中华地方病学杂志
中華地方病學雜誌
중화지방병학잡지
Chinese Journal of Endemiology
2015年
7期
495-500
,共6页
相有章%谭武红%刘源%王秀红%张文明%王静%苏国海
相有章%譚武紅%劉源%王秀紅%張文明%王靜%囌國海
상유장%담무홍%류원%왕수홍%장문명%왕정%소국해
克山病%血清%蛋白质类%质谱法%生物标志物
剋山病%血清%蛋白質類%質譜法%生物標誌物
극산병%혈청%단백질류%질보법%생물표지물
Keshan disease%Serum%Proteins%Mass Spectrometry%Biomarkers
目的 探讨血清蛋白鉴定对克山病临床诊断与发病机制研究的价值.方法 在克山病病区选择65例慢型克山病患者作为克山病(KD)组;同时以29例扩张型心肌病(DCM)患者作为DCM组、62例克山病病区健康人及28例非病区健康人作为对照.采集受检者血清,采用液体芯片飞行时间质谱技术(ClinProtTMMALDI-TOF-MS)检测差异蛋白表达,应用ClinProTools 2.2软件分析确定差异蛋白,以基因遗传(GA)、快速分类(QC)和神经网络(SNN)3种算法筛选标志蛋白.采用MALDI串联飞行时间质谱技术(MALDI-TOF/TOF)鉴定差异多肽;使用flexAnalysis软件标注峰图,MASCOT搜索引擎检索结果.结果 ①KD组与非病区健康对照组比较获得34个差异蛋白/多肽及5个标志蛋白;KD组与病区健康对照组比较获得52个差异蛋白/多肽及5个标志蛋白;KD组与DCM组比较获得67个差异蛋白/多肽及5个标志蛋白,标志蛋白对组间区分的敏感性与特异性分别达98.07% ~ 99.24%、97.15%~99.12%.②二级质谱鉴定获得2个阳性结果,质荷比(m/z)为2 079的肽段匹配β珠蛋白,m/z为l 465的肽段匹配纤维蛋白原.β珠蛋白在克山病呈低表达,纤维蛋白原呈高表达.结论 慢型克山病血清标志蛋白可作为诊断与鉴别的生物标志物,β珠蛋白与纤维蛋白原在克山病心肌损伤的发生发展中扮演了重要角色.
目的 探討血清蛋白鑒定對剋山病臨床診斷與髮病機製研究的價值.方法 在剋山病病區選擇65例慢型剋山病患者作為剋山病(KD)組;同時以29例擴張型心肌病(DCM)患者作為DCM組、62例剋山病病區健康人及28例非病區健康人作為對照.採集受檢者血清,採用液體芯片飛行時間質譜技術(ClinProtTMMALDI-TOF-MS)檢測差異蛋白錶達,應用ClinProTools 2.2軟件分析確定差異蛋白,以基因遺傳(GA)、快速分類(QC)和神經網絡(SNN)3種算法篩選標誌蛋白.採用MALDI串聯飛行時間質譜技術(MALDI-TOF/TOF)鑒定差異多肽;使用flexAnalysis軟件標註峰圖,MASCOT搜索引擎檢索結果.結果 ①KD組與非病區健康對照組比較穫得34箇差異蛋白/多肽及5箇標誌蛋白;KD組與病區健康對照組比較穫得52箇差異蛋白/多肽及5箇標誌蛋白;KD組與DCM組比較穫得67箇差異蛋白/多肽及5箇標誌蛋白,標誌蛋白對組間區分的敏感性與特異性分彆達98.07% ~ 99.24%、97.15%~99.12%.②二級質譜鑒定穫得2箇暘性結果,質荷比(m/z)為2 079的肽段匹配β珠蛋白,m/z為l 465的肽段匹配纖維蛋白原.β珠蛋白在剋山病呈低錶達,纖維蛋白原呈高錶達.結論 慢型剋山病血清標誌蛋白可作為診斷與鑒彆的生物標誌物,β珠蛋白與纖維蛋白原在剋山病心肌損傷的髮生髮展中扮縯瞭重要角色.
목적 탐토혈청단백감정대극산병림상진단여발병궤제연구적개치.방법 재극산병병구선택65례만형극산병환자작위극산병(KD)조;동시이29례확장형심기병(DCM)환자작위DCM조、62례극산병병구건강인급28례비병구건강인작위대조.채집수검자혈청,채용액체심편비행시간질보기술(ClinProtTMMALDI-TOF-MS)검측차이단백표체,응용ClinProTools 2.2연건분석학정차이단백,이기인유전(GA)、쾌속분류(QC)화신경망락(SNN)3충산법사선표지단백.채용MALDI천련비행시간질보기술(MALDI-TOF/TOF)감정차이다태;사용flexAnalysis연건표주봉도,MASCOT수색인경검색결과.결과 ①KD조여비병구건강대조조비교획득34개차이단백/다태급5개표지단백;KD조여병구건강대조조비교획득52개차이단백/다태급5개표지단백;KD조여DCM조비교획득67개차이단백/다태급5개표지단백,표지단백대조간구분적민감성여특이성분별체98.07% ~ 99.24%、97.15%~99.12%.②이급질보감정획득2개양성결과,질하비(m/z)위2 079적태단필배β주단백,m/z위l 465적태단필배섬유단백원.β주단백재극산병정저표체,섬유단백원정고표체.결론 만형극산병혈청표지단백가작위진단여감별적생물표지물,β주단백여섬유단백원재극산병심기손상적발생발전중분연료중요각색.
Objective To investigate the clinical diagnostic value and pathogenesis of serum protein identification in Keshan disease (KD).Methods A total of 65 chronic KD patients were selected as the patient group in KD endemic areas,while 29 cases of dilated cardiomyopathy (the DCM group),62 healthy cases from KD endemic areas (control 1 group) and 28 healthy cases from non-endemic areas (control 2 group) were selected as controls.Liquid chip time of flight mass spectrometry (ClinProtTM MALDI-TOF-MS) was used to determine the expression of proteins/peptide peaks.ClinProTools 2.2 software was used to analyze the protein profiles to determine differentially expressed proteins/peptide peaks.The Genetic Algorithm (GA),QuickClassifer Algorithm (QC) and Supervised Neural Network Algorithm (SNN) methods were used to screen marker proteins.Matrix-assisted laser desorption/ionization time-of-flight Mass Spectrometry technique (MALDI-TOF/TOF) was also used as a secondary mass spectrometry to identify differentially expressed peptides.Results Between the KD and control 1 groups,34 differentially expressed proteins/peptides and 5 marker proteins were identified,while 52 differentially expressed proteins/peptides and 5 marker proteins were identified between the KD and control 2 groups,and there were 67 differentially expressed proteins/peptides and 5 marker proteins between the KD and DCM groups.During secondary mass spectrometry,two peptides for mass-to-charge ratio (m/z) 2 079 and 1 465 were obtained,peptide of matching β-globin showed low expression while peptide of matching fibrinogen showed high expression in the KD patients.Conclusions Serum marker proteins can be used as biomarkers for diagnosis and differentiation of KD.β-globin and fibrinogen play an important role in the development of KD myocardial injury.