医学研究生学报
醫學研究生學報
의학연구생학보
JOURNAL OF MEDICAL POSTGRADUATE
2014年
12期
1290-1293
,共4页
彭瑛%黄远帅%邓正华%程松%温先勇%王开正
彭瑛%黃遠帥%鄧正華%程鬆%溫先勇%王開正
팽영%황원수%산정화%정송%온선용%왕개정
精神分裂症%microRNA%血清
精神分裂癥%microRNA%血清
정신분렬증%microRNA%혈청
Schizophrenia%microRNA%Serum
目的:目前精神分裂症的临床诊断缺乏统一的标准。文中研究精神分裂症患者血清中差异miRNA表达谱,为该病的临床诊断提供依据。方法采用FlashTag TM Biotin RNA芯片技术和SAM软件筛选精神分裂症患者与健康受试者血清中差异表达的miRNA,用实时荧光定量逆转录PCR(RT-PCR)进行验证。结果筛选出3个差异表达的miRNA,其中hsa-miR-1281上调,表达倍数变化为1.50881;hsa-miR-2861、hsa-miR-638下调,表达倍数变化分别为0.64193和0.51624。实时定量PCR结果证实,精神分裂症患者较健康受试者hsa-miR-2861与hsa-miR-638表达下调,分别为[(0.037±0.037) vs (3.159±2.761),χ2=4.089, P<0.05]及[(0.006±0.006) vs (0.689±0.314),χ2=4.083, P<0.05],hsa-miR-1281在精神分裂症患者组呈高表达[(1.221±0.041) vs (0.145±0.036),χ2=5.333,P<0.05)。结论精神分裂症患者血清中存在差异表达的miRNA谱,miR-1281、miR-2861和miR-638可作为诊断精神分裂症的一个新的血清标志物。
目的:目前精神分裂癥的臨床診斷缺乏統一的標準。文中研究精神分裂癥患者血清中差異miRNA錶達譜,為該病的臨床診斷提供依據。方法採用FlashTag TM Biotin RNA芯片技術和SAM軟件篩選精神分裂癥患者與健康受試者血清中差異錶達的miRNA,用實時熒光定量逆轉錄PCR(RT-PCR)進行驗證。結果篩選齣3箇差異錶達的miRNA,其中hsa-miR-1281上調,錶達倍數變化為1.50881;hsa-miR-2861、hsa-miR-638下調,錶達倍數變化分彆為0.64193和0.51624。實時定量PCR結果證實,精神分裂癥患者較健康受試者hsa-miR-2861與hsa-miR-638錶達下調,分彆為[(0.037±0.037) vs (3.159±2.761),χ2=4.089, P<0.05]及[(0.006±0.006) vs (0.689±0.314),χ2=4.083, P<0.05],hsa-miR-1281在精神分裂癥患者組呈高錶達[(1.221±0.041) vs (0.145±0.036),χ2=5.333,P<0.05)。結論精神分裂癥患者血清中存在差異錶達的miRNA譜,miR-1281、miR-2861和miR-638可作為診斷精神分裂癥的一箇新的血清標誌物。
목적:목전정신분렬증적림상진단결핍통일적표준。문중연구정신분렬증환자혈청중차이miRNA표체보,위해병적림상진단제공의거。방법채용FlashTag TM Biotin RNA심편기술화SAM연건사선정신분렬증환자여건강수시자혈청중차이표체적miRNA,용실시형광정량역전록PCR(RT-PCR)진행험증。결과사선출3개차이표체적miRNA,기중hsa-miR-1281상조,표체배수변화위1.50881;hsa-miR-2861、hsa-miR-638하조,표체배수변화분별위0.64193화0.51624。실시정량PCR결과증실,정신분렬증환자교건강수시자hsa-miR-2861여hsa-miR-638표체하조,분별위[(0.037±0.037) vs (3.159±2.761),χ2=4.089, P<0.05]급[(0.006±0.006) vs (0.689±0.314),χ2=4.083, P<0.05],hsa-miR-1281재정신분렬증환자조정고표체[(1.221±0.041) vs (0.145±0.036),χ2=5.333,P<0.05)。결론정신분렬증환자혈청중존재차이표체적miRNA보,miR-1281、miR-2861화miR-638가작위진단정신분렬증적일개신적혈청표지물。
Objective No uniform standards has been established for the clinical diagnosis of schizophrenia .The article was to investigate the differentially expressed microRNA ( miRNA) profile and explore its clinical significance . Methods Differentially expressed miRNAs were screened by FlashTag TM Biotin RNA chips and SAM software in serum of patients with schizophrenia and healthy controls , then the validation was performed by real-time fluorescent quantitative reverse transcription polymerase chain reaction ( RT-PCR) . Results Three differentially expressed miRNAs were screened , including up-regulated hsa-miR-1281 ( fold change =1.50881) and two down-regulated miRNAs:hsa-miR-2861(fold change=0.642) and hsa-miR-638 (fold change=0.516).The com-parative analysis of RT-PCR by SPSS 17.0 Kruskal Wallis H Test validated the expression levels of hsa-miR-2861 and hsa-miR-638 in patients with schizophrenia decreased significantly in comparison to healthy controls (χ2 =4.089,χ2 =4.083, P<0.001).While the expression level of hsa-miR-1281 in patients with schizophrenia was in higher expression level compared with control group (χ2 =5.333, P<0.001). Conclusion There are differentially expressed miRNA profile in serum of patients with schizophrenia , in which miR-1281 , miR-2861 and miR-638 could be new serum markers for diagnosis of schizophrenia .