Ye Ye, Hu Jia-Hui, Xiao Xing-Yu, Ji Ting, Wang Fei, Jia Fu-Jun, Hou Cai-Lan
Guangdong Mental Health Center, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Room 709, Guangdong Mental Health Centre, No.123, Huifuxi Road, Yuexiu District of Guangzhou, Guangzhou, Guangdong Province, 510080, PR China.
The Second School of Clinical Medicine, Southern Medical University, Guangzhou, PR China.
BMC Psychiatry. 2025 Jul 31;25(1):749. doi: 10.1186/s12888-025-07162-y.
To evaluate whether BMI status influences POMC methylation levels and subsequently affects the course of adolescent depression. This study examined the relationship between the methylation levels of different CpG sites in the POMC gene and clinical symptoms across various BMI categories in adolescent depression.
A total of 108 adolescent patients with depressive disorders including 68 with unipolar depression and 40 with bipolar depression participated in the study. They were divided into three groups: 11 underweight individuals (BMI below the age-specific threshold), 75 normal-weight individuals (BMI within the defined normal range), and 22 overweight individuals (BMI between the overweight threshold and obesity threshold). Pyrosequencing methylation analysis was used to assess POMC gene promoter methylation levels
Adolescents in the overweight group exhibited significantly lower methylation levels at CpG6 and CpG8 of the POMC gene compared to their normal-weight and underweight peers. Furthermore, methylation at these sites was associated with clinical and psychological indicators such as Childhood Trauma Questionnaire (CTQ) and Montgomery–Asberg Depression Rating Scale (MADRS) scores. After adjusted for medication use, multivariate linear regression analysis revealed a negative correlation between CpG6 methylation levels and CTQ scores in overweight group.
This study shows the association between POMC methylation levels and depressive symptoms in adolescents across different BMI categories. The findings suggest a potential interaction between epigenetic mechanisms, depression and overweight providing a foundation for further mechanistic investigations.
Not applicable.
The online version contains supplementary material available at 10.1186/s12888-025-07162-y.
评估体重指数(BMI)状态是否会影响阿黑皮素原(POMC)甲基化水平,进而影响青少年抑郁症的病程。本研究调查了青少年抑郁症患者中,不同BMI类别下POMC基因中不同CpG位点的甲基化水平与临床症状之间的关系。
共有108名青少年抑郁症患者参与了本研究,其中68名单相抑郁症患者,40名双相抑郁症患者。他们被分为三组:11名体重过轻个体(BMI低于特定年龄阈值),75名正常体重个体(BMI在规定的正常范围内),以及22名超重个体(BMI在超重阈值和肥胖阈值之间)。采用焦磷酸测序甲基化分析来评估POMC基因启动子甲基化水平。
与正常体重和体重过轻的同龄人相比,超重组青少年的POMC基因CpG6和CpG8位点的甲基化水平显著降低。此外,这些位点的甲基化与儿童创伤问卷(CTQ)和蒙哥马利-艾斯伯格抑郁评定量表(MADRS)评分等临床和心理指标相关。在调整药物使用情况后,多变量线性回归分析显示超重组中CpG6甲基化水平与CTQ评分呈负相关。
本研究表明不同BMI类别的青少年中,POMC甲基化水平与抑郁症状之间存在关联。研究结果表明表观遗传机制、抑郁症和超重之间可能存在相互作用,为进一步的机制研究奠定了基础。
不适用。
在线版本包含可在10.1186/s12888-025-07162-y获取的补充材料。