Literature DB >> 24479577

Increased prevalence of bladder and intestinal dysfunction in amyotrophic lateral sclerosis.

Georg S Nübling1, Eva Mie, Ricarda M Bauer, Mira Hensler, Stefan Lorenzl, Alexander Hapfelmeier, Debra E Irwin, Gian Domenico Borasio, Andrea S Winkler.   

Abstract

Amyotrophic lateral sclerosis (ALS) is predominantly characterized by a progressive loss of motor function. While autonomic dysfunction has been described in ALS, little is known about the prevalence of lower urinary tract symptoms (LUTS) and intestinal dysfunction. We investigated disease severity, LUTS and intestinal dysfunction in 43 patients with ALS attending our outpatient department applying the ALS functional rating scale, the International Consultation on Incontinence Modular Questionnaire, the Urinary Distress Inventory and the Cleveland Clinic Incontinence Score. Results were compared to the German population of a cross-sectional study assessing LUTS in the healthy population, the EPIC study. Results showed that urinary incontinence was increased in patients with ALS aged ≥ 60 years compared to the EPIC cohort (female: 50%/19% (ALS/EPIC), p = 0.026; male: 36%/11% (ALS/EPIC), p = 0.002). No difference was seen at 40-59 years of age. Urge incontinence was the predominant presentation (73% of symptoms). A high symptom burden was stated (ICIQ-SF quality of life subscore 5.5/10). Intake of muscle relaxants and anticholinergics was associated with both urinary incontinence and severity of symptoms. Furthermore, a high prevalence of constipation (46%), but not stool incontinence (9%), was noted. In conclusion, the increased prevalence of urge incontinence and high symptom burden imply that in patients with ALS, LUTS should be increasingly investigated for.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; bladder dysfunction; constipation; motor neuron disease; urinary incontinence

Mesh:

Year:  2014        PMID: 24479577     DOI: 10.3109/21678421.2013.868001

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  14 in total

Review 1.  Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Authors:  Carlayne E Jackson; April L McVey; Stacy Rudnicki; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

2.  Early presentation of lower urinary tract and bowel dysfunction in sporadic amyotrophic lateral sclerosis: A case report.

Authors:  Masataka Nakamura; Kentaro Nakayama; Aya Murakami; Satoshi Morise; Satoshi Kaneko; Hirofumi Kusaka; Yusuke Yakushiji
Journal:  eNeurologicalSci       Date:  2022-06-18

3.  Autonomic system and amyotrophic lateral sclerosis.

Authors:  Ezequiel A Piccione; David M Sletten; Nathan P Staff; Phillip A Low
Journal:  Muscle Nerve       Date:  2015-03-31       Impact factor: 3.217

4.  Patient-reported problematic symptoms in an ALS treatment trial.

Authors:  Divisha Raheja; Helen E Stephens; Erik Lehman; Susan Walsh; Chengwu Yang; Zachary Simmons
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2016-01-29       Impact factor: 4.092

5.  Retinal involvement in amyotrophic lateral sclerosis: a study with optical coherence tomography and diffusion tensor imaging.

Authors:  Annemarie Hübers; Hans Peter Müller; Jens Dreyhaupt; Kathrin Böhm; Florian Lauda; Hayrettin Tumani; Jan Kassubek; Albert C Ludolph; Elmar H Pinkhardt
Journal:  J Neural Transm (Vienna)       Date:  2015-11-18       Impact factor: 3.575

6.  Impairment in Respiratory Function Contributes to Olfactory Impairment in Amyotrophic Lateral Sclerosis.

Authors:  René Günther; Wiebke Schrempf; Antje Hähner; Thomas Hummel; Martin Wolz; Alexander Storch; Andreas Hermann
Journal:  Front Neurol       Date:  2018-02-26       Impact factor: 4.003

7.  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

8.  Aberrant enteric neuromuscular system and dysbiosis in amyotrophic lateral sclerosis.

Authors:  Yongguo Zhang; Destiny Ogbu; Shari Garrett; Yinglin Xia; Jun Sun
Journal:  Gut Microbes       Date:  2021 Jan-Dec

9.  Cognitive Impairment in Chinese Patients with Sporadic Amyotrophic Lateral Sclerosis.

Authors:  Bo Cui; Liying Cui; Jing Gao; Mingsheng Liu; Xiaoguang Li; Caiyan Liu; Junfang Ma; Jia Fang
Journal:  PLoS One       Date:  2015-09-14       Impact factor: 3.240

10.  Non-Motor Symptoms in Patients Suffering from Motor Neuron Diseases.

Authors:  René Günther; Nicole Richter; Anna Sauerbier; Kallol Ray Chaudhuri; Pablo Martinez-Martin; Alexander Storch; Andreas Hermann
Journal:  Front Neurol       Date:  2016-07-25       Impact factor: 4.003

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