adropin和鸢尾素生物标志物在急性心肌梗死和2型糖尿病患者中的动态变化

©M. Yu. Koteliukh
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Serum levels of adropin and irisin were measured by enzyme-linked immunosorbent assay.\nResults. The adropin and irisin serum levels on day 1 of treatment was low in both nondiabetic (I) and diabetic patients (II) compared with those in the control group (p<0.05). On the 10th day of treatment, the levels of adropin in group II patients without early AMI complications were reduced by 13.91 % compared with those in group I (p<0.05). Group II with the presence of early AMI complications showed a reduction of 17.34 % in adropin levels on day 10 compared with group II (p<0.05). On day 10 of treatment, the irisin levels in group II without early AMI complications were reduced by 18.94 % compared with those in group I (p<0.05). In group II with the presence of early AMI complications on the 10th day, the irisin levels were reduced by 23.87 % compared with those in group I (p<0.05).\nConclusions. 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摘要

总结。现代医学迫切关注的是寻找能够影响2型糖尿病(DM)患者急性心肌梗死(AMI)发展和病程的新生物标志物。目的:研究伴有或不伴有AMI并发症的糖尿病患者血清促肾上腺素和鸢尾素水平的动态变化。材料与方法。共有134名AMI患者入组。在60例AMI患者(I组)中,41例未发现AMI的早期心血管(CV)并发症,19例合并AMI。74例AMI合并2型DM患者(II组)中,无AMI早期并发症患者48例,有AMI早期并发症患者26例。对照组由20名其他方面健康的人组成。采用酶联免疫吸附法测定血清adropin和鸢尾素水平。治疗第1天,非糖尿病(I)和糖尿病(II)患者血清adropin和irisin水平均低于对照组(p<0.05)。治疗第10天,无AMI早期并发症的II组患者adropin水平较I组降低13.91% (p<0.05)。有AMI早期并发症的II组第10天adropin水平较II组降低17.34% (p<0.05)。治疗第10天,无AMI早期并发症的II组血清鸢尾素水平较I组降低18.94% (p<0.05)。II组在出现AMI早期并发症的第10天,鸢尾素水平较I组降低23.87% (p<0.05)。第二组患者在住院第1天和第10天adropin和鸢尾素浓度显著降低。在第10天的治疗动态中,有AMI早期CV并发症的II组的adropin和鸢尾素水平仍然很低。
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DYNAMICS OF ADROPIN AND IRISIN BIOMARKERS IN PATIENTS WITH ACUTE MYOCARDIAL INFARCTION AND TYPE 2 DIABETES MELLITUS
summary. A pressing concern of modern medicine is the search for new biomarkers that can influence the development and course of acute myocardial infarction (AMI) in patents with type 2 diabetes mellitus (DM). The aim – To examine the dynamics of adropin and irisin serum levels in diabetic patients with or without AMI complications. Materials and Methods. In total, 134 AMI patients were enrolled. Among 60 examined AMI patients (group I), 41 patients were identified without early cardiovascular (CV) complications of AMI and 19 patients – with complicated AMI. Among 74 AMI patients with type 2 DM (group II), there were 48 patients without early AMI complications and 26 patients with early AMI complications. The control group consisted of 20 otherwise healthy persons. Serum levels of adropin and irisin were measured by enzyme-linked immunosorbent assay. Results. The adropin and irisin serum levels on day 1 of treatment was low in both nondiabetic (I) and diabetic patients (II) compared with those in the control group (p<0.05). On the 10th day of treatment, the levels of adropin in group II patients without early AMI complications were reduced by 13.91 % compared with those in group I (p<0.05). Group II with the presence of early AMI complications showed a reduction of 17.34 % in adropin levels on day 10 compared with group II (p<0.05). On day 10 of treatment, the irisin levels in group II without early AMI complications were reduced by 18.94 % compared with those in group I (p<0.05). In group II with the presence of early AMI complications on the 10th day, the irisin levels were reduced by 23.87 % compared with those in group I (p<0.05). Conclusions. The concentrations of adropin and irisin were significantly low in group II on day 1 and 10 of hospital stay. In the dynamics of treatment on day 10, the levels of adropin and irisin remained low in group II with early CV complications of AMI.
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