Brief communicationTreatment of nocturnal eating syndrome and sleep-related eating disorder with topiramate
Introduction
Over the past 50 years, multiple case series of patients have been described who eat inappropriately during arousals from nocturnal sleep [1], [2], [3], [4], [5]. This behavior has been variably labeled as sleep-related eating disorder (SRED) or nocturnal eating syndrome (NES), depending upon the investigators and specific features of the behavior. Both syndromes are characterized by compulsive eating of high caloric foods at night, poor sleep quality, and morning anorexia. Both SRED and NES are most commonly present in females, usually beginning in young adulthood. SRED has generally been characterized as occurring during partial arousals from sleep, in which consciousness is only partially achieved, and is often associated with amnesia for the event. Primary sleep disorders, most prominently restless legs syndrome (RLS) and somnambulism, have been common in these individuals. On the other hand, NES occurs with maintenance of full awareness, though the binge eating is compulsive and difficult to suppress. Such individuals do not have amnesia, and sleep disorders have not been as prominent.
Treatment of these nocturnal eating behaviors has often been directed towards underlying identifiable sleep disorders (e.g. CPAP for obstructive sleep apnea [3], dopaminergic agonists/benzodiazepines for RLS [3], [6]), or psychiatric disorders (e.g. selective serotonergic reuptake inhibitors for bulimia nervosa). On the other hand, Schenck and Mahowald [7] have described success with combinations of dopaminergic and opioid drugs, at times with the addition of sedatives, even in patients without identified sleep disorders which are responsive to these medications. In two other reports of unblinded trials, the anorectic serotonergic agents fenfluramine [5] and dexfenfluramine [8] were used with good results.
We now describe effective treatment of four cases of nocturnal eating with the GABA agonist, glutamatergic antagonist, topiramate. This agent produced weight loss over periods of 6–12 months in large studies of patients with epilepsy (for which it has FDA indication) [9]. Topiramate was also beneficial in nine of 13 patients with daytime binge eating disorder, with marked reductions in daytime binge episodes [10]. Topiramate has also been associated with weight loss when it has been used as adjunctive treatment for bipolar disorder [11] and migraine [12].
Section snippets
Methods
We reviewed topiramate treatment in four patients with either NES or SRED. Two of the patients had NES, defined as awakenings at night (at least three times per week) with compulsive, binge eating with maintenance of full awareness during the binge, and without subsequent amnesia for the episode. SRED was defined as partial arousals from sleep (at least three times per week) with compulsive, binge eating with partial (or no) awareness of the behavior, and amnesia for at least some of the
Results
Two patients with SRED and two with NES received open-label, naturalistic treatment with topiramate. The clinical characteristics of these patients are described in Table 1. Three of the four patients had tried multiple psychiatric medications for nocturnal eating without benefit over a period of many years. Three patients had been in long-term psychotherapy directed towards this behavior. None of the patients had a current daytime eating disorder, including daytime binging or body image
Discussion
We report four patients with NES or SRED who demonstrated substantial to complete response of nocturnal eating with topiramate administration prior to sleep. Notable weight loss was observed in all patients. These patients had been refractory to multiple previous pharmacotherapy and psychotherapy trials. Efficacy has been maintained over a period averaging 8.5 months. Side effects limited the maximum dosage in two patients, but all patients have continued this treatment.
A number of potential
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2020, Sleep Medicine ClinicsCitation Excerpt :It is unclear how topiramate works to decrease SRED manifestations. It was hypothesized that the drug may work by suppressing arousals produced by underlying sleep disorders or by acting as an anorexigenic agent, either through glutamatergic antagonism or serotonergic agonism.54 Moreover, topiramate has been reported to stimulate insulin release and increase insulin sensitivity, both of which may contribute to appetite regulation and weight loss.56
Drugs Used in Parasomnia
2018, Sleep Medicine ClinicsCitation Excerpt :It is unclear how topiramate works to decrease SRED manifestations. It was hypothesized that the drug may work by suppressing arousals produced by underlying sleep disorders or by acting as an anorexigenic agent, either through glutamatergic antagonism or serotonergic agonism.54 Moreover, topiramate has been reported to stimulate insulin release and increase insulin sensitivity, both of which may contribute to appetite regulation and weight loss.56