Literature DB >> 23849261

Pain in adult patients with Pompe disease: a cross-sectional survey.

D Güngör1, A K Schober, M E Kruijshaar, I Plug, N Karabul, M Deschauer, P A van Doorn, A T van der Ploeg, B Schoser, F Hanisch.   

Abstract

BACKGROUND: Pompe disease is a rare hereditary metabolic myopathy caused by a deficiency of acid-α-glucosidase. We investigated the presence and severity of pain and its interference with daily activities in a large group of adults with Pompe disease, who we compared with an age-matched control group.
METHODS: Data were collected in a cross-sectional survey in Germany and The Netherlands. Pain was assessed using the short-form brief pain inventory (BPI). Patients also completed the Short Form-36 item (SF-36v2), the Hospital Anxiety and Depression Scale (HADS) and the Rotterdam Handicap Scale (RHS).
RESULTS: Forty-five percent of the 124 adult Pompe patients reported having had pain in the previous 24h, against 27% of the 111 controls (p=0.004). The median pain severity score in Pompe patients reporting pain was 3.1 (on a scale from 0 to 10), indicating mild pain; against 2.6 amongst controls (p=0.06). The median score of pain interference with daily activities in patients who reported pain was 3.3, against 1.3 in controls (p=0.001). Relative to patients without pain, those with pain had lower RHS scores (p=0.02), lower SF-36 Physical and Mental component summary scores (p<0.001 and p=0.049), and higher levels of depression and anxiety (p=0.005 and p=0.003).
CONCLUSIONS: To date, this is one of the largest studies on pain in a specific neuromuscular disorder. Nearly one in two Pompe patients had experienced pain in the previous 24h. Although pain severity and its interference with daily life were mild, pain was related to a reduced quality of life, less participation in daily life, and greater depression and anxiety. Its management should therefore be seen as part of clinical practice involving Pompe patients.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acid maltase deficiency; Acid α-glucosidase; Glycogen storage disease type 2; Lysosomal storage disorders; Pain; Pompe disease

Mesh:

Substances:

Year:  2013        PMID: 23849261     DOI: 10.1016/j.ymgme.2013.05.021

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  14 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.  A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene.

Authors:  Jake Plewa; Abhilasha Surampalli; Marie Wencel; Merit Milad; Sandra Donkervoort; Vincent J Caiozzo; Namita Goyal; Tahseen Mozaffar; Virginia Kimonis
Journal:  Neuromuscul Disord       Date:  2018-06-27       Impact factor: 4.296

3.  Ten years of the international Pompe survey: patient reported outcomes as a reliable tool for studying treated and untreated children and adults with non-classic Pompe disease.

Authors:  J C van der Meijden; D Güngör; M E Kruijshaar; A D J Muir; H A Broekgaarden; A T van der Ploeg
Journal:  J Inherit Metab Dis       Date:  2014-08-12       Impact factor: 4.982

4.  Function, structure and quality of striated muscles in the lower extremities in patients with late onset Pompe Disease-an MRI study.

Authors:  Michael Vaeggemose; Rosa Andersen Mencagli; Julie Schjødtz Hansen; Bianca Dräger; Steffen Ringgaard; John Vissing; Henning Andersen
Journal:  PeerJ       Date:  2021-05-06       Impact factor: 2.984

Review 5.  Pain Phenotypes in Rare Musculoskeletal and Neuromuscular Diseases.

Authors:  Anthony Tucker-Bartley; Jordan Lemme; Andrea Gomez-Morad; Nehal Shah; Miranda Veliu; Frank Birklein; Claudia Storz; Seward Rutkove; David Kronn; Alison M Boyce; Eduard Kraft; Jaymin Upadhyay
Journal:  Neurosci Biobehav Rev       Date:  2021-02-10       Impact factor: 9.052

6.  Characteristics of pain in amyotrophic lateral sclerosis.

Authors:  Frank Hanisch; Anika Skudlarek; Janine Berndt; Malte E Kornhuber
Journal:  Brain Behav       Date:  2015-01-21       Impact factor: 2.708

7.  Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group.

Authors:  Fatma Al Jasmi; Mohammed Al Jumah; Fatimah Alqarni; Nouriya Al-Sanna'a; Fawziah Al-Sharif; Saeed Bohlega; Edward J Cupler; Waseem Fathalla; Mohamed A Hamdan; Nawal Makhseed; Shahriar Nafissi; Yalda Nilipour; Laila Selim; Nuri Shembesh; Rawda Sunbul; Seyed Hassan Tonekaboni
Journal:  BMC Neurol       Date:  2015-10-15       Impact factor: 2.474

8.  Risk factors for osteoporosis, falls and fractures in hereditary myopathies and sporadic inclusion body myositis - A cross sectional survey.

Authors:  F Danckworth; N Karabul; A Posa; F Hanisch
Journal:  Mol Genet Metab Rep       Date:  2014-02-11

Review 9.  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

10.  Quality of life and participation in daily life of adults with Pompe disease receiving enzyme replacement therapy: 10 years of international follow-up.

Authors:  Deniz Güngör; Michelle E Kruijshaar; Iris Plug; Dimitris Rizopoulos; Tim A Kanters; Stephan C A Wens; Arnold J J Reuser; Pieter A van Doorn; Ans T van der Ploeg
Journal:  J Inherit Metab Dis       Date:  2015-11-03       Impact factor: 4.982

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