Beths T, Munn R, Bauquier S H, Mitchell P, Whittem T
Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Werribee, Victoria, 3030, Australia.
Aust Vet J. 2020 Dec;98(12):591-595. doi: 10.1111/avj.13024. Epub 2020 Sep 26.
The primary goal of this pilot study was to assess, the efficacy of a new nutraceutical, 4CYTE™ Epiitalis® Forte, containing, as a standalone, a proprietary plant oil extract, Epiitalis, in dogs presenting with signs of osteoarthritis (OA). Fifty dogs aged 9.2 (±3.2) years with signs of naturally occurring OA were included in this report. They were free of other comorbidities and were not on any medications except for those utilised for managing their OA. In these dogs, the current treatments were continued to avoid any sudden changes in their disease management. The effects of the 4CYTE Epiitalis Forte were assessed both at the beginning and at the end of a 1 month-long treatment period. The evaluation consisted of an objective lameness assessment (TPI%[total pressure index]) using a gait analysis (GAITRite® Portable Walkway System) and a subjective quality-of-life questionnaire, the Helsinki Chronic Pain Index (HCPI). Additional exploratory objective measurements included the Symmetry Index (SI) and the fore/hind limb ratio (T/P TPI%). Of dogs, 74% (34/46) registered a numerical improvement in TPI% in their worse limb. In addition, of the 93.5% of the dogs that demonstrated improvement in their HCPI scores by at least 5% on the quality-of-life questionnaire, 79% demonstrated improvements in gait based on TPI%. Finally, there were improvements measured in both exploratory objective endpoints SI and T/P TPI%. These encouraging results will be used to develop a protocol for a follow-up placebo-controlled randomised study to confirm the efficacy of this new nutraceutical for dogs suffering from OA.
这项初步研究的主要目标是评估一种新型营养保健品4CYTE™ Epiitalis® Forte的疗效,该产品单独含有一种专利植物油提取物Epiitalis,用于患有骨关节炎(OA)症状的犬类。本报告纳入了50只年龄为9.2(±3.2)岁、患有自然发生OA症状的犬。它们没有其他合并症,除了用于管理OA的药物外,未服用任何其他药物。在这些犬中,继续采用当前治疗方法以避免其疾病管理出现任何突然变化。在为期1个月的治疗期开始和结束时,均对4CYTE Epiitalis Forte的效果进行评估。评估包括使用步态分析(GAITRite®便携式走道系统)进行客观跛行评估(TPI%[总压力指数])以及主观生活质量问卷——赫尔辛基慢性疼痛指数(HCPI)。额外的探索性客观测量包括对称指数(SI)和前/后肢比率(T/P TPI%)。在犬中,74%(34/46)的较严重肢体的TPI%出现了数值上的改善。此外,在生活质量问卷中HCPI评分至少提高5%的犬中,93.5%的犬基于TPI%显示步态有所改善。最后,在探索性客观终点SI和T/P TPI%方面均测得有所改善。这些令人鼓舞的结果将用于制定一项后续安慰剂对照随机研究方案,以确认这种新型营养保健品对患OA犬类的疗效。