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. 2016 Jul;30(4):1083-9.
doi: 10.1111/jvim.13956. Epub 2016 May 7.

Serum Cystatin C Concentrations in Cats with Hyperthyroidism and Chronic Kidney Disease

Affiliations

Serum Cystatin C Concentrations in Cats with Hyperthyroidism and Chronic Kidney Disease

T L Williams et al. J Vet Intern Med. 2016 Jul.

Abstract

Background: Currently, no test can accurately predict the development of azotemia after treatment of hyperthyroidism. Serum cystatin C concentrations (sCysC) might be less influenced by changes in body muscle mass and so better indicate the presence of concurrent chronic kidney disease (CKD) in hyperthyroidism.

Hypotheses: sCysC will be higher in hyperthyroid cats that develop azotemia compared with hyperthyroid cats that remain nonazotemic after treatment; sCysC will be higher in nonhyperthyroid cats with azotemic CKD than healthy older cats and, sCysC will decrease after treatment of hyperthyroidism.

Animals: Ninety-one cats treated in first opinion practice.

Methods: Case-control study. sCysC were compared between hyperthyroid cats which developed azotemia within 4 months of successful treatment of hyperthyroidism (pre-azotemic group) and hyperthyroid cats which remained nonazotemic after treatment (nonazotemic group), and between nonhyperthyroid cats with azotemic CKD and healthy older cats. sCysC were also compared between hyperthyroid cats before treatment and at time of establishment of euthyroidism. Data are presented as median [25th, 75th percentile].

Results: Baseline sCysC were not different between the pre-azotemic and nonazotemic groups (1.9 [1.4, 2.3] mg/L versus 1.5 [1.1, 2.2] mg/L, respectively; P = .22). sCysC in nonhyperthyroid cats with azotemic CKD and healthy older cats were not significantly different (1.5 [1.0, 1.9] mg/L versus 1.2 [0.8, 1.4] mg/L, respectively; P = .16). sCysC did not change significantly after treatment of hyperthyroidism (pretreatment 1.8 [1.2, 2.3] mg/L, after treatment 1.6 [1.1, 2.4] mg/L; P = .82).

Conclusions and clinical importance: sCysC do not appear to be a reliable marker of renal function in hyperthyroid cats.

Keywords: Azotemia; Clinical chemistry; Clinical pathology; Endocrinology; Renal function; Thyroid; Urinary tract; Validation.

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Figures

Figure 1
Figure 1
Box and whisker plots showing baseline serum cystatin C concentrations in a group of hyperthyroid cats which remained nonazotemic after treatment (n = 34) and initially nonazotemic hyperthyroid cats which developed azotemia within 4 months of successful treatment of hyperthyroidism (n = 21). Whiskers represent the 5th and 95th percentiles and circles represent outliers. Serum cystatin C concentrations were not significantly different between the 2 groups (P = .22).
Figure 2
Figure 2
Line chart showing serum cystatin C concentrations in hyperthyroid cats before treatment (hyperthyroid) and at time of establishment of euthyroidism (euthyroid). Serum cystatin C concentrations were not significantly different between the hyperthyroid and euthyroid time points (P = .82).
Figure 3
Figure 3
Box and whisker plots showing serum cystatin C concentrations in a group of initially nonazotemic (serum creatinine concentration <2.0 mg/dL) hyperthyroid cats (n = 55), healthy nonazotemic older cats (n = 24, serum creatinine concentration <1.7 mg/dL) and nonhyperthyroid cats diagnosed with azotemic CKD (n = 12). Whiskers represent the 5th and 95th percentiles and circles represent outliers. Serum cystatin C concentrations were significantly higher in hyperthyroid cats than healthy nonazotemic older cats (P = .001). Serum cystatin C concentrations were not significantly different between the healthy older cat and nonhyperthyroid azotemic CKD groups (P = .16).

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