Effect of Diflunisal in Patients with Transthyretin Cardiomyopathy: A Pilot Study

Author:

Camblor Blasco Andrea123ORCID,Devesa Ana23ORCID,Nieto Roca Luis12ORCID,Gómez-Talavera Sandra124,Lumpuy-Castillo Jairo56ORCID,Pello Lázaro Ana María1,Llanos Jiménez Lucía7,Sánchez González Javier2,Lorenzo Óscar56ORCID,Tuñón Jose148ORCID,Ibáñez Borja124,Aceña Álvaro18

Affiliation:

1. Department of Cardiology, IIS-Fundación Jiménez Díaz University Hospital-Quiron Salud, 28040 Madrid, Spain

2. Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), 28029 Madrid, Spain

3. Mount Sinai Fuster Heart Hospital, New York, NY 10029, USA

4. Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain

5. Laboratory of Diabetes and Vascular Pathology, IIS-Fundación Jiménez Díaz, Universidad Autónoma, 28040 Madrid, Spain

6. Biomedical Research Network on Diabetes and Associated Metabolic Disorders (CIBERDEM), Carlos III National Health Institute, 28029 Madrid, Spain

7. Clinical Research Unit, Fundación Jiménez Díaz University Hospital, FJD Health Research Institute, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28049 Madrid, Spain

8. Faculty of Medicine, Universidad Autónoma de Madrid, 28049 Madrid, Spain

Abstract

Background: ATTR-CM is becoming more prevalent, and disease-modifying therapy has been investigated in recent years with promising results. Diflunisal has shown TTR-stabilizing properties assessed by biomarkers and echocardiography, but there are no trials addressing the evolution of morphological changes with CMR. Methods and Results: AMILCA-DIFLU is an exploratory pilot study prospective, single-center, non-randomized, open-label clinical trial. Patients diagnosed with ATTR-CM underwent clinical, functional, biochemical and imaging assessment before and one year after diflunisal therapy initiation. Of the twelve ATTR-CM patients included, only nine patients completed treatment and study protocol in 12 months. To increase the sample size, we included seven real-world patients with one year of diflunisal treatment. Among the group of patients who completed treatment, diflunisal therapy did not show improvement in cardiac disease status as assessed by many cardiac and inflammatory biomarkers, 6MWT and CMR parameters after one year of treatment. However, a non-significant trend towards stabilization of CMR parameters such as LVEF, ECV and T2 at one year was found. When comparing the group of patients who completed diflunisal therapy and those who did not, a significant decrease in the distance performed in the 6MWT was found in the group of patients who completed treatment at one year (−14 ± 81.8 vs. −173 ± 122.2; p = 0.032). Diflunisal was overall well tolerated, showing only a statistically significant worsening in renal function in the group of diflunisal-treatment patients with no clinical relevance or need for treatment discontinuation. Conclusions: In patients with ATTR-CM, treatment with diflunisal was overall well tolerated and tended to stabilize or slow down amyloid cardiac disease progression assessed by CMR parameters, cardiac and inflammatory biomarkers and functional capacity.

Funder

Carlos III National Health Institute

European Research Council

Ministry of Science and Innovation

ISCIII, the MCN, and the Pro CNIC Foundation and is a Severo Ochoa Center of Excellence

Publisher

MDPI AG

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