AI Article Synopsis

  • The study aims to understand how cerebral small vessel disease (SVD) impacts prediction models for different types of acute ischemic stroke (AIS).
  • The research involved 573 AIS patients, using methods such as MRI and machine learning to analyze various indicators of SVD and assess functional outcomes after 90 days.
  • Results showed that SVD was a strong predictor of outcomes for small-vessel occlusion strokes (SVO-AIS), while the significance of SVD differed for large artery atherosclerosis strokes (LAA-AIS), with the most effective predictive model being based on eXtreme gradient boosting.

Article Abstract

Aims: Our purpose is to assess the role of cerebral small vessel disease (SVD) in prediction models in patients with different subtypes of acute ischemic stroke (AIS).

Methods: We enrolled 398 small-vessel occlusion (SVO) and 175 large artery atherosclerosis (LAA) AIS patients. Functional outcomes were assessed using the modified Rankin Scale (mRS) at 90 days. MRI was performed to assess white matter hyperintensity (WMH), perivascular space (PVS), lacune, and cerebral microbleed (CMB). Logistic regression (LR) and machine learning (ML) were used to develop predictive models to assess the influences of SVD on the prognosis.

Results: In the feature evaluation of SVO-AIS for different outcomes, the modified total SVD score (Gain: 0.38, 0.28) has the maximum weight, and periventricular WMH (Gain: 0.07, 0.09) was more important than deep WMH (Gain: 0.01, 0.01) in prognosis. In SVO-AIS, SVD performed better than regular clinical data, which is the opposite of LAA-AIS. Among all models, eXtreme gradient boosting (XGBoost) method with optimal index (OI) has the best performance to predict excellent outcome in SVO-AIS. [0.91 (0.84-0.97)].

Conclusions: Our results revealed that different SVD markers had distinct prognostic weights in AIS patients, and SVD burden alone may accurately predict the SVO-AIS patients' prognosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018092PMC
http://dx.doi.org/10.1111/cns.14071DOI Listing

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