Renal amyloid-A amyloidosis in cats: Characterization of proteinuria and biomarker discovery, and associations with kidney histology.

Palizzotto, Carlo; Ferri, Felippo; Callegari, Carolina; Rossi, Francesco; Manfredi, Marcello; Carcangiu, Laura; Gerardi, Gabriele; Ferro, Silvia; Cavicchioli, Laura; Müller, Elizabeth; Weiss, Marco; Vogt, Anne-Cathrine; Lavatelli, Francesca; Ricagno, Stefano; Hurley, Karyl; Zini, Eric (2024). Renal amyloid-A amyloidosis in cats: Characterization of proteinuria and biomarker discovery, and associations with kidney histology. Journal of veterinary internal medicine, 38(1), pp. 205-215. Wiley 10.1111/jvim.16920

[img]
Preview
Text
Veterinary_Internal_Medicne_-_2023_-_Palizzotto_-_Renal_amyloid_A_amyloidosis_in_cats_Characterization_of_proteinuria_and.pdf - Published Version
Available under License Creative Commons: Attribution (CC-BY).

Download (822kB) | Preview

BACKGROUND

Amyloid A (AA) amyloidosis is a protein misfolding disease arising from serum amyloid A (SAA). Systemic AA amyloidosis recently was shown to have a high prevalence in shelter cats in Italy and was associated with azotemia and proteinuria.

OBJECTIVES

Investigate urine protein profiles and diagnostic biomarkers in cats with renal AA amyloidosis.

ANIMALS

Twenty-nine shelter cats.

METHODS

Case-control study. Cats with renal proteinuria that died or were euthanized between 2018 and 2021 with available necropsy kidney, liver and spleen samples, and with surplus urine collected within 30 days before death, were included. Histology was used to characterize renal damage and amyloid amount and distribution; immunohistochemistry was used to confirm AA amyloidosis. Urine protein-to-creatinine (UPC) and urine amyloid A-to-creatinine (UAAC) ratios were calculated, and sodium dodecyl sulfate-agarose gel electrophoresis (SDS-AGE) and liquid chromatography-mass spectrometry (LC-MS) of proteins were performed.

RESULTS

Twenty-nine cats were included. Nineteen had AA amyloidosis with renal involvement. Cats with AA amyloidosis had a higher UPC (median, 3.9; range, 0.6-12.7 vs 1.5; 0.6-3.1; P = .03) and UAAC ratios (median, 7.18 × 10-3 ; range, 23 × 10-3 -21.29 × 10-3 vs 1.26 × 10-3 ; 0.21 × 10-3 -6.33 × 10-3 ; P = .04) than unaffected cats. The SDS-AGE identified mixed-type proteinuria in 89.4% of cats with AA amyloidosis and in 55.6% without AA amyloidosis (P = .57). The LC-MS identified 63 potential biomarkers associated with AA amyloidosis (P < .05). Among these, urine apolipoprotein C-III was higher in cats with AA amyloidosis (median, 1.38 × 107 ; range, 1.85 × 105 -5.29 × 107 vs 1.76 × 106 ; 0.0 × 100 -1.38 × 107 ; P = .01). In the kidney, AA-amyloidosis was associated with glomerulosclerosis (P = .02) and interstitial fibrosis (P = .05).

CONCLUSIONS AND CLINICAL IMPORTANCE

Renal AA amyloidosis is associated with kidney lesions, increased proteinuria and increased urine excretion of SAA in shelter cats. Additional studies are needed to characterize the role of lipid transport proteins in the urine of affected cats.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Rheumatology and Immunology
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Rheumatologie
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Rheumatologie

Graduate School:

Graduate School for Cellular and Biomedical Sciences (GCB)

UniBE Contributor:

Vogt, Anne-Cathrine Sarah

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1939-1676

Publisher:

Wiley

Language:

English

Submitter:

Pubmed Import

Date Deposited:

23 Nov 2023 12:56

Last Modified:

23 Jan 2024 00:14

Publisher DOI:

10.1111/jvim.16920

PubMed ID:

37991136

Uncontrolled Keywords:

chronic kidney disease diagnosis feline fibrils

BORIS DOI:

10.48350/189298

URI:

https://boris.unibe.ch/id/eprint/189298

Actions (login required)

Edit item Edit item
Provide Feedback