Key result
Aneurysm wall enhancement on MRI is linked to ~2.9-fold higher subsequent aneurysm instability.
Why the study?
Aneurysm wall enhancement (AWE) on vessel wall MRI is proposed as an imaging biomarker of instability in unruptured intracranial aneurysms, but its frequent observation in clinically stable aneurysms leaves its longitudinal prognostic value uncertain.
Does baseline aneurysm wall enhancement on vessel wall MRI predict subsequent aneurysm instability in patients with unruptured intracranial aneurysms?
Meta-Analysis (n=2,936)
Does baseline aneurysm wall enhancement on vessel wall MRI predict subsequent aneurysm instability in patients with unruptured intracranial aneurysms?
While baseline aneurysm wall enhancement on MRI is associated with a nearly three-fold increased risk of unruptured intracranial aneurysm instability, its modest diagnostic accuracy means it should be used only as an adjunctive marker rather than a standalone predictor.
Answers are grounded in this paper and cite their sources.
AWE presence signals ~3-fold higher instability risk in UIAs; leaves open its standalone prognostic role pending prospective validation.
Background Aneurysm wall enhancement (AWE) on vessel wall MRI has been proposed as an imaging biomarker of wall inflammation and instability in unruptured intracranial aneurysms (UIAs). However, AWE is frequently observed in aneurysms that remain clinically stable, leaving its prognostic value in longitudinal settings uncertain. We conducted a systematic review and meta-analysis of longitudinal studies to quantify the association between baseline AWE status and subsequent aneurysm instability during follow-up. Methods We searched MEDLINE and Embase for longitudinal studies published between January 1, 2000 and December 13, 2025 that assessed AWE at baseline and reported aneurysm instability during follow-up. Random-effects meta-analyses were performed to estimate pooled risk ratios (RRs), and diagnostic accuracy was evaluated using a bivariate random-effects model. Results Nine studies comprising 2936 UIAs were included. During follow-up, 387 aneurysms (13.2%) demonstrated instability. Newcastle–Ottawa-Scale ranged from 2 to 7, indicating low-to-moderate study quality. Aneurysms with baseline AWE had a higher risk of subsequent instability (pooled RR 2.90; 95% CI 2.2 to 3.81; p<0.001). AWE demonstrated 63% sensitivity and 69% specificity, with a positive likelihood ratio of 2.03 and a negative likelihood ratio of 0.54. Accordingly, AWE positivity increased the post-test probability of instability to 23.5%, whereas AWE negativity reduced it to 7.6%. Conclusions Aneurysms with baseline AWE had an approximately three-fold higher risk of subsequent instability. However, the modest likelihood ratios and limited shifts in post-test probability indicate that AWE should be interpreted cautiously and regarded as an adjunctive marker, rather than a standalone predictor, in individualized UIA risk assessment.
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Goldberg et al. (2026) conducted a meta-analysis in Unruptured intracranial aneurysms (UIAs) (n=2,936). Baseline aneurysm wall enhancement (AWE) positivity on vessel wall MRI vs. Baseline aneurysm wall enhancement (AWE) negativity on vessel wall MRI was evaluated on Subsequent aneurysm instability during follow-up (RR 2.90, 95% CI 2.2-3.81, p=<0.001). Baseline aneurysm wall enhancement on MRI was associated with higher subsequent aneurysm instability (pooled RR 2.90; 95% CI 2.2-3.81; p<0.001).
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