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Chorea (disease)

Chorea (also known as St. Vitus dance) is an abnormal voluntary movement disorder, one of a group of neurological disorders called dyskinesias, which are caused by overactivity of the neurotransmitter dopamine in the areas of the brain that control movement. Chorea is characterized by brief, irregular contractions that are not repetitive or rhythmic, but appear to flow from one muscle to the next. Chorea often occurs with athetosis, which adds twisting and writhing movements. Chorea is a primary feature of Huntington's disease, a progressive, hereditary movement disorder that appears in adults, but it may also occur in a variety of other conditions. more...

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Sydenham's chorea occurs in a small percentage (20 percent) of children and adolescents as a complication of rheumatic fever. Chorea can also be induced by drugs (levodopa, anti-convulsants, and anti-psychotics) metabolic and endocrine disorders and vascular incidents.

When chorea is serious, slight movements will become thrashing motions, this form of severe chorea is referred to as "ballism". Walking may become peculiar, and include odd postures and leg movements. Unlike ataxia and dystonia, which affect the quality of voluntary movements or parkinsonism, which is a hindrance of voluntary movements, the movements of chorea and ballism occur on their own, without conscious effort.

The term chorea is derived from a Greek word khoreia (a kind of dance, see chorea), as the quick movements of the feet or hands are vaguely comparable to dancing or piano playing.

Treatment

There is no standard course of treatment for chorea. Treatment depends on the type of chorea and the associated disease. Treatment for Huntington's disease is supportive, while treatment for Syndenham's chorea usually involves antibiotic drugs to treat the infection, followed by drug therapy to prevent recurrence. Adjusting medication dosages can treat drug-induced chorea. Metabolic and endocrine-related choreas are treated according to the cause(s) of symptoms.

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Energy balance in Huntington Disease
From Nutrition Research Newsletter, 7/1/05

Huntington Disease (HD) is a genetic neurologic disorder characterized by uncontrollable dance-like physical movements, dystonia, impairment in gait and eye movement, cognitive impairment, and psychiatric symptoms.

Predictions of increased basal metabolic rate as a cause of weight loss in HD are consistent with observations of a lower average BMI in presymptomatic carriers of the HD gene and in persons with very early symptoms of liD than in healthy control subjects. However, these previous studies have not ruled out increased energy expenditure (EE) with HD from voluntary movement, such as fidgeting, which may be related to body mass. Therefore, a group of researchers from New York compared 24-hour EE and energy intake in persons with early midstage HD with those of matched controls to determine how HD affects energy balance.

Energy expenditure was measured in 13 subjects with early-stage HD and in 9 controls via indirect calorimetry in a human respiratory chamber. Body composition was assessed to determine fat-flee mass and percentage body fat for each subject by using air-displacement plethysmography. Energy intake was determined by weighing all food provided and all leftovers from an ad libitum diet. Stage of disease was estimated based on the Unified Huntington's Disease Rating Scale and modified Mini-Mental Status examinations.

The 24-hour EE was 11% higher in the HD subjects than in the controls. This difference was due to a higher waking metabolic rate, which was related to a significantly greater displacement of the center of mass by HD subjects than by controls. Both groups were in positive energy balance and exceeded their energy expenditure. However, under flee-living conditions as measured by repeated 24-hour recalls, intake varied much more in the HD subjects than in the controls. The variability in energy intake also increased with the progression of the disease.

Higher 24-hour EE in persons with early midstage HD is due to increased physical activity, both voluntary and involuntary. However, HD subjects are able to maintain positive energy balance when offered adequate amounts of food in a controlled setting. The variability of energy intake are likely related to the weight loss observed with HD and should be taken into account in nutritional evaluations of persons with HD. Further studies of patients with late-stage HD are warranted.

A. M. Gaba, Kuan Zhang, Karen Marder, et al. Energy Balance in Early-Stage Huntington Disease. Am J Clin Nutr; 81:1335-1341 (June, 2005). [Address reprint requests to A. M. Gaba, Department of Food and Nutrition Services, Milstein Hospital Building 8-211, 177 Fort Washington Avenue, New York, NY 10032. E-mail: angaba@worldnet.att.net]

COPYRIGHT 2005 Frost & Sullivan
COPYRIGHT 2005 Gale Group

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