Centre for Youth Bipolar Disorder, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
University of Toronto Faculty of Medicine, Toronto, Ontario, Canada.
J Clin Psychiatry. 2019 Jul 30;80(4):18m12422. doi: 10.4088/JCP.18m12422.
Despite abundant literature demonstrating increased metabolic syndrome (MetS) prevalence and important clinical correlates of MetS among middle-age adults with bipolar disorder, little is known about this topic among adolescents and young adults early in their course of bipolar disorder. We therefore examined this topic in the Course and Outcome of Bipolar Youth (COBY) study.
A cross-sectional, retrospective study was conducted of 162 adolescents and young adults (mean ± SD age = 20.8 ± 3.7 years; range, 13.6-28.3 years) with bipolar disorder (I, II, or not otherwise specified, based on DSM-IV) enrolled in COBY between 2000 and 2006. MetS measures (blood pressure, glucose, high-density lipoprotein cholesterol [HDL-C], triglycerides, and waist circumference), defined using the International Diabetes Federation criteria, were obtained at a single timepoint. Mood, comorbidity, and treatment over the 6 months preceding the MetS assessment were evaluated using the Longitudinal Interval Follow-Up Evaluation.
The prevalence of MetS in the sample was 19.8% (32/162). Low HDL-C (56.5%) and abdominal obesity (46.9%) were the most common MetS criteria. MetS was nominally associated with lower lifetime global functioning at COBY intake (odds ratio [OR] = 0.97, P = .06). MetS was significantly associated with percentage of weeks in full-threshold pure depression (OR = 1.07, P = .02) and percentage of weeks receiving antidepressant medications (OR = 1.06, P = .001) in the preceding 6 months. MetS was not associated with manic symptoms or medications other than antidepressants.
The prevalence of MetS in this sample was at least double compared to the general population. Moreover, MetS is associated with increased burden of depression symptoms in this group. Management of early-onset bipolar disorder should integrate strategies focused on modifying MetS risk factors.
尽管有大量文献表明,患有双相情感障碍的中年成年人中代谢综合征(MetS)的患病率和重要临床相关性增加,但对于疾病早期的青少年和年轻人,人们对此知之甚少。因此,我们在双相青年的病程和预后研究(COBY)中研究了这一课题。
我们对 2000 年至 2006 年间在 COBY 登记的 162 名患有双相情感障碍(基于 DSM-IV,为 I 型、II 型或未特殊说明)的青少年和年轻人(平均年龄 ± 标准差为 20.8 ± 3.7 岁,范围为 13.6-28.3 岁)进行了一项横断面、回顾性研究。使用国际糖尿病联合会标准获得代谢综合征测量值(血压、血糖、高密度脂蛋白胆固醇[HDL-C]、甘油三酯和腰围),并在单个时间点进行测量。使用纵向间隔随访评估,在代谢综合征评估前的 6 个月内评估心境、合并症和治疗情况。
该样本中代谢综合征的患病率为 19.8%(32/162)。低 HDL-C(56.5%)和腹部肥胖(46.9%)是最常见的代谢综合征标准。代谢综合征与 COBY 入院时较低的终生总体功能呈名义相关(优势比[OR] = 0.97,P =.06)。代谢综合征与前 6 个月内完全缓解的纯抑郁周数(OR = 1.07,P =.02)和接受抗抑郁药物治疗的周数(OR = 1.06,P =.001)呈显著相关。代谢综合征与躁狂症状或除抗抑郁药以外的其他药物无关。
该样本的代谢综合征患病率至少是一般人群的两倍。此外,代谢综合征与该组人群抑郁症状负担增加有关。早期双相障碍的管理应整合侧重于改变代谢综合征危险因素的策略。