Evidence map›Paper›PMID 40928765›Full record

ArticleJAMA cardiology2025

Transthyretin Cardiac Amyloidosis in Older Black and Hispanic Individuals With Heart Failure.

Frederick L Ruberg, Sergio Teruya, Stephen Helmke, Dia A Smiley, Denise Fine, Damian Kurian, Farbod Raiszadeh, Tatiana Prokaeva, Brian Spencer, Sherry Wong and 15 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in JAMA cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03812172 (Screening for Cardiac Amyloidosis With Nuclear Cardiology for Minority Populations), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

NCT03812172 completednot on this map

Screening for Cardiac Amyloidosis With Nuclear Cardiology for Minority Populations

TypeobservationalSponsorMathew S. Maurer, MDRan2019 to 2024Enrolled646ConditionsAmyloid Cardiomyopathy, Transthyretin-RelatedArms99mTc-PYP or 99m Tc-HDP
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Fully Automated versus Human Echocardiogram Interpretation in Transthyretin Amyloid Cardiomyopathy: The SCAN-MP Study.Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography · 2026
    Article
  3. Review
  4. Article
  5. Review
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  7. Review
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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

25 authors.

Frederick L RubergSection of Cardiovascular Medicine, Department of Medicine, Boston University Chobanian & Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.
Sergio TeruyaSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Stephen HelmkeSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Dia A SmileySeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Denise FineSection of Cardiovascular Medicine, Department of Medicine, Boston University Chobanian & Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.
Damian KurianDivision of Cardiology, Harlem Hospital Center, New York City Health and Hospital Corporation, New York, New York.
Farbod RaiszadehDivision of Cardiology, Harlem Hospital Center, New York City Health and Hospital Corporation, New York, New York.
Tatiana ProkaevaAmyloidosis Center, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts.
Brian SpencerAmyloidosis Center, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts.
Sherry WongAmyloidosis Center, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts.
Shivda PandeySection of Cardiovascular Medicine, Department of Medicine, Boston University Chobanian & Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.
William S BlanerDepartment of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York.
Albert DeLucaSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Lynne L JohnsonSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Mona P KinkhabwalaSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Jay LebDepartment of Radiology, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Akiva MintzDepartment of Radiology, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Michael P LaValleyDepartment of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Andrew J EinsteinSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.
Elizabeth CohnFeinstein Institutes of Medical Research, Northwell Health, Manhasset, New York.
Cesia GallegosSection of Cardiovascular Medicine, Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Gillian MurtaghAbbott Laboratories, Abbott Park, Illinois.
Jeffery W KellyDepartments of Chemistry and Molecular Medicine, Scripps Research Institute, La Jolla, California.
Edward J MillerSection of Cardiovascular Medicine, Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Mathew S MaurerSeymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York-Presbyterian Hospital, New York, New York.

Funding

Probing the Biochemical Mechanisms of Amyloid DiseaseR01DK046335 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI KELLY, JEFFERY W · 1998 to 2025
$8.8M
SCAN-MP (Screening for Cardiac Amyloidosis with Nuclear imaging in Minority Populations) COVID-19 SuppplementR01HL139671 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAURER, MATHEW S, RUBERG, FREDERICK LIEF · 2019 to 2023
$7.4M
NHLBI NIH HHS R01 HL139671NIDDK NIH HHS R01 DK046335
6 · The paper itself

Abstract

Importance: Transthyretin cardiac amyloidosis (ATTR-CA) is an underdiagnosed but treatable cause of heart failure (HF) in older individuals that occurs in the context of normal wild-type (ATTRwt-CA) or an abnormal inherited (ATTRv-CA) TTR gene variant. While the most common inherited TTR variant, V142I, occurs in 3% to 4% of self-identified Black Americans and is associated with excess morbidity and mortality, the prevalence of ATTR-CA in this at-risk population is unknown. Objective: To define the prevalence of ATTR-CA and proportions attributable to ATTRwt-CA or ATTRv-CA among older Black and Caribbean Hispanic individuals with HF. Design, Setting, and Participants: This prospective, multicenter, cross-sectional study was conducted in several major US cities (Boston, Massachusetts; New York, New York; and New Haven, Connecticut) among individuals who self-identified as Black or Caribbean Hispanic older than 60 years with HF. Participants were enrolled between May 2019 and June 2024, and data analysis was conducted from June 2024 to May 2025. Main Outcomes and Measures: ATTR-CA was determined by radionuclide imaging, with blood testing to exclude light-chain amyloidosis and genotyping to determine TTR gene variant. Echocardiographic, biochemical, physical performance, and quality-of-life data were collected. Results: Among 646 participants, median (IQR) participant age was 73 (66-80) years, 329 (50.6%) were women, 550 (85.1%) identified as Black, and 186 (28.8%) identified as Caribbean Hispanic. Median (IQR) left ventricular wall thickness was 13 (12-14) mm, and median (IQR) left ventricular ejection fraction was 61% (55%-66%). Overall prevalence of ATTR-CA was 6.66% (95% CI, 4.73%-8.58%), of whom 24 (55.8%) had ATTRwt-CA and 19 (44.2%) had ATTRv-CA owing to V142I. Overall prevalence of V142I allele was 5.6%, and of those, 19 (52.8%) had ATTRv-CA. Prevalence of ATTR-CA was 8.15% (95% CI, 5.15%-11.15%) in men and 5.20% (95% CI, 2.79%-7.61%) in women (P = .13). Prevalence of ATTR-CA was 7.82% (95% CI, 5.57%-10.06%) in Black participants and 2.15% (95% CI, 0.07%-4.24%) in Hispanic participants (P = .004). Among Black participants aged 75 years or younger, ATTR-CA was observed in 3.42% of participants (95% CI, 1.43%-5.40%) compared to 14.04% (95% CI, 9.53%-18.54%) of those older than 75 years (P < .001). Among Black male participants older than 75 years, prevalence of ATTR-CA was 17.17% (95% CI, 9.74%-24.60%). Conclusions and Relevance: In this cross-sectional study, ATTR-CA was an important cause of HF in older Black individuals with HF, particularly in men older than 75 years. Approximately half of V142I carriers with HF had ATTR-CA, while 55.8% of all ATTR-CA cases had normal TTR genotype. Trial Registration: ClinicalTrials.gov Identifier: NCT03812172.

Indexed as

Amyloid Neuropathies, FamilialBlack or African AmericanCardiomyopathiesHeart FailureHispanic or LatinoAgedAged, 80 and overCross-Sectional StudiesFemaleHumansMaleMiddle AgedPrealbuminPrevalenceProspective StudiesUnited StatesPrealbumin

Identifiers

PMID40928765
PMCPMC12423950

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Registered trials

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