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The most recent version of this article was published on 1 August 2007

J Neurol Neurosurg Psychiatry. Published Online First: 10 November 2006. doi:10.1136/jnnp.2006.103788
Copyright © 2006 by the BMJ Publishing Group Ltd.

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Original articles

Gender Differences in Parkinson's Disease

Charlotte A. Haaxma 1, Bastiaan R. Bloem 1*, George F. Borm 2, Wim J.G. Oyen 3, Klaus L. Leenders 4, Silvia Eshuis 4, Jan Booij 5, Dean E. Dluzen 6 and Martin W.I.M. Horstink 1

1 Radboud University Nijmegen Medical Centre, Department of Neurology, Netherlands
2 Radboud University Nijmegen, Department of Epidemiology and Biostatistics, Netherlands
3 Radboud University Nijmegen Medical Centre, Department of Nuclear Medicine, Netherlands
4 University Medical Centre Groningen, Department of Neurology, Netherlands
5 Academic Medical Centre Amsterdam, Department of Nuclear Medicine, Netherlands
6 Northeastern Ohio Universities, College of Medicine, Rootstown, Ohio, Department of Anatomy, United States

* To whom correspondence should be addressed. E-mail: b.bloem{at}neuro.umcn.nl.

Accepted 24 October 2006


*  Abstract

Objective. To investigate gender differences in basic disease characteristics, motor deterioration and nigrostriatal degeneration in Parkinson’s disease (PD).

Methods. We studied 253 consecutive PD patients who were not receiving levodopa or dopamine agonists (disease duration <10 years). We investigated the influence of gender and estrogen status on: (1) age at onset, (2) presenting symptom, (3) severity and progression of motor symptoms (UPDRS-III scores), and (4) amount and progression of nigrostriatal degeneration ([123I]FP-CIT SPECT measurements).

Results. Age at onset was 2.1 years later in women (53.4 years) than men (51.3 years). In women, age at onset correlated positively with parity, age at menopause, and fertile life span. Women more often presented with tremor (67%) than men (48%). Overall, patients presenting with tremor had a 3.6 year higher age at onset and a 38% slower UPDRS-III deterioration. Mean UPDRS-III scores at disease onset were equal for both genders, as was the rate of deterioration. Women had a 16% higher striatal [123I]FP-CIT binding than men at symptom onset and throughout the course of PD.

Conclusions. Our results suggest that, in women, the development of symptomatic PD may be delayed by higher physiological striatal dopamine levels, possibly due to the activity of estrogens. This could explain the epidemiological observations of a lower incidence and higher age at onset in women. Women also presented more often with tremor which, in turn, is associated with milder motor deterioration and striatal degeneration. Taken together, these findings suggest a more benign phenotype in women with PD.


Keywords: Parkinson�s disease, UPDRS, [123I]FP-CIT SPECT, estrogens, gender differences


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Sex and Parkinson’s disease: a world of difference?
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