The Plymouth Student Scientist
Document Type
Literature Review
Abstract
Duchenne muscular dystrophy (DMD) is a lethal x-linked recessive disorder, characterised by progressive skeletal muscle weakness, accompanied by cardiac and smooth muscle dysfunction. Although the main cause of death in DMD used to be respiratory problems caused by deterioration of the diaphragm, developments in respiratory care means that cardiac failure is now the major cause of death, despite the introduction of cardio-protective treatment such as angiotensin-converting-enzyme inhibitors and beta-blockers. Once affected, the heart progressively deteriorates over time, with the main problem being due to the death of cardiomyocytes. A loss of dystrophin makes the sarcolemma more susceptible to damage, leading to an influx of calcium ions into the cell, activating proteases and ultimately resulting in cardiomyocyte death. The dead cells are replaced by fibrotic tissue which causes dilated cardiomyopathy. There is at present no cure for DMD, however there is much on-going research producing positive results based around the pathophysiology in DMD patients.
Publication Date
2014-07-01
Publication Title
The Plymouth Student Scientist
Volume
7
Issue
1
First Page
201
Last Page
215
ISSN
1754-2383
Deposit Date
May 2019
Embargo Period
2024-07-03
URI
http://hdl.handle.net/10026.1/14059
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Recommended Citation
Wright, Sophie
(2014)
"A review of Duchenne muscular dystrophy focusing on cardiac involvement,"
The Plymouth Student Scientist: Vol. 7:
Iss.
1, Article 8.
Available at:
https://pearl.plymouth.ac.uk/tpss/vol7/iss1/8
