# Primary angiitis of the central nervous system: predictors of stroke during immunosuppressant treatment

**Authors:** Franca Wagner, Jakob Heimer, Pasquale Mordasini, Thomas Hundsberger, Roman Guggenberger, Anna L. Falkowski, Simon Wildermuth, Sebastian Leschka, Tobias Johannes Dietrich, Tim Steffen Fischer

PMC · DOI: 10.1186/s13244-026-02217-4 · Insights into Imaging · 2026-02-17

## TL;DR

This study identifies risk factors for strokes in patients with central nervous system angiitis during immunosuppressive therapy.

## Contribution

The study reveals a critical timeframe (10-20 days post-therapy) and vessel characteristics linked to stroke risk in primary angiitis patients.

## Key findings

- Most strokes occurred in the territory of inflamed vessels.
- Higher stenosis and circular enhancement significantly increase stroke likelihood.
- Ischemic strokes peak between 10 and 20 days after starting immunosuppressants.

## Abstract

To evaluate predictors of ischemic stroke in patients with primary angiitis of the central nervous system after initiation of immunosuppressive therapy.

This retrospective study included 204 MRI examinations of 23 patients with primary angiitis of the central nervous system, treated with immunosuppressive therapy between 2015 and 2020 at the University Hospital Bern and the Cantonal Hospital St. Gallen, Switzerland. Two senior neuroradiologists evaluated the MRI exams with regard to the occurrence and location of ischemic stroke and hemorrhage, as well as the following characteristics of inflamed vessels on 3D time-of-flight angiography and T1 dark-blood post contrast: signal intensity of vessel walls, length of enhancement, circular extent of enhancement, and stenosis. After matching ischemic strokes to their corresponding vessel, the temporal relationship of vessel alterations in accordance with therapy initiation and stroke onset was calculated.

The majority (77.6%) of observed strokes were in the vascular territory of an inflamed vessel. A significant, non-linear temporal relationship between the timing of MRI and the initiation of immunosuppression was found. The highest predicted probability of ischemic stroke was observed between 10 and 20 days after the initiation of immunosuppressant therapy, reaching approximately 12%. Out of all evaluated vessel characteristics, a higher degree of stenosis (Estimate: 0.93, p = 0.006) and a higher circularity of enhancement (Estimate: 0.76, p = 0.01) were significantly associated with a higher likelihood of stroke.

A better understanding of unfavorable constellations (critical timeframe, characteristic vessel wall changes) in patients treated for primary angiitis of the central nervous system may help to prevent secondary ischemic strokes.

A better understanding of ischemic stroke predictors in patients treated for primary angiitis of the central nervous system may prompt closer monitoring or therapy adjustment.

To evaluate risk factors for ischemic stroke in patients treated for primary angiitis of the central nervous system.Higher degree of stenosis and circular enhancement are associated with a higher likelihood of ischemic strokes, which typically occur between 10 and 20 days after therapy onset.Data obtained from this may prompt closer monitoring or therapy adjustment.

To evaluate risk factors for ischemic stroke in patients treated for primary angiitis of the central nervous system.

Higher degree of stenosis and circular enhancement are associated with a higher likelihood of ischemic strokes, which typically occur between 10 and 20 days after therapy onset.

Data obtained from this may prompt closer monitoring or therapy adjustment.

## Linked entities

- **Diseases:** primary angiitis of the central nervous system (MONDO:0015374), ischemic stroke (MONDO:1060198)

## Full-text entities

- **Genes:** AZIN2 (antizyme inhibitor 2) [NCBI Gene 113451] {aka ADC, AZIB1, ODC-p, ODC1L, ODCp}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}
- **Diseases:** Hemorrhagic infarction (MESH:D007238), PH-2 (MESH:D020803), systemic vasculitis (MESH:D056647), moya-moya disease (MESH:D009072), atherosclerotic plaque (MESH:D058226), PH-1 (MESH:C538557), gliosis (MESH:D005911), Parenchymal hemorrhage (MESH:D002543), MCA stenosis (MESH:D020244), motoric aphasia (MESH:D001039), atherosclerosis (MESH:D050197), artery (MESH:D012078), post-infectious vasculitis (MESH:D000094025), Ischemic stroke (MESH:D002544), hemiparesis (MESH:D010291), lymphomonocytic pleocytosis (MESH:D007964), PACNS (MESH:C535276), Intracranial hemorrhage (MESH:D020300), bleeding (MESH:D006470), dysarthria (MESH:D004401), Acute Stroke (MESH:D020521), small vessel (SV) vasculitis (MESH:C565222), neurologic deficit (MESH:D009461), Stenosis (MESH:D003251), ischemia (MESH:D007511), Primary angiitis of (MESH:D014657), granulomatous inflammation (MESH:D007249), headache (MESH:D006261), reversible cerebral vasoconstriction (MESH:D002547), CNS vasculitis (MESH:D020293), Hematoma (MESH:D006406), vessel (LV) vasculitis (MESH:C536223)
- **Chemicals:** steroids (MESH:D013256), Azathioprin (-), prednisolone (MESH:D011239), Gadobutrol (MESH:C090600), methylprednisolone (MESH:D008775), cyclophosphamide (MESH:D003520), Cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913815/full.md

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Source: https://tomesphere.com/paper/PMC12913815