Cargando…

Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients

Introduction: We aimed to clarify when adult patients with Charcot-Marie-Tooth disease type 1A (CMT1A), especially those diagnosed at middle or advanced ages, first showed symptoms and whether the rate of disease progression is accelerated by aging. Methods: Medical records of CMT1A outpatients betw...

Descripción completa

Detalles Bibliográficos
Autores principales: Kitani-Morii, Fukiko, Noto, Yu-ichi, Tsuji, Yukiko, Shiga, Kensuke, Mizuta, Ikuko, Nakagawa, Masanori, Mizuno, Toshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378731/
https://www.ncbi.nlm.nih.gov/pubmed/32765395
http://dx.doi.org/10.3389/fneur.2020.00626
_version_ 1783562485657239552
author Kitani-Morii, Fukiko
Noto, Yu-ichi
Tsuji, Yukiko
Shiga, Kensuke
Mizuta, Ikuko
Nakagawa, Masanori
Mizuno, Toshiki
author_facet Kitani-Morii, Fukiko
Noto, Yu-ichi
Tsuji, Yukiko
Shiga, Kensuke
Mizuta, Ikuko
Nakagawa, Masanori
Mizuno, Toshiki
author_sort Kitani-Morii, Fukiko
collection PubMed
description Introduction: We aimed to clarify when adult patients with Charcot-Marie-Tooth disease type 1A (CMT1A), especially those diagnosed at middle or advanced ages, first showed symptoms and whether the rate of disease progression is accelerated by aging. Methods: Medical records of CMT1A outpatients between 2012 and 2019 were reviewed. The age at diagnosis, age when symptoms first appeared, and rate of disease progression, assessed based on clinical outcome measures including the CMT Neuropathy Score (CMTNS), Rasch-modified CMTNS (CMTNS-R), CMT Examination Score (CMTES), and Rasch-modified CMTES (CMTES-R) were analyzed. Results: Among 45 adult CMT1A patients, 42% had been diagnosed after 50 years of age, whereas 91% of all patients had exhibited some CMT-related symptoms before 20 years of age. The annual increase of all clinical outcome measures did not differ between patients under and over 50 years. Even when limited to patients whose initial CMTES-R showed mild to moderate severity, the rate of change in CMTES-R did not differ between the two age groups (the annual mean ± standard deviation, under 50 years: 1.1 ± 1.0, and over 50 years: 0.9 ± 1.1, p = 0.68). To determine whether patients with disabilities at a young age have a higher deterioration rate, they were classified into three groups according to their current age and age at diagnosis: patients under 50 years of age, patients over 50 years of age but diagnosed before 50, and patients diagnosed after 50 years of age. The mean annual increase of all clinical outcome measures, however, did not differ among these groups (CMTES-R: 1.03 ± 1.01 vs. 0.94 ± 1.57 vs. 0.81 ± 0.88, respectively, p = 0.87). Discussion: CMT1A patients develop symptoms in childhood and adolescence even if such symptoms are not noticeable until reaching an advanced age. Deterioration rates of clinical outcome measures are constant irrespective of the age in their adulthood, although we cannot rule out the limitation that the difference did not reach significance because of the small number of patients. Being aware of the existence of a considerable number of undiagnosed CMT patients will help promote the avoidance of inadequate medication.
format Online
Article
Text
id pubmed-7378731
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-73787312020-08-05 Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients Kitani-Morii, Fukiko Noto, Yu-ichi Tsuji, Yukiko Shiga, Kensuke Mizuta, Ikuko Nakagawa, Masanori Mizuno, Toshiki Front Neurol Neurology Introduction: We aimed to clarify when adult patients with Charcot-Marie-Tooth disease type 1A (CMT1A), especially those diagnosed at middle or advanced ages, first showed symptoms and whether the rate of disease progression is accelerated by aging. Methods: Medical records of CMT1A outpatients between 2012 and 2019 were reviewed. The age at diagnosis, age when symptoms first appeared, and rate of disease progression, assessed based on clinical outcome measures including the CMT Neuropathy Score (CMTNS), Rasch-modified CMTNS (CMTNS-R), CMT Examination Score (CMTES), and Rasch-modified CMTES (CMTES-R) were analyzed. Results: Among 45 adult CMT1A patients, 42% had been diagnosed after 50 years of age, whereas 91% of all patients had exhibited some CMT-related symptoms before 20 years of age. The annual increase of all clinical outcome measures did not differ between patients under and over 50 years. Even when limited to patients whose initial CMTES-R showed mild to moderate severity, the rate of change in CMTES-R did not differ between the two age groups (the annual mean ± standard deviation, under 50 years: 1.1 ± 1.0, and over 50 years: 0.9 ± 1.1, p = 0.68). To determine whether patients with disabilities at a young age have a higher deterioration rate, they were classified into three groups according to their current age and age at diagnosis: patients under 50 years of age, patients over 50 years of age but diagnosed before 50, and patients diagnosed after 50 years of age. The mean annual increase of all clinical outcome measures, however, did not differ among these groups (CMTES-R: 1.03 ± 1.01 vs. 0.94 ± 1.57 vs. 0.81 ± 0.88, respectively, p = 0.87). Discussion: CMT1A patients develop symptoms in childhood and adolescence even if such symptoms are not noticeable until reaching an advanced age. Deterioration rates of clinical outcome measures are constant irrespective of the age in their adulthood, although we cannot rule out the limitation that the difference did not reach significance because of the small number of patients. Being aware of the existence of a considerable number of undiagnosed CMT patients will help promote the avoidance of inadequate medication. Frontiers Media S.A. 2020-07-16 /pmc/articles/PMC7378731/ /pubmed/32765395 http://dx.doi.org/10.3389/fneur.2020.00626 Text en Copyright © 2020 Kitani-Morii, Noto, Tsuji, Shiga, Mizuta, Nakagawa and Mizuno. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Kitani-Morii, Fukiko
Noto, Yu-ichi
Tsuji, Yukiko
Shiga, Kensuke
Mizuta, Ikuko
Nakagawa, Masanori
Mizuno, Toshiki
Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title_full Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title_fullStr Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title_full_unstemmed Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title_short Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients
title_sort rate of changes in cmt neuropathy and examination scores in japanese adult cmt1a patients
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378731/
https://www.ncbi.nlm.nih.gov/pubmed/32765395
http://dx.doi.org/10.3389/fneur.2020.00626
work_keys_str_mv AT kitanimoriifukiko rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT notoyuichi rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT tsujiyukiko rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT shigakensuke rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT mizutaikuko rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT nakagawamasanori rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients
AT mizunotoshiki rateofchangesincmtneuropathyandexaminationscoresinjapaneseadultcmt1apatients