Dombi Zsófia B, Szendi István, Burnet Philip W J
Department of Psychiatry, University of Oxford, Oxford, United Kingdom.
Medical Division, Gedeon Richter Plc., Budapest, Hungary.
Front Psychiatry. 2022 May 24;13:827322. doi: 10.3389/fpsyt.2022.827322. eCollection 2022.
Cognitive impairment is a core feature of disorders on the schizophrenia-bipolar spectrum, i.e., schizophrenia, bipolar disorder, and schizoaffective disorder. Brain-derived neurotrophic factor (BDNF) has been proposed to be a biomarker of cognitive impairment in these disorders as it plays a critical role in neuroplasticity and proposed to mediate some of the psychotropic effects of medication. However, despite numerous studies investigating the association between circulating BDNF and these disorders, no solid conclusions have been drawn regarding its involvement in cognitive impairment.
The current systematic review and meta-analysis aims to examine blood BDNF levels and cognitive dysfunction in patients on the schizophrenia-bipolar spectrum as well as to evaluate whether circulating BDNF measurements can act as a biomarker for cognitive dysfunction.
Studies were identified by searching Embase and Medline databases for English language articles published in peer-reviewed journals between 2000 January and 2021 June according to the PRISMA guidelines. A total of 815 articles were identified of which 32 met the inclusion criteria for the systematic review - reporting on comparisons between blood BDNF levels and cognitive functions of schizophrenia or bipolar disorder patients versus healthy controls (no studies involving schizoaffective patients were specifically obtained for the time being). Twenty-four of these studies (19 with schizophrenia and 5 with bipolar disorder patients) were eligible to be included in the meta-analysis.
Our findings indicated that circulating BDNF levels were significantly reduced in patients experiencing an acute episode of schizophrenia or bipolar disorder compared to healthy controls. Cognitive function was also found to be significantly worse in patients, however, correlations between BDNF levels and cognitive impairment were not always detected. Interventions, especially pharmacotherapy seemed to improve certain aspects of cognition and increase circulating BDNF levels.
Circulating BDNF alone does not seem to be a valid biomarker of cognitive dysfunction in patients with disorders on the schizophrenia-bipolar spectrum, owing to several confounding factors. Changes of the circulating levels of BDNF should be evaluated in a wider context of other stress-, immune-, and inflammatory-related factors.
认知障碍是精神分裂症-双相情感障碍谱系疾病(即精神分裂症、双相情感障碍和分裂情感性障碍)的核心特征。脑源性神经营养因子(BDNF)被认为是这些疾病中认知障碍的生物标志物,因为它在神经可塑性中起关键作用,并被认为介导了药物的一些精神otropic作用。然而,尽管有大量研究调查循环BDNF与这些疾病之间的关联,但关于其与认知障碍的关系尚未得出确凿结论。
本系统评价和荟萃分析旨在研究精神分裂症-双相情感障碍谱系患者的血液BDNF水平和认知功能障碍,并评估循环BDNF测量是否可作为认知功能障碍的生物标志物。
根据PRISMA指南,通过检索Embase和Medline数据库,查找2000年1月至2021年6月期间发表在同行评审期刊上的英文文章来确定研究。共识别出815篇文章,其中32篇符合系统评价的纳入标准——报告精神分裂症或双相情感障碍患者与健康对照者血液BDNF水平和认知功能的比较(目前尚未专门获得涉及分裂情感性障碍患者的研究)。其中24项研究(19项针对精神分裂症患者,5项针对双相情感障碍患者)符合纳入荟萃分析的条件。
我们的研究结果表明,与健康对照相比,精神分裂症或双相情感障碍急性发作患者的循环BDNF水平显著降低。还发现患者的认知功能明显更差,然而,并非总能检测到BDNF水平与认知障碍之间的相关性。干预措施,尤其是药物治疗似乎改善了认知的某些方面并提高了循环BDNF水平。
由于存在多种混杂因素,仅循环BDNF似乎不是精神分裂症-双相情感障碍谱系疾病患者认知功能障碍的有效生物标志物。应在更广泛的其他与应激、免疫和炎症相关因素的背景下评估BDNF循环水平的变化。