Najar H, Joas E, Kardell M, Pålsson E, Landén M
Institute of Neuroscience and Physiology, Section of Psychiatry and Neurochemistry, University of Gothenburg, Gothenburg, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Acta Psychiatr Scand. 2017 Jun;135(6):606-611. doi: 10.1111/acps.12737. Epub 2017 Apr 13.
Our aim was to investigate the prevalence and magnitude of weight gain in-patients with bipolar disorder when treated with a second-generation antipsychotic as an add-on treatment to a mood stabilizer in routine clinical practice.
Data were derived from the quality register for bipolar disorder in Sweden (BipoläR). Patients with bipolar disorder who started add-on treatment with a SGA (n = 575) were compared at next yearly follow-up with age and sex matched patients who were only treated with a mood stabilizer (n = 566). The primary outcome measure was change in body weight and body mass index (BMI). We also assessed the prevalence of clinically significant weight gain defined as ≥7% gain in body weight.
The group that received add-on treatment with antipsychotics neither gained more weight nor were at higher risk for a clinically significant weight gain than the reference group. Instead, factors associated with clinically significant weight gain were female sex, young age, low-baseline BMI, and occurrence of manic/hypomanic episodes.
We found no evidence of an overall increased risk of weight gain for patients with bipolar disorder after receiving add-on SGA to a mood stabilizer in a routine clinical setting.
我们的目的是调查在常规临床实践中,双相情感障碍患者在使用第二代抗精神病药物作为心境稳定剂的附加治疗时体重增加的患病率和幅度。
数据来源于瑞典双相情感障碍质量登记册(BipoläR)。将开始使用第二代抗精神病药物进行附加治疗的双相情感障碍患者(n = 575)与仅接受心境稳定剂治疗的年龄和性别匹配的患者(n = 566)在次年随访时进行比较。主要结局指标是体重和体重指数(BMI)的变化。我们还评估了临床上显著体重增加的患病率,定义为体重增加≥7%。
接受抗精神病药物附加治疗的组与参照组相比,体重增加并不更多,临床上显著体重增加的风险也不更高。相反,与临床上显著体重增加相关的因素是女性、年轻、基线BMI低以及躁狂/轻躁狂发作的发生。
我们没有发现证据表明在常规临床环境中,双相情感障碍患者在接受心境稳定剂附加第二代抗精神病药物治疗后体重增加的总体风险增加。