2003
DOI: 10.1001/archpsyc.60.11.1109
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A Randomized, Double-blind, Placebo-Controlled Study of Sibutramine in the Treatment of Binge-Eating Disorder

Abstract: Sibutramine is effective and well tolerated in the treatment of obese patients with BED. Its effects address 3 main domains of the BED syndrome, ie, binge eating, weight, and related depressive symptoms.

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Cited by 174 publications
(113 citation statements)
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“…However, topriamate was not found effective on depression and anxiety (15). Important decreases have been recorded in weight loss with sibutramin treatment (average 15 doses mg/day) (16). In the case we presented since the depressive symptoms were clear fluoxetine, as an antidepressant, was given.…”
Section: Discussionmentioning
confidence: 84%
“…However, topriamate was not found effective on depression and anxiety (15). Important decreases have been recorded in weight loss with sibutramin treatment (average 15 doses mg/day) (16). In the case we presented since the depressive symptoms were clear fluoxetine, as an antidepressant, was given.…”
Section: Discussionmentioning
confidence: 84%
“…110 In placebo-controlled studies (total n = 384), sibutramine (10-15 mg/day for 12-24 weeks) reduced body weight and the frequency of binge eating episodes more than placebo. [111][112][113] In one report, depression scores were also reduced more in the sibutramine group. 111 Finally, sibutramine was administered in a small group of obese adults with hypopituitary disease for 11 months.…”
Section: Therapeutic Use Of Sibutramine In Obesity-related Disordersmentioning
confidence: 93%
“…11,18 Positive therapeutic effects on both weight and binge eating have been reported with topiramate (antiepileptic), atomoxetine (norepinephrine reuptake inhibitor), sibutramine (mixed monoamine reuptake inhibitor causing anorexia and thermogenesis), the stimulant phentermine, selective serotonin reuptake inhibitors and rimonabant (cannabinoid receptor 1 inverse agonist). [19][20][21][22][23][24][25] However, safety concerns regarding psychiatric (rimonabant, topiramate) and cardiovascular risks (sibutramine, atomoxetine, phentermine) have hindered the clinical deployment of these treatments [26]. There is a need to explore novel pharmacological approaches, guided by the knowledge of the neurochemical systems implicated in the pathophysiology of abnormal eating.…”
Section: Introductionmentioning
confidence: 99%