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The relation of testosterone levels with fatigue and apathy in Parkinson's disease.

Authors :
Kenangil G
Orken DN
Ur E
Forta H
Celik M
Source :
Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2009 Jun; Vol. 111 (5), pp. 412-4. Date of Electronic Publication: 2009 Jan 08.
Publication Year :
2009

Abstract

Objective: Fatigue and apathy are frequent in patients with Parkinson's disease (PD). Testosterone deficiency in male patients may contribute in development of fatigue and apathy as well. We investigated whether a possible relation exists between serum testosterone levels, fatigue and apathy in male PD patients.<br />Materials and Methods: We included 29 non-demented and non-depressed PD patients and 30 age- and sex-matched healthy subjects. Fatigue Severity Scale (FSS) and Apathy Evaluation Scale (AES-C) were used for the evaluations. In PD patients and healthy subjects, a relationship between FSS, AES-C scores and plasma testosterone levels were assessed. In addition, a correlation between FSS, AES-C and Unified Parkinson's Disease Rating Scale was investigated in PD group.<br />Results: The mean scores of FSS and AES-C were significantly higher in PD patients than those of the control group. The Unified Parkinson's Disease Rating Scale (UPDRS) scores were significantly correlated with FSS and AES-C scores. Mean free testosterone level was significantly lower in PD patients than controls (p=0.008). f-Testosterone levels of PD patients were not correlated with FSS or AES-C scores.<br />Conclusion: Apathy and fatigue are frequent in PD and show significant correlation with the severity of the disease. f-Testosterone levels are not related with apathy or fatigue in male PD patients and the role of testosterone in the pathophysiology of these non-motor symptoms is still controversial.

Details

Language :
English
ISSN :
1872-6968
Volume :
111
Issue :
5
Database :
MEDLINE
Journal :
Clinical neurology and neurosurgery
Publication Type :
Academic Journal
Accession number :
19131155
Full Text :
https://doi.org/10.1016/j.clineuro.2008.11.019