Literature DB >> 26806216

Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations.

K R Servelhere1, I Faber1, J A M Saute2, M Moscovich3, A D'Abreu1, L B Jardim2, H A G Teive3, I Lopes-Cendes4, M C Franca1.   

Abstract

BACKGROUND AND
PURPOSE: Non-motor manifestations are frequently overlooked in degenerative disorders and little is known about their frequency and clinical relevance in SPG4 hereditary spastic paraplegia (SPG4-HSP).
METHODS: Thirty patients with SPG4-HSP and 30 healthy controls answered the Modified Fatigue Impact Scale, Epworth Sleepiness Scale, Brief Pain Inventory and Beck Depression Inventory. Student's t test was used to compare groups and linear regression was used to assess correlations.
RESULTS: Patients had higher fatigue scores than controls (31.0 ± 16.5 vs. 14.5 ± 16.0, P = 0.002) as well as pain (3.4 ± 2.7 vs. 1.0 ± 1.6, P = 0.001) and depression (12.7 ± 8.9 vs. 4.4 ± 3.8, P < 0.001, respectively). Fatigue was associated with depression and possibly with disease severity (P = 0.008 and 0.07, respectively).
CONCLUSIONS: Fatigue, pain and depression are frequent and often severe manifestations in patients with SPG4-HSP.
© 2016 EAN.

Entities:  

Keywords:  SPG4; depression; fatigue; non-motor symptoms; pain; spastic paraplegia

Mesh:

Substances:

Year:  2016        PMID: 26806216     DOI: 10.1111/ene.12839

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  7 in total

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Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Intern Emerg Med       Date:  2017-03-09       Impact factor: 3.397

2.  Fatigue and Its Associated Factors in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.

Authors:  Alberto R M Martinez; Marcelo B Nunes; Ingrid Faber; Anelyssa D'Abreu; Íscia Lopes-Cendes; Marcondes C França
Journal:  Cerebellum       Date:  2017-02       Impact factor: 3.847

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.  Ascending Axonal Degeneration of the Corticospinal Tract in Pure Hereditary Spastic Paraplegia: A Cross-Sectional DTI Study.

Authors:  Julia List; Zacharias Kohl; Juergen Winkler; Franz Marxreiter; Arnd Doerfler; Manuel A Schmidt
Journal:  Brain Sci       Date:  2019-10-09

5.  Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia: a web-based survey in the Netherlands.

Authors:  Bas J H van Lith; Hans C J W Kerstens; Laura A C van den Bemd; Maria W G Nijhuis-van der Sanden; Vivian Weerdesteyn; Rob J E M Smeets; Klemens Fheodoroff; Bart P C van de Warrenburg; Alexander C H Geurts
Journal:  Orphanet J Rare Dis       Date:  2020-03-04       Impact factor: 4.123

Review 6.  Recent advances in understanding hereditary spastic paraplegias and emerging therapies.

Authors:  Pauline Lallemant-Dudek; Frederic Darios; Alexandra Durr
Journal:  Fac Rev       Date:  2021-03-10

Review 7.  Cognitive dysfunction in hereditary spastic paraplegias and other motor neuron disorders.

Authors:  Ingrid Faber; Lucas Melo T Branco; Marcondes Cavalvante França Júnior
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  7 in total

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