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Peer-reviewed veterinary case report

Serum SDMA and urine protein patterns in dogs with ACTH

By Menard, M et al.·Published in Veterinary journal (London, England : 1997)·2024·Ecole Nationale V&#xe9, France·View original on PubMed

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Original publication title: Description of serum symmetric dimethylarginine concentration and of urinary SDS-AGE pattern in dogs with ACTH dependent hyperadrenocorticism.

Species:
dog

Plain-English summary

A group of dogs with a condition called Cushing's disease (ACTH-dependent hyperadrenocorticism) were tested to see if certain blood and urine markers could help identify kidney issues. The study included 35 dogs, some with protein in their urine and some without. While the kidney function marker serum creatinine was lower in dogs with Cushing's compared to healthy dogs, the other marker, symmetric dimethylarginine (SDMA), did not show significant differences. The findings suggest that while urinary tests can provide useful information, more research is needed to see if they can help guide treatment for dogs with kidney problems related to Cushing's disease.

People also search for: dog Cushing's disease symptoms · dog kidney problems treatment · dog protein in urine causes

Abstract

Serum symmetric dimethylarginine (SDMA) and patterns of urinary protein separated by sodium dodecyl sulfate agarose gel electrophoresis (SDS-AGE) have not been investigated as biomarkers in dogs with ACTH-dependent hyperadrenocorticism (ADHAC). This exploratory prospective study aimed to evaluate SDMA, serum creatinine (sCR), and SDS-AGE in dogs with ADHAC with and without proteinuria (ADHAC-P and ADHAC-nP, respectively). Thirty-five pet dogs classified as ADHAC-P (n=16), ADHAC-nP (n=6) and healthy (n=13) were included. Renal biomarkers were evaluated in all dogs at diagnosis. Baseline concentration of SDMA was not significantly different between the three groups (P = 0.15) whereas sCr was significantly lower in dogs in ADHAC dogs compared to healthy dogs (88.0 µmol/L [70.4-132.6; 79.2-114.4]) whether they had proteinuria or not (P = 0.014 and 0.002, respectively). However, baseline concentrations of sCr and SDMA were not significantly different between dogs with ADHAC-P dogs (SDMA, 8 µg/dL [5-12; 7-9]; sCr, 57.2 µmol/L [35.2-212.2; 52.8-92.4]) and ADHAC-nP dogs (SDMA, 8.5 µg/dL [7-13; 8-10]; sCr, 70.4 µmol/L [61.6-79.2; 61.6-70.4]) (P = 0.35 and P = 0.41, respectively). Proteinuria in dogs with ADHAC-P was mainly of glomerular origin (SDS-AGE pattern: glomerular in 10/16 dogs; mixed glomerular/tubular in four dogs). In our study, SDMA was neither significantly different in dogs with ADHAC whether they were proteinuric or not, nor between ADHAC and healthy dogs. Urinary electrophoresis provides additional information to the UPC and further investigations are needed to determine whether it may help identify dogs with ADHAC-P requiring specific antiproteinuric treatment.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/38580156/