Cevher Binici Nagihan, Inal Emiroğlu Fatma Neslihan, Resmi Halil, Ellidokuz Hülya
Clinic of Child and Adolescent Psychiatry, Dr. Behçet Uz Pediatrics and Surgery Training and Research Hospital, İzmir, Turkey.
Department of Child and Adolescent Psychiatry, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Noro Psikiyatr Ars. 2016 Sep;53(3):267-271. doi: 10.5152/npa.2015.8832. Epub 2016 Sep 1.
Bipolar disorder (BD) has been increasingly associated with abnormalities in neuroplasticity and cellular resilience in brain regions that are involved in mood and that affect regulation. Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family that regulates neuroplasticity. The aims of the current study were to compare serum BDNF levels in euthymic adolescents with BD type I with those in controls and to investigate the relationship between clinical variables and serum BDNF levels in adolescents with BD type I.
Twenty-five adolescents diagnosed with BD type I and 17 healthy control subjects within the age range of 15-19 years were recruited. Diagnoses were made by two experienced research clinicians using the Kiddie and Young Adult Schedule for Affective Disorders and Schizophrenia Present and Lifetime Version and the affective module of Washington University in St. Louis Kiddie and Young Adult Schedule for Affective Disorders and Schizophrenia-Present State and Lifetime. Blood samples were taken during euthymia, which was defined as Young Mania Rating Scale and Hamilton Depression Rating Scale scores below 7.
The comparison of BDNF serum levels between the case and healthy control groups revealed no significant differences. In the case group, BDNF levels were significantly lower in patients being currently treated with lithium.
Similar to normal BDNF levels in adult patients with BD, the normal BDNF serum levels that we found in the euthymic state in adolescents and early adulthood may be related to the developmental brain stage in our study group. It may also show a common neurobiological basis of pediatric and adult BD. Further investigations evaluating BDNF levels in different mood states could help identify the role of BDNF in the underlying pathophysiology of BD.
双相情感障碍(BD)越来越多地与参与情绪调节的脑区神经可塑性和细胞弹性异常相关。脑源性神经营养因子(BDNF)是调节神经可塑性的神经营养因子家族成员。本研究的目的是比较I型双相情感障碍青少年缓解期患者与对照组的血清BDNF水平,并探讨I型双相情感障碍青少年临床变量与血清BDNF水平之间的关系。
招募了25名年龄在15 - 19岁之间被诊断为I型双相情感障碍的青少年和17名健康对照者。由两名经验丰富的研究临床医生使用《儿童和青少年情感障碍及精神分裂症现症和终生版量表》以及圣路易斯华盛顿大学儿童和青少年情感障碍及精神分裂症现症和终生版量表的情感模块进行诊断。在缓解期采集血样,缓解期定义为杨氏躁狂评定量表和汉密尔顿抑郁评定量表得分低于7分。
病例组与健康对照组的BDNF血清水平比较无显著差异。在病例组中,目前正在接受锂治疗的患者BDNF水平显著较低。
与成年双相情感障碍患者正常的BDNF水平相似,我们在青少年和成年早期缓解状态下发现正常的BDNF血清水平可能与我们研究组的脑发育阶段有关。它也可能显示儿童和成人双相情感障碍的共同神经生物学基础。进一步评估不同情绪状态下BDNF水平的研究有助于确定BDNF在双相情感障碍潜在病理生理学中的作用。