An analysis of POMC gene methylation and expression in patients with schizophrenia

Author:

Chen Xuanyu12ORCID,Qing Lili12,Zou Tiantian12,Wang Jia123,Yin Wensa4,Wang Zhiyong12,Cheng Tiantian12,Lu Yumei12,Hu Liping12,Liu Linlin12ORCID,Nie Shengjie12

Affiliation:

1. School of Forensic Medicine Kunming Medical University Kunming Yunnan China

2. NHC Key Laboratory of Drug Addiction Medicine Kunming Medical University Kunming Yunnan China

3. Kunming Yan'an Hospital Kunming Yunnan China

4. Dept. of Medical, Mental Hospital of Yunnan Province Mental Health Center Affiliated to Kunming Medical University Kunming Yunnan China

Abstract

AbstractSchizophrenia is a chronic mental disorder that affects millions of people and is believed to be caused by both environmental and genetic factors. Despite extensive research, the exact mechanisms underlying schizophrenia are still unclear. Studies have shown that numerous psychiatric disorders are associated with methylation of the POMC gene, which encodes adrenocorticotropic hormone, a critical player in the hypothalamic–pituitary–adrenal axis. However, the association between DNA methylation in POMC patients and schizophrenia remains unclear. In this study, we evaluated three fragments of the POMC promoter region, including 51 CpG sites, in the peripheral blood of schizophrenia patients and healthy controls. The POMC protein level was measured via enzyme‐linked immunosorbent assay (ELISA). The schizophrenia group exhibited significantly greater levels of methylation of the POMC gene than those in the control group. The methylation level of the POMC‐2 fragment was significantly greater in the patient group than in the control group. There were 17 significantly hypermethylated CpG sites in the patient group. After stratification by sex, POMC methylation levels were found to be significantly greater in male schizophrenia patients than in healthy controls; the methylation levels of POMC‐2 fragments were greater in the male patient group; nine CpG sites were significantly hypermethylated in the male patient group; and only one CpG site was significantly hypermethylated in the female patient group. The POMC protein level in patients was significantly lower than that in healthy controls. These findings demonstrate that the DNA methylation of POMC might be associated with the pathophysiology of schizophrenia. Overall, studying the correlation between POMC methylation and schizophrenia may contribute to the diagnosis and evaluation of neuropsychiatric disorders.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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