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Original research
Prevalence of unruptured intracranial aneurysms: impact of different definitions – the Tromsø Study
  1. Liv-Hege Johnsen1,2,
  2. Marit Herder1,2,
  3. Torgil Vangberg2,3,
  4. Roar Kloster2,4,
  5. Tor Ingebrigtsen2,4,
  6. Jørgen Gjernes Isaksen2,4,
  7. Ellisiv B Mathiesen2,5
  1. 1Department of Radiology, University Hospital of North Norway, Tromso, Norway
  2. 2Department of Clinical Medicine, UiT The Arctic University, Tromso, Norway
  3. 3PET Imaging Center, University Hospital of North Norway, Tromso, Norway
  4. 4Department of Neurosurgery, Ophthalmology, and Otorhinolaryngology, University Hospital of North Norway, Tromso, Norway
  5. 5Department of Neurology, University Hospital of North Norway, Tromso, Norway
  1. Correspondence to Liv-Hege Johnsen, Department of Radiology, University Hospital of North Norway, Tromso, Norway; liv.hege.johnsen{at}gmail.com

Abstract

Background Management of incidental unruptured intracranial aneurysms (UIAs) remains challenging and depends on their risk of rupture, estimated from the assumed prevalence of aneurysms and the incidence of aneurysmal subarachnoid haemorrhage. Reported prevalence varies, and consistent criteria for definition of UIAs are lacking. We aimed to study the prevalence of UIAs in a general population according to different definitions of aneurysm.

Methods Cross-sectional population-based study using 3-dimensional time-of-flight 3 Tesla MR angiography to identify size, type and location of UIAs in 1862 adults aged 40–84 years. Size was measured as the maximal distance between any two points in the aneurysm sac. Prevalence was estimated for different diameter cutoffs (≥1, 2 and 3 mm) with and without inclusion of extradural aneurysms.

Results The overall prevalence of intradural saccular aneurysms ≥2 mm was 6.6% (95% CI 5.4% to 7.6%), 7.5% (95% CI 5.9% to 9.2%) in women and 5.5% (95% CI 4.1% to 7.2%) in men. Depending on the definition of an aneurysm, the overall prevalence ranged from 3.8% (95% CI 3.0% to 4.8%) for intradural aneurysms ≥3 mm to 8.3% (95% CI 7.1% to 9.7%) when both intradural and extradural aneurysms ≥1 mm were included.

Conclusion Prevalence in this study was higher than previously observed in other Western populations and was substantially influenced by definitions according to size and extradural or intradural location. The high prevalence of UIAs sized <5 mm may suggest lower rupture risk than previously estimated. Consensus on more robust and consistent radiological definitions of UIAs is warranted.

  • EPIDEMIOLOGY
  • CEREBROVASCULAR DISEASE
  • STROKE
  • SUBARACHNOID HAEMORRHAGE

Data availability statement

Data are available on reasonable request. Data may be obtained from a third party and are not publicly available. Data availability are restricted due to their sensitive nature. Deidentified data can be obtained by application to the Tromsø Study, please contact tromsous@uit.no for details.

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Data availability statement

Data are available on reasonable request. Data may be obtained from a third party and are not publicly available. Data availability are restricted due to their sensitive nature. Deidentified data can be obtained by application to the Tromsø Study, please contact tromsous@uit.no for details.

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Footnotes

  • JGI and EBM contributed equally.

  • Contributors Study conception and design: EBM, JGI; data collection: L-HJ; Imaging analysis: L-HJ, MH; analysis and interpretation of the results: L-HJ, EBM, JGI, TI, TV; manuscript draft: L-HJ. All authors provided critical review, edited and approved the final manuscript. EBM is guarantor of the study.

  • Funding L-HJ received funding from the Northern Norway Regional Health Authority (Grant SFP 1283-16). The MRI/MRA study was funded by the Northern Norway Regional Health Authority (Grant SFP 1271-16).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.