspected cases of cardiac amyloidosis is underway.

Indexed as

biomarkerscardiac amyloidosis

Identifiers

PMID33283202
PMCPMC7717591

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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.