Jess G Fiedorowicz, Lisa Brown, James Li, Sagar V Parikh, Boadie W Dunlop, Brent P Forester, Richard C Shelton, Michael E Thase, Matthew Macaluso, Kunbo Yu, John F Greden
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We compared weight gain between those on versus not on medications with high risk for weight gain, including a subgroup receiving combination treatment with bupropion. A second analysis evaluated weight gain across traditional medication classes, adjusting for potential confounding variables. Those on medications identified as high risk for weight gain were significantly more likely to experience clinically significant weight gain (≥3%) at 12 weeks (29.3% vs. 16.3%, <i>p</i> < .001) and 24 weeks (33.5% vs. 23.5%, <i>p</i> = .015). No protection from clinically significant weight gain was observed among patients treated with a high-risk medication concomitantly with bupropion (N = 31, 35% and 52% with clinically significant weight gain at 12 and 24 weeks). Antipsychotic medications and tricyclic antidepressants were most often associated with clinically significant weight gain. This study helps quantify the real-world risk of weight gain for patients with MDD on medications with high risk for weight gain, especially for patients taking antipsychotics. 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We sought to estimate the frequency of weight gain for obesogenic medications prescribed for MDD and to evaluate if bupropion mitigated risk for weight gain. We analyzed a prospective cohort of patients with weight available at baseline and 12 weeks (n = 1,032) or 24 weeks (n = 871) in a post hoc analysis of the <b>G</b>enomics <b>U</b>sed to <b>I</b>mprove <b>DE</b>pression <b>D</b>ecisions (GUIDED) study of patients with MDD who failed at least one medication trial. We compared weight gain between those on versus not on medications with high risk for weight gain, including a subgroup receiving combination treatment with bupropion. A second analysis evaluated weight gain across traditional medication classes, adjusting for potential confounding variables. Those on medications identified as high risk for weight gain were significantly more likely to experience clinically significant weight gain (≥3%) at 12 weeks (29.3% vs. 16.3%, <i>p</i> < .001) and 24 weeks (33.5% vs. 23.5%, <i>p</i> = .015). No protection from clinically significant weight gain was observed among patients treated with a high-risk medication concomitantly with bupropion (N = 31, 35% and 52% with clinically significant weight gain at 12 and 24 weeks). Antipsychotic medications and tricyclic antidepressants were most often associated with clinically significant weight gain. This study helps quantify the real-world risk of weight gain for patients with MDD on medications with high risk for weight gain, especially for patients taking antipsychotics. 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引用次数: 0
摘要
体重增加是用于治疗重度抑郁症(MDD)的药物的常见副作用。我们试图估计服用致肥药物治疗重度抑郁症患者体重增加的频率,并评估安非他酮是否能减轻体重增加的风险。我们分析了在基线和12周(n = 1032)或24周(n = 871)时体重可用的患者的前瞻性队列,对至少一次药物试验失败的MDD患者进行了基因组学用于改善抑郁决策(引导)研究的后分析。我们比较了体重增加高风险药物治疗组和未治疗组的体重增加情况,包括接受安非他酮联合治疗的亚组。第二项分析评估了传统药物类别的体重增加情况,调整了潜在的混杂变量。在12周(29.3% vs. 16.3%, p < 0.001)和24周(33.5% vs. 23.5%, p = 0.015)时,那些被确定为体重增加高风险药物的患者更有可能出现临床显著的体重增加(≥3%)。在高危药物同时使用安非他酮治疗的患者中,没有观察到对临床显著体重增加的保护作用(N = 31、35%和52%在12周和24周时出现临床显著体重增加)。抗精神病药物和三环类抗抑郁药物通常与临床显著的体重增加有关。这项研究有助于量化MDD患者在实际生活中体重增加的风险,尤其是服用抗精神病药物的患者。同时服用安非他酮并不能减轻体重增加的风险。
Obesogenic Medications and Weight Gain Over 24 Weeks in Patients with Depression: Results from the GUIDED Study.
Weight gain is a common side-effect of medications used to treat major depressive disorder (MDD). We sought to estimate the frequency of weight gain for obesogenic medications prescribed for MDD and to evaluate if bupropion mitigated risk for weight gain. We analyzed a prospective cohort of patients with weight available at baseline and 12 weeks (n = 1,032) or 24 weeks (n = 871) in a post hoc analysis of the Genomics Used to Improve DEpression Decisions (GUIDED) study of patients with MDD who failed at least one medication trial. We compared weight gain between those on versus not on medications with high risk for weight gain, including a subgroup receiving combination treatment with bupropion. A second analysis evaluated weight gain across traditional medication classes, adjusting for potential confounding variables. Those on medications identified as high risk for weight gain were significantly more likely to experience clinically significant weight gain (≥3%) at 12 weeks (29.3% vs. 16.3%, p < .001) and 24 weeks (33.5% vs. 23.5%, p = .015). No protection from clinically significant weight gain was observed among patients treated with a high-risk medication concomitantly with bupropion (N = 31, 35% and 52% with clinically significant weight gain at 12 and 24 weeks). Antipsychotic medications and tricyclic antidepressants were most often associated with clinically significant weight gain. This study helps quantify the real-world risk of weight gain for patients with MDD on medications with high risk for weight gain, especially for patients taking antipsychotics. Concurrent treatment with bupropion does not appear to mitigate the weight gain risk.