Literature DB >> 27306634

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

Nicholas E Johnson1, Russell Butterfield2, Kiera Berggren2, Man Hung2, Wei Chen2, Deanna DiBella2, Melissa Dixon2, Heather Hayes2, Evan Pucillo2, Jerry Bounsanga2, Chad Heatwole2, Craig Campbell2.   

Abstract

OBJECTIVE: Herein, we describe the disease burden and age-related changes of congenital-onset myotonic dystrophy (CDM) in childhood.
METHODS: Children with CDM and age-matched controls aged 0 to 13 years were enrolled. Participants were divided into cohorts based on the following age groups: 0-2, 3-6, and 7-13 years. Each cohort received age-appropriate evaluations including functional testing, oral facial strength testing, neuropsychological testing, quality-of-life measurements, and ECG. Independent-samples t test or Wilcoxon 2-sample test was used to compare the differences between children with CDM and controls. Probability values less than 0.05 are reported as significant.
RESULTS: Forty-one participants with CDM and 29 healthy controls were enrolled. The 6-minute walk was significantly different between CDM (258.3 m [SD 176.0]) and control participants (568.2 m [SD 73.2]). The mean lip force strength was significantly different in CDM (2.1 N [SD 2.8)] compared to control participants (17.8 N [SD 7.6]). In participants with CDM, the mean IQ (65.8; SD 18.4) was 3 SDs below the mean compared to standardized norms. Measurements of grip strength, sleep quality, and quality of life were also significantly different. Strength measures (oral facial strength, grip strength, and 6-minute walk) correlated with each other but not with participant IQ.
CONCLUSIONS: This work identifies important phenotypes associated with CDM during childhood. Several measures of strength and function were significantly different between participants with CDM and controls and may be useful during future therapeutic trials.
© 2016 American Academy of Neurology.

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Year:  2016        PMID: 27306634      PMCID: PMC4940062          DOI: 10.1212/WNL.0000000000002845

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  12 in total

1.  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

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

Authors:  Nicholas E Johnson; Anne-Berit Ekstrom; Craig Campbell; Man Hung; Heather R Adams; Wei Chen; Elizabeth Luebbe; James Hilbert; Richard T Moxley; Chad R Heatwole
Journal:  Dev Med Child Neurol       Date:  2015-10-28       Impact factor: 5.449

3.  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

4.  An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Authors:  Y H Fu; A Pizzuti; R G Fenwick; J King; S Rajnarayan; P W Dunne; J Dubel; G A Nasser; T Ashizawa; P de Jong
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

5.  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

6.  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

Review 7.  Myotonic dystrophy: from bench to bedside.

Authors:  Nicholas E Johnson; Chad R Heatwole
Journal:  Semin Neurol       Date:  2012-11-01       Impact factor: 3.420

8.  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

9.  Reference values for the 6-minute walk test in healthy children and adolescents in Switzerland.

Authors:  Silvia Ulrich; Florian F Hildenbrand; Ursula Treder; Manuel Fischler; Stephan Keusch; Rudolf Speich; Margrit Fasnacht
Journal:  BMC Pulm Med       Date:  2013-08-05       Impact factor: 3.317

10.  The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study.

Authors:  Craig M McDonald; Erik K Henricson; R Ted Abresch; Julaine M Florence; Michelle Eagle; Eduard Gappmaier; Allan M Glanzman; Robert Spiegel; Jay Barth; Gary Elfring; Allen Reha; Stuart Peltz
Journal:  Muscle Nerve       Date:  2013-06-26       Impact factor: 3.217

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  11 in total

Review 1.  Repeat-associated RNA structure and aberrant splicing.

Authors:  Melissa A Hale; Nicholas E Johnson; J Andrew Berglund
Journal:  Biochim Biophys Acta Gene Regul Mech       Date:  2019-07-16       Impact factor: 4.490

2.  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

3.  Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1.

Authors:  Siham Ait Benichou; Dominic Jauvin; Thiéry De Serres-Bérard; Marion Pierre; Karen K Ling; C Frank Bennett; Frank Rigo; Genevieve Gourdon; Mohamed Chahine; Jack Puymirat
Journal:  Gene Ther       Date:  2022-01-25       Impact factor: 5.250

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.  Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy.

Authors:  James D Thomas; Łukasz J Sznajder; Olgert Bardhi; Faaiq N Aslam; Zacharias P Anastasiadis; Marina M Scotti; Ichizo Nishino; Masayuki Nakamori; Eric T Wang; Maurice S Swanson
Journal:  Genes Dev       Date:  2017-07-11       Impact factor: 11.361

Review 6.  Hard ways towards adulthood: the transition phase in young people with myotonic dystrophy.

Authors:  Sigrid Baldanzi; Giulia Ricci; Costanza Simoncini; Mirna Cosci O Di Coscio; Gabriele Siciliano
Journal:  Acta Myol       Date:  2016-12

Review 7.  Walking and weakness in children: a narrative review of gait and functional ambulation in paediatric neuromuscular disease.

Authors:  Rachel A Kennedy; Kate Carroll; Jennifer L McGinley; Kade L Paterson
Journal:  J Foot Ankle Res       Date:  2020-03-02       Impact factor: 2.303

8.  Reversible cardiac disease features in an inducible CUG repeat RNA-expressing mouse model of myotonic dystrophy.

Authors:  Ashish N Rao; Hannah M Campbell; Xiangnan Guan; Tarah A Word; Xander Ht Wehrens; Zheng Xia; Thomas A Cooper
Journal:  JCI Insight       Date:  2021-03-08

9.  Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing.

Authors:  Silvie Franck; Edouard Couvreu De Deckersberg; Jodi L Bubenik; Christina Markouli; Lise Barbé; Joke Allemeersch; Pierre Hilven; Geoffrey Duqué; Maurice S Swanson; Alexander Gheldof; Claudia Spits; Karen D Sermon
Journal:  Biol Open       Date:  2022-01-12       Impact factor: 2.643

10.  Determining correlations between hand grip strength and anthropometric measurements in preschool children.

Authors:  Amira G Mahmoud; Eman I Elhadidy; Mohamed S Hamza; Nanees E Mohamed
Journal:  J Taibah Univ Med Sci       Date:  2020-02-05
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