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Tardive dyskinesia: clinical and neuroendocrine response to low dose bromocriptine.

AbstractTwelve patients with a long-standing history of moderate to severe symptoms of tardive dyskinesia, which had remained stable for several months, participated in a 6-week trial with bromocriptine. All patients were receiving a concomitant neuroleptic medication and were treated with a low dose of bromocriptine (0.75 to 7.5 mg). Patients showed a modest overall improvement of 16.6%, with a trend for greater improvement in male patients (23.6%). Baseline prolactin levels in the female patients showed a positive correlation with age and duration of tardive dyskinesia symptomatology. Plasma prolactin levels 4 hours following administration of bromocriptine were negatively correlated with the dose of bromocriptine. There appears to be a differential sensitivity for prolactin and growth hormone response to bromocriptine at these low doses in the presence of chronic neuroleptic treatment.
AuthorsR H Lenox, L A Weaver, B M Saran
JournalJournal of clinical psychopharmacology (J Clin Psychopharmacol) Vol. 5 Issue 5 Pg. 286-92 (Oct 1985) ISSN: 0271-0749 UNITED STATES
PMID4044881 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bromocriptine
  • Prolactin
  • Growth Hormone
Topics
  • Bromocriptine (therapeutic use)
  • Dyskinesia, Drug-Induced (blood, drug therapy)
  • Female
  • Growth Hormone (blood)
  • Humans
  • Male
  • Prolactin (blood)