Literature DB >> 31378431

Muscle biopsies in clinical trials for Duchenne muscular dystrophy - Patients' and caregivers' perspective.

Ingrid E C Verhaart1, Alex Johnson2, Sejal Thakrar2, Elizabeth Vroom3, Fernanda De Angelis4, Francesco Muntoni5, Annemieke M Aartsma-Rus6, Erik H Niks7.   

Abstract

The number of clinical trials for Duchenne muscular dystrophy is increasing. Many trials require muscle biopsies, which involve an invasive surgical procedure. Little is known about short- and long-term impacts of muscle biopsies as perceived by patients and caregivers. Therefore a survey was held among patients and their caregivers who participated in trials involving muscle biopsies, in seven countries. Seventy-eight responses were received. Analysis revealed that many patients and parents had significant anxiety before the biopsy. The main concern of caregivers was the required general anaesthesia. In most cases biopsies caused pain and temporarily hampered daily activities. The main long-term impact was scarring, although large variation in size was reported. Seventy-nine percent of caregivers were little bothered and 21% were moderately or severely bothered by the scar. Willingness to consider another biopsy in future protocols was higher for open-label studies than for placebo-controlled trials. Caregivers stressed the importance of knowing the results of biopsy analyses; only a minority actually received this information. Recommendations are made on the informed consent procedure regarding risks and consequences of muscle biopsies, and communication of results. Furthermore, efforts should be made to minimise the impact of biopsies through pain management and by considering plastic surgery.
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Clinical trials; Duchenne muscular dystrophy; Muscle biopsy; Patient perspective; Scarring

Year:  2019        PMID: 31378431     DOI: 10.1016/j.nmd.2019.06.004

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  9 in total

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Authors:  Anthony Tucker-Bartley; Jordan Lemme; Andrea Gomez-Morad; Nehal Shah; Miranda Veliu; Frank Birklein; Claudia Storz; Seward Rutkove; David Kronn; Alison M Boyce; Eduard Kraft; Jaymin Upadhyay
Journal:  Neurosci Biobehav Rev       Date:  2021-02-10       Impact factor: 9.052

Review 2.  The Art of Muscle Biopsy in the New Genetic Era: A Narrative Review.

Authors:  Yalda Nilipour
Journal:  Iran J Child Neurol       Date:  2019

Review 3.  The use of genetically humanized animal models for personalized medicine approaches.

Authors:  Annemieke Aartsma-Rus; Maaike van Putten
Journal:  Dis Model Mech       Date:  2019-10-01       Impact factor: 5.758

4.  Quantitative immuno-mass spectrometry imaging of skeletal muscle dystrophin.

Authors:  David P Bishop; Mika T Westerhausen; Florian Barthelemy; Thomas Lockwood; Nerida Cole; Elizabeth M Gibbs; Rachelle H Crosbie; Stanley F Nelson; M Carrie Miceli; Philip A Doble; Jonathan Wanagat
Journal:  Sci Rep       Date:  2021-01-13       Impact factor: 4.379

5.  The Role of Patient Involvement When Developing Therapies.

Authors:  Annemieke Aartsma-Rus; Elizabeth Vroom; Daniel O'Reilly
Journal:  Nucleic Acid Ther       Date:  2021-10-01       Impact factor: 4.244

6.  Modeling Patient-Specific Muscular Dystrophy Phenotypes and Therapeutic Responses in Reprogrammed Myotubes Engineered on Micromolded Gelatin Hydrogels.

Authors:  Florian Barthélémy; Jeffrey W Santoso; Laura Rabichow; Rongcheng Jin; Isaiah Little; Stanley F Nelson; Megan L McCain; M Carrie Miceli
Journal:  Front Cell Dev Biol       Date:  2022-04-06

7.  Low dystrophin variability between muscles and stable expression over time in Becker muscular dystrophy using capillary Western immunoassay.

Authors:  Z Koeks; A A Janson; C Beekman; M Signorelli; H A van Duyvenvoorde; J C van den Bergen; M T Hooijmans; I Alleman; I M Hegeman; J J G M Verschuuren; J C V Deutekom; P Spitali; N A Datson; E H Niks
Journal:  Sci Rep       Date:  2021-03-15       Impact factor: 4.379

8.  miRNome profiling in Duchenne muscular dystrophy; identification of asymptomatic and manifesting female carriers.

Authors:  Nahla O Mousa; Ahmed A Sayed; Nagia Fahmy; Mariam G Elzayat; Usama Bakry; Ahmed Abdellatif; Waheed K Zahra; Ahmed Osman
Journal:  Biosci Rep       Date:  2021-09-30       Impact factor: 3.840

9.  Study of Clinical Features and Diagnosis Pattern of Duchene Muscular Dystrophy in Southern India.

Authors:  Nigama Chandra Sattenapalli; Anka Rao Areti; S N Koteswara Rao G; Uma Sankar Kulandaivelu; Rajasekhar Reddy Alavala; Ravi Manne
Journal:  J Neurosci Rural Pract       Date:  2022-01-05
  9 in total

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