Adult spinal muscular atrophy: problems of early diagnosis

Background. Spinal muscular atrophy (SMA) associated with chromosome 5q is an autosomal recessive neuromuscular disease caused by a mutation in the SMN1 gene. Adult forms of SMA are relatively rarer and associated with significant diagnostic difficulties and pronounced delay in diagnosis. The availa...

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Main Authors: Yu. A. Shpilyukova, S. N. Illarioshkin
Format: Article
Language:Russian
Published: ABV-press 2022-12-01
Series:Нервно-мышечные болезни
Subjects:
Online Access:https://nmb.abvpress.ru/jour/article/view/507
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author Yu. A. Shpilyukova
S. N. Illarioshkin
author_facet Yu. A. Shpilyukova
S. N. Illarioshkin
author_sort Yu. A. Shpilyukova
collection DOAJ
description Background. Spinal muscular atrophy (SMA) associated with chromosome 5q is an autosomal recessive neuromuscular disease caused by a mutation in the SMN1 gene. Adult forms of SMA are relatively rarer and associated with significant diagnostic difficulties and pronounced delay in diagnosis. The available pathogenetic therapy for SMA has the greatest effect with an earlier start of treatment, so timely diagnosis of the disease significantly improves the overall prognosis.Aim. To evaluate the features of diagnosis of the adult SMA and summarize the first experience of such diagnosis in Russian patients.Materials and methods. We analyzed the archived medical records of 50 adult patients with SMA consulted at the Research Center of Neurology (Moscow).Results. The data of patients with SMA type 2 (n = 26), SMA type 3 (n = 21), SMA type 4 (n = 3) were analyzed. The delay time for diagnosis in SMA type 2 is 35 (0–270) months, with SMA types 3 and 4 – 108 (0–408) months. The diagnosis of SMA was the first diagnosis in SMA type 2 in 69 % of cases, in SMA types 3 and 4 in 29 % of cases. The most common first diagnosis in patients with SMA is myopathy, accounting for 52 % of all misdiagnosed cases. A small percentage of the use of needle electromyography in the diagnostic process was noted (1/3 of cases); in cases of its use, this did not accelerate the correct diagnosis. Creatine phosphokinase activity is often elevated in patients with SMA types 3 and 4 compared with SMA type 2 (p <0.05). Conclusions. To reduce the delay in the correct diagnosis of SMA and earlier initiation of pathogenetic therapy, it is necessary to increase the awareness of specialists about the features of diagnosis the disease and focus on alternative erroneous diagnoses, among which adult patients with SMA may “hide”. The key to confirming the diagnosis is DNA testing.
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spelling doaj.art-5e29129b8336446c8f26630c248a4d342023-09-03T09:22:25ZrusABV-pressНервно-мышечные болезни2222-87212413-04432022-12-01124374510.17650/2222-8721-2022-12-4-37-45332Adult spinal muscular atrophy: problems of early diagnosisYu. A. Shpilyukova0S. N. Illarioshkin1ФГБНУ «Научный центр неврологии»ФГБНУ «Научный центр неврологии»Background. Spinal muscular atrophy (SMA) associated with chromosome 5q is an autosomal recessive neuromuscular disease caused by a mutation in the SMN1 gene. Adult forms of SMA are relatively rarer and associated with significant diagnostic difficulties and pronounced delay in diagnosis. The available pathogenetic therapy for SMA has the greatest effect with an earlier start of treatment, so timely diagnosis of the disease significantly improves the overall prognosis.Aim. To evaluate the features of diagnosis of the adult SMA and summarize the first experience of such diagnosis in Russian patients.Materials and methods. We analyzed the archived medical records of 50 adult patients with SMA consulted at the Research Center of Neurology (Moscow).Results. The data of patients with SMA type 2 (n = 26), SMA type 3 (n = 21), SMA type 4 (n = 3) were analyzed. The delay time for diagnosis in SMA type 2 is 35 (0–270) months, with SMA types 3 and 4 – 108 (0–408) months. The diagnosis of SMA was the first diagnosis in SMA type 2 in 69 % of cases, in SMA types 3 and 4 in 29 % of cases. The most common first diagnosis in patients with SMA is myopathy, accounting for 52 % of all misdiagnosed cases. A small percentage of the use of needle electromyography in the diagnostic process was noted (1/3 of cases); in cases of its use, this did not accelerate the correct diagnosis. Creatine phosphokinase activity is often elevated in patients with SMA types 3 and 4 compared with SMA type 2 (p <0.05). Conclusions. To reduce the delay in the correct diagnosis of SMA and earlier initiation of pathogenetic therapy, it is necessary to increase the awareness of specialists about the features of diagnosis the disease and focus on alternative erroneous diagnoses, among which adult patients with SMA may “hide”. The key to confirming the diagnosis is DNA testing.https://nmb.abvpress.ru/jour/article/view/507спинальная мышечная атрофияsmn1диагностикадифференциальный диагноз
spellingShingle Yu. A. Shpilyukova
S. N. Illarioshkin
Adult spinal muscular atrophy: problems of early diagnosis
Нервно-мышечные болезни
спинальная мышечная атрофия
smn1
диагностика
дифференциальный диагноз
title Adult spinal muscular atrophy: problems of early diagnosis
title_full Adult spinal muscular atrophy: problems of early diagnosis
title_fullStr Adult spinal muscular atrophy: problems of early diagnosis
title_full_unstemmed Adult spinal muscular atrophy: problems of early diagnosis
title_short Adult spinal muscular atrophy: problems of early diagnosis
title_sort adult spinal muscular atrophy problems of early diagnosis
topic спинальная мышечная атрофия
smn1
диагностика
дифференциальный диагноз
url https://nmb.abvpress.ru/jour/article/view/507
work_keys_str_mv AT yuashpilyukova adultspinalmuscularatrophyproblemsofearlydiagnosis
AT snillarioshkin adultspinalmuscularatrophyproblemsofearlydiagnosis