# Hyperbilirubinemia and neurologic signs in dogs with non-associative immune-mediated hemolytic anemia: 81 cases (2015–2024)

**Authors:** Sasha Chapman, John M Angles, Christine Griebsch, Jane Yu

PMC · DOI: 10.1093/jvimsj/aalaf034 · Journal of Veterinary Internal Medicine · 2026-01-21

## TL;DR

This study shows that high bilirubin levels in dogs with immune-mediated hemolytic anemia are linked to neurological symptoms like seizures and paralysis.

## Contribution

The study identifies a significant association between bilirubin concentrations and neurological signs in dogs with IMHA, emphasizing the importance of monitoring bilirubin levels.

## Key findings

- 20% of dogs with IMHA developed neurological signs such as stupor, tetraparesis, and seizures.
- Higher baseline and peak bilirubin concentrations were strongly associated with increased odds of neurological signs.
- Dogs with peak bilirubin ≥13.9 mg/dL had 93.3 times higher odds of neurological symptoms.

## Abstract

Bilirubin encephalopathy is a poorly recognized complication in dogs with immune-mediated hemolytic-anemia (IMHA).

Assess serial trends of hyperbilirubinemia and the association between bilirubin concentrations and neurologic signs in dogs with IMHA.

Eighty one dogs with non-associative IMHA and hyperbilirubinemia.

Multicenter retrospective cohort study. The signalment, clinical signs, clinicopathological data, treatment, and outcome were evaluated. Bilirubin concentrations were recorded at the baseline, peak, initial decrease, and normalization. Univariable logistic regression was used to determine the association between neurologic signs and hyperbilirubinemia.

The median bilirubin concentrations at the baseline, peak, and initial decrease were 2.5 (IQR, 1.4–4.8), 3.7 (IQR, 1.8–24.2), and 1.1 mg/dL (IQR, 0.5–4.3; 43, 64, and 19 μmol/L), respectively. Twenty percent (16/81) of dogs developed neurologic signs. Neurologic signs included stupor, non-ambulatory tetraparesis, and generalized seizures. A significant association was found between the presence of neurologic signs and the baseline, peak, and fold-change of bilirubin concentration (P < .001). The odds of having neurologic signs were 12.2 (95% CI, 3.1-48.2) for dogs with baseline bilirubin concentrations ≥3.3 mg/dL (≥57.5 μmol/L), and 93.3 (95% CI, 11.0-795.5) for dogs with peak bilirubin concentrations ≥13.9 mg/dL (≥239.5 μmol/L).

Although the causation of the neurologic signs cannot be attributed solely to bilirubin based on our study, these findings emphasize the importance of monitoring serum bilirubin concentrations and the development of neurologic signs in dogs with IMHA. The results reflect findings in our study population and may not be directly applicable to all dogs with IMHA.

## Full-text entities

- **Genes:** SLC6A3 (solute carrier family 6 member 3) [NCBI Gene 609304] {aka DAT}, ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 403548] {aka ALP}
- **Diseases:** vomiting (MESH:D014839), hypoxia (MESH:D000860), systemic diseases (MESH:D034721), stupor (MESH:D053608), hemolysis (MESH:D006461), extrahepatic biliary duct obstruction (MESH:D001651), seizure (MESH:D012640), ischemia (MESH:D007511), neurologic compromise (MESH:D009461), pulmonary thromboembolism (MESH:D011655), acute (MESH:D000208), respiratory distress (MESH:D012128), tetraparesis (MESH:C565722), rotary, horizontal, or vertical nystagmus (MESH:D009759), IMHA (MESH:C567355), secondary neurologic compromise (MESH:D000068376), diarrhea (MESH:D003967), hypoalbuminemia (MESH:D034141), hypercoagulability (MESH:D019851), acute kidney injury (MESH:D058186), hypoxic brain injury (MESH:D002534), neurologic disease (MESH:D020271), autoimmune disease (MESH:D001327), circulatory overload (MESH:D065227), cardiac arrest (MESH:D006323), spherocytosis (MESH:C567159), leptospirosis (MESH:D007922), pancreatitis (MESH:D010195), Neurologic complications (MESH:D002493), inflammatory response syndrome (MESH:D018746), ABE (MESH:D007647), proprioceptive deficits (MESH:D020886), rickettsial diseases (MESH:D012282), intracranial tumors (MESH:D009369), cerebral ischemia (MESH:D002545), inflammation (MESH:D007249), associative disease (MESH:D004194), babesiosis (MESH:D001404), volume overload (MESH:D019190), hepatic or renal insufficiency (MESH:D048550), comatose (MESH:D003128), infectious diseases (MESH:D003141), sepsis (MESH:D018805), -hepatic biliary duct obstruction (MESH:D008105), Hyperbilirubinemia (MESH:D006932), ocular disease (MESH:D005128), vector-borne diseases (MESH:D000079426), erythema (MESH:D004890), thromboembolic renal disease (MESH:D013923), hemolytic anemia (MESH:D000743), miosis (MESH:D015877), ACVIM (MESH:D000034), systemic (MESH:D015619), renal disease (MESH:D007674), heartworm (MESH:D004184), hypertonia (MESH:D009122), inflammatory encephalitis (MESH:D004660), uremic (MESH:D006463), ischemic stroke (MESH:D002544), thrombocytopenia (MESH:D013921)
- **Chemicals:** sucralfate (MESH:D013392), metronidazole (MESH:D008795), Bilirubin (MESH:D001663), amoxicillin-clavulanate (MESH:D019980), saline (MESH:D012965), ondansetron (MESH:D017294), Creatinine (MESH:D003404), metoclopramide (MESH:D008787), lipid (MESH:D008055), urea nitrogen (MESH:C530477), misoprostol (MESH:D016595), maropitant (MESH:C518176), omeprazole (MESH:D009853), methadone (MESH:D008691), ABE (-)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Neospora caninum (species) [taxon 29176], Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685]

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881973/full.md

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Source: https://tomesphere.com/paper/PMC12881973