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Arch Neurol 1999 Jan;56(1):98-102

Clinical correlates of Vascular Parkinsonism.

Winikates J, Jankovic J
Department of Neurology, Baylor College of Medicine, Houston, Tex 77030,
USA.

BACKGROUND: Parkinsonism may be due to other causes besides Parkinson
disease (PD). Vascular parkinsonism (VP) has not been well defined and the
clinical correlates of VP have not been clarified.

OBJECTIVES: To seek evidence for or against the role of cerebrovascular
disease in parkinsonism, and to identify clinical features that suggest a
vascular origin.

DESIGN: Retrospective chart review of patients with parkinsonism. A vascular
rating scale was used to identify 2 patient groups, 1 with strong evidence
of cerebrovascular disease (VP), and 1 with idiopathic PD. Clinical features
of parkinsonism were then compared between the 2 patient groups.

SETTING: A Movement Disorders Clinic, Baylor College of Medicine, Houston,
Tex, a tertiary referral center.

PATIENTS: Three hundred forty-six patients, 69 with VP and 277 with PD.

RESULTS: The VP and PD groups were clearly differentiated in terms of
evidence of cerebrovascular disease (P<.001 to P<.00001). Patients with VP
were older, more likely to present with gait difficulty rather than tremor,
and less likely to respond to the use of levodopa compared with patients
with PD (P<.00001). Patients with VP were also significantly more likely to
have predominant lower body involvement, postural instability, a history of
falling, dementia, corticospinal findings, incontinence (P<.00001), and
pseudobulbar effect (P<.05).

CONCLUSIONS: These differences in clinical features suggest a different
pathogenesis of parkinsonism in these 2 patient groups. The strong evidence
of cerebrovascular disease in the VP group and the differences in clinical
features support the concept of VP as a distinct clinical entity. We
conclude that compared with PD, patients with parkinsonism associated with
vascular disease are more likely to present with gait difficulty and
postural instability rather than tremor, have a history of stroke and risk
factors for stroke, and fail to respond to levodopa therapy.

PMID: 9923767, UI: 99120642
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