Aberrant Expression of Long Non-Coding RNAs in Schizophrenia Patients

被引:37
作者
Chen, Shengdong [1 ,2 ]
Sun, Xinyang [3 ]
Niu, Wei [4 ]
Kong, Lingming [5 ]
He, Mingjun [5 ]
Li, Wanshuai [6 ]
Zhong, Aifang [7 ]
Lu, Jim [6 ,8 ]
Zhang, Liyi [1 ,5 ]
机构
[1] Second Mil Med Univ, Dept Psychiat & Psychol, Shanghai, Peoples R China
[2] 102 Hosp Chinese Peoples Liberat Army, Dept Neurol, Changzhou, Jiangsu, Peoples R China
[3] PingAn Hlth Cloud Co Ltd China, Dept Psychiat & Psychol, Shanghai, Peoples R China
[4] 102 Hosp Chinese Peoples Liberat Army, Dept Rehabil, Changzhou, Jiangsu, Peoples R China
[5] 102 Hosp Chinese Peoples Liberat, Prevent & Treatment Ctr Psychol Dis, Changzhou, Jiangsu, Peoples R China
[6] GoPath Diagnost Lab Co Ltd, Changzhou, Jiangsu, Peoples R China
[7] 102 Hosp Chinese Peoples Liberat Army, Dept Lab, Changzhou, Jiangsu, Peoples R China
[8] GoPath Labs LLC, Buffalo Grove, IL 60089 USA
来源
MEDICAL SCIENCE MONITOR | 2016年 / 22卷
关键词
Drug Therapy; Microarray Analysis; RNA; Long Noncoding; Schizophrenia; BIOMARKER DISCOVERY; DISEASE; BRAIN; DISORDERS;
D O I
10.12659/MSM.896927
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Dysfunction of long non-coding RNAs (lncRNAs) has been demonstrated to be involved in psychiatric diseases. However, the expression patterns and functions of the regulatory lncRNAs in schizophrenia (SZ) patients have rarely been systematically reported. Material/Methods: The lncRNAs in peripheral blood mononuclear cells (PBMCs) were screened and compared between the SZ patients and demographically-matched healthy controls using microarray analysis, and then were validated by quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) method. Three verified significantly dysregulated lncRNAs of PBMCs were selected and then measured in SZ patients before and after the antipsychotic treatment. SZ symptomatology improvement was measured by Positive And Negative Syndrome Scale (PANSS) scores. Results: One hundred and twenty-five lncRNAs were significantly differentially expressed in SZ patients compared with healthy controls, of which 62 were up-regulated and 63 were down-regulated. Concurrent with the significant decrease of the PANSS scores of patients after the treatment, the PBMC levels of lncRNA NONHSAT089447 and NONHSAT041499 were strikingly decreased (P<0.05). Down-regulation of PBMC expression of NONHSAT041499 was significantly correlated to the improvement of positive and activity symptoms of patients (r=-0.444 and -0.423, respectively, P<0.05, accounting for 16.9% and 15.1%, respectively), and was also significantly associated with better outcomes (odds ratio 2.325 for positive symptom and 12.340 for activity symptom). Conclusions: LncRNA NONHSAT089447 and NONHSAT041499 might be involved in the pathogenesis and development of SZ, and the PBMC level of NONHSAT041499 is significantly associated with the treatment outcomes of SZ.
引用
收藏
页码:3340 / 3351
页数:12
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