Literature DB >> 28545342

Echocardiographic and clinical findings in patients with Fabry disease during long-term enzyme replacement therapy: a nationwide Danish cohort study.

Christoffer Valdorff Madsen1, Henning Bundgaard2, Åse Krogh Rasmussen1, Søren Schwartz Sørensen3, Jørgen Holm Petersen4, Lars Køber5, Ulla Feldt-Rasmussen1, Helle Petri5.   

Abstract

OBJECTIVES: In patients with Fabry disease (FD), left ventricular hypertrophy and arrhythmias are frequently observed and cardiac involvement is the leading cause of death. Long-term efficacy of enzyme replacement therapy (ERT) on cardiac involvement is unclear. We assessed and compared long-term progression of cardiac involvement according to ERT and non-ERT.
METHODS: We retrospectively assessed and compared long-term progression of cardiac involvement in adult patients with FD in the nationwide Danish cohort. We followed clinical signs, symptoms and findings by echocardiography, electrocardiography and Holter-monitoring.
RESULTS: We included 66 patients; 47 patients (27 women) received ERT (ERT group) and 19 patients (15 women) did not (non-ERT group). The groups were followed for a median of 8 [0-12] years and 6 [0-13] years, respectively. Comparison between ERT and non-ERT receiving patients by left ventricular mass (echocardiographic assessment) and Sokolow-Lyon voltage- and Cornell product criteria (electrocardiographic assessment) revealed no significant differences. In the ERT group, we observed no change in left ventricular mass but a decrease in Sokolow-Lyon voltage- and Cornell product criteria from baseline to follow-up; 30 mm [15-53] vs. 25 mm [3-44], p < 0.005 and 1710 mm·ms [480-3740] vs. 1520 mm·ms [550-5740], p < .05, respectively. There were no changes within the non-ERT group. During follow-up, cardiac symptoms and use of cardiovascular procedures and -medication increased significantly in the ERT group, whereas no differences were observed within the non-ERT group. DISCUSSION: We raise concerns regarding the efficacy and benefit of ERT on cardiac involvement in Fabry disease and stress the need for further research.

Entities:  

Keywords:  Fabry disease; enzyme replacement therapy; familial cardiomyopathies; hypertrophic cardiomyopathy

Mesh:

Substances:

Year:  2017        PMID: 28545342     DOI: 10.1080/14017431.2017.1332383

Source DB:  PubMed          Journal:  Scand Cardiovasc J        ISSN: 1401-7431            Impact factor:   1.589


  5 in total

1.  Cognitive Impairments and Subjective Cognitive Complaints in Fabry Disease: A Nationwide Study and Review of the Literature.

Authors:  Josefine Loeb; Ulla Feldt-Rasmussen; Christoffer Valdorff Madsen; Asmus Vogel
Journal:  JIMD Rep       Date:  2018-04-14

2.  A pilot study of circulating microRNAs as potential biomarkers of Fabry disease.

Authors:  Giuseppe Cammarata; Simone Scalia; Paolo Colomba; Carmela Zizzo; Antonio Pisani; Eleonora Riccio; Michaela Montalbano; Riccardo Alessandro; Antonello Giordano; Giovanni Duro
Journal:  Oncotarget       Date:  2018-06-08

3.  Significant hearing loss in Fabry disease: Study of the Danish nationwide cohort prior to treatment.

Authors:  Puriya Daniel Yazdanfard; Christoffer Valdorff Madsen; Lars Holme Nielsen; Åse Krogh Rasmussen; Jørgen Holm Petersen; Alka Seth; Søren Schwartz Sørensen; Lars Køber; Ulla Feldt-Rasmussen
Journal:  PLoS One       Date:  2019-12-06       Impact factor: 3.240

4.  Serial Analysis of Cardiopulmonary Fitness and Echocardiography in Patients with Fabry Disease Undergoing Enzyme Replacement Therapy.

Authors:  Sheng-Hui Tuan; Pao-Chin Chiu; I-Hsiu Liou; Wen-Hsien Lu; Hung-Ya Huang; Shin-Yi Wu; Guan-Bo Chen; Ko-Long Lin
Journal:  J Rehabil Med Clin Commun       Date:  2020-02-27

5.  Anderson-Fabry disease presenting with atrial fibrillation as earlier sign in a young patient: A case report.

Authors:  Hangyul Kim; Min Gyu Kang; Hyun Woong Park; Jeong-Rang Park; Jin-Yong Hwang; Kyehwan Kim
Journal:  World J Clin Cases       Date:  2021-06-26       Impact factor: 1.337

  5 in total

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