Literature DB >> 25155777

Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey.

Nesrin Karabul1, Anika Skudlarek, Janine Berndt, Cornelia Kornblum, Rudolf A Kley, Stephan Wenninger, Nikolaus Tiling, Eugen Mengel, Ursula Plöckinger, Matthias Vorgerd, Marcus Deschauer, Benedikt Schoser, Frank Hanisch.   

Abstract

OBJECTIVE: To determine the frequency and impact of gastrointestinal symptoms, and bowel and urinary incontinence, as this is currently unknown in adults with Pompe disease.
METHODS: Adult German Pompe patients and age- and gender-matched controls were asked about symptoms in the upper and lower intestinal tract as well as urinary incontinence using the Gastrointestinal Symptoms Questionnaire and the International Consultation on Incontinence Questionnaires for Bowel Symptoms and Urinary Incontinence.
RESULTS: The overall response rate was 78%; 57 patients and 57 controls participated. The mean age of the patients was 48.3 years ±14.7 (28 female, 29 male). 84% of patients were receiving enzyme replacement therapy. Stool urgency, diarrhoea, and urinary urge incontinence were reported significantly more frequently in patients compared to the age- and gender-matched controls (55%, 56%, 33% vs. 20%, 18%, 7%). 20% of Pompe patients used loperamide daily against diarrhoea. No other gastrointestinal tract-related symptoms were reported to occur more frequently in Pompe patients than in controls.
CONCLUSIONS: Compared to age- and gender-matched controls, both urinary and bowel incontinence occur in a higher frequency in adults with Pompe disease and have a major impact on daily life.

Entities:  

Year:  2014        PMID: 25155777      PMCID: PMC4241205          DOI: 10.1007/8904_2014_334

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  35 in total

1.  Pathological features of glycogen storage disease type II highlighted in the knockout mouse model.

Authors:  A G Bijvoet; H Van Hirtum; M Vermey; D Van Leenen; A T Van Der Ploeg; W J Mooi; A J Reuser
Journal:  J Pathol       Date:  1999-11       Impact factor: 7.996

2.  The pattern of involvement of adult-onset acid maltase deficiency at autopsy.

Authors:  J D van der Walt; M Swash; J Leake; E L Cox
Journal:  Muscle Nerve       Date:  1987 Mar-Apr       Impact factor: 3.217

3.  Gaucher's disease: a pilot study of the symptomatic responses to enzyme replacement therapy.

Authors:  C L Verderese; O C Graham; C A Holder-McShane; N E Harnett; N W Barton
Journal:  J Neurosci Nurs       Date:  1993-10       Impact factor: 1.230

4.  Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 months.

Authors:  Ilka Schneider; Frank Hanisch; Tobias Müller; Bernd Schmidt; Stephan Zierz
Journal:  Wien Med Wochenschr       Date:  2012-11-19

5.  Prognostic factors for the late onset Pompe disease with enzyme replacement therapy: from our experience of 4 cases including an autopsy case.

Authors:  Hiroshi Kobayashi; Yohta Shimada; Masahiro Ikegami; Toshinao Kawai; Ken Sakurai; Takashi Urashima; Masatoshi Ijima; Masako Fujiwara; Eiko Kaneshiro; Toya Ohashi; Yoshikatsu Eto; Keiko Ishigaki; Makiko Osawa; Sandra Obikawa Kyosen; Hiroyuki Ida
Journal:  Mol Genet Metab       Date:  2010-02-04       Impact factor: 4.797

6.  Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tract.

Authors:  P F Chinnery; S Jones; L Sviland; R M Andrews; T J Parsons; D M Turnbull; L A Bindoff
Journal:  Gut       Date:  2001-01       Impact factor: 23.059

7.  Multisystem disorder in late-onset chronic progressive external ophthalmoplegia.

Authors:  Gerald Pfeffer; Sandra Sirrs; N Kevin Wade; Michelle M Mezei
Journal:  Can J Neurol Sci       Date:  2011-01       Impact factor: 2.104

8.  Adult onset acid maltase deficiency. Distribution and progression of clinical and pathological abnormality in a family.

Authors:  M Swash; M S Schwartz; M C Apps
Journal:  J Neurol Sci       Date:  1985-04       Impact factor: 3.181

9.  Impact of enzyme replacement therapy on survival in adults with Pompe disease: results from a prospective international observational study.

Authors:  Deniz Güngör; Michelle E Kruijshaar; Iris Plug; Ralph B D'Agostino; Marloes L C Hagemans; Pieter A van Doorn; Arnold J J Reuser; Ans T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2013-03-27       Impact factor: 4.123

10.  Glycogenosome accumulation in the arrector pili muscle in Pompe disease.

Authors:  Istvan Katona; Joachim Weis; Frank Hanisch
Journal:  Orphanet J Rare Dis       Date:  2014-02-05       Impact factor: 4.123

View more
  6 in total

Review 1.  Multisystem late onset Pompe disease (LOPD): an update on clinical aspects.

Authors:  Antonio Toscano; Carmelo Rodolico; Olimpia Musumeci
Journal:  Ann Transl Med       Date:  2019-07

2.  Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment.

Authors:  Federica Montagnese; E Barca; O Musumeci; S Mondello; A Migliorato; A Ciranni; C Rodolico; P De Filippi; C Danesino; A Toscano
Journal:  J Neurol       Date:  2015-02-12       Impact factor: 4.849

3.  Lower Urinary Tract Symptoms and Incontinence in Children with Pompe Disease.

Authors:  Divya Ajay; Erin R McNamara; Stephanie Austin; John S Wiener; Priya Kishnani
Journal:  JIMD Rep       Date:  2015-11-05

4.  Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD).

Authors:  Federica Montagnese; Francesca Granata; Olimpia Musumeci; Carmelo Rodolico; Stefania Mondello; Emanuele Barca; Maria Cucinotta; Anna Ciranni; Marcello Longo; Antonio Toscano
Journal:  J Inherit Metab Dis       Date:  2016-02-01       Impact factor: 4.982

5.  Early-onset of symptoms and clinical course of Pompe disease associated with the c.-32-13 T > G variant.

Authors:  Mrudu Herbert; Laura E Case; Mugdha Rairikar; Heidi Cope; Lauren Bailey; Stephanie L Austin; Priya S Kishnani
Journal:  Mol Genet Metab       Date:  2018-08-23       Impact factor: 4.204

Review 6.  The humanistic burden of Pompe disease: are there still unmet needs? A systematic review.

Authors:  Benedikt Schoser; Deborah A Bilder; David Dimmock; Digant Gupta; Emma S James; Suyash Prasad
Journal:  BMC Neurol       Date:  2017-11-22       Impact factor: 2.474

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.