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

Frederick L Ruberg1,2, Sergio Teruya3, Stephen Helmke3

  • 1Section of Cardiovascular Medicine, Department of Medicine, Boston University Chobanian & Avedisian School of Medicine and Boston Medical Center, Boston, Massachusetts.

JAMA Cardiology
|September 10, 2025
PubMed

Insights

Transthyretin cardiac amyloidosis (ATTR-CA) is a significant cause of heart failure in older Black individuals, especially men over 75. This study found ATTR-CA prevalence was 7.82% in Black participants, highlighting its underdiagnosis.

Area of Science:

  • Cardiology
  • Genetics
  • Epidemiology

Background:

  • Transthyretin cardiac amyloidosis (ATTR-CA) is an underdiagnosed cause of heart failure (HF) in older adults.
  • It can be wild-type (ATTRwt-CA) or hereditary (ATTRv-CA) due to TTR gene variants.
  • The V142I variant is common in Black Americans, but ATTR-CA prevalence in this population is unknown.

Purpose of the Study:

  • To determine the prevalence of ATTR-CA in older Black and Caribbean Hispanic individuals with HF.
  • To identify the proportion of ATTR-CA cases due to wild-type (ATTRwt-CA) or variant (ATTRv-CA) TTR genes.

Main Methods:

  • Prospective, multicenter, cross-sectional study of individuals >60 years with HF.
  • ATTR-CA diagnosis via radionuclide imaging, excluding light-chain amyloidosis with blood tests.
  • Genotyping to identify TTR gene variants; collection of echocardiographic, biochemical, and quality-of-life data.

Main Results:

  • Overall ATTR-CA prevalence was 6.66% in 646 participants.
  • Prevalence was higher in Black (7.82%) vs. Hispanic (2.15%) individuals (P=.004).
  • Among Black participants, ATTR-CA was more common in men (8.15%) and those >75 years (14.04%).

Conclusions:

  • ATTR-CA is a significant cause of HF in older Black individuals, particularly men over 75.
  • Approximately half of V142I carriers with HF had ATTR-CA.
  • Over half of all ATTR-CA cases in this cohort had a normal TTR genotype.
Abstract

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