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Peer-reviewed veterinary case report

Gene changes in calcium receptor linked to bone disorder in cats

By Geddes, R F et al.·Published in Veterinary journal (London, England : 1997)·2018·Department of Clinical Sciences and Services, United Kingdom·View original on PubMed

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Original publication title: Associations between single nucleotide polymorphisms in the calcium sensing receptor and chronic kidney disease-mineral and bone disorder in cats.

Species:
cat

Plain-English summary

A group of older cats with chronic kidney disease (CKD) were studied to see if certain genetic variations in a calcium receptor could explain differences in their bone and mineral health. Researchers found that one specific genetic change was linked to higher levels of parathyroid hormone, which can affect calcium levels in the body. However, they concluded that these genetic factors likely do not account for most of the differences in bone and mineral disorders seen in cats with CKD. This means that other factors are probably more important in managing these conditions.

People also search for: cat chronic kidney disease symptoms · cat calcium levels treatment · cat kidney disease and bone health

Abstract

Feline chronic kidney disease (CKD) is associated with high variability in severity of CKD-mineral and bone disorder (CKD-MBD). The calcium sensing receptor (CaSR) regulates circulating parathyroid hormone (PTH) and calcium concentrations. Single nucleotide polymorphisms (SNPs) in the CaSR are associated with severity of secondary renal hyperparathyroidism and total calcium concentrations in human patients receiving haemodialysis. The objective of this study was to explore associations between polymorphisms in the feline CaSR (fCaSR) and biochemical changes observed in CKD-MBD. Client owned cats (&#x2265;9years) were retrospectively included. SNP discovery was performed in 20 cats with azotaemic CKD and normal or dysregulated calcium concentrations. Non-pedigree cats (n=192) (125 with azotaemic CKD and 66 healthy), Persians (n=40) and Burmese (n=25) were genotyped for all identified SNPs using KASP. Biochemical parameters from the date of CKD diagnosis or from first visit to the clinic (healthy cats) were used. Associations between genotype and ionized calcium, total calcium, phosphate, PTH and FGF-23 were performed for non-pedigree cats using logistic regression. Sequence alignment against the fCaSR sequence revealed eight novel exonic SNPs. KASP genotyping had high accuracy (99.6%) and a low failure rate (<6%) for all SNPs. Allele frequencies varied between breeds. In non-pedigree cats, one synonymous SNP CaSR:c.1269G>A was associated with logPTH concentration (adjusted for plasma creatinine concentration), with a recessive model having the best fit (G/G vs A/A-G/A, P=0.031). Genetic variation in the fCaSR is unlikely to explain the majority of the variability in presence and severity of CKD-MBD in cats.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29704936/