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      Prognostic Value of a 6-Minute Walk Test in Patients With Transthyretin Cardiac Amyloidosis

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          Abstract

          Background

          The 6-minute walk test (6MWT) represents a comprehensive functional assessment that is commonly used in patients with heart failure; however, data are lacking in patients with transthyretin cardiac amyloidosis (ATTR-CA).

          Objectives

          This study aimed to assess the prognostic importance of the 6MWT in patients with ATTR-CA.

          Methods

          A retrospective analysis of patients diagnosed with ATTR-CA at the National Amyloidosis Centre who underwent a baseline 6MWT between 2011 and 2023 identified 2,141 patients, of whom 1,118 had follow-up at 1 year.

          Results

          The median baseline 6MWT distance was 347 m (Q1-Q3: 250-428 m) and analysis by quartiles demonstrated an increased death rate with each distance reduction (deaths per 100 person-years: 6.3 vs 9.2 vs 13.6 vs 19.0; log-rank P < 0.001). A 6MWT distance of <350 m was associated with a 2.2-fold higher risk of mortality (HR: 2.15; 95% CI: 1.85-2.50; P < 0.001), with a similar increased risk across National Amyloidosis Centre disease stages ( P for interaction = 0.761) and genotypes ( P for interaction = 0.172). An absolute (reduction of >35 m) and relative worsening (reduction of >5%) of 6MWT at 1 year was associated with an increased risk of mortality (HR: 1.80; 95% CI: 1.51-2.15; P < 0.001 and HR: 1.89; 95% CI: 1.59-2.24; P < 0.001, respectively), which was similar across the aforementioned subgroups. When combined with established measures of disease progression (N-terminal pro–B-type natriuretic peptide progression and outpatient diuretic intensification), each incremental increase in progression markers was associated with an increased death rate (deaths per 100 person-years: 7.6 vs 13.9 vs 22.4 vs 32.9; log-rank P < 0.001).

          Conclusions

          The baseline 6MWT distance can refine risk stratification beyond traditional prognosticators. A worsening 6MWT distance can stratify disease progression and, when combined with established markers, identifies patients at the highest risk of mortality.

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          Most cited references21

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          ATS statement: guidelines for the six-minute walk test.

          (2002)
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            Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy

            Transthyretin amyloid cardiomyopathy is caused by the deposition of transthyretin amyloid fibrils in the myocardium. The deposition occurs when wild-type or variant transthyretin becomes unstable and misfolds. Tafamidis binds to transthyretin, preventing tetramer dissociation and amyloidogenesis.
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              A new staging system for cardiac transthyretin amyloidosis

              Cardiac transthyretin (ATTR) amyloidosis is an increasingly recognized, progressive, and fatal cardiomyopathy, the natural history of which remains unclear. We sought to establish and validate a new prognostic staging system applicable to patients with both wild-type ATTR (ATTRwt) and hereditary variant ATTR (ATTRv) amyloid cardiomyopathy.
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                Author and article information

                Contributors
                Journal
                J Am Coll Cardiol
                J Am Coll Cardiol
                Journal of the American College of Cardiology
                Elsevier Biomedical
                0735-1097
                1558-3597
                02 July 2024
                02 July 2024
                : 84
                : 1
                : 43-58
                Affiliations
                [a ]National Amyloidosis Centre, University College London, Royal Free Campus, London, United Kingdom
                [b ]Tuscan Regional Amyloidosis Centre, Careggi University Hospital, Florence, Italy
                [c ]Center for Diagnosis and Treatment of Cardiomyopathies, Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste, Trieste, Italy
                [d ]Department of Cardiology, Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom
                [e ]Institute of Cardiovascular Sciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom
                [f ]University College London, London, United Kingdom
                [g ]Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA
                Author notes
                [] Address for correspondence: Dr Marianna Fontana, National Amyloidosis Centre, University College London, Royal Free Hospital, Rowland Hill Street, London NW3 2PF, United Kingdom. m.fontana@ 123456ucl.ac.uk
                [∗]

                Drs Ioannou and Fumagalli contributed equally to this work as first authors.

                [†]

                Drs Gioomore and Fontana contributed equally to this work as last authors.

                Article
                S0735-1097(24)06893-1
                10.1016/j.jacc.2024.04.011
                11218050
                38739065
                cd8c3bf7-d445-4ae2-8620-b2cbbf71d62e
                © 2024 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 13 March 2024
                : 3 April 2024
                : 10 April 2024
                Categories
                Original Research

                Cardiovascular Medicine
                6-minute walk test,cardiac attr amyloidosis,prognosis
                Cardiovascular Medicine
                6-minute walk test, cardiac attr amyloidosis, prognosis

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