Back to results
Bibliographic record · Consultation and access
Artículo

Risk factors and implications associated with renal mineralization in chronic kidney disease in cats

Pak‐Kan Tang et al · Oxford University Press · 2022

Open access available
Quick overview. Review the resource’s basic details, then access the content using the main button. This page shows only the information needed to identify, cite, and open the work.
Serial publication

A de novo nonsense variant in the DMD gene associated with X‐linked dystrophin‐deficient muscular dystrophy in a cat

This serial publication contains 149 related contents.

Resource access

Open the content from the main option or choose another available source.

DOAJ DOAJ Articles
Entrar por DOAJ
Main access

Open access available

Recurso identificado como acceso abierto, sin confirmar automáticamente si es texto completo directo.
Open resource

Summary

Descripción general del contenido del recurso.

Abstract Background Nephrocalcinosis is a pathological feature of chronic kidney disease (CKD). Its pathophysiological implications for cats with CKD are unexplored. Objectives Identify nephrocalcinosis risk factors and evaluate its influence on CKD progression and all‐cause mortality. Animals Fifty‐one euthyroid client‐owned cats with International Renal Interest Society (IRIS) stages 2‐3 azotemic CKD. Methods Retrospective cohort study. Histopathological kidney sections were assessed for nephrocalcinosis (von Kossa stain). Nephrocalcinosis severity was determined by image analysis (ImageJ). Ordinal logistic regressions were performed to identify nephrocalcinosis risk factors. The influence of nephrocalcinosis on CKD progression and mortality risk were assessed using linear mixed model and Cox regression, respectively. Cats were categorized by their owner‐reported time‐averaged phosphate‐restricted diet (PRD) intake, where PRD comprised ≥50%, 10‐50%, or none of food intake. Results Nephrocalcinosis was rated as mild‐to‐severe in 78.4% and absent‐to‐minimal in 21.6% of cases. Higher baseline plasma total calcium concentration (tCa; odds ratio [OR] = 3.07 per 1 mg/dL; P = .02) and eating a PRD (10%‐50%: OR = 8.35; P = .01; ≥50%: OR = 5.47; P = .01) were independent nephrocalcinosis risk factors. Cats with absent‐to‐minimal nephrocalcinosis had increasing plasma creatinine (0.250 ± 0.074 mg/dL/month; P = .002), urea (5.06 ± 1.82 mg/dL/month; P = .01), and phosphate (0.233 ± 0.115 mg/dL/month; P = .05) concentrations over a 1‐year period, and had shorter median survival times than cats with mild‐to‐severe nephrocalcinosis. Conclusion and Clinical Importance Higher plasma tCa at CKD diagnosis and PRD intake are independently associated with nephrocalcinosis. However, nephrocalcinosis is not associated with rapid CKD progression in cats.

How to cite

Elegí el formato que necesitás y copiá la referencia al portapapeles.

APA 7

al, P. T. E. (2022). Risk factors and implications associated with renal mineralization in chronic kidney disease in cats. https://doi.org/10.1111/jvim.16363

MLA

al, Pak‐Kan Tang et. "Risk factors and implications associated with renal mineralization in chronic kidney disease in cats." 2022. https://doi.org/10.1111/jvim.16363.

Chicago

al, Pak‐Kan Tang et. 2022. "Risk factors and implications associated with renal mineralization in chronic kidney disease in cats.". https://doi.org/10.1111/jvim.16363.

Harvard

al, P. T. E. 2022, Risk factors and implications associated with renal mineralization in chronic kidney disease in cats, Oxford University Press, available at: https://doi.org/10.1111/jvim.16363 [Accessed 7 Aug. 2026].

Share and print

Save the record, copy its permanent link, or print it as a PDF.

Export reference

You can export the record in common formats for use in a reference manager.

Resource details

Bibliographic information to help confirm that this is the correct material.

Title
Risk factors and implications associated with renal mineralization in chronic kidney disease in cats
Author / contributors
Pak‐Kan Tang et al
Publisher
Oxford University Press
Publication year
2022
ISSN
0891-6640
ISSN
0891-6640
Language
English

Subjects

Explore related resources through these subjects.

Copied