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首页> 外文期刊>Psychopharmacology >An increase in plasma brain derived neurotrophic factor levels is related to n-3 polyunsaturated fatty acid efficacy in first episode schizophrenia: secondary outcome analysis of the OFFER randomized clinical trial
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An increase in plasma brain derived neurotrophic factor levels is related to n-3 polyunsaturated fatty acid efficacy in first episode schizophrenia: secondary outcome analysis of the OFFER randomized clinical trial

机译:血浆脑衍生的神经营养因子水平的增加与第一次发作精神分裂症中的N-3多不饱和脂肪酸疗效有关:促进随机临床试验的次要结果分析

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摘要

Rationale N-3 polyunsaturated fatty acids (n-3 PUFA) influence multiple biochemical mechanisms postulated in the pathogenesis of schizophrenia that may influence BDNF synthesis. Objectives A randomized placebo-controlled study was designed to compare the efficacy of a 26-week intervention composed of either 2.2 g/day of n-3 PUFA or olive oil placebo, with regard to symptom severity in first-episode schizophrenia patients. The secondary outcome measure of the study was to describe the association between n-3 PUFA clinical effect and changes in peripheral BDNF levels. Methods Seventy-one patients aged 16-35 were enrolled in the study and randomly assigned to the following study arms: 36 to the EPA + DHA group and 35 to the placebo group. Plasma BDNF levels were assessed three times, at baseline and at weeks 8 and 26 of the intervention. BDNF levels were determined in plasma samples using Quantikine Human BDNF ELISA kit. Plasma BDNF level changes were further correlated with changes in the severity of symptoms in different clinical domains. Results A significantly greater increase in plasma BDNF levels was observed in the intervention compared to the placebo group (Cohen's d = 1.54). Changes of BDNF levels inversely correlated with change in depressive symptoms assessed using the Calgary Depression Rating Scale in Schizophrenia (Pearson's r = - 0.195; p = 0.018). Conclusions The efficacy of a six-month intervention with n-3 PUFA observed in first-episode schizophrenia may be related to an increase in BDNF levels, which may be triggered by the activation of intracellular signaling pathways including transcription factors such as cAMP-reactive element binding protein.
机译:理论N-3多不饱和脂肪酸(N-3 PUFA)影响在可影响BDNF合成的精神分裂症发病机制中的多种生化机制。目的是一项随机安慰剂对照研究旨在比较26周干预的疗效,该疗效由2.2克/天的N-3 PUFA或橄榄油安慰剂组成,关于初始发作精神分裂症患者的症状严重程度。该研究的二次结果测量是描述N-3 PUFA临床疗效和外周BDNF水平的变化之间的关联。方法七十一位患者16-35岁患者注册了研究,并随机分配到以下研究武器:36至EPA + DHA集团和35次。血浆BDNF水平在基线和第8周和第26周的干预时进行评估三次。使用Quankine人BDNF ELISA试剂盒在血浆样品中测定BDNF水平。血浆BDNF水平变化与不同临床结构域中症状严重程度的变化进一步相关。结果与安慰剂组(Cohen的D = 1.54)相比,在干预中观察到血浆BDNF水平显着提高。 BDNF水平的变化与使用精神分裂症中的卡尔加里抑郁率评级评定评估的抑郁症状变化(Pearson的R = - 0.195; P = 0.018)。结论六个月干预患者在第一集中的精神分裂症中观察到的六个月干预的功效可能与BDNF水平的增加有关,其可以通过在包括转录因子(如CAMP-反应元件)的转录因子的激活来引发结合蛋白。

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