Department of Psychiatry, University of Toronto, Toronto, Canada; Centre for Addiction and Mental Health, 100 Stokes Street, Toronto, ON M6J 1H4, Canada.
Department of Psychiatry, University of Toronto, Toronto, Canada.
J Affect Disord. 2022 Feb 15;299:135-141. doi: 10.1016/j.jad.2021.11.032. Epub 2021 Nov 16.
Metabolic dysfunction is prevalent in bipolar disorder (BD) and associated with illness severity and treatment outcomes. There is little research exploring this relationship in low and middle-income countries (LMICs) and little is known about the moderating effect of metabolic health on treatment response to anti-inflammatory drugs in BD.
MINDCARE, a randomized-controlled-trial conducted in Pakistan, investigated the efficacy of minocycline and celecoxib in 266 adults with bipolar depression. This secondary analysis evaluated the association between depression severity at baseline and treatment outcome with metabolic parameters including body mass index (BMI), waist circumference (WC), heart rate (HR), systolic blood pressure (s-BP), and diastolic blood pressure (d-BP). Depression severity was measured using the Hamilton Depression Rating Scale-17. The exploratory aim was to assess whether treatment impacted change in metabolic variables. Associations were evaluated using linear regression.
Higher BMI (B=-0.38, 95%CI: -0.55 to -0.21) and WC (B=-0.68, 95%CI: -0.97 to -0.39) were associated with lower baseline depression severity in both the unadjusted and the adjusted models. Baseline metabolic parameters were not associated with treatment response to minocycline or celecoxib nor did treatment significantly impact metabolic variables.
Our sample represents patients in an RCT and may not be fully representative of the overall BD population in Pakistan.
Our findings indicate a potential association of poor metabolic health and lower severity of bipolar depression but not treatment outcomes. Future work should evaluate potential relationships of metabolic parameters and BD in diverse populations to increase the transferability of this line of work.
代谢功能障碍在双相情感障碍(BD)中很常见,与疾病严重程度和治疗结果相关。在中低收入国家(LMICs)中,很少有研究探索这种关系,也不知道代谢健康对 BD 中抗炎药物治疗反应的调节作用。
MINDCARE 是在巴基斯坦进行的一项随机对照试验,研究了米诺环素和塞来昔布在 266 名双相抑郁患者中的疗效。这项二次分析评估了基线时抑郁严重程度与治疗结果与代谢参数之间的关系,包括体重指数(BMI)、腰围(WC)、心率(HR)、收缩压(s-BP)和舒张压(d-BP)。抑郁严重程度采用汉密尔顿抑郁评定量表-17 进行测量。探索性目的是评估治疗是否影响代谢变量的变化。使用线性回归评估相关性。
在未调整和调整模型中,较高的 BMI(B=-0.38,95%CI:-0.55 至 -0.21)和 WC(B=-0.68,95%CI:-0.97 至 -0.39)与基线抑郁严重程度较低相关。基线代谢参数与米诺环素或塞来昔布的治疗反应无关,治疗也未显著影响代谢变量。
我们的样本代表 RCT 中的患者,可能无法完全代表巴基斯坦总体 BD 人群。
我们的发现表明,代谢健康不良和双相抑郁严重程度较低之间可能存在关联,但与治疗结果无关。未来的工作应评估代谢参数与不同人群中 BD 的潜在关系,以提高这项工作的可转移性。