Literature DB >> 19726407

Bladder dysfunction in hereditary spastic paraplegia: what to expect?

Mark Braschinsky1, Inga Zopp, Mart Kals, Sulev Haldre, Katrin Gross-Paju.   

Abstract

BACKGROUND: Hereditary spastic paraplegia (HSP) comprises a group of rare neurodegenerative disorders characterised by progressive spasticity and hyperreflexia of the legs. Neurogenic bladder dysfunction is a well recognised problem in patients with HSP but it has not yet been described systematically in the literature. The aim of this study was to provide an evidential overview of the ways in which urinary dysfunction presents in HSP.
METHODS: 49 patients with HSP were included and underwent evaluation. A history was followed by a semi-structured interview and, in those patients who consented, measurement of residual volume of urine (PVR) and urodynamic evaluation.
RESULTS: 38 subjects (77.6%) reported some type of urinary symptom. Subjective complaints of bladder problems showed a correlation with verified urinary dysfunction. There were no significant differences in the occurrence of urinary disturbances between the pure and complex forms of HSP. The most frequent symptoms were incontinence (69.4%), hesitancy (59.2%), increased frequency of micturition (55.1%) and urgency (51.0%). Incomplete bladder emptying was the rarest (36.7%). The most common combination of symptoms was to have all of them (14.3%). Incomplete bladder emptying as a complaint was associated with an increased risk of PVR. Women had a higher risk of increased voiding frequency.
CONCLUSIONS: To our knowledge, this work is the first systematic and disease oriented overview of neurogenic bladder disturbances in patients with HSP. Our results may be useful to the clinicians who work with HSP patients, allowing them to make appropriate screening and management decisions.

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Year:  2009        PMID: 19726407     DOI: 10.1136/jnnp.2009.180331

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  7 in total

1.  A De Novo BSCL2 Gene S90L Mutation in a Progressive Tetraparesis with Urinary Dysfunction and Corpus Callosum Involvement.

Authors:  Joana Ramos-Lopes; Joana Ribeiro; Mário Laço; Cristina Alves; Anabela Matos; Cármen Costa
Journal:  J Pediatr Genet       Date:  2020-07-08

2.  Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.

Authors:  Mark Braschinsky; Riin Tamm; Christian Beetz; Elena Sachez-Ferrero; Elve Raukas; Siiri-Merike Lüüs; Katrin Gross-Paju; Catherine Boillot; Federico Canzian; Andres Metspalu; Sulev Haldre
Journal:  BMC Neurol       Date:  2010-03-09       Impact factor: 2.474

3.  Health survey of adults with hereditary spastic paraparesis compared to population study controls.

Authors:  Krister W Fjermestad; Øivind J Kanavin; Eva E Næss; Lise B Hoxmark; Grete Hummelvoll
Journal:  Orphanet J Rare Dis       Date:  2016-07-13       Impact factor: 4.123

4.  Gastrointestinal and urinary complaints in adults with hereditary spastic paraparesis.

Authors:  Øivind J Kanavin; Krister W Fjermestad
Journal:  Orphanet J Rare Dis       Date:  2018-04-16       Impact factor: 4.123

5.  Beyond gait and balance: urinary and bowel dysfunction in X-linked adrenoleukodystrophy.

Authors:  Camille S Corre; Natalie Grant; Reza Sadjadi; Douglas Hayden; Catherine Becker; Pablo Gomery; Florian S Eichler
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

6.  A novel mutation in the UBAP1 gene causing hereditary spastic paraplegia: A case report and overview of the genotype-phenotype correlation.

Authors:  Peiqiang Li; Xiande Huang; Senmao Chai; Dalin Zhu; Huirong Huang; Fengdie Ma; Shasha Zhang; Xiaodong Xie
Journal:  Front Genet       Date:  2022-07-14       Impact factor: 4.772

7.  Clinical and genetic study of hereditary spastic paraplegia in Canada.

Authors:  Nicolas Chrestian; Nicolas Dupré; Ziv Gan-Or; Anna Szuto; Shiyi Chen; Anil Venkitachalam; Jean-Denis Brisson; Jodi Warman-Chardon; Sohnee Ahmed; Setareh Ashtiani; Heather MacDonald; Noreen Mohsin; Karim Mourabit-Amari; Pierre Provencher; Kym M Boycott; Dimitri J Stavropoulos; Patrick A Dion; Peter N Ray; Oksana Suchowersky; Guy A Rouleau; Grace Yoon
Journal:  Neurol Genet       Date:  2016-12-05
  7 in total

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