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MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?
MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?
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MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?
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MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?
MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?
Journal Article

MIAs (Mirror Intracranial Aneurysms): symmetry-related patient risk or consequence of multiplicity?

2025
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Overview
Purpose Determine whether mirror intracranial aneurysms (MIAs) confer risk beyond aneurysm multiplicity and describe their distribution and longitudinal change. Methods Retrospective two-centre UK cohort of unruptured intracranial aneurysms (UIAs) diagnosed 2006–2020; outcomes to 2022. Endpoints: first rupture, SAH-specific/all-cause mortality, time to treatment, and lesion-level growth/morphology change. Rates used Poisson models with person-time offsets; lesion-level risks used GEE (modified Poisson). Rupture-free survival used inverse-probability-weighted Kaplan–Meier. Models adjusted for baseline aneurysm count. Results 1,985 UIAs were identified; 289 (14.6%) were MIAs. MIAs clustered at the MCA bifurcation (57.8%) and ICA terminus (34.6%). First-rupture incidence was higher in MIAs (1.74/100 person-years (PY)) than aMIAs (0.76/100 PY) or SIAs (0.39/100 PY); MIA > SIA IRR 4.46 ( q  = 0.0003), MIA > aMIA IRR 2.29 ( q  = 0.0044). SAH-specific mortality incidence was higher in MIAs (1.21/100 PY) than SIAs (0.36/100 PY; IRR 3.36, q  = 0.0057) and aMIAs (0.19/100 PY; IRR 6.37, q  = 0.0002). IPW survival was poorer for MIAs vs aMIAs (weighted log-rank χ 2  = 9.95, p  = 0.0016) and vs SIAs (χ 2  = 18.09, p  = 2.11 × 10⁻ 5 ). Lesion-level GEE showed no symmetry-specific increase in rupture risk (omnibus p  = 0.72). Lesion-level growth ≥ 1 mm (RR 1.67, q  = 0.0380) and morphology change (RR 2.10, q  = 0.0121) were higher in MIAs. With aneurysm count adjustment, effects attenuated with wide CIs, consistent with limited power. Conclusion MIAs were associated with higher patient-time rupture and SAH-specific mortality and greater lesion-level instability, but not with an independent per-aneurysm rupture hazard. The excess patient-level risk is largely explained by exposure (multiplicity); a symmetry-related effect remains plausible but unconfirmed. Larger, prospectively harmonised datasets are needed.