Clinical Phenotype and Prognostic Significance of Frailty in Transthyretin Cardiac Amyloidosis
- Carlo Fumagalli 1, Adam Ioannou 2, Francesco Cappelli 3, Mathew S Maurer 4, Yousuf Razvi 2, Aldostefano Porcari 5, Mattia Zampieri 6, Federico Perfetto 3, Muhammad U Rauf 2, Ana Martinez-Naharro 2, Lucia Venneri 2, Aviva Petrie 7, Carol Whelan 2, Ashutosh Wechalekar 2, Helen Lachmann 2, Philip N Hawkins 2, Iacopo Olivotto 8, Raffaele Marfella 9, Andrea Ungar 10, Niccolò Marchionni 10, Julian D Gillmore 2, Marianna Fontana 2
- 1National Amyloidosis Centre, University College London, London, United Kingdom; Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy; Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.
- 2National Amyloidosis Centre, University College London, London, United Kingdom.
- 3Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy.
- 4Cardiac Amyloidosis Program, New York-Presbyterian Hospital, Columbia University Irving Medical Center, New York, New York, USA.
- 5National Amyloidosis Centre, University College London, London, United Kingdom; Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste, Trieste, Italy.
- 6Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy; Meyer Children's Hospital, IRCCS, Florence, Italy.
- 7University College London, London, United Kingdom.
- 8Meyer Children's Hospital, IRCCS, Florence, Italy.
- 9Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.
- 10Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
- 0National Amyloidosis Centre, University College London, London, United Kingdom; Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy; Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.
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View abstract on PubMed
Summary
This summary is machine-generated.Frailty is common in transthyretin cardiac amyloidosis (ATTR-CA), affecting over half of patients. Assessing frailty improves mortality risk prediction in ATTR-CA patients.
Area Of Science
- Cardiology
- Geriatrics
- Amyloidosis Research
Background
- Frailty prevalence and impact in transthyretin cardiac amyloidosis (ATTR-CA) are not well understood.
- ATTR-CA is a progressive disease affecting the heart.
Purpose Of The Study
- To determine the prevalence of frailty in a large ATTR-CA cohort.
- To identify factors associated with frailty.
- To assess the prognostic value of frailty for mortality.
Main Methods
- 880 ATTR-CA patients were assessed using the Clinical Frailty Scale (CFS).
- Frailty was analyzed continuously and categorically.
- Predictors and mortality associations were evaluated.
Main Results
- 57.1% of patients were frail (CFS ≥ 4).
- Older age, female sex, specific genetic variants, and advanced disease stage predicted frailty.
- Mortality risk increased significantly with higher frailty scores (log-rank P < 0.001).
Conclusions
- Frailty is highly prevalent in ATTR-CA.
- Frailty is an independent predictor of mortality in ATTR-CA.
- Integrating frailty assessment enhances prognostication, especially for short-term risk.
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