Evidence map›Paper›PMID 41742492›Full record

ArticleJournal of veterinary internal medicine2026

Association between PCV and degree of azotemia with serum hepcidin concentration in cats with chronic kidney disease.

Sarah Spencer, Gabriella Lynn, Caroline Wheeler-Jones, Jonathan Elliott

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Article in Journal of veterinary internal medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sarah SpencerComparative Biological Sciences, Royal Veterinary College, London NW1 0TU,  United Kingdom.
Gabriella LynnRoyal Veterinary College, London NW1 0TU,  United Kingdom.
Caroline Wheeler-JonesComparative Biological Sciences, Royal Veterinary College, London NW1 0TU,  United Kingdom.
Jonathan ElliottComparative Biological Sciences, Royal Veterinary College, London NW1 0TU,  United Kingdom.

Funding

BBSRC BB/M009513/1Biotechnology and Biological Sciences Research CouncilBoehringer IngelheimCEVA Santé AnimaleIdexx Ltd.Royal Canin SAS
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) in cats is common and often leads to anemia. Hepcidin, an acute-phase protein and regulator of iron metabolism, is a potential biomarker for CKD-associated anemia. HYPOTHESIS/

objectivesTo validate a hepcidin-25 ELISA for cats. To compare serum hepcidin concentrations in cats with CKD grouped by PCV, and explore associations between hepcidin and other clinicopathological variables. ANIMALS: One hundred client-owned cats with naturally occurring CKD.

methodsRetrospective cross-sectional study. Cats with azotemic CKD were categorized by PCV: anemic (<28%), low-normal (LN-PCV, 28%-33%), or normal PCV (N-PCV, 35%-43%). LN-PCV and N-PCV groups were matched for plasma creatinine concentration, age, bodyweight, body and muscle condition scores. Associations between serum hepcidin concentrations, serum amyloid A (SAA), and clinicopathological variables were evaluated. Multiple regression analysis identified independent associations with hepcidin.

resultsThe hepcidin-25 ELISA demonstrated acceptable precision, reproducibility, and specificity. Hepcidin was higher in anemic cats (median [range], 3.1 ng/mL [1.17-6.58]) compared to LN-PCV (2.21 ng/mL [1.24-6.94]) and N-PCV cats (2.29 ng/mL [1.41-7.72) (P = .007), with no difference between the latter two groups (P > .99). Hepcidin was weakly positively correlated with plasma creatinine (r = 0.265, P = .008) and plasma phosphate (r = 0.214, P = .034); no significant correlations were observed between hepcidin and PCV, SAA, or other clinicopathological variables. Plasma creatinine alone was associated with hepcidin in multivariable analysis, explaining <15% of the variance. CONCLUSIONS AND CLINICAL IMPORTANCE: Serum hepcidin concentration is higher in cats with CKD once anemia is established. Its association with plasma creatinine suggests kidney dysfunction influences its excretion, although additional factors not assessed in this study likely contribute.

Indexed as

anemiahypoxiainflammationiron metabolismvalidation

Identifiers

PMID41742492
PMCPMC12881961

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