Imaging phenotype is more strongly associated with early neurological deterioration after acute isolated pontine infarction: a retrospective cohort study.
Chen Y, Li X, Wang H, Zhou G • Frontiers in neurology • 2026
In this retrospective cohort of 162 patients with acute isolated pontine infarction, BAD and LAA imaging phenotypes (relative to SAD) were independently associated with early neurological deterioration, TyG was not, and the imaging model's discrimination advantage over the metabolic/coagulation model was not statistically established; the full model and nomogram need external validation.
Key Findings
Results
Early neurological deterioration occurred in about 30% of patients with acute isolated pontine infarction.
END occurred in 49 of 162 patients (30.2%).
END was defined as a ≥2-point increase in total NIHSS or a ≥1-point increase in NIHSS motor item 5 or 6 from admission baseline within 7 days of admission.
The study was a retrospective analysis of patients with acute IPI.
Results
The BAD imaging phenotype was very strongly associated with END relative to SAD.
In the full Firth logistic model, BAD had OR 20.70 (95% CI 7.10-70.04; P < 0.001).
Imaging was modeled nominally (BAD, LAA, SAD) with SAD as the reference.
Firth logistic regression was used for the primary associations.
Results
The LAA imaging phenotype was independently associated with END relative to SAD.
In the full Firth model, LAA had OR 5.06 (95% CI 1.84-15.41; P = 0.001).
SAD was the reference category.
Results
Thrombin time was associated with END, but this association is described as exploratory.
TT had OR 1.34 per second (95% CI 1.04-1.73; P = 0.020) in the full Firth model.
The authors state the association with TT is exploratory.
Results
TyG was not independently associated with END, and diabetes showed only borderline evidence of association.
TyG P = 0.603 in the full Firth model.
Diabetes P = 0.057.
Results
Adding imaging phenotype to a base model improved discrimination more than adding metabolic/coagulation markers did, but the difference between the two was not statistically significant.
Apparent AUC was 0.652 (95% CI 0.562-0.742) for the base model, 0.814 (0.745-0.883) for base-plus-imaging, 0.716 (0.631-0.802) for base-plus-metabolic/coagulation, and 0.852 (0.792-0.911) for the full model.
ΔAUC between base-plus-imaging and base-plus-metabolic/coagulation was 0.098 (bootstrap 95% CI -0.015 to 0.180); paired DeLong P = 0.066.
Four prespecified Firth models were compared by AUC.
Results
The full model showed good discrimination after bootstrap validation, with reasonable calibration.
All 1,000 bootstrap iterations succeeded.
The optimism-corrected AUC was 0.818.
The calibration intercept was -0.023, the calibration slope 0.870, and the Brier score 0.162.
Conclusions
The authors conclude that the prediction model and nomogram require external validation before clinical use.
The model was developed as exploratory, in a single retrospective cohort of 162 patients.
The direct discrimination advantage of the imaging model over the metabolic/coagulation model was not statistically established.
What This Means
This study looked back at the records of 162 patients who had a stroke in one specific part of the brainstem, the pons. About 3 in 10 of them got worse neurologically within the first week in hospital. The researchers wanted to know whether the way the stroke looked on brain imaging, or blood markers related to metabolism and clotting, were more closely linked to this early worsening.
Patients whose scans showed a particular pattern involving blockage of a branch of the basilar artery (BAD) or large-artery disease (LAA) were much more likely to get worse than those with small-vessel disease (SAD). The link was especially strong for BAD. A longer thrombin time, a clotting test, was also linked to worsening, though the authors consider this finding exploratory. A blood sugar and fat measure called TyG was not independently linked to worsening, and diabetes showed only a borderline link.
A prediction model that combined all the factors performed fairly well, even after internal testing. However, the study could not show statistically that imaging predicted worsening better than the metabolic and clotting markers did. The study was retrospective, small, and from a single group of patients. This research suggests that imaging pattern may help identify patients at higher risk, but the model needs testing in other groups of patients before it could be used in clinical practice.
Chen Y, Li X, Wang H, Zhou G. (2026). Imaging phenotype is more strongly associated with early neurological deterioration after acute isolated pontine infarction: a retrospective cohort study.. Frontiers in neurology. https://doi.org/10.3389/fneur.2026.1913826