岭南急诊医学杂志
嶺南急診醫學雜誌
령남급진의학잡지
LINGNAN JOURNAL OF EMERGENCY MEDICINE
2015年
4期
271-272,293
,共3页
微小核糖核苷酸%急性心肌梗死%早期%诊断价值
微小覈糖覈苷痠%急性心肌梗死%早期%診斷價值
미소핵당핵감산%급성심기경사%조기%진단개치
microRNA%acute myocardial infarction%early stage%diagnostic value
目的:探讨微小核糖核苷酸(miRNA)在急性心肌梗死(AMI)早期诊断中的价值。方法:将发病时间<3h的胸痛患者60例根据其诊断结果分为AMI组(n=30)和非AMI组(n=30),另选择正常对照组(n=30),在入院即刻测定miR-208a、肌钙蛋白、肌红蛋白、磷酸肌酸心肌同工酶(CK-MB),比较各组生化标记物的变化。在AMI组动态监测miR-208a和肌钙蛋白的波动情况;以实时荧光定量聚合酶链反应测定miR-208a。结果:入院即刻AMI组miR-208a明显高于对照组(P<0.05),但肌钙蛋白和CK-MB与对照组无明显差异;发病1h时的miR-208a显著高于对照组(P<0.05),肌钙蛋白浓度尚处于正常范围内。 miR-208a的峰值出现于发病12h,峰值明显早于肌钙蛋白。结论:miR-208a在早期AMI诊断中具备高特异性和高敏感性。
目的:探討微小覈糖覈苷痠(miRNA)在急性心肌梗死(AMI)早期診斷中的價值。方法:將髮病時間<3h的胸痛患者60例根據其診斷結果分為AMI組(n=30)和非AMI組(n=30),另選擇正常對照組(n=30),在入院即刻測定miR-208a、肌鈣蛋白、肌紅蛋白、燐痠肌痠心肌同工酶(CK-MB),比較各組生化標記物的變化。在AMI組動態鑑測miR-208a和肌鈣蛋白的波動情況;以實時熒光定量聚閤酶鏈反應測定miR-208a。結果:入院即刻AMI組miR-208a明顯高于對照組(P<0.05),但肌鈣蛋白和CK-MB與對照組無明顯差異;髮病1h時的miR-208a顯著高于對照組(P<0.05),肌鈣蛋白濃度尚處于正常範圍內。 miR-208a的峰值齣現于髮病12h,峰值明顯早于肌鈣蛋白。結論:miR-208a在早期AMI診斷中具備高特異性和高敏感性。
목적:탐토미소핵당핵감산(miRNA)재급성심기경사(AMI)조기진단중적개치。방법:장발병시간<3h적흉통환자60례근거기진단결과분위AMI조(n=30)화비AMI조(n=30),령선택정상대조조(n=30),재입원즉각측정miR-208a、기개단백、기홍단백、린산기산심기동공매(CK-MB),비교각조생화표기물적변화。재AMI조동태감측miR-208a화기개단백적파동정황;이실시형광정량취합매련반응측정miR-208a。결과:입원즉각AMI조miR-208a명현고우대조조(P<0.05),단기개단백화CK-MB여대조조무명현차이;발병1h시적miR-208a현저고우대조조(P<0.05),기개단백농도상처우정상범위내。 miR-208a적봉치출현우발병12h,봉치명현조우기개단백。결론:miR-208a재조기AMI진단중구비고특이성화고민감성。
Objective:To explore the value of miR208a in the early diagnosis of acute myocardial infarction (AMI). Methods:60 Patients with chest discomfort within 3 hours were included, 30 in the AMI group and 30 in the non-AMI group. Another 30 healthy people were also included as the control group. Plasma miR-208a,cardiac troponin I, myoglobin and CK-MB were determined once the patients arrived and then compared to the basic level in the control group. MiR-208a was detected at series times thereafter in the AMI group. In the study,miR-208a was determined by quantitative RT-PCR. Results:MiR-208a was higher in the AMI group than the control group with the first plasma sample(P<0.05). At the first hour after the onset of symptoms miR-208a elevated significantly (P<0.05), while cardiac troponin I was normal. The peak level of miR-208a appeared within 12 hours. Conclusions:It is confirmed that the novel biomarker miR-208a had great specificity and sensitivity in the early diagnosis of AMI.