Uceyler N, Offenbacher M, Petzke F, Hauser W, Sommer C
Department of Neurology, University of Würzburg Germany.
Fibromyalgia
syndrome (FMS) is a chronic condition characterized by widespread pain,
tender points, fatigue, and sleep disturbance. FMS leads to high
disability levels, poor quality of life, and extensive use of medical
care. Effective pharmacological treatment options are rare, and
treatment effects are often of limited duration. Duloxetine is a new
selective serotonin and norepinephrine reuptake inhibitor that is
licensed for the treatment of pain in diabetic neuropathy. So far two
randomized, placebo-controlled trials have investigated the short-term
safety and efficacy of duloxetine 60 mg/day and 120 mg/day in patients
suffering from FMS over a period of 12 weeks. Both dosages were
superior to placebo in pain relief, and improvement in quality of life
and depressive symptoms. The analgesic effect was largely independent
of the antidepressant action of duloxetine. The higher dose of 120
mg/day further reduced the tender point count and elevated the tender
point pain thresholds. Only mild to moderate adverse effects were
reported. Duloxetine 60 mg/day and 120 mg/day has proven to be
beneficial in the treatment of FMS symptoms. As true for other
antidepressants further studies are needed to assess the long-term
efficacy and safety of duloxetine as an additional pharmacological
treatment option in FMS.