Tyrosine is a non essential amino acid that is the precursor of the neurotransmitter, dopamine. Tyrosine is converted into Levodihydrophenylalanine (L-Dopa) and L-Dopa is subsequently and avidly converted into dopamine. It is well known that dopamine deficiency leads to the manifestations of restless legs syndrome (RLS). Studies have shown dopamine agonists and L-dopa to be effective in controlling symptoms. No studies to date have been done to determine the role of tyrosine in RLS. This open-label pilot study aims to determine the efficacy and tolerability of tyrosine in RLS, as current agents have limitations in treating RLS in addition to adding another possible agent to the investigators arsenal of treating RLS that maybe more cost efficient. In this pilot study, the dose of tyrosine will be escalated from 750 mg once daily by mouth (PO) up to 3000 mg once daily PO, as tolerated, in increments of 750 mg every week in patients who meet the inclusion criteria for RLS. Patients' symptoms will be monitored on a weekly basis for six weeks.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
L-Tyrosine 750 mg PO every day for 7 days, then increase to 1500 mg PO every day for 7 days, then increase to 2250 mg PO every day for 7 days, then increase to 3000 mg PO every day for remainder of the study.
Seton Family of Hospitals
Austin, Texas, United States
International RLS Survey Group (IRLSSG20) Score
Use of this survey to be used as a marker for severity of RLS symptoms and therefore efficacy of this medication.
Time frame: 6 weeks
Clinical global impression-global improvement (CGI-I) scale
Use of the CGI-I scale as a secondary outcome measure to determine severity of RLS symptoms and efficacy of medication.
Time frame: 6 weeks
Medical Outcomes Study - Sleep Scale (MOS-SS)
Use of the MOS-SS to determine severity of RLS symptoms and efficacy of medication.
Time frame: 6 weeks
Case Report Form
Use of a history and physical examination (limited neurological exam) to be used as a secondary assessment measure of RLS symptom severity and medication efficacy. They will be charted in case report format.
Time frame: 6 weeks
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