Literature DB >> 27618855

Afro-Caribbean Heart Failure in the United Kingdom: Cause, Outcomes, and ATTR V122I Cardiac Amyloidosis.

Jason N Dungu1, Sofia A Papadopoulou2, Katharine Wykes2, Ihtisham Mahmood2, Joseph Marshall2, Oswaldo Valencia2, Marianna Fontana2, Carol J Whelan2, Julian D Gillmore2, Philip N Hawkins2, Lisa J Anderson2.   

Abstract

BACKGROUND: It has been reported that subjects of African descent present with heart failure at a younger age and because of different causes than whites. We present contemporary data from UK Afro-Caribbean patients in London. METHODS AND
RESULTS: All patients with heart failure presenting to St George's Hospital Heart Failure clinic between 2005 and 2012 were included (n=1392). Patients were predominantly white (71%) and male (67%), and median age at presentation was 73 years (range, 18-100 years). In 211 Afro-Caribbean patients, the most common cause of heart failure was nonischemic dilated cardiomyopathy in 27.5% (whites, 19.9%; P<0.001). Lower rates of ischemic cardiomyopathy were observed (13% versus 41%; P<0.001). The fourth most common cause of heart failure in Afro-Caribbeans was cardiac amyloidosis (11.4%). The prevalence may have been even higher as not all patients were tested for amyloidosis. Patients with ATTR V122I had the worst prognosis compared with other causes of Afro-Caribbean heart failure and white patients. To better understand this condition, we analyzed data from the largest international cohort of ATTR V122I patients, followed up at the UK National Amyloidosis Center (n=72). Patients presented with cardiac failure (median age, 75 [range, 59-90] years). Median survival was 2.6 years from diagnosis.
CONCLUSIONS: In London, the cause of heart failure varies depending on ethnicity and affects age of presentation and outcomes. In Afro-Caribbean patients, ATTR V122I is an underappreciated cause of heart failure, and cardiomyopathy is often misattributed to hypertension. As promising TTR therapies are in development, increased awareness and proactive detection are needed.
© 2016 American Heart Association, Inc.

Entities:  

Keywords:  amyloid; blacks; ethnology; heart failure; prognosis

Mesh:

Substances:

Year:  2016        PMID: 27618855     DOI: 10.1161/CIRCHEARTFAILURE.116.003352

Source DB:  PubMed          Journal:  Circ Heart Fail        ISSN: 1941-3289            Impact factor:   8.790


  20 in total

1.  Estimating cancer risk from 99mTc pyrophosphate imaging for transthyretin cardiac amyloidosis.

Authors:  Andrew J Einstein; Igor Shuryak; Adam Castaño; Akiva Mintz; Mathew S Maurer; Sabahat Bokhari
Journal:  J Nucl Cardiol       Date:  2018-05-30       Impact factor: 5.952

2.  Epidemiology of Cardiac Amyloidosis-Associated Heart Failure Hospitalizations Among Fee-for-Service Medicare Beneficiaries in the United States.

Authors:  Lauren G Gilstrap; Francesca Dominici; Yun Wang; M Samir El-Sady; Amitoj Singh; Marcelo F Di Carli; Rodney H Falk; Sharmila Dorbala
Journal:  Circ Heart Fail       Date:  2019-06-07       Impact factor: 8.790

Review 3.  Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.

Authors:  Frederick L Ruberg; Martha Grogan; Mazen Hanna; Jeffery W Kelly; Mathew S Maurer
Journal:  J Am Coll Cardiol       Date:  2019-06-11       Impact factor: 24.094

4.  ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: Part 1 of 2-evidence base and standardized methods of imaging.

Authors:  Sharmila Dorbala; Yukio Ando; Sabahat Bokhari; Angela Dispenzieri; Rodney H Falk; Victor A Ferrari; Marianna Fontana; Olivier Gheysens; Julian D Gillmore; Andor W J M Glaudemans; Mazen A Hanna; Bouke P C Hazenberg; Arnt V Kristen; Raymond Y Kwong; Mathew S Maurer; Giampaolo Merlini; Edward J Miller; James C Moon; Venkatesh L Murthy; C Cristina Quarta; Claudio Rapezzi; Frederick L Ruberg; Sanjiv J Shah; Riemer H J A Slart; Hein J Verberne; Jamieson M Bourque
Journal:  J Nucl Cardiol       Date:  2019-12       Impact factor: 5.952

Review 5.  A systematic review and meta-analysis of the prevalence of transthyretin amyloidosis in heart failure with preserved ejection fraction.

Authors:  Mohamed Magdi; Mostafa Reda Mostafa; Waiel Abusnina; Ahmad Al-Abdouh; Ramy Doss; Sarah Mohamed; Chidera Philippa Ekpo; Richard Alweis; Bipul Baibhav
Journal:  Am J Cardiovasc Dis       Date:  2022-06-15

6.  Prevalence and Outcomes of p.Val142Ile TTR Amyloidosis Cardiomyopathy: A Systematic Review.

Authors:  Pranav Chandrashekar; Laith Alhuneafat; Meghan Mannello; Lana Al-Rashdan; Morris M Kim; Jason Dungu; Kevin Alexander; Ahmad Masri
Journal:  Circ Genom Precis Med       Date:  2021-08-31

7.  Prevalence of mutant ATTR cardiac amyloidosis in elderly African Americans with heart failure.

Authors:  Marios Arvanitis; Gloria G Chan; Daniel R Jacobson; John L Berk; Lawreen H Connors; Frederick L Ruberg
Journal:  Amyloid       Date:  2017-10-20       Impact factor: 7.141

8.  Geographic Disparities in Reported US Amyloidosis Mortality From 1979 to 2015: Potential Underdetection of Cardiac Amyloidosis.

Authors:  Kevin M Alexander; John Orav; Avinainder Singh; Sophia A Jacob; Adil Menon; Robert F Padera; Marie F Kijewski; Ronglih Liao; Marcelo F Di Carli; Jacob P Laubach; Rodney H Falk; Sharmila Dorbala
Journal:  JAMA Cardiol       Date:  2018-09-01       Impact factor: 14.676

9.  Clinical comparison of V122I genotypic variant of transthyretin amyloid cardiomyopathy with wild-type and other hereditary variants: a systematic review.

Authors:  Amandeep Goyal; Shubham Lahan; Tarun Dalia; Sagar Ranka; Venugopal Brijmohan Bhattad; Ronak R Patel; Zubair Shah
Journal:  Heart Fail Rev       Date:  2021-03-25       Impact factor: 4.214

10.  Diagnosing Transthyretin Cardiac Amyloidosis by Technetium Tc 99m Pyrophosphate: A Test in Evolution.

Authors:  Timothy J Poterucha; Pierre Elias; Sabahat Bokhari; Andrew J Einstein; Albert DeLuca; Mona Kinkhabwala; Lynne L Johnson; Kathleen R Flaherty; Sunil E Saith; Jan M Griffin; Adler Perotte; Mathew S Maurer
Journal:  JACC Cardiovasc Imaging       Date:  2020-11-18
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