Exon Array Biomarkers for the Differential Diagnosis of Schizophrenia and Bipolar Disorder.

Molecular Neuropsychiatry Pub Date : 2018-05-01 Epub Date: 2018-04-10 DOI:10.1159/000485800
Marquis Philip Vawter, Robert Philibert, Brandi Rollins, Patricia L Ruppel, Terry W Osborn
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引用次数: 4

Abstract

This study developed potential blood-based biomarker tests for diagnosing and differentiating schizophrenia (SZ), bipolar disorder type I (BD), and normal control (NC) subjects using mRNA gene expression signatures. A total of 90 subjects (n = 30 each for the three groups of subjects) provided blood samples at two visits. The Affymetrix exon microarray was used to profile the expression of over 1.4 million probesets. We selected potential biomarker panels using the temporal stability of the probesets and also back-tested them at two different visits for each subject. The 18-gene biomarker panels, using logistic regression modeling, correctly differentiated the three groups of subjects with high accuracy across the two different clinical visits (83-88% accuracy). The results are also consistent with the actual data and the "leave-one-out" analyses, indicating that the models should be predictive when applied to independent data cohorts. Many of the SZ and BD subjects were taking antipsychotic and mood stabilizer medications at the time of blood draw, raising the possibility that these drugs could have affected some of the differential transcription signatures. Using an independent Illumina data set of gene expression data from antipsychotic medication-free SZ subjects, the 18-gene biomarker panels produced a receiver operating characteristic curve accuracy greater than 0.866 in patients that were less than 30 years of age and medication free. We confirmed select transcripts by quantitative PCR and the nCounter® System. The episodic nature of psychiatric disorders might lead to highly variable results depending on when blood is collected in relation to the severity of the disease/symptoms. We have found stable trait gene panel markers for lifelong psychiatric disorders that may have diagnostic utility in younger undiagnosed subjects where there is a critical unmet need. The study requires replication in subjects for ultimate proof of the utility of the differential diagnosis.

Abstract Image

Abstract Image

外显子阵列生物标志物用于精神分裂症和双相情感障碍的鉴别诊断。
这项研究开发了潜在的基于血液的生物标志物测试,用于诊断和区分精神分裂症(SZ)、双相情感障碍I型(BD)和正常对照(NC)受试者,使用mRNA基因表达特征。共90名受试者(三组各30名)在两次访问时提供血液样本。Affymetrix外显子微阵列被用于分析超过140万个问题集的表达。我们利用问题集的时间稳定性选择了潜在的生物标志物组,并对每个受试者在两次不同的访问中进行了回测。使用逻辑回归模型的18个基因生物标志物面板在两次不同的临床就诊中正确区分了三组受试者,准确率很高(83-88%)。结果也与实际数据和“留一”分析相一致,表明该模型在应用于独立数据队列时应该具有预测性。许多SZ和BD受试者在抽血时正在服用抗精神病药物和情绪稳定药物,这增加了这些药物可能影响一些差异转录特征的可能性。使用独立的Illumina数据集收集无抗精神病药物SZ受试者的基因表达数据,18个基因生物标志物面板在年龄小于30岁且无药物的患者中产生的受试者工作特征曲线精度大于0.866。我们通过定量PCR和nCounter®系统确认选择的转录本。精神疾病的发作性可能导致高度可变的结果,这取决于采集血液的时间与疾病/症状的严重程度有关。我们已经发现了终身精神疾病的稳定性状基因面板标记,这些标记可能对年轻的未被诊断的受试者具有诊断效用,因为这些受试者存在严重的未满足需求。该研究需要在受试者中进行复制,以最终证明鉴别诊断的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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