Effectiveness of a Feed Supplement in Advanced Stages of Feline Chronic Kidney Disease

Authors

  • Diana Vergnano Department of Veterinary Science, University of Turin (UNITO), Grugliasco, TO, Italy.
  • Emanuela Valle Department of Veterinary Science, University of Turin (UNITO), Grugliasco, TO, Italy.
  • Natascia Bruni Istituto Farmaceutico Candioli S.p.A., Beinasco, TO.
  • Rita Rizzi Department of Veterinary Science and Public Health, Milano, MI, Italy.
  • Mauro Bigliati Istituto Farmaceutico Candioli S.p.A., Beinasco, TO.
  • Tiziana Cocca Clinica Veterinaria Napolivet, Napoli, NA, Italy.

DOI:

https://doi.org/10.22456/1679-9216.81082

Keywords:

cats, chronic kidney disease, hyperphosphatemia, metabolic acidosis, feed supplement, phosphate binder.

Abstract

Background: Chronic kidney disease (CKD) is a very common pathology in cats, especially in the geriatric age. A proper renal diet is considered the current standard of care to enhance patients’ long-term survival and quality of life. However, when diet alone is not sufficient, it is necessary to supplement it with specific substances: these are phosphate binders and alkalinizing agents. The aim of this study was to evaluate the effectiveness of a feed supplement containing calcium carbonate, calcium lactate gluconate, chitosan and sodium bicarbonate in controlling hyperphosphatemia and metabolic acidosis in cats with severe CKD (IRIS, International Renal Interest Society, stage 3 and 4).

Materials, Methods & Results: 10 cats (median BW 4.00 (3.20; 5.70) Kg, BCS 3/5 (2.25; 3.75), 11 (8.25;12.00) years) fed with a balanced renal diet were included in the study. To be enrolled in the study cats had to be affected by CKD in stages 3 or 4 and show hyperphosphatemia. Treatment consisted in oral administration of the product (Renal, Candioli Pharma) at 0.2 g/kg/day mixed with the food for 60 days. The animals were evaluated at the beginning of the study and at 15, 30, 60 days (T0, T15, T30, T60) for: clinical condition, BW, BCS, blood pressure and for routinely hematochemical, biochemical and urinary parameters. Owners were asked to assess appetite of the cat, palatability of the supplement, presence of vomit and/or diarrhoea, general health and vitality. All statistical analyses were performed using SAS software. After checking normality data were analyzed using Kruskal-Wallis and Wilcoxon tests. Results are expressed as median (interquartile range). For the parameters P (P < 0.0001), iCa (P = 0.0008) and HCO3 (P = 0.0002) there were statistically significant differences among times of supplementation (T0, T15, T30, T60). Statistically significant reduction of serum phosphorus concentration was obtained through the study (reduction of 59% at T60 vs T0). Also a statistically significant increase of bicarbonate was seen (7% from T0 to T60). At T60 was also recorded an increase of ionized calcium level, which however was in normal range. For the other laboratory parameters, no statistical difference was recorded. All the owners reported a good palatability of the product. The decrease of vomit and diarrhea episodes and the increase of the appetite reported were statistically significant (P < 0.05).

Discussion: The restriction of available dietary phosphorus is now recognised as one of the major contributors in slowing the disease progression and improving survival rates. Phosphate binders are able to absorb phosphate (P) in the intestine, forming insoluble products that are eliminated with the faeces, thus decreasing serum phosphate levels. The phosphate binders contained in the product tested in the present trial were chitosan, calcium lactate gluconate and calcium carbonate. During the study P decreased significantly from T0 to T60, reaching the target post-treatment plasma P concentration for IRIS stage 3 after 30 days. Another important recommendation for CKD treatment is to use alkalinisation therapy if metabolic acidosis is present. The feed supplement tested in this study also contained sodium bicarbonate. In our study, 90% of the patients at the inclusion examination had metabolic acidosis. At the end of the study, the median blood bicarbonate concentration was in the normal range, thus reaching the IRIS treatment target. The feed supplement tested was therefore effective in reducing blood phosphate levels and in increasing blood bicarbonate levels, thus improving the cats’ clinical conditions for the duration of the study without any adverse effect.

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References

Adeva-Andany M.M., Fernández-Fernández C., Mouriño-Bayolo D., Castro-Quintela E. & Domínguez-Montero A. 2014. Sodium bicarbonate therapy in patients with metabolic acidosis. The Scientific World Journal. 2014: 627-673.

Bernachon N., Fournel S., Gatto H., Monginoux P. & Mcgahie D. 2014. Comparative palatability of five supplements designed for cats suffering from chronic renal disease. Irish Veterinary Journal. 67: 10-15.

Brown S.A., Rickertsen M. & Sheldon S. 2008. Effects of an intestinal phosphorus binder on serum phosphorus and parathyroid hormone concentration in cats with reduced renal function. International Journal of Applied Research in Veterinary Medicine. 6: 155-160.

Chakrabarti S., Syme H.M. & Elliott J. 2012. Clinicopathological variables predicting progression of azotemia in cats with chronic kidney disease. Journal of Veterinary Internal Medicine. 26: 275-281.

Chen W. & Abramowitz M.K. 2014. Metabolic acidosis and the progression of chronic kidney disease. BMC Nephrology. 15: 55-62.

Elliott J. 2008. Retrospective analysis of dietary management of hyperphosphatemia in cats with CKD. Veterinary Focus. 18: 45-47.

Elliott J. 2008. Hyperphosphataemia and CKD. Veterinary Times. 38: 12-16.

Elliott J., Rawlings J.M., Markwell P.J. & Barber P.J. 2000. Survival of cats with naturally occurring chronic renal failure: effect of dietary management. Journal of Small Animal Practice. 41: 235-242.

Emmett M. 2006. A comparison of calcium-based phosphorus binders for patients with chronic kidney disease. Dialysis & Transplantation. 35 (5): 284-293.

Fédération européenne de l’industrie des aliments pour animaux familiers (FEDIAF). 2014. Nutritional Guidelines For Complete And Complementary Pet Food For Cats And Dogs. Disponível em: http://www.fediaf.org/self-regulation/ nutrition/. [Accessed December 2015].

Ferlizza E., Campos A., Neagu A., Cuoghi A., Bellei E., Monari E., Dondi F., Almeida A.M. & Isani G. 2015. The effect of chronic kidney disease on the urine proteome in the domestic cat (Felis catus). Veterinary Journal. 204: 73-81.

Forrester S.D., Adams L.G. & Allen T.A. 2010. Chronic Kidney Disease. In: Hand M., Thatcher C., Remillard R., Roudebush P. & Novotny B.J. (Eds). Small Animal Clinical Nutrition. 5th edn. Topeka: Mark Morris Institute, pp.765-810.

Fritsch D.A., Jewell D.E., Leventhal P.S., Brejda J., Ahle N.W., Schiefelbein H.M. & Forrester S.D. 2015. Acceptance and effects of a therapeutic renal food in pet cats with chronic kidney disease. Veterinary Record Open. 13:2(2): e000128-e000134.

Geddes R.F., Finch N.C., Syme H.M. & Elliott J. 2013. The role of phosphorus in the pathophysiology of chronic kidney disease. Journal of Veterinary Emergency and Critical Care. 23: 122-133.

Greene J.P., Lefebvre S.L., Wang M., Yang M., Lund E.M. & Polzin D.J. 2014. Risk factors associated with the development of chronic kidney disease in cats evaluated at primary care veterinary hospitals. Journal of the American Veterinary Medicine Association. 244: 320-327.

Hill K.M., Martin B.R., Wastney M.E., McCabe G.P., Moe S.M., Weaver C.M. & Peacock M. 2013. Oral calcium carbonate affects calcium but not phosphorus balance in stage 3-4 chronic kidney disease. Kidney International. 83(5): 959-66.

International Renal Interest Society (IRIS). 2013. Elanco Animal Health. Treatment Recommendations for CKD in Cats (2013). Disponível em: http://iris-kidney.com/guidelines/recommendations.aspx. [Accessed December 2015].

International Renal Interest Society (IRIS). 2013. Elanco Animal Health. CKD Staging in Cats (2013). Disponível em: http://iris-kidney.com/guidelines/staging.aspx. [Accessed December 2015].

Kalaitzidis R.G. & Elisaf M.S. 2014. Hyperphosphatemia and phosphate binders: effectiveness and safety. Current Medical Research and Opinion. 30: 109-112.

King J.N., Tasker S., Gunn-Moore D.A., Strehlau G. & the BENRIC (Benazepril In Renal Insufficiency In Cats) Study Group. 2007. Prognostic factors in cats with chronic kidney disease. Journal of Veterinary Internal Medicine. 21: 906-916.

Korman R.M. & White J.D. 2013. Feline CKD: Current therapies - what is achievable? Journal of Feline Medicine and Surgery. 15(Suppl 1): 29-44.

Lawson J., Elliott J., Wheeler-Jones C., Syme H. & Jepson R. 2015. Renal fibrosis in feline chronic kidney disease: known mediators and mechanisms of injury. Veterinary Journal. 203: 18-26.

Oh M.S. & Uribarri J. 2014. What can we learn from the saga of chitosan gums in hyperphosphatemia therapy? Clinical Journal of the American Society of Nephrology. 9: 967-970.

Pettifer G. 2002. Fluids, Electrolytes, and Acid-Base Therapy. In: Slatter D.H. (Ed). Textbook of Small Animal Surgery. 3rd edn. Philadelphia: Saunders, pp.17-43.

Polzin D.J. 2011. Chronic kidney disease in small animals. Veterinary Clinics of North America: Small Animal Practice. 41: 15-30.

Polzin D.J. 2013. Evidence-based step-wise approach to managing chronic kidney disease in dogs and cats. Journal of Veterinary Emergency and Critical Care. 23: 205-215.

Takashima T., Sanai T., Miyazono M., Fukuda M., Kishi T., Nonaka Y., Yoshizaki M., Sato S. & Ikeda Y. 2014. A comparison of the long-term effects of lanthanum carbonate and calcium carbonate on the course of chronic renal failure in rats with adriamycin-induced nephropathy. PLoS One 9(5): e97859.

Thatcher C.D., Hand M.S. & Remillard R.L. 2010. Small Animal Clinical Nutrition: An Iterative Process. In: Hand M., Thatcher C., Remillard R., Roudebush P. & Novotny B.J. (Eds). Small Animal Clinical Nutrition. 5th edn. Topeka: Mark Morris Institute, pp.3-21.

Wagner E., Schwendenwein I. & Zentek J. 2004. Effects of a dietary chitosan and calcium supplement on Ca and P metabolism in cats. Berliner und Münchener Tierärztliche Wochenschrift. 117: 310-315.

Zatelli A., Pierantozzi M., D’ippolito P., Bigliati M. & Zini E. 2012. Effect of dietary supplements in reducing probability of death for uremic crises in dogs affected by chronic kidney disease (masked RCCT). The Scientific World Journal. 2012: 219082-219088.

Published

2016-01-01

How to Cite

Vergnano, D., Valle, E., Bruni, N., Rizzi, R., Bigliati, M., & Cocca, T. (2016). Effectiveness of a Feed Supplement in Advanced Stages of Feline Chronic Kidney Disease. Acta Scientiae Veterinariae, 44(1), 8. https://doi.org/10.22456/1679-9216.81082

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Articles