Peer-reviewed veterinary case report
Inflammation and oxidative stress linked to heart failure in dogs
By Nemec Svete, Alenka et al.·Published in BMC veterinary research·2021·Small Animal Clinic·View original on PubMed →
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Original publication title: Inflammation and its association with oxidative stress in dogs with heart failure.
- Species:
- dog
Plain-English summary
A group of dogs with heart failure, specifically those with dilated cardiomyopathy and myxomatous mitral valve disease, showed higher levels of inflammation and oxidative stress markers compared to healthy dogs. The study found that dogs with congestive heart failure had significantly elevated levels of certain proteins and white blood cells, indicating inflammation. These markers were linked to the severity of heart failure, suggesting that inflammation and oxidative stress may play a role in the progression of the disease. Understanding these connections could help veterinarians better manage heart failure in dogs.
People also search for: dog heart failure symptoms · inflammation in dogs with heart disease · treatment for congestive heart failure in dogs
Abstract
BACKGROUND: Inflammation and oxidative stress can contribute to the development and progression of heart failure. This study aimed to investigate the association between inflammatory and oxidative stress markers in dogs with congestive heart failure (CHF). Associations between the disease severity marker N-terminal pro-B-type natriuretic peptide (NT-proBNP) and markers of inflammation and oxidative stress were also determined. RESULTS: Thirty-seven dogs with cardiovascular diseases (dilated cardiomyopathy, DCM (16 dogs), myxomatous mitral valve disease, MMVD (21 dogs)) and ten healthy dogs were included in this prospective study. The patients were further divided into groups with (26) and without CHF (11). We found a significantly higher serum concentration of C-reactive protein (P = 0.012), white blood cell (P = 0.001), neutrophil (P = 0.001) and monocyte counts (P = 0.001) in patients with CHF compared to control dogs. The concentration of tumor necrosis factor-alpha (TNF-α) was significantly higher in patients with CHF compared to patients without CHF (P = 0.030). No significant difference was found in most of the measured parameters between MMVD and DCM patients, except for glutathione peroxidase (GPX) and NT-proBNP. In patients with CHF, TNF-α correlated positively with malondialdehyde (P = 0.014, r = 0.474) and negatively with GPX (P = 0.026, r = - 0.453), and interleukin-6 correlated negatively with GPX (P = 0.046, r = - 0.412). NT-proBNP correlated positively with malondialdehyde (P = 0.011, r = 0.493). In patients without CHF none of the inflammatory and oxidative stress markers correlated significantly. Furthermore, in the group of all cardiac patients, GPX activity significantly negatively correlated with NT-proBNP (P = 0.050, r = - 0.339) and several markers of inflammation, including TNF-α (P = 0.010, r = - 0.436), interleukin-6 (P = 0.026, r = - 0.382), white blood cell (P = 0.032, r = - 0.369), neutrophil (P = 0.027, r = - 0.379) and monocyte counts (P = 0.024, r = - 0.386). CONCLUSION: Inflammatory and oxidative stress markers are linked in canine CHF patients, but not in patients without CHF. These results suggest complex cross communication between the two biological pathways in advanced stages of CHF.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/33902566/