𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Fluvoxamine and sulpiride in comorbid obsessive–compulsive disorder and gilles de la tourette syndrome

✍ Scribed by Mark S. George; Michael R. Trimble; Mary M. Robertson


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
637 KB
Volume
8
Category
Article
ISSN
0885-6222

No coin nor oath required. For personal study only.

✦ Synopsis


Recently interest has arisen concerning the genetic, pharmacologic and phenomenologic links between Gilles de la Tourette Syndrome (GTS) and Obsessive-Compulsive Disorder (OCD). Some theorize the two disorders may be phenotypic variations of the same neurobiologic defect. Previous studies have demonstrated serotonin (5HT) abnormalities in OCD patients and dopamine dysfunction in patients with tics and GTS. We probed the relationship between 5HT and dopamine in these disorders with a Wweek, double-blind, placebo-controlled crossover trial of fluvoxamine (a specific 5HT reuptake inhibitor) versus sulpiride (a dopamine (D2) antagonist) followed by single-blind combined therapy (4 weeks) in 11 subjects with comorbid OCD and GTS.

Sulpiride monotherapy significantly reduced tics and non-significantly improved OC symptoms. Fluvoxamine, either alone or combined with sulpiride, non-significantly ameliorated tics and reduced OCD symptoms. Additionally, tics and OC symptoms covaried. These results are consistent with a possible coupling of dopaminergic and 5HT systems in cornorbid OCD/GTS subjects.


📜 SIMILAR VOLUMES


Obsessive compulsive symptoms in Gilles
✍ Eapen, Valsamma; Robertson, Mary M.; Alsobrook, John P.; Pauls, David L. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 56 KB 👁 2 views

The distribution of obsessive compulsive symptoms was compared in 16 individuals with primary obsessive compulsive disorder (OCD) and 16 individuals with Gilles de la Tourette syndrome (GTS) and associated obsessive compulsive behaviors (OCB). The two groups showed significant differences in the dis

Examination of the SGCE gene in Tourette
✍ Patricia De Carvalho Aguiar; Melissa Fazzari; Joseph Jankovic; Laurie J. Ozelius 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 49 KB

## Abstract Mutations in the ϵ‐sarcoglycan gene (SGCE) have been reported in families with myoclonus–dystonia (M‐D). In addition to abnormal movements, obsessive–compulsive disorder (OCD) has also been described in families with M‐D. OCD is a common feature in another movement disorder, namely Tour