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一项关于体内方法测定幼猪骨软骨状态性能的纵向研究。

A longitudinal study on the performance of in vivo methods to determine the osteochondrotic status of young pigs.

作者信息

Bertholle Christian P, Meijer Ellen, Back Willem, Stegeman Arjan, van Weeren P René, van Nes Arie

机构信息

Department of Farm Animal Health, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 7, NL-3584 CL, Utrecht, The Netherlands.

Department of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 112-114, NL-3584 CM, Utrecht, The Netherlands.

出版信息

BMC Vet Res. 2016 Mar 24;12:62. doi: 10.1186/s12917-016-0682-z.

Abstract

BACKGROUND

In today's porcine industry, lameness has a major welfare and economic impact, and is often caused by osteochondrosis (OC). The etiological factors of the disease have been studied in depth, however, to this day, little is known about the natural course of the disorder and how it can be detected at an early stage in pigs. The aim of this pilot study was to assess the potential of three non-invasive techniques for the detection and monitoring of early OC processes in piglets. A group of weaned piglets (n = 19) were examined longitudinally using radiographs, a visual lameness scoring scheme and a quantitative pressure-mat based locomotion analysis system to detect OC in the humeroradial, femoropatellar and tarsocrural joints. At several time points, a selection of animals was euthanized for post-mortem examinations, including histology, which was the gold standard.

RESULTS

In this study, clear signs of subclinical signs of OC were observed, however, we were unsuccessful in producing clinical OC. Lesions were observed to be commonly bilaterally symmetric in the joints examined in 80% of cases. The radiographic examinations showed a clear correlation with the gold standard, particularly when subclinical lesions were of a high histological score. Moreover, radiography was also able to detect the early repair processes, which appeared to take place at least until 14 weeks of age. Both visual scoring and pressure mat analyses showed good intra-assay reproducibility, with the pressure mat showing intra-class correlation values between 0.44 and 0.6 and the inter-observer agreement of visual scoring method was between 88 and 96%, however their correlation to OC lesions detected by histology was very weak, with only 2 out of 12 traits for the visual scoring method showing significant and biologically logical relations to a specific joint having histological OC lesions. For the pressure mat, only a maximum of 5 associations for specific joints with histological OC lesions were found out of a possible 8.

CONCLUSION

All tested in-vivo methods showed good reproducibility. Radiography was the most reliable technique to detect and monitor longitudinally the earliest signs of OC in these piglets. It also demonstrated that the "Point of No Return" (PNR) of the disease, when repair processes end, might be later than anticipated, after 13 weeks of age. All in all, our study shows that the timing of the use of these in-vivo methods is critical to detect and monitor OC, especially in the early phases of the disease. It also shows the difficulty in producing OC regardless of the optimization of the experimental settings in relation to the etiological factors known to induce OC.

摘要

背景

在当今的养猪业中,跛行对猪的健康福利和经济效益有重大影响,且常由骨软骨病(OC)引起。该疾病的病因已得到深入研究,然而,时至今日,对于这种病症的自然发展过程以及如何在猪的早期阶段检测到它,人们知之甚少。这项初步研究的目的是评估三种非侵入性技术在检测和监测仔猪早期骨软骨病过程中的潜力。使用X射线照片、视觉跛行评分方案和基于定量压力垫的运动分析系统对一组断奶仔猪(n = 19)进行纵向检查,以检测肱桡关节、股髌关节和跗关节的骨软骨病。在几个时间点,挑选一些动物实施安乐死以进行尸检,包括组织学检查,组织学检查是金标准。

结果

在本研究中,观察到了骨软骨病亚临床症状的明显迹象,然而,我们未能成功诱发临床骨软骨病。在80%的病例中,在所检查的关节中观察到病变通常呈双侧对称。X射线检查显示与金标准有明显相关性,特别是当亚临床病变具有高组织学评分时。此外,X射线摄影还能够检测到早期修复过程,这种修复过程似乎至少持续到14周龄。视觉评分和压力垫分析均显示出良好的批内重复性,压力垫的组内相关值在0.44至0.6之间,视觉评分方法的观察者间一致性在88%至96%之间,然而它们与通过组织学检测到的骨软骨病病变的相关性非常弱,视觉评分方法的12个特征中只有2个显示出与具有组织学骨软骨病病变的特定关节有显著且符合生物学逻辑的关系。对于压力垫,在可能的8种关联中,最多只发现了5种与具有组织学骨软骨病病变的特定关节的关联。

结论

所有测试的体内方法均显示出良好的重复性。X射线摄影是检测和纵向监测这些仔猪骨软骨病最早迹象的最可靠技术。它还表明,疾病的“不可逆转点”(PNR),即修复过程结束时,可能比预期的要晚,在13周龄之后。总而言之,我们的研究表明,使用这些体内方法的时机对于检测和监测骨软骨病至关重要,尤其是在疾病的早期阶段。它还表明,无论与已知诱发骨软骨病的病因相关的实验设置如何优化,诱发骨软骨病都存在困难。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4964/4807589/ce90f7e75bdb/12917_2016_682_Fig1_HTML.jpg

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