Literature DB >> 26581301

Patient-Reported Impact of Symptoms in Myotonic Dystrophy Type 2 (PRISM-2).

Chad Heatwole1, Nicholas Johnson2, Rita Bode2, Jeanne Dekdebrun2, Nuran Dilek2, James E Hilbert2, Elizabeth Luebbe2, William Martens2, Michael P McDermott2, Christine Quinn2, Nan Rothrock2, Charles Thornton2, Barbara G Vickrey2, David Victorson2, Richard T Moxley2.   

Abstract

OBJECTIVE: To determine the frequency and relative importance of the most life-affecting symptoms in myotonic dystrophy type 2 (DM2) and to identify the factors that have the strongest association with these symptoms.
METHODS: We conducted a cross-sectional study of adult patients with DM2 from a National Registry of DM2 Patients to assess the prevalence and relative importance of 310 symptoms and 21 symptomatic themes. Participant responses were compared by age categories, sex, educational attainment, employment status, and duration of symptoms.
RESULTS: The symptomatic themes with the highest prevalence in DM2 were the inability to do activities (94.4%), limitations with mobility or walking (89.2%), hip, thigh, or knee weakness (89.2%), fatigue (89.2%), and myotonia (82.6%). Participants identified the inability to do activities and fatigue as the symptomatic themes that have the greatest overall effect on their lives. Unemployment, a longer duration of symptoms, and less education were associated with a higher average prevalence of all symptomatic themes (p < 0.01). Unemployment, a longer duration of symptoms, sex, and increased age were associated with a higher average effect of all symptomatic themes among patients with DM2 (p < 0.01).
CONCLUSIONS: The lives of patients with DM2 are affected by a variety of symptoms. These symptoms have different levels of significance and prevalence in this population and vary across DM2 subgroups in different demographic categories.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 26581301      PMCID: PMC4691689          DOI: 10.1212/WNL.0000000000002225

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


  27 in total

1.  Changes in pain-related beliefs, coping, and catastrophizing predict changes in pain intensity, pain interference, and psychological functioning in individuals with myotonic muscular dystrophy and facioscapulohumeral dystrophy.

Authors:  Rubén Nieto; Katherine A Raichle; Mark P Jensen; Jordi Miró
Journal:  Clin J Pain       Date:  2012-01       Impact factor: 3.442

2.  Laboratory abnormalities in patients with myotonic dystrophy type 2.

Authors:  Chad Heatwole; Nicholas Johnson; Bradley Goldberg; William Martens; Richard Moxley
Journal:  Arch Neurol       Date:  2011-09

3.  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

4.  Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2).

Authors:  C Gaul; T Schmidt; G Windisch; T Wieser; T Müller; S Vielhaber; S Zierz; B Leplow
Journal:  Neurology       Date:  2006-07-25       Impact factor: 9.910

5.  Poor sleep quality and fatigue but no excessive daytime sleepiness in myotonic dystrophy type 2.

Authors:  Alide A Tieleman; Hans Knoop; Anne-Els van de Logt; Gijs Bleijenberg; Baziel G M van Engelen; Sebastiaan Overeem
Journal:  J Neurol Neurosurg Psychiatry       Date:  2010-09       Impact factor: 10.154

6.  Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.

Authors:  J W Day; K Ricker; J F Jacobsen; L J Rasmussen; K A Dick; W Kress; C Schneider; M C Koch; G J Beilman; A R Harrison; J C Dalton; L P W Ranum
Journal:  Neurology       Date:  2003-02-25       Impact factor: 9.910

Review 7.  Cerebral involvement in myotonic dystrophies.

Authors:  Giovanni Meola; Valeria Sansone
Journal:  Muscle Nerve       Date:  2007-09       Impact factor: 3.217

8.  Chronic pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy.

Authors:  Mark P Jensen; Amy J Hoffman; Brenda L Stoelb; Richard T Abresch; Gregory T Carter; Craig M McDonald
Journal:  Arch Phys Med Rehabil       Date:  2008-02       Impact factor: 3.966

9.  Impact of biopsychosocial factors on chronic pain in persons with myotonic and facioscapulohumeral muscular dystrophy.

Authors:  Jordi Miró; Katherine A Raichle; Gregory T Carter; Sarah A O'Brien; Richard T Abresch; Craig M McDonald; Mark P Jensen
Journal:  Am J Hosp Palliat Care       Date:  2009-05-04       Impact factor: 2.500

10.  The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease.

Authors:  Martina Minnerop; Bernd Weber; Jan-Christoph Schoene-Bake; Sandra Roeske; Sandra Mirbach; Christian Anspach; Christiane Schneider-Gold; Regina C Betz; Christoph Helmstaedter; Marc Tittgemeyer; Thomas Klockgether; Cornelia Kornblum
Journal:  Brain       Date:  2011-11-29       Impact factor: 13.501

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  9 in total

Review 1.  Sleep Complaints, Sleep and Breathing Disorders in Myotonic Dystrophy Type 2.

Authors:  Andrea Romigi; Michelangelo Maestri; Carmine Nicoletta; Giuseppe Vitrani; Marco Caccamo; Gabriele Siciliano; Enrica Bonanni; Diego Centonze; Alessandro Sanduzzi
Journal:  Curr Neurol Neurosci Rep       Date:  2019-02-09       Impact factor: 5.081

2.  A Qualitative Approach to Health Related Quality-of-Life in Congenital Muscular Dystrophy.

Authors:  Kylie M Cornwall; Russell J Butterfield; Antonio Hernandez; Chad Heatwole; Nicholas E Johnson
Journal:  J Neuromuscul Dis       Date:  2018

Review 3.  Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2.

Authors:  Andrea Romigi; Valentina Franco; Fabio Placidi; Claudio Liguori; Emanuele Rastelli; Giuseppe Vitrani; Diego Centonze; Roberto Massa
Journal:  Curr Neurol Neurosci Rep       Date:  2018-10-31       Impact factor: 5.081

4.  Patient-Reported Symptoms in Facioscapulohumeral Muscular Dystrophy (PRISM-FSHD).

Authors:  Johanna Hamel; Nicholas Johnson; Rabi Tawil; William B Martens; Nuran Dilek; Michael P McDermott; Chad Heatwole
Journal:  Neurology       Date:  2019-08-13       Impact factor: 9.910

5.  Patient-identified impact of symptoms in spinal and bulbar muscular atrophy.

Authors:  Robert D Guber; Angela D Kokkinis; Alice B Schindler; Roxanna M Bendixen; Chad R Heatwole; Kenneth H Fischbeck; Christopher Grunseich
Journal:  Muscle Nerve       Date:  2017-09-25       Impact factor: 3.217

Review 6.  Myotonic Dystrophies: State of the Art of New Therapeutic Developments for the CNS.

Authors:  Genevieve Gourdon; Giovanni Meola
Journal:  Front Cell Neurosci       Date:  2017-04-20       Impact factor: 5.505

7.  Patient Reported Impact of Symptoms in Spinal Muscular Atrophy (PRISM-SMA).

Authors:  Phillip Mongiovi; Nuran Dilek; Connie Garland; Michael Hunter; John T Kissel; Elizabeth Luebbe; Michael P McDermott; Nicholas Johnson; Chad Heatwole
Journal:  Neurology       Date:  2018-08-24       Impact factor: 11.800

8.  Transcriptome alterations in myotonic dystrophy frontal cortex.

Authors:  Brittney A Otero; Kiril Poukalov; Ryan P Hildebrandt; Charles A Thornton; Kenji Jinnai; Harutoshi Fujimura; Takashi Kimura; Katharine A Hagerman; Jacinda B Sampson; John W Day; Eric T Wang
Journal:  Cell Rep       Date:  2021-01-19       Impact factor: 9.995

Review 9.  Core Clinical Phenotypes in Myotonic Dystrophies.

Authors:  Stephan Wenninger; Federica Montagnese; Benedikt Schoser
Journal:  Front Neurol       Date:  2018-05-02       Impact factor: 4.003

  9 in total

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