Brownley Kimberly A, Berkman Nancy D, Peat Christine M, Lohr Kathleen N, Cullen Katherine E, Bann Carla M, Bulik Cynthia M
From University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; RTI International, Research Triangle Park, North Carolina; and Karolinska Institutet, Stockholm, Sweden.
Ann Intern Med. 2016 Sep 20;165(6):409-20. doi: 10.7326/M15-2455. Epub 2016 Jun 28.
The best treatment options for binge-eating disorder are unclear.
To summarize evidence about the benefits and harms of psychological and pharmacologic therapies for adults with binge-eating disorder.
English-language publications in EMBASE, the Cochrane Library, Academic OneFile, CINAHL, and ClinicalTrials.gov through 18 November 2015, and in MEDLINE through 12 May 2016.
9 waitlist-controlled psychological trials and 25 placebo-controlled trials that evaluated pharmacologic (n = 19) or combination (n = 6) treatment. All were randomized trials with low or medium risk of bias.
2 reviewers independently extracted trial data, assessed risk of bias, and graded strength of evidence.
Therapist-led cognitive behavioral therapy, lisdexamfetamine, and second-generation antidepressants (SGAs) decreased binge-eating frequency and increased binge-eating abstinence (relative risk, 4.95 [95% CI, 3.06 to 8.00], 2.61 [CI, 2.04 to 3.33], and 1.67 [CI, 1.24 to 2.26], respectively). Lisdexamfetamine (mean difference [MD], -6.50 [CI, -8.82 to -4.18]) and SGAs (MD, -3.84 [CI, -6.55 to -1.13]) reduced binge-eating-related obsessions and compulsions, and SGAs reduced symptoms of depression (MD, -1.97 [CI, -3.67 to -0.28]). Headache, gastrointestinal upset, sleep disturbance, and sympathetic nervous system arousal occurred more frequently with lisdexamfetamine than placebo (relative risk range, 1.63 to 4.28). Other forms of cognitive behavioral therapy and topiramate also increased abstinence and reduced binge-eating frequency and related psychopathology. Topiramate reduced weight and increased sympathetic nervous system arousal, and lisdexamfetamine reduced weight and appetite.
Most study participants were overweight or obese white women aged 20 to 40 years. Many treatments were examined only in single studies. Outcomes were measured inconsistently across trials and rarely assessed beyond end of treatment.
Cognitive behavioral therapy, lisdexamfetamine, SGAs, and topiramate reduced binge eating and related psychopathology, and lisdexamfetamine and topiramate reduced weight in adults with binge-eating disorder.
Agency for Healthcare Research and Quality.
暴饮暴食症的最佳治疗方案尚不清楚。
总结针对成年暴饮暴食症患者心理治疗和药物治疗的益处及危害的证据。
截至2015年11月18日在EMBASE、Cochrane图书馆、Academic OneFile、CINAHL和ClinicalTrials.gov上的英文出版物,以及截至2016年5月12日在MEDLINE上的英文出版物。
9项等待列表对照的心理试验和25项安慰剂对照试验,这些试验评估了药物治疗(n = 19)或联合治疗(n = 6)。所有试验均为随机试验,偏倚风险低或中等。
两名审阅者独立提取试验数据、评估偏倚风险并对证据强度进行分级。
治疗师主导的认知行为疗法、赖氨酸右旋安非他命和第二代抗抑郁药(SGA)降低了暴饮暴食频率并提高了暴饮暴食戒断率(相对风险分别为4.95 [95%CI,3.06至8.00]、2.61 [CI,2.04至3.33]和1.67 [CI,1.24至2.26])。赖氨酸右旋安非他命(平均差[MD],-6.50 [CI,-8.82至-4.18])和SGA(MD,-3.84 [CI,-6.55至-1.13])减少了与暴饮暴食相关的强迫观念和强迫行为,SGA减轻了抑郁症状(MD,-1.97 [CI,-3.67至-0.28])。与安慰剂相比,赖氨酸右旋安非他命引起的头痛、胃肠道不适、睡眠障碍和交感神经系统兴奋更为频繁(相对风险范围为1.63至4.28)。其他形式的认知行为疗法和托吡酯也提高了戒断率,降低了暴饮暴食频率和相关精神病理学症状。托吡酯减轻了体重并增加了交感神经系统兴奋,赖氨酸右旋安非他命减轻了体重和食欲。
大多数研究参与者为年龄在20至40岁之间的超重或肥胖白人女性。许多治疗仅在单一研究中进行了检验。各试验对结果的测量不一致,且很少在治疗结束后进行评估。
认知行为疗法、赖氨酸右旋安非他命、SGA和托吡酯减少了成年暴饮暴食症患者的暴饮暴食及相关精神病理学症状,赖氨酸右旋安非他命和托吡酯减轻了体重。
医疗保健研究与质量局。