Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers
Emery–Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD...
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Published in | Neuromuscular disorders : NMD Vol. 8; no. 2; pp. 67 - 71 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
01.04.1998
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Subjects | |
Online Access | Get full text |
ISSN | 0960-8966 1873-2364 |
DOI | 10.1016/S0960-8966(97)00147-8 |
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Abstract | Emery–Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the
STA gene (Xq28). Emerin is normally localised in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive. |
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AbstractList | Emery-Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the STA gene (Xq28). Emerin is normally localized in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive. Emery-Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the STA gene (Xq28). Emerin is normally localized in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive.Emery-Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the STA gene (Xq28). Emerin is normally localized in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive. Emery–Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with humeroperoneal distribution. Cardiac arrhythmia and heart conduction block are also important characteristics of this disease. The X-linked form of EMD is caused by the absence of emerin, encoded by the STA gene (Xq28). Emerin is normally localised in muscle and other tissues at the nuclear rim. Currently, muscle and skin biopsies are used for the immunohistochemical diagnosis. We demonstrate that emerin is present in the cheek oral mucosa, in the exfoliating epithelial cells, and we propose the collection of these cells as a new method for the diagnosis of X-linked EMD patients and the detection of carriers by immunofluorescence techniques: smears from healthy subjects contained about 98% emerin-positive cells, those from X-linked EMD patients contained none and those from carriers contained about 45%. The technique is completely non-invasive, simple, repeatable and inexpensive. |
Author | Cobianchi, F Petrini, S Maraldi, N.M Sabatelli, P Squarzoni, S Toniolo, D Ognibene, A Cartegni, L Capanni, C Merlini, L |
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Keywords | Immunohistochemistry Immunoblotting Emery–Dreifuss Muscular dystrophy (EMD) Emerin SDS-polyacrylamide gel electrophoresis (SDS-PAGE) |
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References_xml | – reference: Online Mendellian inheritance in man (OMIM) home page 1997; http://www3.ncbi.nlm.nih.gov/omim/ – volume: 29 start-page: 338 year: 1966 end-page: 342 ident: BIB1 article-title: Unusual type of benign X-linked muscular dystrophy publication-title: J Neurol Neurosurg Psychiatry – volume: 4 start-page: 1859 year: 1995 end-page: 1863 ident: BIB4 article-title: Identification of new mutations in the `Emery–Dreifuss' muscular dystrophy gene and evidence for genetic heterogeneity of the disease publication-title: Hum Mol Gen – volume: 9 start-page: 481 year: 1986 end-page: 485 ident: BIB2 article-title: `Emery–Dreifuss' muscular dystrophy: report of five cases in a family and review of the literature publication-title: Muscle Nerve – volume: 8 start-page: 323 year: 1994 end-page: 327 ident: BIB6 article-title: Identification of a novel X-linked gene responsible for `Emery–Dreifuss' muscular dystrophy publication-title: Nature Genet – volume: 4 start-page: 2003 year: 1995 end-page: 2004 ident: BIB12 article-title: SSCP detection of novel mutations in patients with `Emery–Dreifuss' muscular dystrophy: definition of a small C-terminal region required for emerin function publication-title: Hum Mol Genet – volume: 74 start-page: 409 year: 1986 end-page: 416 ident: BIB11 article-title: A linkage study of `Emery–Dreifuss' muscular dystrophy publication-title: Hum Genet – volume: 14 start-page: 411 year: 1991 end-page: 416 ident: BIB3 article-title: Progression of cardiac disease in `Emery–Dreifuss' muscular dystrophy publication-title: Clin Cardiol – volume: 5 start-page: 801 year: 1996 end-page: 808 ident: BIB8 article-title: The `Emery–Dreifuss' muscular dystrophy protein, emerin, is a nuclear membrane protein publication-title: Hum Mol Gen – volume: 12 start-page: 254 year: 1996 end-page: 259 ident: BIB7 article-title: Emerin deficiency at the nuclear membrane in patients with `Emery–Dreifuss' muscular dystrophy publication-title: Nature Genet – volume: 7 start-page: 63 year: 1997 end-page: 66 ident: BIB9 article-title: Diagnosis of X-linked `Emery–Dreifuss' muscular dystrophy by protein analysis of leukocytes and skin with monoclonal antibodies publication-title: Neuromusc Disord – volume: 42 start-page: 249 year: 1997 end-page: 253 ident: BIB10 article-title: X-Linked `Emery–Dreifuss' muscular dystrophy can be diagnosed from skin biopsy or blood sample publication-title: Ann Neurol – volume: 4 start-page: 1859 issue: 10 year: 1995 ident: 10.1016/S0960-8966(97)00147-8_BIB4 article-title: Identification of new mutations in the `Emery–Dreifuss' muscular dystrophy gene and evidence for genetic heterogeneity of the disease publication-title: Hum Mol Gen doi: 10.1093/hmg/4.10.1859 – volume: 5 start-page: 801 year: 1996 ident: 10.1016/S0960-8966(97)00147-8_BIB8 article-title: The `Emery–Dreifuss' muscular dystrophy protein, emerin, is a nuclear membrane protein publication-title: Hum Mol Gen doi: 10.1093/hmg/5.6.801 – volume: 7 start-page: 63 year: 1997 ident: 10.1016/S0960-8966(97)00147-8_BIB9 article-title: Diagnosis of X-linked `Emery–Dreifuss' muscular dystrophy by protein analysis of leukocytes and skin with monoclonal antibodies publication-title: Neuromusc Disord doi: 10.1016/S0960-8966(96)00405-1 – volume: 14 start-page: 411 issue: 5 year: 1991 ident: 10.1016/S0960-8966(97)00147-8_BIB3 article-title: Progression of cardiac disease in `Emery–Dreifuss' muscular dystrophy publication-title: Clin Cardiol doi: 10.1002/clc.4960140509 – volume: 4 start-page: 2003 year: 1995 ident: 10.1016/S0960-8966(97)00147-8_BIB12 article-title: SSCP detection of novel mutations in patients with `Emery–Dreifuss' muscular dystrophy: definition of a small C-terminal region required for emerin function publication-title: Hum Mol Genet doi: 10.1093/hmg/4.10.2003 – volume: 8 start-page: 323 year: 1994 ident: 10.1016/S0960-8966(97)00147-8_BIB6 article-title: Identification of a novel X-linked gene responsible for `Emery–Dreifuss' muscular dystrophy publication-title: Nature Genet doi: 10.1038/ng1294-323 – volume: 42 start-page: 249 issue: 2 year: 1997 ident: 10.1016/S0960-8966(97)00147-8_BIB10 article-title: X-Linked `Emery–Dreifuss' muscular dystrophy can be diagnosed from skin biopsy or blood sample publication-title: Ann Neurol doi: 10.1002/ana.410420218 – volume: 29 start-page: 338 year: 1966 ident: 10.1016/S0960-8966(97)00147-8_BIB1 article-title: Unusual type of benign X-linked muscular dystrophy publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.29.4.338 – ident: 10.1016/S0960-8966(97)00147-8_BIB5 – volume: 9 start-page: 481 year: 1986 ident: 10.1016/S0960-8966(97)00147-8_BIB2 article-title: `Emery–Dreifuss' muscular dystrophy: report of five cases in a family and review of the literature publication-title: Muscle Nerve doi: 10.1002/mus.880090602 – volume: 12 start-page: 254 year: 1996 ident: 10.1016/S0960-8966(97)00147-8_BIB7 article-title: Emerin deficiency at the nuclear membrane in patients with `Emery–Dreifuss' muscular dystrophy publication-title: Nature Genet doi: 10.1038/ng0396-254 – volume: 74 start-page: 409 issue: 4 year: 1986 ident: 10.1016/S0960-8966(97)00147-8_BIB11 article-title: A linkage study of `Emery–Dreifuss' muscular dystrophy publication-title: Hum Genet doi: 10.1007/BF00280495 |
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Snippet | Emery–Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with... Emery-Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with... |
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SubjectTerms | Adolescent Adult Case-Control Studies Cheek Child Cytodiagnosis Emerin Emery–Dreifuss Muscular dystrophy (EMD) Female Genetic Carrier Screening Genetic Linkage Humans Immunoblotting Immunohistochemistry Male Middle Aged Mouth Mucosa - pathology Muscular Dystrophies - genetics Muscular Dystrophies - pathology Muscular Dystrophy, Emery-Dreifuss SDS-polyacrylamide gel electrophoresis (SDS-PAGE) X Chromosome |
Title | Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers |
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