Literature DB >> 26510705

Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy.

Nicholas E Johnson1, Anne-Berit Ekstrom2, Craig Campbell3, Man Hung4,5, Heather R Adams6, Wei Chen5, Elizabeth Luebbe6, James Hilbert6, Richard T Moxley6, Chad R Heatwole6.   

Abstract

AIM: The frequency and impact of symptoms experienced by patients with congenital, childhood, and juvenile-onset myotonic dystrophy (CDM/ChDM/JDM) is not documented. This report identifies symptomatic areas with the greatest disease burden in an international population of patients with early-onset myotonic dystrophy type-1 (DM1).
METHOD: We distributed surveys to parents of patients with CDM/ChDM/JDM. Patients with CDM/ChDM/JDM were members of the US National Registry of DM1 Patients and Family Members, the Canadian Neuromuscular Disease Registry, or the Swedish Health System. Surveys inquired about 325 symptoms and 20 themes associated with CDM/ChDM/JDM. Parents identified the importance of each symptom and theme to their affected child. The prevalence of each symptom and theme were compared across subgroups of patients. The statistical analysis was performed using Fisher's exact and Kruskal-Wallis tests.
RESULTS: One hundred and fifty parents returned surveys. The most frequently reported symptomatic themes in children were issues involving communication (81.7%) and problems with hands or fingers (79.6%). Problems with communication and fatigue were the issues that were reported to have the greatest impact on childrens' lives, while 24.1% of children reported cardiac disorders and 15.8% had problems with anesthesia.
INTERPRETATION: A range of symptoms contribute to the burden of disease faced by children with DM1. Many of these symptoms are under-recognized.
© 2015 Mac Keith Press.

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Year:  2015        PMID: 26510705      PMCID: PMC4848162          DOI: 10.1111/dmcn.12948

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  22 in total

1.  Genetic risks for children of women with myotonic dystrophy.

Authors:  M C Koch; T Grimm; H G Harley; P S Harper
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Orofacial dysfunction in children and adolescents with myotonic dystrophy.

Authors:  Lotta Sjögreen; Monica Engvall; Anne-Berit Ekström; Anette Lohmander; Stavros Kiliaridis; Már Tulinius
Journal:  Dev Med Child Neurol       Date:  2007-01       Impact factor: 5.449

3.  If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD).

Authors:  James E Hilbert; John T Kissel; Elizabeth A Luebbe; William B Martens; Michael P McDermott; Donald B Sanders; Rabi Tawil; Charles A Thornton; Richard T Moxley
Journal:  Contemp Clin Trials       Date:  2011-11-26       Impact factor: 2.226

4.  A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1).

Authors:  Nathalie Angeard; Aurélia Jacquette; Marcela Gargiulo; Hélène Radvanyi; Sylvain Moutier; Bruno Eymard; Delphine Héron
Journal:  Neuromuscul Disord       Date:  2011-05-17       Impact factor: 4.296

5.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors:  M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

6.  The impact of congenital and childhood myotonic dystrophy on quality of life: a qualitative study of associated symptoms.

Authors:  Nicholas E Johnson; Elizabeth Luebbe; Eileen Eastwood; Nancy Chin; Richard T Moxley; Chad R Heatwole
Journal:  J Child Neurol       Date:  2013-04-22       Impact factor: 1.987

7.  Cognition and adaptive skills in myotonic dystrophy type 1: a study of 55 individuals with congenital and childhood forms.

Authors:  Anne-Berit Ekström; Louise Hakenäs-Plate; Már Tulinius; Elisabet Wentz
Journal:  Dev Med Child Neurol       Date:  2009-04-21       Impact factor: 5.449

8.  Congenital myotonic dystrophy: assisted ventilation duration and outcome.

Authors:  Craig Campbell; Rebecca Sherlock; Pierre Jacob; Marc Blayney
Journal:  Pediatrics       Date:  2004-04       Impact factor: 7.124

9.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

10.  Diffusion tensor imaging reveals widespread white matter abnormalities in children and adolescents with myotonic dystrophy type 1.

Authors:  Jeffrey R Wozniak; Bryon A Mueller; Christopher J Bell; Ryan L Muetzel; Kelvin O Lim; John W Day
Journal:  J Neurol       Date:  2012-11-29       Impact factor: 4.849

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  12 in total

1.  Physical function and mobility in children with congenital myotonic dystrophy.

Authors:  Evan M Pucillo; Deanna L Dibella; Man Hung; Jerry Bounsanga; Becky Crockett; Melissa Dixon; Russell J Butterfield; Craig Campbell; Nicholas E Johnson
Journal:  Muscle Nerve       Date:  2017-02-13       Impact factor: 3.217

2.  12-Month progression of motor and functional outcomes in congenital myotonic dystrophy.

Authors:  Kellen H Quigg; Kiera N Berggren; Melissa McIntyre; Kameron Bates; Francesca Salmin; Jacopo L Casiraghi; Adele DʼAmico; Guja Astrea; Federica Ricci; Marnee J McKay; Jennifer N Baldwin; Joshua Burns; Craig Campbell; Valeria A Sansone; Nicholas E Johnson
Journal:  Muscle Nerve       Date:  2021-01-10       Impact factor: 3.217

3.  Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional study.

Authors:  Nicholas E Johnson; Russell Butterfield; Kiera Berggren; Man Hung; Wei Chen; Deanna DiBella; Melissa Dixon; Heather Hayes; Evan Pucillo; Jerry Bounsanga; Chad Heatwole; Craig Campbell
Journal:  Neurology       Date:  2016-06-15       Impact factor: 9.910

4.  Orofacial strength, dysarthria, and dysphagia in congenital myotonic dystrophy.

Authors:  Kiera N Berggren; Man Hung; Melissa M Dixon; Jerry Bounsanga; Becky Crockett; Mary D Foye; Yushan Gu; Craig Campbell; Russell J Butterfield; Nicholas E Johnson
Journal:  Muscle Nerve       Date:  2018-09       Impact factor: 3.217

5.  The Charcot-Marie-Tooth Health Index: Evaluation of a Patient-Reported Outcome.

Authors:  Nicholas E Johnson; Chad Heatwole; Peter Creigh; Michael P McDermott; Nuran Dilek; Man Hung; Jerry Bounsanga; Wan Tang; Michael E Shy; David N Herrmann
Journal:  Ann Neurol       Date:  2018-08-29       Impact factor: 10.422

6.  CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.

Authors:  Lise Barbé; Stella Lanni; Arturo López-Castel; Silvie Franck; Claudia Spits; Kathelijn Keymolen; Sara Seneca; Stephanie Tomé; Ioana Miron; Julie Letourneau; Minggao Liang; Sanaa Choufani; Rosanna Weksberg; Michael D Wilson; Zdenek Sedlacek; Cynthia Gagnon; Zuzana Musova; David Chitayat; Patrick Shannon; Jean Mathieu; Karen Sermon; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025

7.  PREPUBERTAL GYNECOMASTIA: A RARE MANIFESTATION OF MYOTONIC DYSTROPHY TYPE 1.

Authors:  Patrícia Sofia Ferreira Miranda; Ester Preciosa Maio Nunes Pereira; Joana Serra Caetano Baltazar Barreto; Margarida Maria Videira Henriques; Maria Alice Santos Cordeiro Mirante; Lina Maria Jesus Ferreira Cardoso Ramos
Journal:  Rev Paul Pediatr       Date:  2020-02-14

Review 8.  DM1 Phenotype Variability and Triplet Repeat Instability: Challenges in the Development of New Therapies.

Authors:  Stéphanie Tomé; Geneviève Gourdon
Journal:  Int J Mol Sci       Date:  2020-01-10       Impact factor: 5.923

9.  The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities.

Authors:  Yi Wei; Anna McCormick; Alex MacKenzie; Erin O'Ferrall; Shannon Venance; Jean K Mah; Kathryn Selby; Hugh J McMillan; Garth Smith; Maryam Oskoui; Gillian Hogan; Laura McAdam; Gracia Mabaya; Victoria Hodgkinson; Josh Lounsberry; Lawrence Korngut; Craig Campbell
Journal:  Paediatr Child Health       Date:  2017-12-08       Impact factor: 2.253

10.  Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study.

Authors:  Mieke Kooi-van Es; Corrie E Erasmus; Bert J M de Swart; Nicoline B M Voet; Philip J van der Wees; Imelda J M de Groot; Lenie van den Engel-Hoek
Journal:  J Neuromuscul Dis       Date:  2020
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