{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T14:18:33Z","timestamp":1740147513351,"version":"3.37.3"},"reference-count":18,"publisher":"Akademiai Kiado Zrt.","issue":"41","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Orvosi Hetilap"],"published-print":{"date-parts":[[2014,10]]},"abstract":"<jats:p>Introduction: Idiopathic inflammatory myopathy (called also myositis) is a systemic autoimmune disease mainly characterised with proximal muscle weakness. The most frequent subsets are polymyositis and dermatomyositis. The epidemiology of these diseases is not entirely explored. There is a need to build national and international registries which may help to obtain more data. The Myositis Team at the Department of Clinical Immunology, University of Debrecen, has been established in 1975. Aim: The aim of the authors was to obtain epidemiological data on this disease. Method: The authors analysed the database of the National Health Insurance Fund Administration of Hungary which included 1119 patients with myositis, of which 289 patients were followed up by the authors. Results: The average incidence of the disease was found to be 0.95\/100.000\/year. The male\/female ratio was 1\/2. Dermatomyositis occurred both in children and adult, but polymyositis was found mainly in adults. These epidemiological data partly correlate with those published in the international literature. Conclusions: The authors propose to establish a National Myositis Registry in the frame of multicentric collaboration in order to have more information about the disease. Orv. Hetil., 2014, 155(41), 1643\u20131646.<\/jats:p>","DOI":"10.1556\/oh.2014.29993","type":"journal-article","created":{"date-parts":[[2014,10,5]],"date-time":"2014-10-05T01:00:55Z","timestamp":1412470855000},"page":"1643-1646","source":"Crossref","is-referenced-by-count":1,"title":["Epidemiology of idiopathic inflammatory myopathy in Hungary"],"prefix":"10.1556","volume":"155","author":[{"given":"Melinda","family":"Nagy-Vincze","sequence":"first","affiliation":[{"name":"Debreceni Egyetem, Klinikai K\u00f6zpont, \u00c1ltal\u00e1nos Orvostudom\u00e1nyi Kar Klinikai Immunol\u00f3gia Tansz\u00e9k Debrecen M\u00f3ricz Zs. u. 22. 4032"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Levente","family":"Bodoki","sequence":"additional","affiliation":[{"name":"Debreceni Egyetem, Klinikai K\u00f6zpont, \u00c1ltal\u00e1nos Orvostudom\u00e1nyi Kar Klinikai Immunol\u00f3gia Tansz\u00e9k Debrecen M\u00f3ricz Zs. u. 22. 4032"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zolt\u00e1n","family":"Griger","sequence":"additional","affiliation":[{"name":"Debreceni Egyetem, Klinikai K\u00f6zpont, \u00c1ltal\u00e1nos Orvostudom\u00e1nyi Kar Klinikai Immunol\u00f3gia Tansz\u00e9k Debrecen M\u00f3ricz Zs. u. 22. 4032"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katalin","family":"Dank\u00f3","sequence":"additional","affiliation":[{"name":"Debreceni Egyetem, Klinikai K\u00f6zpont, \u00c1ltal\u00e1nos Orvostudom\u00e1nyi Kar Klinikai Immunol\u00f3gia Tansz\u00e9k Debrecen M\u00f3ricz Zs. u. 22. 4032"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"425","reference":[{"key":"1","unstructured":"<i>Plotz, P. H., Rider, L. G., Targoff, I. N., et al.:<\/i> NIH Conference. Myositis: immunologic contributions to understanding cause, pathogenesis, and therapy. Ann. Intern. Med., 1995, <i>122<\/i>(9), 715\u2013724."},{"key":"2","doi-asserted-by":"crossref","unstructured":"<i>Vincze, M., Danko, K.:<\/i> Idiopathic inflammatory myopathies. Best Pract. Res. Clin. Rheumatol., 2012, <i>26<\/i>(1), 25\u201345.","DOI":"10.1016\/j.berh.2012.01.013"},{"key":"3","doi-asserted-by":"crossref","unstructured":"<i>Rider, L. G., Miller, F. W.:<\/i> Idiopathic inflammatory muscle disease: clinical aspects. Baillieres Best Pract. Res. Clin. Rheumatol., 2000, <i>14<\/i>(1), 37\u201354.","DOI":"10.1053\/berh.1999.0076"},{"key":"4","doi-asserted-by":"crossref","unstructured":"<i>Dalakas, M. C., Hohlfeld, R.:<\/i> Polymyositis and dermatomyositis. Lancet, 2003, <i>362<\/i>(9388), 971\u2013982.","DOI":"10.1016\/S0140-6736(03)14368-1"},{"key":"5","doi-asserted-by":"crossref","unstructured":"<i>Dorph, C., Lundberg, I. E.:<\/i> Idiopathic inflammatory myopathies \u2013 myositis. Best Pract. Res. Clin. Rheumatol., 2002, <i>16<\/i>(5), 817\u2013832.","DOI":"10.1053\/berh.2002.0261"},{"key":"6","doi-asserted-by":"crossref","unstructured":"<i>Vargas-Legu\u00e1s, H., Selva-O\u2019Callaghan, A., Campins-Mart\u00ed, M., et al.:<\/i> Polymyositis-dermatomyositis: incidence in Spain (1997\u20132004). Med. Clin. (Barc), 2007, <i>129<\/i>(19), 721\u2013724.","DOI":"10.1157\/13113285"},{"key":"7","doi-asserted-by":"crossref","unstructured":"<i>Kuo, C. F., See, L. C., Yu, K. H., et al.:<\/i> Incidence, cancer risk and mortality of dermatomyositis and polymyositis in Taiwan: a nationwide population study. Br. J. Dermatol., 2011, <i>165<\/i>(6), 1273\u20131279.","DOI":"10.1111\/j.1365-2133.2011.10595.x"},{"key":"8","doi-asserted-by":"crossref","unstructured":"<i>Mendez, E. P., Lipton, R., Ramsey-Goldman, R., et al.:<\/i> US incidence of juvenile dermatomyositis, 1995\u20131998: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry. Arthritis Rheum., 2003, <i>49<\/i>(3), 300\u2013305.","DOI":"10.1002\/art.11122"},{"key":"9","unstructured":"<i>Oddis, C. V., Conte, C. G., Steen, V. D., et al.:<\/i> Incidence of polymyositis-dermatomyositis: a 20-year study of hospital diagnosed cases in Allegheny County, PA 1963\u20131982. J. Rheumatol., 1990, <i>17<\/i>(10), 1329\u20131334."},{"key":"10","doi-asserted-by":"crossref","unstructured":"<i>Furst, D. E., Amato, A. A., Iorga, \u015e. R., et al.:<\/i> Epidemiology of adult idiopathic inflammatory myopathies in a U.S. managed care plan. Muscle Nerve, 2012, <i>45<\/i>(5), 676\u2013683.","DOI":"10.1002\/mus.23302"},{"key":"11","doi-asserted-by":"crossref","unstructured":"<i>Bendewald, M. J., Wetter, D. A., Li, X., et al.:<\/i> Incidence of dermatomyositis and clinically amyopathic dermatomyositis: a population-based study in Olmsted County, Minnesota. Arch. Dermatol., 2010, <i>146<\/i>(1), 26\u201330.","DOI":"10.1001\/archdermatol.2009.328"},{"key":"12","doi-asserted-by":"crossref","unstructured":"<i>Bernatsky, S., Joseph, L., Pineau, C. A., et al.:<\/i> Estimating the prevalence of polymyositis and dermatomyositis from administrative data: age, sex and regional differences. Ann. Rheum. Dis., 2009, <i>68<\/i>(7), 1192\u20131196.","DOI":"10.1136\/ard.2008.093161"},{"key":"13","doi-asserted-by":"crossref","unstructured":"<i>Barnabe, C., Joseph, L., B\u00e9lisle, P., et al.:<\/i> Prevalence of autoimmune inflammatory myopathy in the first nations population of Alberta, Canada. Arthritis Care Res. (Hoboken), 2012, <i>64<\/i>(11), 1715\u20131719.","DOI":"10.1002\/acr.21743"},{"key":"14","doi-asserted-by":"crossref","unstructured":"<i>Rosa, J., Garrot, L. F., Navarta, D. A., et al.:<\/i> Incidence and prevalence of polymyositis and dermatomyositis in a health management organization in Buenos Aires. J. Clin. Rheumatol., 2013, <i>19<\/i>(6), 303\u2013307.","DOI":"10.1097\/RHU.0b013e3182a21ba8"},{"key":"15","doi-asserted-by":"crossref","unstructured":"<i>Tan, J. A., Roberts-Thomson, P. J., Blumbergs, P., et al.:<\/i> Incidence and prevalence of idiopathic inflammatory myopathies in South Australia: a 30-year epidemiologic study of histology-proven cases. Int. J. Rheum. Dis., 2013, <i>16<\/i>(3), 331\u2013338.","DOI":"10.1111\/j.1756-185X.2011.01669.x"},{"key":"16","unstructured":"<i>Hiketa, T., Ohashi, M.:<\/i> Juvenile dermatomyositis \u2013 statistical observation of 105 patients with dermatomyositis. Nihon Hifuka Gakkai Zasshi, 1991, <i>101<\/i>(8), 825\u2013830."},{"key":"17","doi-asserted-by":"crossref","unstructured":"<i>Ohta, A., Nagai, M., Nishina, M., et al.:<\/i> Prevalence and incidence of polymyositis and dermatomyositis in Japan. Mod. 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