将透明质酸、III型胶原蛋白N端肽和基质金属蛋白酶组织抑制剂-1作为犬肝纤维化的血清标志物进行评估。

IF 0.8 Q3 VETERINARY SCIENCES
Jonathan A Lidbury, Aline Rodrigues Hoffmann, Joanna K Fry, Jan S Suchodolski, Jörg M Steiner
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引用次数: 0

摘要

诊断狗肝纤维化的唯一方法是对肝活检标本进行组织学评估。由于这种技术具有侵入性,而且容易受取样变化的影响,因此人类使用血清生物标记物来检测肝纤维化。本研究旨在评估透明质酸(HA)、III型胶原蛋白N端肽(PIIINP)和基质金属蛋白酶-1组织抑制剂(TIMP-1)作为犬肝纤维化血清标志物的效用。采集了 47 只经组织学证实患有肝胆疾病的狗和 24 只健康狗的血清样本,以测定 HA、PIIINP 和 TIMP-1 的浓度。肝纤维化采用 5 点评分法进行分期。血清中 HA 或 PIIINP 的浓度与肝纤维化的严重程度没有相关性。血清中 TIMP-1 的浓度与肝纤维化的严重程度呈负相关(rs = -0.33;P = 0.036)。无法利用血清中 HA、PIIINP 或 TIMP-1 的浓度来区分没有肝纤维化到中度肝纤维化的狗和肝纤维化明显到非常明显的狗。本研究结果不支持测量血清中的 HA、PIIINP 或 TIMP-1 浓度来诊断犬肝纤维化。还需要进一步的研究来支持这一发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of hyaluronic acid, procollagen type III N-terminal peptide, and tissue inhibitor of matrix metalloproteinase-1 as serum markers of canine hepatic fibrosis.

The only way to diagnose hepatic fibrosis in dogs is by histological assessment of a liver biopsy specimen. As this technique is invasive and susceptible to sampling variation, serum biomarkers are used to detect hepatic fibrosis in humans. The objective of this study was to assess the utility of hyaluronic acid (HA), procollagen type III N-terminal peptide (PIIINP), and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) as serum markers of canine hepatic fibrosis. Serum samples were collected from 47 dogs with histologically confirmed hepatobiliary disease and 24 healthy dogs in order to measure concentrations of HA, PIIINP, and TIMP-1. Hepatic fibrosis was staged using a 5-point scoring scheme. There was no correlation between serum concentrations of HA or PIIINP and the severity of hepatic fibrosis. There was a negative correlation between serum concentration of TIMP-1 and the severity of hepatic fibrosis (rs = -0.33; P = 0.036). It was not possible to use serum concentrations of HA, PIIINP, or TIMP-1 to discriminate between dogs with absent-to-moderate hepatic fibrosis and those with marked-to-very-marked fibrosis. The results of this study do not support the utility of measuring serum concentrations of HA, PIIINP, or TIMP-1 for diagnosing canine hepatic fibrosis. Further studies are needed to support this finding.

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