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Racial and Ethnic Disparities in Transthyretin Cardiac Amyloidosis.

Authors :
Spencer-Bonilla G
Njoroge JN
Pearson K
Witteles RM
Aras MA
Alexander KM
Source :
Current cardiovascular risk reports [Curr Cardiovasc Risk Rep] 2021 Jun; Vol. 15 (6). Date of Electronic Publication: 2021 Apr 04.
Publication Year :
2021

Abstract

Purpose of Review: Transthyretin amyloid cardiomyopathy (ATTR-CM) is a life-threatening disease that disproportionately affects older adults and people of African descent. This review discusses current knowledge regarding racial and ethnic disparities in the diagnosis and management of ATTR-CM.<br />Recent Findings: Historically, ATTR-CM was thought to be a rare cause of heart failure. Recent evidence has shown that ATTR-CM is more common among older adults, men, and people of African descent. In addition, significant geographic variation exists in the identification of amyloid cardiomyopathy. Despite the high burden of ATTR-CM among Black individuals, most clinical data for ATTR-CM are from North America and Europe. Moreover, only a minority of clinical trial participants thus far have been Black patients. In addition to racial differences, socioeconomic disparities may be further compounded by the potentially prohibitive cost and limited accessibility of disease-modifying ATTR therapies.<br />Summary: ATTR-CM is an important cause of heart failure that disproportionately affects people of African descent. Efforts to promote earlier identification of ATTR-CM in general practice will likely improve clinical outcomes for all groups. Future trials should strive to enroll a higher proportion of Black patients. Furthermore, enhanced efforts are warranted to improve treatment accessibility among racial and ethnic minority groups that may be more likely to be affected by ATTR-CM.

Details

Language :
English
ISSN :
1932-9520
Volume :
15
Issue :
6
Database :
MEDLINE
Journal :
Current cardiovascular risk reports
Publication Type :
Academic Journal
Accession number :
35280930
Full Text :
https://doi.org/10.1007/s12170-021-00670-y