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Evaluation of renal values during treatment for heartworm disease in 27 client-owned dogs
C Autumn M Vetter1, Alison G Meindl2, Bianca N Lourenço3
1Department of Small Animal Medicine and Surgery, College of Veterinary Medicine, University of Georgia, Athens, GA, USA. cam18@uga.edu.
Insights
Canine heartworm disease (CHD) treatment using the American Heartworm Society (AHS) protocol did not significantly impact renal function markers, including symmetric dimethylarginine (SDMA). This study monitored SDMA and creatinine levels during adulticide therapy, finding no substantial changes in kidney function.
Area of Science:
- Veterinary Medicine
- Parasitology
- Nephrology
Background:
- Canine heartworm disease (CHD) caused by Dirofilaria immitis is a prevalent and growing concern in the USA.
- Current American Heartworm Society (AHS) treatment involves macrocyclic lactones, doxycycline, and melarsomine, with potential for complications.
- Renal damage is a known systemic effect of CHD, indicated by elevated renal biomarkers, but changes in symmetric dimethylarginine (SDMA) during treatment are unstudied.
Purpose of the Study:
- To evaluate renal function in dogs undergoing adulticide treatment for CHD.
- To measure serum creatinine and symmetric dimethylarginine (SDMA) concentrations at various stages of treatment.
Main Methods:
- Serum creatinine and SDMA were measured in 27 dogs with CHD at baseline, during antibiotic therapy, and at multiple points during melarsomine administration.
- Measurements were also taken at a follow-up visit 1-6 months post-treatment.
- A mixed effects linear model was used to compare biomarker concentrations between time points.
Main Results:
- Mean SDMA concentrations were significantly lower after the second dose of melarsomine compared to baseline (-1.80 ug/dL, P=0.00829).
- No other statistically significant differences in creatinine or SDMA were observed between baseline and other treatment time points.
- These findings suggest minimal impact on renal function markers during the AHS protocol.
Conclusions:
- The current AHS treatment protocol for canine heartworm disease appears to have no substantial impact on renal function.
- Monitoring SDMA and creatinine provides insight into kidney health during CHD treatment.
- Further research may explore long-term renal effects or alternative treatment impacts.
Background:
Canine heartworm disease (CHD) caused by Dirofilaria immitis remains a common preventable disease with increasing incidence in some parts of the USA. The treatment guidelines of the American Heartworm Society (AHS) currently recommend monthly macrocyclic lactone administration, 28 days of doxycycline given orally every 12 h and three injections of melarsomine dihydrochloride (1 injection on day 2 of treatment followed 30 days later by 2 injections 24 h apart). Minocycline has also been utilized when doxycycline is unavailable. The systemic effects of CHD, which particularly impact cardiac and renal function, have been described, with infected dogs often experiencing renal damage characterized by an increase in serum concentrations of renal biomarkers. Although the AHS treatment protocol for CHD has been shown to be safe and effective in most cases, the potential for complications remains. No study as of yet has evaluated changes in symmetric dimethylarginine (SDMA), a sensitive marker of renal function, during treatment for CHD. The purpose of the present study was to evaluate renal function in dogs by measuring serum creatinine and SDMA concentrations during the adulticide treatment period.
Methods:
Serum creatinine and SDMA concentrations were measured in 27 client-owned dogs affected by CHD at the following time points: prior to starting doxycycline or minocycline therapy (baseline), during doxycycline or minocycline therapy (interim), at the time of the first dose of melarsomine (first dose), at the time of the second dose of melarsomine (second dose) and at the dog's follow-up visit after treatment, occurring between 1 and 6 months after completion of therapy (post-treatment). Concentrations of creatinine and SDMA were compared between time points using a mixed effects linear model.
Results:
Mean SDMA concentrations following the second dose of melarsomine were significantly lower (-1.80 ug/dL, t-test, df = 99.067, t = -2.694, P-Value = 0.00829) than baseline concentrations. There were no other statistically significant differences in the concentration of either biomarker between the baseline and the other time points in CHD dogs undergoing treatment.
Conclusions:
The results suggest that the current AHS protocol may not have a substantial impact on renal function.
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