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Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran

BACKGROUND: The epidemiologic data on demographic features of early-onset multiple sclerosis (EOMS) are rare in the Middle East, and no previous study has explored it. We aim to perform a neuroepidemiologic analysis to emphasize on the demographic features of EOMS in Tehran, Iran, during 2005–2015....

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Detalles Bibliográficos
Autores principales: Omrani, Fateme, Sahraian, Mohamamad Ali, Saeen, Amirreza Azim, Omrani, Zahra, Hayeri, Ghazal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057173/
https://www.ncbi.nlm.nih.gov/pubmed/30090125
http://dx.doi.org/10.4103/jpn.JPN_122_17
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author Omrani, Fateme
Sahraian, Mohamamad Ali
Saeen, Amirreza Azim
Omrani, Zahra
Hayeri, Ghazal
author_facet Omrani, Fateme
Sahraian, Mohamamad Ali
Saeen, Amirreza Azim
Omrani, Zahra
Hayeri, Ghazal
author_sort Omrani, Fateme
collection PubMed
description BACKGROUND: The epidemiologic data on demographic features of early-onset multiple sclerosis (EOMS) are rare in the Middle East, and no previous study has explored it. We aim to perform a neuroepidemiologic analysis to emphasize on the demographic features of EOMS in Tehran, Iran, during 2005–2015. MATERIALS AND METHODS: Our study was performed in Tehran, Iran; the research included patients with EOMS who had experienced their first symptoms before the age of 18 years and those who were referred to Iranian Multiple Sclerosis Society in Tehran during 2005–2015. A total of 300 patients were contacted and filled the checklists by themselves or the physician. The checklist contained data about gender, age at the onset, the first symptom, time interval between the first presentation and the diagnosis, clinical course, family history of MS, and history of smoking in parents. RESULTS: Among the patients with EOMS, 78% were female and 22% were male. Average age of disease onset was 15.6 years (standard deviation, 2.6 years), mean time interval between the first symptoms and disease diagnosis was 16.8 months, the shortest time interval measured was 0.1 month, and the longest time interval was 144 months. The first symptom at the onset of the disease was ocular in 140 patients and sensory in 82 patients. Approximately 16.7% of the patients had a positive family history for MS. The most common clinical course of disease was relapsing-remitting MS (RRMS). Parental smoking history was negative in 63.3% of the patients. CONCLUSION: In our study, the EOMS was higher in females. Despite the earlier studies, it was found that the polysymptomatic onset was not very common. Optic neuritis was the most initial presentation and RRMS was the most frequent course.
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spelling pubmed-60571732018-08-08 Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran Omrani, Fateme Sahraian, Mohamamad Ali Saeen, Amirreza Azim Omrani, Zahra Hayeri, Ghazal J Pediatr Neurosci Original Article BACKGROUND: The epidemiologic data on demographic features of early-onset multiple sclerosis (EOMS) are rare in the Middle East, and no previous study has explored it. We aim to perform a neuroepidemiologic analysis to emphasize on the demographic features of EOMS in Tehran, Iran, during 2005–2015. MATERIALS AND METHODS: Our study was performed in Tehran, Iran; the research included patients with EOMS who had experienced their first symptoms before the age of 18 years and those who were referred to Iranian Multiple Sclerosis Society in Tehran during 2005–2015. A total of 300 patients were contacted and filled the checklists by themselves or the physician. The checklist contained data about gender, age at the onset, the first symptom, time interval between the first presentation and the diagnosis, clinical course, family history of MS, and history of smoking in parents. RESULTS: Among the patients with EOMS, 78% were female and 22% were male. Average age of disease onset was 15.6 years (standard deviation, 2.6 years), mean time interval between the first symptoms and disease diagnosis was 16.8 months, the shortest time interval measured was 0.1 month, and the longest time interval was 144 months. The first symptom at the onset of the disease was ocular in 140 patients and sensory in 82 patients. Approximately 16.7% of the patients had a positive family history for MS. The most common clinical course of disease was relapsing-remitting MS (RRMS). Parental smoking history was negative in 63.3% of the patients. CONCLUSION: In our study, the EOMS was higher in females. Despite the earlier studies, it was found that the polysymptomatic onset was not very common. Optic neuritis was the most initial presentation and RRMS was the most frequent course. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6057173/ /pubmed/30090125 http://dx.doi.org/10.4103/jpn.JPN_122_17 Text en Copyright: © 2018 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Omrani, Fateme
Sahraian, Mohamamad Ali
Saeen, Amirreza Azim
Omrani, Zahra
Hayeri, Ghazal
Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title_full Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title_fullStr Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title_full_unstemmed Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title_short Early-Onset Multiple Sclerosis: Reports of 300 Patients from Iran
title_sort early-onset multiple sclerosis: reports of 300 patients from iran
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057173/
https://www.ncbi.nlm.nih.gov/pubmed/30090125
http://dx.doi.org/10.4103/jpn.JPN_122_17
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