Open AccessAssociation of Intracranial Aneurysms With Aortic Aneurysms in 125 Patients With Fusiform and 4253 Patients With Saccular Intracranial Aneurysms and Their Family Members and Population Controls
Author(s) -
Kurtelius Arttu,
Väntti Nelli,
Rezai Jahromi Behnam,
Tähtinen Olli,
Manninen Hannu,
Koskenvuo Juha,
Tulamo Riikka,
Kotikoski Satu,
Nurmonen Heidi,
Kämäräinen OlliPekka,
Huttunen Terhi,
Huttunen Jukka,
Fraunberg Mikael,
Koivisto Timo,
Jääskeläinen Juha E.,
Lindgren Antti E.
Publication year - 2019
Publication title -
journal of the american heart association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.494
H-Index - 85
ISSN - 2047-9980
DOI - 10.1161/jaha.119.013277
Subject(s) - medicine , aneurysm , population , hazard ratio , vascular disease , surgery , gastroenterology , pathology , radiology , confidence interval , environmental health
Background Varying degrees of co‐occurrence of intracranial aneurysms ( IA ) and aortic aneurysms ( AA ) have been reported. We sought to compare the risk for AA in fusiform intracranial aneurysms ( fIA ) and saccular intracranial aneurysms ( sIA ) disease and evaluate possible genetic connection between the fIA disease and AA s. Additionally, the characteristics and aneurysms of the fIA and sIA patients were compared. Methods and Results The Kuopio Intracranial Aneurysm Database includes all 4253 sIA and 125 fIA patients from its Eastern Finnish catchment population, and 13 009 matched population controls and 18 455 first‐degree relatives to the IA patients were identified, and the Finnish national registers were used to identify the individuals with AA . A total of 33 fIA patients were studied using an exomic gene panel of 37 genes associated with AA s. Seventeen (14.4%) fIA patients and 48 (1.2%) sIA patients had a diagnosis of AA . Both fIA and sIA patients had AA s significantly more often than their controls (1.2% and 0.5%) or relatives (0.9% and 0.3%). In a competing risks Cox regression model, the presence of fIA was the strongest risk factor for AA (subdistribution hazard ratio 7.6, 95% CI 3.9–14.9, P <0.0005). One likely pathogenic variant in COL 5A2 and 3 variants of unknown significance were identified in MYH 11 , COL 11A1 , and FBN 1 in 4 fIA patients. Conclusions The prevalence of AA s is increased slightly in sIA patients and significantly in fIA patients. fIA patients are older and have more comorbid diseases than sIA patients but this alone does not explain their clinically significant AA risk.