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Serum vitamin D status in sick cats with and without cholestatic liver disease
Lesli Kibler1, Cailin R Heinze1, Cynthia Rl Webster1
1Department of Clinical Sciences, Cummings School of Veterinary Medicine at Tufts University, North Grafton, MA, USA.
Insights
Many cats with chronic liver disease (CLD) have low vitamin D levels, with one-third falling below the reference range. Further research is needed to understand the clinical impact and potential benefits of vitamin D supplementation in feline CLD.
Area of Science:
- Veterinary Medicine
- Biochemistry
- Comparative Pathology
Background:
- Vitamin D deficiency is common in human patients with chronic cholestatic liver disease (CLD).
- The vitamin D status in cats suffering from CLD remains largely uninvestigated.
- This study aims to elucidate vitamin D levels in cats with CLD.
Purpose of the Study:
- To assess serum vitamin D concentrations in cats diagnosed with CLD.
- To investigate the correlation between vitamin D levels and indicators of liver disease severity in cats.
- To compare vitamin D status in cats with CLD versus sick cats without liver disease.
Main Methods:
- Prospective enrollment of 36 cats with CLD and 23 sick control cats.
- Measurement of serum 25-hydroxyvitamin D (25[OH]D), parathyroid hormone (PTH), and ionized calcium.
- Collection of clinical data, including signalment, comorbidities, diet, and liver-specific biomarkers.
Main Results:
- Median serum 25(OH)D levels were comparable between cats with CLD and sick controls.
- A significant proportion of cats with CLD (33%) exhibited vitamin D levels below the reference interval.
- Cats with CLD showed higher median PTH concentrations and a greater prevalence of elevated PTH compared to controls.
- Vitamin D levels did not correlate with standard liver disease markers but showed a negative correlation with white blood cell count in cats with CLD.
- Hepatic lipidosis was associated with the highest incidence of vitamin D deficiency.
Conclusions:
- A substantial number of cats with CLD present with sub-optimal serum 25(OH)D concentrations.
- The clinical significance of these low vitamin D levels in feline CLD requires further investigation.
- The potential therapeutic benefits of vitamin D supplementation in cats with CLD warrant additional research.
Objectives:
Vitamin D deficiency accompanies chronic cholestatic liver disease (CLD) in humans. The vitamin D status of cats with CLD is unknown. The objectives of this study were to describe serum vitamin D concentrations in cats with CLD and to determine if they correlated with indices of liver disease severity.
Methods:
Thirty-six cats with CLD, defined by increases in serum bilirubin and serum alanine aminotransferase, and 23 sick cats with non-hepatobiliary diseases were prospectively enrolled. Serum 25-hydroxyvitamin D (25[OH]D), parathyroid hormone (PTH) and ionized calcium were measured. Signalment, clinical signs, comorbidities, diet history, serum bilirubin, liver enzyme activity, albumin, phosphorus, white blood cell count, prothrombin time and final hepatic cytologic/histopathologic diagnosis, when available, were recorded.
Results:
Median serum 25(OH)D levels were similar in cats with CLD (89.5 nmol/l; range 21-112 nmol/l) and sick cats (89.0 nmol/l; range 49-115 nmol/l). Overall 12/36 (33%) cats with CLD and 4/23 (17%) sick cats had 25(OH)D levels below the lower limit of the reference interval (<65 nmol/l). Median PTH concentrations in cats with CLD were significantly higher (0.95 pmol/l; range 0-11.3 pmol/l) than in sick cats (0.70 pmol/l; range 0.5-6 pmol/l). In cats with CLD, 6/36 (17%) had high PTH levels in contrast to only 1/23 (4%) sick cats. In cats with CLD, 25(OH)D concentrations did not correlate with serum bilirubin, albumin or serum liver enzymes but were moderately negatively correlated with white blood cell count (r = - 0.402, P = 0.013). Cats with hepatic lipidosis had the highest prevalence of 25(OH)D concentrations that fell below the reference interval.
Conclusions And Relevance:
Many cats with CLD have serum 25(OH)D concentrations below the lower limit of the reference interval. Further study is warranted to determine the clinical relevance and whether supplementation would provide benefits.
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