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Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan

BACKGROUND: There was no nationwide epidemiological study of Lambert-Eaton myasthenic syndrome (LEMS) in Japan; therefore, we conducted a nationwide survey. METHODS: For the first survey, we sent survey sheets to randomly selected medical departments (n=7545) to obtain the number of LEMS who visited...

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Autores principales: Yoshikawa, Hiroaki, Adachi, Yumi, Nakamura, Yosikazu, Kuriyama, Nagato, Murai, Hiroyuki, Nomura, Yoshiko, Sakai, Yasunari, Iwasa, Kazuo, Furukawa, Yutaka, Kuwabara, Satoshi, Matsui, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445827/
https://www.ncbi.nlm.nih.gov/pubmed/36110924
http://dx.doi.org/10.1136/bmjno-2022-000291
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author Yoshikawa, Hiroaki
Adachi, Yumi
Nakamura, Yosikazu
Kuriyama, Nagato
Murai, Hiroyuki
Nomura, Yoshiko
Sakai, Yasunari
Iwasa, Kazuo
Furukawa, Yutaka
Kuwabara, Satoshi
Matsui, Makoto
author_facet Yoshikawa, Hiroaki
Adachi, Yumi
Nakamura, Yosikazu
Kuriyama, Nagato
Murai, Hiroyuki
Nomura, Yoshiko
Sakai, Yasunari
Iwasa, Kazuo
Furukawa, Yutaka
Kuwabara, Satoshi
Matsui, Makoto
author_sort Yoshikawa, Hiroaki
collection PubMed
description BACKGROUND: There was no nationwide epidemiological study of Lambert-Eaton myasthenic syndrome (LEMS) in Japan; therefore, we conducted a nationwide survey. METHODS: For the first survey, we sent survey sheets to randomly selected medical departments (n=7545) to obtain the number of LEMS who visited medical departments between 1 January 2017 and 31 December 2017. For the second survey, we sent survey sheets to the corresponding medical departments to obtain clinical information on LEMS. RESULTS: We received 2708 responses (recovery rate: 35.9%) to the first survey. We estimated the number of LEMS as 348 (95% CI 247 to 449). The prevalence was 2.7 (95% CI 1.9 to 3.5) in 1 000 000 population. As a result of the second survey, we obtained 30 case records of 16 men and 14 women. Fourteen patients (46.7%) had a tumour, and 10 out of 14 tumours were small-cell lung carcinoma (71.4%). There was a predominance of men in the LEMS with tumour (paraneoplastic LEMS, P-LEMS) (n=11, 78.6%) and women in the LEMS without tumour (a primary autoimmune form of LEMS, AI-LEMS) (n=11, 68.8%) (p=0.0136). The onset age (mean (SD)) for the P-LEMS was 67.1 (9.0), and that for AI-LEMS was 57.8 (11.2) years old (p=0.0103). The disease duration (median) for P-LEMS was 2 years, and for AI-LEMS was 7.5 years (p=0.0134). CONCLUSIONS: The prevalence of LEMS in Japan is similar to that in other countries. There are predominances of men in P-LEMS and women in AI-LEMS.
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spelling pubmed-94458272022-09-14 Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan Yoshikawa, Hiroaki Adachi, Yumi Nakamura, Yosikazu Kuriyama, Nagato Murai, Hiroyuki Nomura, Yoshiko Sakai, Yasunari Iwasa, Kazuo Furukawa, Yutaka Kuwabara, Satoshi Matsui, Makoto BMJ Neurol Open Original Research BACKGROUND: There was no nationwide epidemiological study of Lambert-Eaton myasthenic syndrome (LEMS) in Japan; therefore, we conducted a nationwide survey. METHODS: For the first survey, we sent survey sheets to randomly selected medical departments (n=7545) to obtain the number of LEMS who visited medical departments between 1 January 2017 and 31 December 2017. For the second survey, we sent survey sheets to the corresponding medical departments to obtain clinical information on LEMS. RESULTS: We received 2708 responses (recovery rate: 35.9%) to the first survey. We estimated the number of LEMS as 348 (95% CI 247 to 449). The prevalence was 2.7 (95% CI 1.9 to 3.5) in 1 000 000 population. As a result of the second survey, we obtained 30 case records of 16 men and 14 women. Fourteen patients (46.7%) had a tumour, and 10 out of 14 tumours were small-cell lung carcinoma (71.4%). There was a predominance of men in the LEMS with tumour (paraneoplastic LEMS, P-LEMS) (n=11, 78.6%) and women in the LEMS without tumour (a primary autoimmune form of LEMS, AI-LEMS) (n=11, 68.8%) (p=0.0136). The onset age (mean (SD)) for the P-LEMS was 67.1 (9.0), and that for AI-LEMS was 57.8 (11.2) years old (p=0.0103). The disease duration (median) for P-LEMS was 2 years, and for AI-LEMS was 7.5 years (p=0.0134). CONCLUSIONS: The prevalence of LEMS in Japan is similar to that in other countries. There are predominances of men in P-LEMS and women in AI-LEMS. BMJ Publishing Group 2022-09-05 /pmc/articles/PMC9445827/ /pubmed/36110924 http://dx.doi.org/10.1136/bmjno-2022-000291 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Yoshikawa, Hiroaki
Adachi, Yumi
Nakamura, Yosikazu
Kuriyama, Nagato
Murai, Hiroyuki
Nomura, Yoshiko
Sakai, Yasunari
Iwasa, Kazuo
Furukawa, Yutaka
Kuwabara, Satoshi
Matsui, Makoto
Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title_full Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title_fullStr Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title_full_unstemmed Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title_short Nationwide survey of Lambert-Eaton myasthenic syndrome in Japan
title_sort nationwide survey of lambert-eaton myasthenic syndrome in japan
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445827/
https://www.ncbi.nlm.nih.gov/pubmed/36110924
http://dx.doi.org/10.1136/bmjno-2022-000291
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