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THERIOGENOLOGY AND LAMENESS


phonates have been reported, but none of the studies performed long-term follow-up on the infants. In growing laboratory animals, bisphosphonate administration was associated with a transient dis- ruption of physeal microscopic morphology, reten- tion of cartilaginous remnants in the cortical bone, and a mild decrease in tibial length.42 Thus, bis- phosphonates seem to affect endochondral ossifica- tion, but it is unclear whether this has any lasting effects.


How Long Are Tiludronate or Clodronate Decreasing Bone Turnover After Administration? Is This Dependent on Exercise, Age of the Animal, or Other Factors? Is it Important to Obtain a Sustained Decrease in Bone Turnover for Therapeutic Effectiveness?


The answers to these questions remain open. The bone resorption marker CTX-1 (a peptide that is cleaved off type I collagen by osteoclasts during bone resorption) was measured up to 60 days after treat- ment of horses with either a single dose of tiludro- nate at 1 mg/kg IV or with 10 daily doses of tiludronate at 0.1 mg/kg IV.16 Significant de- creases were seen only transiently within the first 3 days after treatment was started in either group. This study was performed in sound horses that were not exercised, and CTX-1 response in horses in training with musculoskeletal diseases that affect bone turnover may be different. One could con- clude from this study that sustained suppression of CTX-1 may not be necessary to obtain a treatment effect after IV tiludronate administration, but to prove or disprove this statement, measurements of CTX-1 in horses with navicular disease before and after treatment with bisphosphonates would need to be performed.


Where Does the Dosing Regimen to Treat Every 2 Months Come From?


The author is not certain how this dosing regimen was derived, but an abstract presented at the Ninth International Congress of the European Association for Veterinary Pharmacology and Toxicology43 sug- gested that radioactivity from radioactively labeled tiludronate in equine bones decreased relatively lit- tle for the first 3 months after administration at 1 mg/kg IV, and then decreased more rapidly 3–6 months after administration. Based on extrapola- tion from data in rats it was concluded that tiludro- nate concentrations in equine bone at 6 months were probably not high enough to inhibit bone resorption by 50%.


12. Summary


A subset of horses with lameness due to navicular syndrome seems to improve after IV administration of tiludronate or IM administration of clodronate, but resolution of lameness may not be achieved. Assessment of response should be performed 2–6 months post-treatment and in horses with failure to improve, an additional treatment may result in im-


proved lameness. Horses with a lameness history of less than 6 months are more likely to respond to treatment.


Bisphosphonates can be nephrotoxic and a renal


panel should be obtained prior to treatment. Horses with compromised kidney function are poor candidates for bisphosphonate treatment due to likely worsening of the condition. Bisphosphonates should not be administered con- currently with NSAIDs or other nephrotoxic drugs. Colic is the most common adverse effect of bisphos- phonate administration, but most horses improve with walking only. If medical treatment is war- ranted, N-butylscopolamine, xylazine, detomidine or butorphanol, or a mixture of these can be used. NSAID administration is not recommended. Bisphosphonate administration may be associated


with HYPP episodes in heterozygotes, although the FDA did not come to the same conclusion. No in- formation is available for safety of bisphosphonate treatment in homozygous carriers. The author rec- ommends analyzing the electrolyte status of horses with muscle fasciculations and/or colic signs that do not resolve with walking exercise. According to the FDA approval studies, tiludro-


nate administration (1 mg/kg in 1 L saline IV over 60–90 min) may be accompanied more often with colic signs or alterations of clinical pathologic vari- ables of kidney function and electrolyte homeostasis than clodronate administration (1.4 mg/kg up to 900 mg total distributed into three different injection sites), but these studies were not peer reviewed and their description is incomplete in the FDA Freedom of Information Summaries. Administration of bisphosphonates via routes


other than what is approved by the FDA may not be innocuous or clinically effective and is not currently recommended.


Acknowledgments


Declaration of Ethics The Author has adhered to the Principles of the Veterinary Medical Ethics of the AVMA.


Conflict of Interest The Author declares no conflicts of interest.


References and Footnotes


1. Ohnishi H, Nakamura T, Narusawa K, et al. Bisphospho- nate tiludronate increases bone strength by improving mass and structure in established osteopenia after ovariectomy in rats. Bone 1997;21:335–343. ¨nkko


2. Mo ¨nen J, Koponen HM, Ylitalo P. comparison of the


distribution of three bisphosphonates in mice. Pharmacol Toxicol 1990;66:294–298.


3. Lin JH, Duggan DE, Chen IW, et al. Physiological disposi- tion of alendronate, a potent anti-osteolytic bisphosphonate, in laboratory animals. Drug Metab Dispos 1991;19:926– 932.


4. Gertz BJ, Holland SD, Kline WF, et al. Clinical pharmacol- ogy of alendronate sodium. Osteopor Int 1993;(suppl 3):513– 516.


AAEP PROCEEDINGS  Vol. 62  2016 377


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