Long Non-Coding RNA: Potential Diagnostic and Therapeutic Biomarker for Major Depressive Disorder

被引:66
作者
Cui, Xuelian [1 ]
Sun, Xinyang [2 ]
Niu, Wei [3 ]
Kong, Lingming [4 ]
He, Mingjun [4 ]
Zhong, Aifang [5 ]
Chen, Shengdong [6 ]
Jiang, Kunhong [4 ]
Zhang, Liyi [4 ]
Cheng, Zaohuo [7 ]
机构
[1] Nanjing Med Univ, Changzhou Matern & Child Hlth Care Hosp, Dept Women Hlth Care, Changzhou, Jiangsu, Peoples R China
[2] PingAn Hlth Cloud Co Ltd China, Dept Psychiat & Psychol, Shanghai, Peoples R China
[3] Chinese Peoples Liberat Army, Hosp 102, Dept Rehabil, Changzhou, Jiangsu, Peoples R China
[4] Chinese Peoples Liberat Army, Hosp 102, Prevent & Treatment Ctr Psychol Dis, Changzhou, Jiangsu, Peoples R China
[5] Chinese Peoples Liberat Army, Hosp 102, Dept Lab, Changzhou, Jiangs, Peoples R China
[6] Chinese Peoples Liberat Army, Hosp 102, Dept Neurol, Changzhou, Jiangsu, Peoples R China
[7] Nanjing Med Univ, Wuxi Mental Hlth Ctr, Wuxi, Jiangsu, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2016年 / 22卷
关键词
Biological Markers; Depressive Disorder; Major; RNA; Long Noncoding; DIFFERENTIAL EXPRESSION; MICRORNA EXPRESSION; MONONUCLEAR-CELLS; RISK-FACTORS; AGE; PROFILES; PLASMA; FUTURE; SEX;
D O I
10.12659/MSM.899372
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: The criteria for diagnosing depression are based on behavioral observation and self-reporting of symptoms by the patients or guardians without any biological validation of the disease. This study aimed to identify long non-coding RNAs (lncRNAs) in peripheral blood mononuclear cells (PBMCs) as robust and predictive biomarkers for diagnosis and therapy response in major depressive disorder (MDD). Material/Methods: We used human lncRNA 3.0 microarray profiling (which covers 30,586 human lncRNAs), using PBMCs from five MDD patients and five controls. Differentially expressed lncRNAs in the PBMCs of MDD patients were identified, of which 10 candidate lncRNAs were selected for real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) analysis in a larger cohort of 138 MDD patients and 63 healthy controls. Then among the 138 MDD patients who received standard antidepressant treatment, 30 were randomly selected for lncRNAs expression retesting and symptomatology assessments after three-weeks and six-weeks of antidepressant treatment. Results: Six lncRNAs (TCONS_00019174, ENST00000566208, NONHSAG045500, ENST00000517573, NONHSAT034045, and NONHSAT142707) were significantly downregulated in MDD patients compared to control patients, and the area under the receiver operator curve (ROC) of these six lncRNAs cases, combined, was 0.719 (95% confidence interval (CI): 0.617-0.821). There was no difference in the expression of these six lncRNAs based on gender (p>0.05) or age (p>0.05). Conclusions: These results suggest that the combined expression of six lncRNAs in PBMCs may serve as a potential biomarker for diagnosis and therapy response of MDD in the clinical setting.
引用
收藏
页码:5240 / 5248
页数:9
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