Evidence map›Paper›PMID 30566191›Full record

Observational studyJAMA cardiology2019

Association of Cardiac Injury and Malignant Left Ventricular Hypertrophy With Risk of Heart Failure in African Americans: The Jackson Heart Study.

Ambarish Pandey, Neil Keshvani, Colby Ayers, Adolfo Correa, Mark H Drazner, Alana Lewis, Carlos J Rodriguez, Michael E Hall, Ervin R Fox, Robert J Mentz and 6 more

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in JAMA cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  14. Validation of the WATCH-DM and TRS-HFJournal of the American Heart Association · 2022
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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

16 authors at 7 institutions in 1 country.

Ambarish PandeyDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Neil KeshvaniDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Colby AyersDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Adolfo CorreaDepartment of Medicine, University of Mississippi Medical Center, Jackson.
Mark H DraznerDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Alana LewisDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Carlos J RodriguezDivision of Cardiology, Department of Internal Medicine, Wake Forest University, Winston-Salem, North Carolina.
Michael E HallDepartment of Medicine, University of Mississippi Medical Center, Jackson.
Ervin R FoxDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Robert J MentzDivision of Cardiology, Duke Clinical Research Institute, Durham, North Carolina.
Christopher deFilippiInova Heart and Vascular Institute, Falls Church, Virginia.
Stephen L SeligerDivision of Nephrology, University of Maryland School of Medicine, Baltimore.
Christie M BallantyneSection of Cardiology and Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, Texas.
Ian J NeelandDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
James A de LemosDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
Jarett D BerryDivision of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.
The University of Texas Southwestern Medical Center · USUniversity of Mississippi Medical Center · USAlaska Heart and Vascular Institute · USBaylor College of Medicine · USClinical Research Institute · USUniversity of Maryland, Baltimore · USWake Forest University · US

Funding

Renal Sinus Fat, Hypertension, and Altered Kidney FunctionK08DK099415 · NIDDK · UNIVERSITY OF MISSISSIPPI MED CTR · PI HALL, MICHAEL EDWARD · 2015 to 2019
$791k
NIDDK NIH HHS K08 DK099415
6 · The paper itself

Abstract

Importance: African Americans have a higher burden of heart failure (HF) risk factors and clinical HF than other racial/ethnic groups. However, the factors underlying the transition from at-risk to clinical HF in African Americans are not well understood. Objective: To evaluate the contributions of left ventricular hypertrophy (LVH) and subclinical myocardial injury as determined by abnormal high-sensitivity cardiac troponin-I (hs-cTnI) measurements toward HF risk among African Americans. Design, Setting, and Participants: This prospective, community-based cohort study was conducted between July 2016 and September 2018 and included African American participants from Jackson, Mississippi enrolled in the Jackson Heart Study without prevalent HF who had hs-cTnI measurements and an echocardiographic examination at baseline. Participants were stratified into categories based on the presence or absence of LVH and subclinical myocardial injury (category 1: hs-cTnI <4 ng/L in women and <6 ng/L in men; category 2: 4-10 ng/L in women and 6-12 ng/L in men; category 3: >10 ng/L in women and >12 ng/L in men). Main Outcomes and Measures: Adjusted associations between LVH, subclinical myocardial injury, and the risk of incident HF hospitalization were assessed using Cox proportional hazards models. Results: The study included 3987 participants (2552 women [64%]; 240 (6.0%) with LVH; 1003 (25.1%) with myocardial injury) with 285 incident HF events over a median follow-up of 9.8 years (interquartile range, 8.9-10.6 years). In adjusted analyses, higher LV mass and subclinical myocardial injury were independently associated with the risk of HF with a significant interaction between the 2 (Pint < 0.001). The highest risk of HF was noted among individuals with both LVH and myocardial injury (absolute incidence, 35%; adjusted hazard ratio [aHR; vs no LVH and no myocardial injury], 5.35; 95% CI, 3.66-7.83). A significant interaction by sex was also observed. Men with LVH and subclinical myocardial injury had an almost 15-fold higher risk of HF (aHR, 14.62; 95% CI, 7.61-28.10) vs those with neither LVH nor injuries. By contrast, women with this phenotype had a nearly 4-fold higher risk of HF (aHR, 3.81; 95% CI, 2.40-6.85). Conclusions and Relevance: The combination of LVH and subclinical myocardial injury identifies a malignant, preclinical HF phenotype in African Americans with a very high risk of HF, particularly among men. This finding could have implications for future screening strategies that are designed to prevent HF in the population.

Indexed as

AdultAgedBlack or African AmericanEchocardiographyFemaleHeart FailureHumansHypertrophy, Left VentricularLongitudinal StudiesMaleMiddle AgedMississippiMyocardial Reperfusion InjuryPrevalenceProspective StudiesRisk FactorsTroponin I

Identifiers

PMID30566191
PMCPMC6439681
OpenAlexW2905154463

What OpenQuestion holds

Textmetadata
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.