Literature DB >> 28855409

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.

James E Hilbert1, Richard J Barohn2, Paula R Clemens2, Elizabeth A Luebbe2, William B Martens2, Michael P McDermott2, Amy L Parkhill2, Rabi Tawil2, Charles A Thornton2, Richard T Moxley.   

Abstract

OBJECTIVE: To analyze gastrointestinal (GI) manifestations, their progression over time, and medications being used to treat GI symptoms in a large cohort of patients with myotonic dystrophy types 1 (DM1) and 2 (DM2).
METHODS: We analyzed patient-reported data and medical records in a national registry cohort at baseline and 5 years.
RESULTS: At baseline, the majority of patients reported trouble swallowing in DM1 (55%; n = 499 of 913) and constipation in DM2 (53%; n = 96 of 180). Cholecystectomy occurred in 16.5% of patients with DM1 and 12.8% of patients with DM2, on average before 45 years of age. The use of medications indicated for gastroesophageal reflux disease was reported by 22.5% of DM1 and 18.9% of patients with DM2. Greater risk of a GI manifestation was associated with higher body mass index and longer disease duration in DM1 and female sex in DM2. At the 5-year follow-up, the most common new manifestations were trouble swallowing in patients with DM1 and constipation in patients with DM2.
CONCLUSIONS: GI manifestations were common in both DM1 and DM2, with a relatively high frequency of gallbladder removal in DM1 and DM2 occurring at a younger age compared to normative data in the literature. Studies are needed to determine the pathomechanism of how sex, weight gain, and duration of disease contribute to GI manifestations and how these manifestations affect quality of life and clinical care for patients with DM1 and DM2.
© 2017 American Academy of Neurology.

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Year:  2017        PMID: 28855409      PMCID: PMC5649763          DOI: 10.1212/WNL.0000000000004420

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


  37 in total

1.  SMOOTH MUSCLE INVOLVEMENT IN MYOTONIC DYSTROPHY.

Authors:  J C HARVEY; D H SHERBOURNE; C I SIEGEL
Journal:  Am J Med       Date:  1965-07       Impact factor: 4.965

2.  Consensus on cerebral involvement in myotonic dystrophy: workshop report: May 24-27, 2013, Ferrere (AT), Italy.

Authors:  E Bugiardini; G Meola
Journal:  Neuromuscul Disord       Date:  2014-02-07       Impact factor: 4.296

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.  Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.

Authors:  C L Liquori; K Ricker; M L Moseley; J F Jacobsen; W Kress; S L Naylor; J W Day; L P Ranum
Journal:  Science       Date:  2001-08-03       Impact factor: 47.728

Review 5.  Myotonic dystrophy: approach to therapy.

Authors:  Charles A Thornton; Eric Wang; Ellie M Carrell
Journal:  Curr Opin Genet Dev       Date:  2017-04-01       Impact factor: 5.578

6.  Gastric emptying in myotonic dystrophic patients.

Authors:  M Bellini; P Alduini; F Costa; C Tosetti; L Pasquali; F Pucciani; A Tornar; C Mammini; G Siciliano; G Maltinti; S Marchi
Journal:  Dig Liver Dis       Date:  2002-07       Impact factor: 4.088

7.  Gastric and esophageal emptying in dystrophia myotonica. Effect of metoclopramide.

Authors:  M Horowitz; A Maddox; G J Maddern; J Wishart; P J Collins; D J Shearman
Journal:  Gastroenterology       Date:  1987-03       Impact factor: 22.682

8.  A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1.

Authors:  R Cardani; E Mancinelli; G Saino; L Bonavina; G Meola
Journal:  Neuromuscul Disord       Date:  2008-07-23       Impact factor: 4.296

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.  Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.

Authors:  Celine Dogan; Marie De Antonio; Dalil Hamroun; Hugo Varet; Marianne Fabbro; Felix Rougier; Khadija Amarof; Marie-Christine Arne Bes; Anne-Laure Bedat-Millet; Anthony Behin; Remi Bellance; Françoise Bouhour; Celia Boutte; François Boyer; Emmanuelle Campana-Salort; Françoise Chapon; Pascal Cintas; Claude Desnuelle; Romain Deschamps; Valerie Drouin-Garraud; Xavier Ferrer; Helene Gervais-Bernard; Karima Ghorab; Pascal Laforet; Armelle Magot; Laurent Magy; Dominique Menard; Marie-Christine Minot; Aleksandra Nadaj-Pakleza; Sybille Pellieux; Yann Pereon; Marguerite Preudhomme; Jean Pouget; Sabrina Sacconi; Guilhem Sole; Tanya Stojkovich; Vincent Tiffreau; Andoni Urtizberea; Christophe Vial; Fabien Zagnoli; Gilbert Caranhac; Claude Bourlier; Gerard Riviere; Alain Geille; Romain K Gherardi; Bruno Eymard; Jack Puymirat; Sandrine Katsahian; Guillaume Bassez
Journal:  PLoS One       Date:  2016-02-05       Impact factor: 3.240

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  12 in total

1.  Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2.

Authors:  Federica Montagnese; Stefania Mondello; Stephan Wenninger; Wolfram Kress; Benedikt Schoser
Journal:  J Neurol       Date:  2017-10-30       Impact factor: 4.849

2.  Gender difference in clinical conditions among hospitalized adults with myotonic dystrophy.

Authors:  Lijing Ouyang; Yinding Wang; Rodolfo Valdez; Nicholas Johnson; Laurie Gutmann; Natalie Street; Julie Bolen
Journal:  Muscle Nerve       Date:  2019-01-13       Impact factor: 3.217

3.  Myotonic dystrophy type 1 presenting with dyspnea: A case report.

Authors:  Yu-Xi Jia; Chun-Ling Dong; Jia-Wei Xue; Xiao-Qin Duan; Ming-Yu Xu; Xiao-Min Su; Ping Li
Journal:  World J Clin Cases       Date:  2022-07-16       Impact factor: 1.534

Review 4.  Myotonic Dystrophies: Targeting Therapies for Multisystem Disease.

Authors:  Samantha LoRusso; Benjamin Weiner; W David Arnold
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

Review 5.  Gastrointestinal motility disorders in neurologic disease.

Authors:  Michael Camilleri
Journal:  J Clin Invest       Date:  2021-02-15       Impact factor: 14.808

6.  High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study.

Authors:  Alessia Perna; Daria Maccora; Salvatore Rossi; Tommaso Filippo Nicoletti; Maria Assunta Zocco; Vittorio Riso; Anna Modoni; Antonio Petrucci; Venanzio Valenza; Antonio Grieco; Luca Miele; Gabriella Silvestri
Journal:  Front Neurol       Date:  2020-06-12       Impact factor: 4.003

7.  Myotonic Dystrophy Type 1 Complicated by Colonic Obstruction Due to a Bezoar.

Authors:  Aaron de Souza; Sanjeev Gupta
Journal:  Ann Indian Acad Neurol       Date:  2019-10-25       Impact factor: 1.383

8.  Myotonic dystrophy type 2: the 2020 update.

Authors:  Giovanni Meola
Journal:  Acta Myol       Date:  2020-12-01

Review 9.  Consensus-based care recommendations for adults with myotonic dystrophy type 2.

Authors:  Benedikt Schoser; Federica Montagnese; Guillaume Bassez; Barbara Fossati; Josep Gamez; Chad Heatwole; James Hilbert; Cornelia Kornblum; Anne Kostera-Pruszczyk; Ralf Krahe; Anna Lusakowska; Giovanni Meola; Richard Moxley; Charles Thornton; Bjarne Udd; Paul Formaker
Journal:  Neurol Clin Pract       Date:  2019-08

10.  Zebrafish mbnl mutants model physical and molecular phenotypes of myotonic dystrophy.

Authors:  Melissa N Hinman; Jared I Richardson; Rose A Sockol; Eliza D Aronson; Sarah J Stednitz; Katrina N Murray; J Andrew Berglund; Karen Guillemin
Journal:  Dis Model Mech       Date:  2021-06-14       Impact factor: 5.758

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