Hayat Mian Rohail, Umair Muhammad, Ikhtiar Hina, Wazir Shandana, Palwasha Ameena, Shah Maheen
Department of Psychiatry, Mardan Medical Complex, Medical Teaching Institution (MTI), Mardan, PAK.
Department of Physiology, Gomal Medical College, Medical Teaching Institution (MTI), Dera Ismail Khan, PAK.
Cureus. 2024 Oct 2;16(10):e70728. doi: 10.7759/cureus.70728. eCollection 2024 Oct.
Background Mood disorders like major depressive disorder (MDD) and bipolar disorder (BD) involve complex interactions between brain-derived neurotrophic factor (BDNF) and serotonin. While extensive research has explored these factors individually, their combined effects and interactions in these disorders are less understood. This study uniquely addresses this gap by examining how BDNF and serotonin interact and relate to mood disorder severity, providing new insights into their joint role in MDD and BD. Objectives The objective of this study was to examine the correlation between serum BDNF and plasma serotonin levels and to assess how these correlations relate to the severity of symptoms and overall disease severity in MDD and BD. Methodology This cross-sectional study, conducted at the Khyber Medical University, Peshawar, from January to September 2023, examined the correlation between BDNF and serotonin in individuals with MDD and BD. Participants (n = 63) aged 18-65 were recruited based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria, excluding those with neurological disorders, substance abuse, or severe medical illness. A control group of 21 healthy individuals was matched by age and gender. Data collection involved demographic details, clinical history, and comorbid diagnoses assessed using the Mini International Neuropsychiatric Interview (MINI). Mood disorder severity was measured using the Hamilton Depression Rating Scale (HAM-D) for MDD and the Young Mania Rating Scale (YMRS) for BD, along with additional assessments (Beck Depression Inventory, Global Assessment of Functioning). Serum BDNF and serotonin levels were analyzed using enzyme-linked immunosorbent assay (ELISA) kits. Statistical analyses included t-tests, Mann-Whitney U tests, Pearson correlations, and subgroup analyses to assess relationships between biomarkers, mood disorder severity, and influencing factors. Results BDNF levels were found to be 20.1 ± 5.3 ng/mL in MDD, 18.5 ± 4.7 ng/mL in BD, and 25.9 ± 6.2 ng/mL in controls. Serotonin levels were 45.8 ± 12.6 ng/mL in MDD, 43.2 ± 11.4 ng/mL in BD, and 52.1 ± 14.3 ng/mL in controls. In the MDD group, significant negative correlations were observed between BDNF levels and mood disorder severity (r = -0.32, p = 0.045), whereas serotonin levels did not show significant correlations (r = -0.21, p = 0.23). In the BD group, BDNF levels also showed a significant negative correlation with manic symptoms (r = -0.28, p = 0.048), but serotonin levels showed no significant correlation. Subgroup analyses revealed that participants under 40 years had higher BDNF levels (22.8 ± 5.6 ng/mL) compared to those aged 40 and above (19.7 ± 4.3 ng/mL). Females showed higher BDNF levels (24.5 ± 6.3 ng/mL) than males (19.3 ± 3.8 ng/mL). Participants not on medication had higher BDNF levels (23.6 ± 5.1 ng/mL) compared to those on medication (17.9 ± 4.2 ng/mL). Those without comorbidities also had higher BDNF levels (23.8 ± 5.9 ng/mL) than those with comorbidities (18.2 ± 4.5 ng/mL), while serotonin levels varied similarly across these subgroups. Conclusion Lower BDNF levels are associated with mood disorders and symptom severity, indicating their potential as a biomarker.
重度抑郁症(MDD)和双相情感障碍(BD)等情绪障碍涉及脑源性神经营养因子(BDNF)和血清素之间的复杂相互作用。虽然已有广泛研究分别探讨了这些因素,但它们在这些疾病中的联合作用和相互作用仍鲜为人知。本研究通过研究BDNF和血清素如何相互作用以及与情绪障碍严重程度的关系,独特地填补了这一空白,为它们在MDD和BD中的联合作用提供了新的见解。
本研究的目的是检测血清BDNF和血浆血清素水平之间的相关性,并评估这些相关性与MDD和BD中症状严重程度和整体疾病严重程度的关系。
这项横断面研究于2023年1月至9月在白沙瓦的开伯尔医科大学进行,研究了MDD和BD患者中BDNF和血清素之间的相关性。根据《精神疾病诊断与统计手册》第五版(DSM-5)标准招募了年龄在18-65岁之间的参与者(n = 63),排除患有神经系统疾病、药物滥用或严重内科疾病的人。选取21名健康个体作为对照组,按年龄和性别进行匹配。数据收集包括人口统计学细节、临床病史以及使用迷你国际神经精神访谈(MINI)进行的共病诊断评估。使用汉密尔顿抑郁量表(HAM-D)评估MDD的情绪障碍严重程度,使用杨氏躁狂量表(YMRS)评估BD的情绪障碍严重程度,并进行其他评估(贝克抑郁量表、功能总体评估)。使用酶联免疫吸附测定(ELISA)试剂盒分析血清BDNF和血清素水平。统计分析包括t检验、曼-惠特尼U检验、皮尔逊相关性分析和亚组分析,以评估生物标志物、情绪障碍严重程度和影响因素之间的关系。
发现MDD患者的BDNF水平为20.1±5.3 ng/mL,BD患者为18.5±4.7 ng/mL,对照组为25.9±6.2 ng/mL。MDD患者的血清素水平为45.8±12.6 ng/mL,BD患者为43.2±11.4 ng/mL,对照组为52.1±14.3 ng/mL。在MDD组中,观察到BDNF水平与情绪障碍严重程度之间存在显著负相关(r = -0.32,p = 0.045),而血清素水平未显示出显著相关性(r = -0.21,p = 0.23)。在BD组中,BDNF水平与躁狂症状也存在显著负相关(r = -0.28,p = 0.048),但血清素水平未显示出显著相关性。亚组分析显示,40岁以下的参与者BDNF水平(22.8±5.6 ng/mL)高于40岁及以上的参与者(19.7±4.3 ng/mL)。女性的BDNF水平(24.5±6.3 ng/mL)高于男性(19.3±3.8 ng/mL)。未服药的参与者BDNF水平(23.6±5.1 ng/mL)高于服药的参与者(17.9±4.2 ng/mL)。无共病的参与者BDNF水平(23.8±5.9 ng/mL)也高于有共病的参与者(18.2±4.5 ng/mL),而血清素水平在这些亚组中的变化情况类似。
较低的BDNF水平与情绪障碍及症状严重程度相关,表明其有可能作为一种生物标志物。