Abstract
It has been reported that wet foods for dogs and cats have high levels of sodium and phosphorus due to their composition. Therefore, this study aimed to evaluate the sodium and phosphorus contents in wet pet foods, and compare it to daily requirements for both species. Twenty‐five commercial wet foods for adult animals were evaluated, 13 for dogs and 12 for cats. The analyses’ results were compared to the European Pet Food Industry Federation (FEDIAF 2018) recommendations. All foods contained phosphorus and sodium amounts above minimum requirements. Three wet foods for dogs exceeded the safe upper limit for phosphorus, and four wet foods for dogs and three for cats exceeded 3.75 g of sodium/1,000 kcal metabolizable energy (ME), considered safe by FEDIAF. No studies were found at the present time evaluating whether higher sodium levels are safe for dogs and cats; however, consumption of high phosphorus diets has been associated with adverse effects on renal function parameters. Therefore, more studies are necessary to investigate the health implications of phosphorus and sodium concentrations observed in some foods evaluated in this research.
Keywords: minerals, nutritional profile, pet food, phosphate, safe upper limit
It has been reported that wet foods for dogs and cats have high levels of sodium and phosphorus due to their composition. Therefore, this study aimed to evaluate the sodium and phosphorus contents in wet pet foods, and compared to daily requirements for both species.
1. INTRODUCTION
Studies point out that offering wet foods may be an important way to increase water intake, especially for cats and some small dog breeds, such as Miniature Schnauzer, and this may be a key factor in the prevention and treatment of uroliths (Buckley, Hawthorne, Colyer, & Stevenson, 2011; Seefeldt & Chapman, 1979).
Another way to stimulate water intake is increasing dietary sodium intake (Chandler, 2008; Hawthorne & Markwell, 2004). However, increasing sodium may be contradictory due to its possible harmful effects such as hypertension, progression of renal and heart diseases, hypercalciuria, and increased risk of urolith formation (Nguyen, Reynolds, Zentek, Paßlack, & Leray, 2017). In this context, phosphorus may also be a key factor as its increased intake may be related to increased risk of urolith formation (Lulich et al., 2016) and development of chronic kidney disease (CKD) (Böswald, Kienzle, & Dobenecker, 2018; Dobenecker, Webel, Reese, & Kienzle, 2018), as well as speeding progression of this disease in dogs and cats (Osborne, 1995).
It has been reported that wet foods for dogs and cats have high levels of sodium and phosphorus due to their composition of mainly fresh meats (Crane et al., 2011). However, in the literature, there is only one study that evaluated levels of phosphorus and sodium in wet foods commercialized in the United Kingdom (Davies et al., 2017). These authors observed that concentrations of both minerals were higher in wet foods when compared to dry foods.
Due to a lack of information in the literature regarding the nutritional profile of wet foods, the present study aimed to analyse phos European Pet Food Industry phorus and sodium contents and compare them to FEDIAF (2018) nutritional requirements.
2. MATERIAL AND METHODS
2.1. Wet foods
Twenty‐five wet foods were selected based on the availability in major pet stores in the cities of Pirassununga and Campinas (Sao Paulo/Brazil). Thirteen of these wet foods were products for adult dogs and 12 were for adult cats, and were all manufactured by 13 different companies. Of the 25 wet foods, 11 were international brands and 14 were national brands.
2.2. Chemical analysis
Analyses of sodium and phosphorus contents were performed at the Multiuser Laboratory of Animal Nutrition and Bromatology at the Department of Animal Nutrition and Production of the School of Veterinary Medicine and Animal Science, and the Agrarian Laboratory of the Department of the School of Animal Science and Food Engineering, both of the University of Sao Paulo.
Phosphorus concentrations were measured by spectrophotometry (Caputi, 2013) and sodium concentrations were obtained by atomic absorption spectrophotometry (AOAC, 2007). All analyses were performed in duplicate and repeated when variation over 5% was observed.
Phosphorus and sodium contents were calculated in grams (g) per 1,000 kilocalories (kcal) of metabolizable energy (ME). ME was estimated by the most current method, described in NRC (2006), which consists of different methods for estimating metabolizable energy for dog and cat foods.
3. RESULTS
Based on FEDIAF (2018) daily requirements, all 13 wet foods for dogs and 12 for cats presented higher phosphorus concentrations than these recommendations (Tables 1 and 2), considering energy intake of 95 kcal/kg BW0.75 for dogs and 100 kcal/kg BW0.67 for cats, which are the most commonly used equations to calculate daily energy requirement of these species. Of all foods analysed, 10 for dogs and seven for cats had phosphorus concentrations over twice the recommendations (Tables 1 and 2). Three of the diets for adult dogs presented phosphorus concentrations higher than 4 g/1,000 kcal ME, which is the nutritional limit for healthy adult dogs according to FEDIAF (2018).
Table 1.
Phosphorus (g /1,000 Kcal ME) | Phosphorus supplya (%) | Sodium (g/1,000 Kcal ME) | Sodium supplya (%) | |
---|---|---|---|---|
FEDIAF for dogsb (minimum/maximum) | 1.16/4.00 | – | 0.29/3.75 | – |
Food A | 3.60 | 310 | 4.04 | 1,394 |
Food B | 3.35 | 289 | 4.38 | 1,512 |
Food C | 1.10 | 95 | 2.88 | 994 |
Food D | 4.34 | 374 | 3.51 | 1,211 |
Food E | 3.63 | 313 | 4.66 | 1,608 |
Food F | 3.65 | 315 | 3.29 | 1,134 |
Food G | 2.70 | 233 | 1.95 | 672 |
Food H | 4.26 | 367 | 3.20 | 1,104 |
Food I | 1.83 | 158 | 2.59 | 894 |
Food J | 1.64 | 141 | 1.87 | 646 |
Food K | 3.26 | 281 | 3.39 | 1,167 |
Food L | 4.08 | 351 | 3.53 | 1,216 |
Food M | 3.24 | 279 | 4.44 | 1,532 |
Mean ± SD c | 3.13 ± 1.03 | 270 ± 89 | 3.36 ± 0.89 | 1,160 ± 306 |
Table 2.
Phosphorus (g /1,000 Kcal ME) | Phosphorus supplya (%) | Sodium (g/1,000 Kcal ME) | Sodium supplya (%) | |
---|---|---|---|---|
FEDIAF for catsb (minimum/maximum) | 1.25/− | 0.19/3.75 | ||
Food A | 2.13 | 170 | 1.68 | 885 |
Food B | 3.55 | 284 | 2.39 | 1,259 |
Food C | 2.74 | 219 | 3.11 | 1,638 |
Food D | 5.29 | 423 | 3.07 | 1,617 |
Food E | 2.25 | 180 | 0.86 | 451 |
Food F | 4.36 | 349 | 4.11 | 2,162 |
Food G | 3.96 | 317 | 4.67 | 2,460 |
Food H | 1.67 | 134 | 2.12 | 1,114 |
Food I | 1.74 | 139 | 1.06 | 557 |
Food J | 4.89 | 392 | 5.64 | 2,966 |
Food K | 1.88 | 150 | 1.40 | 738 |
Food L | 2.64 | 211 | 2.97 | 1,561 |
Media ± SD c | 3.09 ± 1.28 | 247 ± 102 | 2.76 ± 1.48 | 1,451 ± 779 |
Sodium concentrations of all wet foods were above recommended intake according to FEDIAF (2018) (Tables 1 and 2). Nine wet foods for dogs and eight for cats exceeded by more than 10 times the recommendations of sodium (Tables 1 and 2). Seven of the 25 wet foods (four for dogs and three for cats) had sodium amounts higher than 3.75 g/1,000 kcal, the safe upper limit for both dogs and cats established by FEDIAF (2018).
4. DISCUSSION
This study showed that high sodium values were present in the wet foods evaluated, and seven of the 25 products had sodium levels above the safe upper limit according to FEDIAF (2018). However, FEDIAF (2018) states that perhaps higher levels may be safe, but no scientific data are available.
Despite the potential benefit of increased water intake associated with higher sodium contents in pet food (Chandler, 2008), excessive ingestion of sodium by humans has been associated with increased risk of developing systemic arterial hypertension, cardiac disease (Institute of Medicine, 2004; Strazzullo, D'Elia, Kandala, & Cappuccio, 2009; WHO, 2007), nephropathies (Ritz, Koleganova, & Piecha, 2009), damage to gastric mucosa and gastric tumours (Kono, Ikeda, & Ogata, 1983; Tsugane & Sasazuki, 2007).
Short‐ and medium‐term studies using either healthy adult cats, healthy older cats and dogs or cats with induced chronic kidney disease did not observe harmful effects of high sodium intake (2.9–3.2 g Na/1,000 kcal) on blood pressure (Buranakarl, Mathur, & Brown, 2004; Cowgill, Segev, & Bandt, 2007; Greco, Lees, Dzendzel, Komkov, & Carter, 1994; Kirk, Jewell, & Lowry, 2006; Xu, Laflamme, & Long, 2009). The absence of negative effects despite high sodium intake may be explained by the presence of mechanisms that control the organism's sodium balance, like the interaction between vascular pressure receptors, renal sympathetic enervation and vasopressin hormone, renin‐angiotensin‐aldosterone system, and natriuretic peptides (Bartges, 2012). This may also explain the range between minimum recommendation (0.29 g/1,000 kcal for dogs and 0.19 g/1,000 kcal for cats) and safe upper limit (3.75 g/1,000 kcal for both dogs and cats) according to FEDIAF (2018).
The effect of high sodium content in pet foods is controversial, especially for pets that have systemic arterial hypertension, and the consensus of management of this disease recommends avoiding the excessive consumption without necessarily indicating decreasing this mineral's intake (Brown et al., 2007).
In older cats, a sodium intake of 3.1 g/1,000 kcal did not increase the risk of myocardial dysfunction or glomerular filtration rate (Chetboul et al., 2014; Reynolds et al., 2013). However, dogs diagnosed with congestive heart failure seem to benefit from diets with low sodium levels (0.4 g/1,000 kcal) when compared to moderate sodium levels (0.7 g/1,000 kcal) (Rush et al., 2000). None of the studies above‐mentioned have used more than 3.75 g of sodium per 1,000 kcal content considered safe by FEDIAF differently from our study, in which seven wet foods exceeded this amount.
The safe upper limit for sodium intake is also suggested by the consensus for treatment and prevention of urolith formation in dogs and cats (Lulich et al., 2016). High sodium intake has been associated with hypercalciuria, which may pre‐dispose patients to formation of calcium and struvite uroliths (Kirk et al., 2006). Lekcharoensuk et al. (2001) observed that out of 290 cats, those who had high sodium intake (1.42–3.71 g/1,000 kcal) for 6 months presented 4.1 times more chances of developing struvite uroliths when compared to cats that had an intake of 0.48–0.77 g/1,000 kcal. However, there was a correlation found between high sodium and high phosphorus contents, which may have influenced the results.
Regarding phosphorus content, in the present study, three wet foods for dogs presented levels above the safe upper limit according to FEDIAF (2018). There is no established safe upper limit by FEDIAF (2018) for phosphorus in cats.
As water intake by consuming wet foods is increased which therefore decreases dehydration and increases diuresis, this type of food may be prescribed for patients with uroliths (Buckley et al., 2011; Seefeldt & Chapman, 1979). However, of the 25 wet foods evaluated in this study, three products for dogs had phosphorus levels above the safe upper limit recommended by FEDIAF (2018), which can be pre‐judicial because high phosphorus intake is associated with struvite uroliths and may even make it harder to dissolve these uroliths (Abdullahi, Osborne, Leininger, Fletcher, & Griffith, 1984; Osborne, Lulich, Forrester, & Albasan, 2009).
The consumption of high phosphorus diets is associated with adversely affecting renal function parameters in healthy cats (Dobenecker et al., 2018) and also with an increased risk of developing chronic kidney disease (CKD) in this species (Böswald et al., 2018). Dobenecker et al. (2018) observed that cats consuming a diet with a phosphorus content five times higher (1.6% phosphorus in dry matter) than the minimum requirement had decreased creatinine clearance and increased renal phosphorus excretion when compared to the control group which consumed a diet with 0.56% of phosphorus in dry matter. These authors also observed glycosuria and microalbuminuria in nine of the 13 cats in the high phosphorus diet group. In a retrospective study, Böswald et al. (2018) observed that cats with CKD consumed a greater amount of phosphorus in the period prior to diagnosis, compared to older cats who did not present with CKD.
It is important to consider the type of phosphorus involved when establishing and evaluating its content in foods, because organic and inorganic forms have different physiological effects. While the organic form binds to proteins resulting in lower absorption, the inorganic phosphorus is absorbed much more readily, making its excess potentially more harmful to animals. Coltherd et al. (2018) observed that addition of inorganic phosphorous salts in the diet at levels from 0.5 g/1,000 kcal is able to increase plasma phosphorus in cats. Meanwhile, the authors did not verify changes in plasma phosphorus concentration after the ingestion of organic phosphorus. A harmful effect of the inorganic form of phosphorus was described by Alexander et al. (2018) in a study evaluating high inclusion of inorganic phosphorus in a diet for healthy cats. Authors observed loss of renal function and changes in echogenicity suggestive of renal pathology, observed by ultrasonography, after high phosphorus intake.
In dogs, Herbst and Dobenecker (2018) also observed that diets containing inorganic sources of phosphorus (2.1% in dry matter) were more efficient in increasing postprandial serum concentrations of phosphorus and parathyroid hormone (PTH) when compared to organic sources, as well as in increasing the area under the curve of PTH. Dogs fed diets with inorganic phosphorus sources had calcium vs. phosphorus serum product exceeding 2.1 times the recommended (55 mg2/dl2).
Furthermore, hyperphosphataemia is related to progression of CKD, because it stimulates parathyroid hormone secretion and consequently secondary renal hyperparathyroidism (SRHP), which increases nephron loss (Osborne, 1995). Several studies showed that phosphorus restriction is beneficial to dogs and cats with induced and naturally acquired CKD (Barber, Rawlings, Markweu, & Elliott, 1999; Bonder et al., 2016; Brunetto et al., 2016; Lopez‐Hilker, Dusso, Rapp, Martin, & Slatopolsky, 1990; Ross et al., 2006; Ross, Finco, & Crowell, 1982; Slatopolsky et al., 1971). Moreover, there is evidence that dogs and cats with low phosphorus intake had an increase in survival time (Elliott, Rawlings, Markwell, & Barber, 2000; Jacob et al., 2002; Ross et al., 2006).
The limitations of the present study are the small number of foods evaluated, the fact that calcium content of the products was not analysed, and estimating metabolizable energy with the use of a prediction equation rather than analysing.
5. CONCLUSION
High phosphorus and sodium concentrations were observed in most of the evaluated foods. Some of them exceeded safe upper limits established by the European Pet Food Industry (FEDIAF 2018). With regard to phosphorus, this high content might be harmful when consumed in long term. On the other hand, in relation to sodium, further studies are needed to investigate whether concentrations found in this study are safe for dogs and cats. Therefore, several wet foods evaluated in the present study are not recommended, although available in the pet food market. This study provides a stimulus for the pet food industry to review its formulations and inclusion of mineral supplements as well as to promote constant assessments of their products.
CONFLICT OF INTEREST
The authors declare that they have no conflict of interest.
ETHICAL APPROVAL
The authors confirm that the ethical policies of the journal, as noted on the journal's author guidelines page, have been adhered to. No ethical approval was required as this is an article that does not use animals or their tutors.
CONTRIBUTIONS
Study design was performed by R.V.A.Z. and M.A.B. All authors participated in the manuscript writing and review process. Laboratorial analyses were performed by R.V.A.Z.
ACKNOWLEDGEMENTS
We thank Renata Maria Consentino Conti, Simi Luisa Durante Aflalo and Marcos Roberto Ferraz for technical assistance.
Brunetto MA, Zafalon RVA, Teixeira FA, et al. Phosphorus and sodium contents in commercial wet foods for dogs and cats. Vet Med Sci. 2019;5:494–499. 10.1002/vms3.183
Funding Information
This study was supported by FUNEP fund.
REFERENCES
- Abdullahi, S. U. , Osborne, C. A. , Leininger, J. R. , Fletcher, T. F. , & Griffith, D. P. (1984). Evaluation of a calculolytic diet in female dogs with induced struvite urolithiasis. American Journal of Veterinary Research, 45, 1508–1519. [PubMed] [Google Scholar]
- Alexander, J. , Stockman, J. , Atwal, J. , Butterwick, R. , Colyer, A. , Elliott, D. , Gilham, M. , Morris, P. , Staunton, R. , Renfrew, H. , Elliott, J. , & Watson, P. (2018). Effects of the long‐term feeding of diets enriched with inorganic phosphorus on the adult feline kidney and phosphorus metabolism. British Journal of Nutrition, 21, 1–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- AOAC (2007). Official Methods of Analysis, 16th ed. Washington, DC: Association of Official Analytical Chemists. [Google Scholar]
- Barber, P. J. , Rawlings, J. M. , Markweu, P. J. , & Elliott, J. (1999). Effect of dietary phosphate restriction on renal secondary hyperparathyroidism in the cat. Journal of Small Animal Practice, 40, 62–70. [DOI] [PubMed] [Google Scholar]
- Bartges, J. W. (2012). Chronic kidney disease in dogs and cats. Veterinary Clinics of North America: Small Animal Practice, 42, 669–692. [DOI] [PubMed] [Google Scholar]
- Bonder, B. S. , Halfen, D. P. , Caragelasco, D. S. , Pontieri, C. F. F. , Jeremias, J. T. , Kogika, M. M. , & Brunetto, M. A. (2016). Influence of renal enriched diet in inflammatory profile and antioxidant capacity in dogs with chronic kidney disease. Chicago: WALTHAM International Nutritional Sciences Symposium. [Google Scholar]
- Böswald, L. F. , Kienzle, E. , & Dobenecker, B. (2018). Observation about phosphorus and protein supply in cats and dogs prior to the diagnosis of chronic kidney disease. Journal of animal physiology and animal nutrition, 102, 31–36. [DOI] [PubMed] [Google Scholar]
- Brown, S. , Atkins, C. , Bagley, R. , Carr, A. , Cowgill, L. , Davidson, M. , & Littman, M. (2007). Guidelines for the identification, evaluation, and management of systemic hypertension in dogs and cats. Journal of Veterinary Internal Medicine, 21, 542–558. [DOI] [PubMed] [Google Scholar]
- Brunetto, M. , Caragelasco, D. S. , Kogika, M. M. , Halfen, D. P. , Pontieri, C. F. F. , Jeremias, J. T. , & Sucupira, M. C. A. (2016). Evaluation of phosphorus metabolism in dogs with chronic kidney disease under renal diet: Serum parathormone and fibroblast growth factor 23 (FGF‐23). Chicago: WALTHAM International Nutritional Sciences Symposium. [Google Scholar]
- Buckley, C. M. , Hawthorne, A. , Colyer, A. , & Stevenson, A. E. (2011). Effect of dietary water intake on urinary output, specific gravity and relative supersaturation for calcium oxalate and struvite in the cat. British Journal of Nutrition, 106, 128–130. [DOI] [PubMed] [Google Scholar]
- Buranakarl, C. , Mathur, S. , & Brown, S. A. (2004). Effects of dietary sodium chloride intake on renal function and blood pressure in cats with normal and reduced renal function. American Journal of Veterinary Research, 65, 620–627. [DOI] [PubMed] [Google Scholar]
- Caputi, B. (2013). Compêndio Brasileiro de Alimentação Animal, 4th ed. São Paulo: Sindirações. [Google Scholar]
- Chandler, M. L. (2008). Pet food safety: Sodium in pet foods. Topics in Companion Animal Medicine, 23, 148–153. [DOI] [PubMed] [Google Scholar]
- Chetboul, V. , Reynolds, B. S. , Trehiou‐Sechi, E. , Nguyen, P. , Concordet, D. , Sampedrano, C. C. , Testault, I. , Elliott, J. , Abadie, J. , Biourge, V. , & Lefebvre, H. P. (2014). Cardiovascular effects of dietary salt intake in aged healthy cats: A 2‐year prospective randomized, blinded, and controlled study. PLoS ONE, 9, e97862. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coltherd, J. C. , Staunton, R. , Colyer, A. , Thomas, G. , Gilham, M. , Logan, D. W. , Butterwick, R. , & Watson, P. (2018). Not all forms of dietary phosphorus are equal: An evaluation of postprandial phosphorus concentrations in the plasma of the cat. British Journal of Nutrition, 121, 270–284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cowgill, L. D. , Segev, G. , & Bandt, C. (2007). Effects of dietary salt intake on body fluid volume and renal function in healthy cats. Journal of Veterinary Internal Medicine, 21, 600. [Google Scholar]
- Crane, S. W. , Cowell, C. S. , Stout, N. P. , Moser, E. A. , Mellican, J. , & Romano, P . (2011). Commercial pet foods In Hand M. S., Thatcher C. D., Remillard R. L., Roudebush P. & Novotny B. J. (Eds.), Small animal clinical nutrition (pp. 157–190). 5th ed Topeka, KS: Mark Morris Institute. [Google Scholar]
- Davies, M. , Alborough, R. , Jones, L. , Davis, C. , Williams, C. , & Gardner, D. S. (2017). Mineral analysis of complete dog and cat foods in the UK and compliance with European guidelines. Scientific Reports, 7(1), 17107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dobenecker, B. , Webel, A. , Reese, S. , & Kienzle, E. (2018). Effect of a high phosphorus diet on indicators of renal health in cats. Journal of feline medicine and surgery, 20(4), 339–343. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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. [DOI] [PubMed] [Google Scholar]
- FEDIAF (2018). Nutritional guidelines for complete and complementary pet food for cats and dogs. Belgium: European Pet Food Industry Federation Brussels. [Google Scholar]
- Greco, D. S. , Lees, G. E. , Dzendzel, G. S. , Komkov, A. , & Carter, A. B. (1994). Effect of dietary sodium intake on glomerular filtration rate in partially nephrectomized dogs. American Journal of Veterinary Research, 55, 152–159. [PubMed] [Google Scholar]
- Hawthorne, A. J. , & Markwell, P. J. (2004). Dietary sodium promotes increased water intake and urine volume in cats. The Journal of Nutrition, 134, 2128–2129. [DOI] [PubMed] [Google Scholar]
- Herbst, S. , & Dobenecker, B. (2018). Effects of phosphorus addition from organic and inorganic sources on kinetics of selected blood parameters in dogs. Munich: ESVCN European society of Veterinary & Comparative Nutrition Congress. [Google Scholar]
- Institute of Medicine (2004). Dietary reference intakes for water, potassium, sodium, chloride, and sulfate. Washington, DC, USA: The National Academies Press. [Google Scholar]
- Jacob, F. , Polzin, D. J. , Osborne, C. A. , Allen, T. A. , Kirk, C. A. , Neaton, J. D. , Lekcharoensuk, C. , & Swanson, L. L. (2002). Clinical evaluation of dietary modification for treatment of spontaneous chronic renal failure in dogs. Journal of the American Veterinary Medical Association, 220, 1163–1170. [DOI] [PubMed] [Google Scholar]
- Kirk, C. A. , Jewell, D. E. , & Lowry, S. R. (2006). Effects of sodium chloride on selected parameters in cats. Veterinary Therapeutics, 7, 333e46.. [PubMed] [Google Scholar]
- Kono, S. , Ikeda, M. , & Ogata, M. (1983). Salt and geographical mortality of gastric cancer and stroke in Japan. Journal of Epidemiology & Community Health, 37, 43–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lekcharoensuk, C. , Osborne, C. A. , Lulich, J. P. , Pusoonthornthum, R. , Kirk, C. A. , Ulrich, L. K. , Koehler, L. A. , Carpenter, K. A. , & Swanson, L. L. (2001). Association between dietary factors and calcium oxalate and magnesium ammonium phosphate urolithiasis in cats. Journal of the American Veterinary Medical Association, 219, 1228–1237. [DOI] [PubMed] [Google Scholar]
- Lopez‐Hilker, S. , Dusso, A. S. , Rapp, N. S. , Martin, K. J. , & Slatopolsky, E. (1990). Phosphorus restriction reverses hyperparathyroidism in uremia independent of changes in calcium and calcitriol. American Journal of Physiology‐Renal Physiology, 259, F432–F437. [DOI] [PubMed] [Google Scholar]
- Lulich, J. P. , Berent, A. C. , Adams, L. G. , Westropp, J. L. , Bartges, J. W. , & Osborne, C. A. (2016). ACVIM small animal consensus recommendations on the treatment and prevention of uroliths in dogs and cats. Journal of Veterinary Internal Medicine, 30, 1564–1574. [DOI] [PMC free article] [PubMed] [Google Scholar]
- National Research Council (2006). Nutrient requirements of dogs and cats. Washington, D.C. : National Academies Press. [Google Scholar]
- Nguyen, P. , Reynolds, B. , Zentek, J. , Paßlack, N. , & Leray, V. (2017). Sodium in feline nutrition. Journal of Animal Physiology and Animal Nutrition, 101, 403–420. [DOI] [PubMed] [Google Scholar]
- Osborne, C. A . (1995). Canine and feline nephrology and urology. A clinician's analysis of Urinarysis, 136–205.
- Osborne, C. A. , Lulich, J. P. , Forrester, D. , & Albasan, H. (2009). Paradigm changes in the role of nutrition for the management of canine and feline urolithiasis. Veterinary Clinics of North America: Small Animal Practice, 39, 127–141. [DOI] [PubMed] [Google Scholar]
- Reynolds, B. S. , Chetboul, V. , Nguyen, P. , Testault, I. , Concordet, D. V. , Carlos, S. C. , Elliott, J. , Trehiou‐Sechi, E. , Abadie, J. , Biourge, V. , & Lefebvre, H. P. (2013). Effects of dietary salt intake on renal function: A 2‐year study in healthy aged cats. Journal of Veterinary Internal Medicine, 27, 507–515. [DOI] [PubMed] [Google Scholar]
- Ritz, E. , Koleganova, N. , & Piecha, G. (2009). Role of sodium intake in the progression of chronic kidney disease. Journal of Renal Nutrition, 19, 61–62. [DOI] [PubMed] [Google Scholar]
- Ross, L. A. , Finco, D. R. , & Crowell, W. A. (1982). Effect of dietary phosphorus restriction on the kidneys of cats with reduced renal mass. American Journal of Veterinary Research, 43, 1023–1026. [PubMed] [Google Scholar]
- Ross, S. J. , Osborne, C. A. , Kirk, C. A. , Lowry, S. R. , Koehler, L. A. , & Polzin, D. J. (2006). Clinical evaluation of dietary modification for treatment of spontaneous chronic kidney disease in cats. Journal of the American Veterinary Medical Association, 229, 949–957. [DOI] [PubMed] [Google Scholar]
- Rush, J. E. , Freeman, L. M. , Brown, D. J. , Brewer, B. P. , Ross, J. N. , & Markwell, P. J. (2000). Clinical, echocardiographic, and neurohormonal effects of a sodium‐restricted diet in dogs with heart failure. Journal of Veterinary Internal Medicine, 14, 513–520. [DOI] [PubMed] [Google Scholar]
- Seefeldt, S. L. , & Chapman, T. E. (1979). Body water content and turnover in cats fed dry and canned rations. American Journal of Veterinary Research, 40, 183–185. [PubMed] [Google Scholar]
- Slatopolsky, E. , Caglar, S. , Pennell, J. P. , Taggart, D. D. , Canterbury, J. M. , Reiss, E. , & Bricker, N. S. (1971). On the pathogenesis of hyperparathyroidism in chronic experimental renal insufficiency in the dog. Journal of Clinical Investigation, 50, 492–499. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strazzullo, P. , D'Elia, L. , Kandala, N. B. , & Cappuccio, F. P. (2009). Salt intake, stroke, and cardiovascular disease: Meta‐analysis of prospective studies. BMJ, 339, b4567. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsugane, S. , & Sasazuki, S. (2007). Diet and the risk of gastric cancer: Review of epidemiological evidence. Gastric Cancer, 10, 75–83. [DOI] [PubMed] [Google Scholar]
- World Health Organization (2007). Prevention of cardiovascular disease. Geneva, Switzerland: : World Health Organization. [Google Scholar]
- Xu, H. , Laflamme, D. P. L. , & Long, G. L. (2009). Effects of dietary sodium chloride onhealth parameters in mature cats. Journal of Feline Medicine and Surgery, 11, 435–441. [DOI] [PMC free article] [PubMed] [Google Scholar]