首页> 外文期刊>BMC Veterinary Research >A canine-specific anti-nerve growth factor antibody alleviates pain and improves mobility and function in dogs with degenerative joint disease-associated pain
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A canine-specific anti-nerve growth factor antibody alleviates pain and improves mobility and function in dogs with degenerative joint disease-associated pain

机译:犬特异性抗神经生长因子抗体可减轻与退行性关节疾病相关性疼痛的狗的疼痛并改善其活动能力和功能

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Background There is a critical need for proven drugs other than non-steroidal anti-inflammatory drugs for treatment of degenerative joint disease (DJD) pain in dogs. Antibodies against nerve growth factor (NGF) are analgesic in rodent models and in humans with DJD. This pilot study aimed to evaluate the efficacy of a novel caninised anti-NGF antibody (NV-01) for the treatment of DJD pain in dogs. In a randomized, parallel group, stratified, double masked, placebo controlled, proof of principle clinical pilot study design, 26 dogs with DJD received NV-01 (200 mcg/kg IV) or placebo on day 0 (D0). In addition to objective accelerometry measures, owners completed clinical metrology instruments (Client-Specific Outcome Measures [CSOM], Canine Brief Pain Inventory [CBPI] and Liverpool Osteoarthritis in Dogs Index [LOAD]) on D0, D14 and D28. CBPI subscales (pain severity [PS] and pain interference [PI]), CSOM and LOAD scores were evaluated within and between groups for change over time. Recognized success/failure criteria were applied and success compared between groups. Results CBPI PS and PI scores significantly improved in the NV-01 group (PS: D0-14, P?=?0.012 and D0-28, P?=?0.019; PI: D0-14, P?=?0.012 and D0-28, P?=?0.032) but not in the placebo group. CSOM scores showed similar patterns with a significant difference between within-group changes at D14 and D28 (P?=?0.038 and P?=?0.009, respectively), and significantly more successes at D28 (P?=?0.047). LOAD scores significantly improved in the NV-01 group (D0-14, P = 0.004 and D0-28, P?=?0.002) but not in the placebo group. There were significant differences between the groups for change in LOAD score at D14 (P?=?0.014) and D28 (P?=?0.033). No side effects were noted. Activity in the NV-01 group increased over the study period compared to placebo (P?=?0.063) and the difference between the groups for change in activity over the time period 9am-5pm (8 hours) was significant (P?=?0.006). Conclusions These pilot data demonstrate a positive analgesic effect of anti-NGF antibody in dogs suffering from chronic pain. The magnitude of the effect appeared identical to that expected with an NSAID.
机译:背景技术除非甾体抗炎药以外,迫切需要用于狗的退行性关节病(DJD)疼痛的经验证的药物。抗神经生长因子(NGF)的抗体在啮齿动物模型和患有DJD的人中具有镇痛作用。这项初步研究旨在评估新型犬化抗NGF抗体(NV-01)在犬DJD疼痛治疗中的功效。在随机,平行,分层,双掩蔽,安慰剂对照的安慰剂对照的原则性临床试验研究设计中,有26例DJD犬在第0天(D0)接受NV-01(200 mcg / kg IV)或安慰剂。除了客观的加速度测量方法外,所有者还分别在D0,D14和D28上完成了临床计量工具(特定于客户的结果度量[CSOM],犬简短疼痛量表[CBPI]和利物浦犬骨关节炎指数[LOAD])。 CBPI分量表(疼痛严重度[PS]和疼痛干扰[PI]),CSOM和LOAD评分在组内和组之间随时间的变化进行了评估。应用公认的成功/失败标准,并在组之间比较成功。结果NV-01组的CBPI PS和PI得分显着提高(PS:D0-14,P?=?0.012和D0-28,P?=?0.019; PI:D0-14,P?=?0.012和D0 -28,P≥0.032),但不在安慰剂组中。 CSOM评分显示出相似的模式,在D14和D28时组内变化之间存在显着差异(分别为P?=?0.038和P?=?0.009),而在D28时的成功率显着更高(P?=?0.047)。 NV-01组(D0-14,P = 0.004和D0-28,P1 =?0.002)的LOAD评分显着改善,而安慰剂组则没有。两组之间在D14(P?=?0.014)和D28(P?=?0.033)时LOAD评分的变化之间存在显着差异。没有发现副作用。与安慰剂相比,NV-01组的活性在研究期间有所增加(P <= 0.063),并且两组之间在上午9点至下午5点(8小时)的时间段内活动变化的差异是显着的(P <=? 0.006)。结论这些初步数据证明抗NGF抗体对患有慢性疼痛的犬有积极的镇痛作用。效果的程度似乎与NSAID预期的相同。

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