Bifurcation geometry remodelling of vessels in de novo and growing intracranial aneurysms: a multicenter study.

Julien Boucherit, Basile Kerleroux, Gregoire Boulouis, Guillaume Tessier, Christine Rodriguez, Peter B Sporns, Haroun Ghannouchi, Eimad Shotar, Florent Gariel, Gaultier Marnat, Julien Burel, Heloise Ifergan, Géraud Forestier, Aymeric Rouchaud, Hubert Desal, Anass Nouri, Florent Autrusseau, Gervaise Loirand, Romain Bourcier, Vincent L'Allinec
J NeuroIntervent Surg. 2022-05-13; 15(6): 566-571
DOI: 10.1136/neurintsurg-2021-018487

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BackgroundGeometrical parameters, including arterial bifurcation angle, tortuosity, and arterial diameters, have been associated with the pathophysiology of intracranial aneurysm (IA) formation. The aim of this study was to investigate whether these parameters were present before or if they resulted from IA formation and growth.MethodsPatients from nine academic centers were retrospectively identified if they presented with a de novo IA or a significant IA growth on subsequent imaging. For each patient, geometrical parameters were extracted using a semi-automated algorithm and compared between bifurcations with IA formation or growth (aneurysmal group), and their contralateral side without IA (control group). These parameters were compared at two different times using univariable models, multivariable models, and a sensitivity analysis with paired comparison.Results46 patients were included with 21 de novo IAs (46%) and 25 significant IA growths (54%). The initial angle was not different between the aneurysmal and control groups (129.7±42.1 vs 119.8±34.3; p=0.264) but was significantly wider at the final stage (140.4±40.9 vs 121.5±34.1; p=0.032), with a more important widening of the aneurysmal angle (10.8±15.8 vs 1.78±7.38; p=0.001). Variations in other parameters were not significant. These results were confirmed by paired comparisons.ConclusionOur study suggests that wider bifurcation angles that have long been deemed causal factors for IA formation or growth may be secondary to IA formation at pathologic bifurcation sites. This finding has implications for our understanding of IA formation pathophysiology.

Auteurs Bordeaux Neurocampus