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A systematic review of population based epidemiological studies in Myasthenia Gravis
BACKGROUND: The aim was to collate all myasthenia gravis (MG) epidemiological studies including AChR MG and MuSK MG specific studies. To synthesize data on incidence rate (IR), prevalence rate (PR) and mortality rate (MR) of the condition and investigate the influence of environmental and technical...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905354/ https://www.ncbi.nlm.nih.gov/pubmed/20565885 http://dx.doi.org/10.1186/1471-2377-10-46 |
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author | Carr, Aisling S Cardwell, Chris R McCarron, Peter O McConville, John |
author_facet | Carr, Aisling S Cardwell, Chris R McCarron, Peter O McConville, John |
author_sort | Carr, Aisling S |
collection | PubMed |
description | BACKGROUND: The aim was to collate all myasthenia gravis (MG) epidemiological studies including AChR MG and MuSK MG specific studies. To synthesize data on incidence rate (IR), prevalence rate (PR) and mortality rate (MR) of the condition and investigate the influence of environmental and technical factors on any trends or variation observed. METHODS: Studies were identified using multiple sources and meta-analysis performed to calculate pooled estimates for IR, PR and MR. RESULTS: 55 studies performed between 1950 and 2007 were included, representing 1.7 billion population-years. For All MG estimated pooled IR (eIR): 5.3 per million person-years (C.I.:4.4, 6.1), range: 1.7 to 21.3; estimated pooled PR: 77.7 per million persons (C.I.:64.0, 94.3), range 15 to 179; MR range 0.1 to 0.9 per millions person-years. AChR MG eIR: 7.3 (C.I.:5.5, 7.8), range: 4.3 to 18.0; MuSK MG IR range: 0.1 to 0.32. However marked variation persisted between populations studied with similar methodology and in similar areas. CONCLUSIONS: We report marked variation in observed frequencies of MG. We show evidence of increasing frequency of MG with year of study and improved study quality. This probably reflects improved case ascertainment. But other factors must also influence disease onset resulting in the observed variation in IR across geographically and genetically similar populations. |
format | Text |
id | pubmed-2905354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29053542010-07-17 A systematic review of population based epidemiological studies in Myasthenia Gravis Carr, Aisling S Cardwell, Chris R McCarron, Peter O McConville, John BMC Neurol Research Article BACKGROUND: The aim was to collate all myasthenia gravis (MG) epidemiological studies including AChR MG and MuSK MG specific studies. To synthesize data on incidence rate (IR), prevalence rate (PR) and mortality rate (MR) of the condition and investigate the influence of environmental and technical factors on any trends or variation observed. METHODS: Studies were identified using multiple sources and meta-analysis performed to calculate pooled estimates for IR, PR and MR. RESULTS: 55 studies performed between 1950 and 2007 were included, representing 1.7 billion population-years. For All MG estimated pooled IR (eIR): 5.3 per million person-years (C.I.:4.4, 6.1), range: 1.7 to 21.3; estimated pooled PR: 77.7 per million persons (C.I.:64.0, 94.3), range 15 to 179; MR range 0.1 to 0.9 per millions person-years. AChR MG eIR: 7.3 (C.I.:5.5, 7.8), range: 4.3 to 18.0; MuSK MG IR range: 0.1 to 0.32. However marked variation persisted between populations studied with similar methodology and in similar areas. CONCLUSIONS: We report marked variation in observed frequencies of MG. We show evidence of increasing frequency of MG with year of study and improved study quality. This probably reflects improved case ascertainment. But other factors must also influence disease onset resulting in the observed variation in IR across geographically and genetically similar populations. BioMed Central 2010-06-18 /pmc/articles/PMC2905354/ /pubmed/20565885 http://dx.doi.org/10.1186/1471-2377-10-46 Text en Copyright ©2010 Carr et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Carr, Aisling S Cardwell, Chris R McCarron, Peter O McConville, John A systematic review of population based epidemiological studies in Myasthenia Gravis |
title | A systematic review of population based epidemiological studies in Myasthenia Gravis |
title_full | A systematic review of population based epidemiological studies in Myasthenia Gravis |
title_fullStr | A systematic review of population based epidemiological studies in Myasthenia Gravis |
title_full_unstemmed | A systematic review of population based epidemiological studies in Myasthenia Gravis |
title_short | A systematic review of population based epidemiological studies in Myasthenia Gravis |
title_sort | systematic review of population based epidemiological studies in myasthenia gravis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905354/ https://www.ncbi.nlm.nih.gov/pubmed/20565885 http://dx.doi.org/10.1186/1471-2377-10-46 |
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