Paraffin wax embedded muscle is suitable for the diagnosis of muscular dystrophy
Open Access
- 1 July 2001
- journal article
- research article
- Published by BMJ in Journal of Clinical Pathology
- Vol. 54 (7), 517-520
- https://doi.org/10.1136/jcp.54.7.517
Abstract
Aim—At present, the diagnosis of muscular dystrophy is made by means of immunohistochemistry on frozen sections. The aim of this study was to develop a sensitive and reproducible immunohistochemical method for use on formalin fixed, paraffin wax embedded sections for the demonstration of dystrophin associated proteins and other muscle associated antigens. Methods—All the cases studied were from the files of the department of histopathology, Great Ormond Street Hospital for Children NHS Trust. Immunohistochemistry was performed on paraffin wax embedded sections with heat mediated antigen retrieval and overnight incubation with the antibodies at room temperature. Four different pretreatment buffers were tested in the attempt to optimise the immunostaining. Frozen sections were run in parallel for direct comparison. Results—All the antibodies except δ sarcoglycan gave strong, consistent immunostaining in paraffin wax embedded sections, comparable with the frozen sections. The most consistent results were obtained using citrate/EDTA as the pretreatment buffer. Conclusion—A reliable and reproducible technique has been established, using a heat mediated citrate/EDTA buffer antigen retrieval method, which works well for most of the antibodies needed to make the diagnosis of muscular dystrophy in formalin fixed, paraffin wax embedded sections. This technique overcomes some of the inherent problems encountered using frozen muscle tissue and it could become a valuable tool for the diagnosis of muscular dystrophy.Keywords
This publication has 10 references indexed in Scilit:
- Making sense of the limb-girdle muscular dystrophiesBrain, 1999
- The sarcoglycan complex in limb–girdle muscular dystrophyCurrent Opinion in Neurology, 1998
- From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophyMuscle & Nerve, 1998
- Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.Journal of Medical Genetics, 1997
- 30th and 31st ENMC international workshops, Naarden, The Netherlands, Held 6–8 January 1995Neuromuscular Disorders, 1995
- Congenital muscular dystrophy with merosin deficiency.1994
- Dystrophin or a “related protein” in Duchenne muscular dystrophy?Acta Neurologica Scandinavica, 1992
- The Wellcome Lecture, 1988 - Muscular dystrophy: a time of hopeProceedings of the Royal Society of London. B. Biological Sciences, 1989
- Eine neue x-chromosomale MuskeldystrophieArchiv Fur Psychiatrie Und Nervenkrankheiten, 1955
- ON THE CLASSIFICATION, NATURAL HISTORY AND TREATMENT OF THE MYOPATHIESBrain, 1954