Department of Clinical Sciences, Veterinary Health Center, Kansas State University, Manhattan, Kansas, United States of America.
PLoS One. 2020 Apr 9;15(4):e0231306. doi: 10.1371/journal.pone.0231306. eCollection 2020.
To determine if a commercial myostatin reducer (Fortetropin®) would inhibit disuse muscle atrophy in dogs after a tibial plateau leveling osteotomy.
A prospective randomized, double-blinded, placebo-controlled clinical trial.
One hundred client-owned dogs presenting for surgical correction of cranial cruciate ligament rupture by tibial plateau leveling osteotomy.
Patients were randomly assigned into the Fortetropin® or placebo group and clients were instructed to add the assigned supplement to the dog's normal diet once daily for twelve weeks. Enrolled patients had ultrasound measurements of muscle thickness, tape measure measurements of thigh circumference, serum myostatin level assays, and static stance analysis evaluated at weeks 0, 8, and 12.
From week 0 to week 8, there was no change for thigh circumference in the Fortetropin® group for the affected limb (-0.54cm, P = 0.31), but a significant decrease in thigh circumference for the placebo group (-1.21cm, P = 0.03). There was no significant change in serum myostatin levels of dogs in the Fortetropin® group at any time point (P>0.05), while there was a significant rise of serum myostatin levels of dogs in placebo group during the period of forced exercise restriction (week 0 to week 8; +2,892 pg/ml, P = 0.02). The percent of body weight supported by the affected limb increased in dogs treated with Fortetropin® (+7.0%, P<0.01) and the placebo group (+4.9%, P<0.01) at the end of the period of forced exercise restriction. The difference in weight bearing between the Fortetropin® and placebo groups was not statistically significant (P = 0.10).
Dogs receiving Fortetropin® had a similar increase in stance force on the affected limb, no significant increase in serum myostatin levels, and no significant reduction in thigh circumference at the end of the period of forced exercise restriction compared to the placebo. These findings support the feeding of Fortetropin® to prevent disuse muscle atrophy in canine patients undergoing a tibial plateau leveling osteotomy.
确定一种商业性肌肉生长抑制素减少剂(Fortetropin®)是否会抑制胫骨平台平整截骨术后犬的废用性肌肉萎缩。
前瞻性随机、双盲、安慰剂对照临床试验。
100 只因前十字韧带断裂而接受胫骨平台平整截骨术的客户所有犬。
患者被随机分配到 Fortetropin®或安慰剂组,客户被指示将分配的补充剂添加到犬的正常饮食中,每天一次,持续 12 周。入组患者在第 0、8 和 12 周进行肌肉厚度超声测量、大腿周径卷尺测量、血清肌肉生长抑制素水平检测和静态站立分析。
从第 0 周到第 8 周,Fortetropin®组受影响肢体的大腿周径没有变化(-0.54cm,P=0.31),但安慰剂组的大腿周径显著减小(-1.21cm,P=0.03)。在任何时间点,Fortetropin®组犬的血清肌肉生长抑制素水平均无显著变化(P>0.05),而安慰剂组犬在强制运动限制期间(第 0 周到第 8 周)血清肌肉生长抑制素水平显著升高(+2892pg/ml,P=0.02)。接受 Fortetropin®治疗的犬受影响肢体的体重支持百分比增加(+7.0%,P<0.01),安慰剂组也增加(+4.9%,P<0.01),在强制运动限制结束时。Fortetropin®和安慰剂组之间的承重差异无统计学意义(P=0.10)。
与安慰剂相比,接受 Fortetropin®治疗的犬在强制运动限制结束时,受影响肢体的站立力有类似的增加,血清肌肉生长抑制素水平无显著升高,大腿周径无显著减小。这些发现支持在接受胫骨平台平整截骨术的犬患者中喂养 Fortetropin®以预防废用性肌肉萎缩。