Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 10 10 2019
accepted: 05 03 2020
entrez: 24 3 2020
pubmed: 24 3 2020
medline: 1 7 2020
Statut: epublish

Résumé

The advent of new therapies has increased the need to achieve early diagnosis in Spinal Muscular Atrophy (SMA). The aim of the present study was to define the age of diagnosis in the three main types of SMA with pediatric-onset and the timing between the recognition of clinical signs and confirmed genetic diagnosis. All patients with a confirmed diagnosis of type I, II, III SMA followed in 5 Italian centers were included in this study, assessing age at symptoms onset, presenting sign or symptom, age at diagnosis, interval between clinical onset and diagnosis and type of medical investigations conducted in order to obtain the diagnosis. The cohort included 480 patients, 191 affected by SMA type I, 210 by type II and 79 by type III. The mean age at diagnosis was 4.70 months (SD ±2.82) in type I, 15.6 months (SD±5.88) in type II, and 4.34 years (SD±4.01) in type III. The mean time between symptom onset and diagnosis was 1.94 months (SD±1.84) in type I, 5.28 months (SD±4.68) in type II and 16.8 months (SD±18.72) in type III. Our results suggest that despite improved care recommendations there is still a marked diagnostic delay, especially in type III. At the time new therapies are becoming available more attention should be devoted to reducing such delay as there is consistent evidence of the benefit of early treatment.

Sections du résumé

BACKGROUND
The advent of new therapies has increased the need to achieve early diagnosis in Spinal Muscular Atrophy (SMA). The aim of the present study was to define the age of diagnosis in the three main types of SMA with pediatric-onset and the timing between the recognition of clinical signs and confirmed genetic diagnosis.
METHODS
All patients with a confirmed diagnosis of type I, II, III SMA followed in 5 Italian centers were included in this study, assessing age at symptoms onset, presenting sign or symptom, age at diagnosis, interval between clinical onset and diagnosis and type of medical investigations conducted in order to obtain the diagnosis.
RESULTS
The cohort included 480 patients, 191 affected by SMA type I, 210 by type II and 79 by type III. The mean age at diagnosis was 4.70 months (SD ±2.82) in type I, 15.6 months (SD±5.88) in type II, and 4.34 years (SD±4.01) in type III. The mean time between symptom onset and diagnosis was 1.94 months (SD±1.84) in type I, 5.28 months (SD±4.68) in type II and 16.8 months (SD±18.72) in type III.
CONCLUSIONS
Our results suggest that despite improved care recommendations there is still a marked diagnostic delay, especially in type III. At the time new therapies are becoming available more attention should be devoted to reducing such delay as there is consistent evidence of the benefit of early treatment.

Identifiants

pubmed: 32203538
doi: 10.1371/journal.pone.0230677
pii: PONE-D-19-28344
pmc: PMC7089564
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0230677

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Maria Carmela Pera (MC)

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.

Giorgia Coratti (G)

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.

Beatrice Berti (B)

Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Adele D'Amico (A)

Department of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.

Maria Sframeli (M)

Department of Neurosciences, and Centro Clinico Nemo Sud, University of Messina, Messina, Italy.

Emilio Albamonte (E)

Neurorehabilitation Unit, Neuromuscular Omnicentre Clinical Center, Niguarda Hospital, University of Milan, Milan, Italy.

Roberto de Sanctis (R)

Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Sonia Messina (S)

Department of Neurosciences, and Centro Clinico Nemo Sud, University of Messina, Messina, Italy.

Michela Catteruccia (M)

Department of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.

Giorgia Brigati (G)

Center of Experimental and Translational Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Laura Antonaci (L)

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.

Simona Lucibello (S)

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.

Claudio Bruno (C)

Center of Experimental and Translational Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Valeria A Sansone (VA)

Neurorehabilitation Unit, Neuromuscular Omnicentre Clinical Center, Niguarda Hospital, University of Milan, Milan, Italy.

Enrico Bertini (E)

Department of Neurosciences, Unit of Neuromuscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.

Danilo Tiziano (D)

Institute of Genomic Medicine, Università Cattolica del Sacro Cuore Fondazione, Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Marika Pane (M)

Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Eugenio Mercuri (E)

Pediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

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