医学
心肌梗塞
内科学
不稳定型心绞痛
心脏病学
脱氧核糖核酸酶
肌酸激酶
心绞痛
脱氧核糖核酸酶ⅰ
基础(医学)
胃肠病学
酶
DNA
生物
胰岛素
基序列
遗传学
生物化学
化学
作者
Yasuyuki Kawai,Masahiro Yoshida,Kenichiro Arakawa,Teruhiko Kumamoto,Norihiro Morikawa,Katsuhiko Masamura,Hiroshi Tada,Sachiko Ito,Hiroshi Hoshizaki,Shigeru Oshima,Koichi Taniguchi,Hidekazu Terasawa,Isamu Miyamori,Koichiro Kishi,Toshihiro Yasuda
出处
期刊:Circulation
[Ovid Technologies (Wolters Kluwer)]
日期:2004-05-18
卷期号:109 (20): 2398-2400
被引量:68
标识
DOI:10.1161/01.cir.0000129232.61483.43
摘要
Background— The delayed release of serum cardiac markers such as creatine kinase isoenzyme MB and equivocal early electrocardiographic changes have hampered a diagnosis of acute myocardial infarction (AMI) in the early phase after its onset. Therefore, a reliable serum biochemical marker for the diagnosis of AMI in the very early phase is desirable. Methods and Results— Serum samples were collected from the patients with AMI, unstable angina pectoris, stable angina pectoris, and other diseases. Levels of serum deoxyribonuclease I (DNase I) activity in the patients were determined. An abrupt elevation of serum DNase I activity was observed within approximately 3 hours of the onset of symptoms in patients with AMI, with significantly higher activity levels (21.7±5.10 U/L) in this group compared with the other groups with unstable angina pectoris (10.4±4.41 U/L), angina pectoris (10.8±3.70 U/L), and other diseases (9.22±4.16 U/L). Levels of the DNase I activity in serum then exhibited a marked time-dependent decline within 12 hours and had returned to basal levels within 24 hours. Conclusions— We suggest that serum DNase I activity could be used as a new diagnostic marker for the early detection of AMI.
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