血清、唾液和尿液中鸢尾素伴与不伴急性阑尾炎和腹痛。

Biochemistry Insights Pub Date : 2016-06-15 eCollection Date: 2016-01-01 DOI:10.4137/BCI.S39671
Unal Bakal, Suleyman Aydin, Mehmet Sarac, Tuncay Kuloglu, Mehmet Kalayci, Gokhan Artas, Meltem Yardim, Ahmet Kazez
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引用次数: 18

摘要

鸢尾素(irisin, IRI)是一种由112个氨基酸组成的蛋白,在许多器官中广泛表达,但目前尚不清楚阑尾组织和血细胞是否表达它。如果阑尾组织和中性粒细胞表达IRI,测量其在生物体液中的浓度可能有助于诊断急性阑尾炎(AA),因为中性粒细胞是目前诊断AA的金标准实验室参数。因此,本研究的目的是探讨基于酶联免疫吸附试验的肌因子IRI测量方法在区分AA患者与急性腹痛(AP)患者和健康对照者中的适用性。此外,研究了阑尾组织和血细胞对IRI的免疫反应性。术后T1-T3对应的疑似AA患者和AP患者于入院时(T1)、24小时(T2)和72小时(T3)采集血样,对照受试者在T1对应一次血样。采用酶联免疫吸附法测定血清、唾液和尿液中的IRI,采用免疫组织化学法检测阑尾组织和血细胞中的IRI。阑尾组织和血细胞(红细胞除外)是IRI的新来源。与术后T2水平相比,AA患儿的基础唾液、尿液和血清水平较高,术后T2水平开始下降。这与研究结果一致,AA患儿的IRI水平高于AP患儿或对照组,这很可能是由于AA中大量中性粒细胞浸润,将IRI释放到体液中。AA患儿IRI的测量与中性粒细胞计数的增加或减少平行。这一新发现表明,IRI和中性粒细胞计数的测量可以共同提高AA的诊断,并可以将其与AP区分。IRI可以作为诊断AA的候选标志物,并为中性粒细胞计数提供了额外的参数。有希望的接收操作曲线结果表明,IRI的敏感性和特异性分别为:血清90%和55%,唾液90%和60%,尿液90%和50%。血清中性粒细胞计数的敏感性为90%,特异性为90%。这一有希望的结果现在需要在更大的患者群体中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum, Saliva, and Urine Irisin with and Without Acute Appendicitis and Abdominal Pain.

A 112-amino-acid protein irisin (IRI) is widely expressed in many organs, but we currently do not know whether appendix tissue and blood cells express it. If appendix tissue and neutrophil cells express IRI, measuring its concentration in biological fluids might be helpful in the diagnosis of acute appendicitis (AA), since neutrophil cells are the currently gold-standard laboratory parameters for the diagnosis of AA. Therefore, the purpose of this study was to investigate the suitability of enzyme-linked immunosorbent assay-based measurements of the proposed myokine IRI for the discrimination of patients with AA from those with acute abdominal pain (AP) and healthy controls. Moreover, immunoreactivity to IRI was investigated in appendix tissues and blood cells. Samples were collected on admission (T1), 24 hours (T2), and 72 hours (T3) postoperatively from patients with suspected AA and from patients with AP corresponding to T1-T3, whereas control subject blood was once corresponding to T1. IRI was measured in serum, saliva, and urine by using enzyme-linked immunosorbent assay, whereas in appendix tissue and blood cells, IRI was detected by immunohistohcemistry. Appendix tissue and blood cells (except for erythrocytes) are new sources of IRI. Basal saliva, urine, and serum levels were higher in children with AA compared with postoperative levels (T2) that start to decline after surgery. This is in line with the finding that IRI levels are higher in children with AA when compared with those with AP or control subject levels, most likely due to a large infiltration of neutrophil cells in AA that release its IRI into body fluids. Measurement of IRI in children with AA parallels the increase or decrease in the neutrophil count. This new finding shows that the measurement of IRI and neutrophil count can together improve the diagnosis of AA, and it can distinguish it from AP. IRI can be a candidate marker for the diagnosis of AA and offers an additional parameter to neutrophil count. The promising receiving operating curve results indicate the following sensitivities and specificities, respectively, for IRI: serum 90% and 55%, saliva 90% and 60%, and urine 90% and 50%. Serum neutrophil count gave a sensitivity of 90% and a specificity of 90%. This promising result now needs to be confirmed in a larger group of patients.

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Biochemistry Insights
Biochemistry Insights BIOCHEMISTRY & MOLECULAR BIOLOGY-
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