Abstract |
In order to evaluate the efficacy of L-phenylalanine (L-Phe) in combination with UVA therapy for vitiligo an open trial (149 patients, 18 months) and a small double-blind trial (32 patients, 6 months) were conducted. Oral L-Phe loading resulted in peak plasma levels of L-Phe after 30-60 min and a slight increase in the plasma tyrosine level. Response to L-Phe plus UVA irradiation was positive, and various grades of repigmentation not exceeding 77% in the open and 60% in the blind trial were observed. An increased L-Phe dose resulted in increased L-Phe plasma levels but not in improved clinical results. The optimal L-Phe dose appears to be lower than 50 mg/kg/day. Although it is difficult to draw firm conclusions from the present investigation, we think that L-Phe may have a place in the treatment of vitiligo and its role merits further investigation.
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Authors | A H Siddiqui, L M Stolk, R Bhaggoe, R Hu, R B Schutgens, W Westerhof |
Journal | Dermatology (Basel, Switzerland)
(Dermatology)
Vol. 188
Issue 3
Pg. 215-8
( 1994)
ISSN: 1018-8665 [Print] Switzerland |
PMID | 8186511
(Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article)
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Chemical References |
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Topics |
- Administration, Oral
- Adolescent
- Adult
- Combined Modality Therapy
- Dose-Response Relationship, Drug
- Double-Blind Method
- Humans
- Middle Aged
- Phenylalanine
(therapeutic use)
- Tyrosine
(blood)
- Ultraviolet Therapy
- Vitiligo
(blood, therapy)
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