An incomplete Circle of Willis is not a risk factor for white matter hyperintensities: The Tromso Study

被引:4
作者
Hindenes, Lars B. [1 ,2 ]
Haberg, Asta K. [3 ,4 ]
Mathiesen, Ellisiv B. [1 ,5 ]
Vangberg, Torgil R. [1 ,2 ]
机构
[1] UiT Arctic Univ Norway, Fac Hlth Sci, Dept Clin Med, Postboks 6050, N-9037 Tromso, Norway
[2] Univ Hosp North Norway, PET Ctr, N-9038 Tromso, Norway
[3] St Olavs Univ Hosp, Dept Radiol & Nucl Med, Postboks 3250, N-7030 Trondheim, Norway
[4] Norwegian Univ Sci & Technol NTNU, Dept Neuromed & Movement Sci, NTNU, N-7491 Trondheim, Norway
[5] Univ Hosp North Norway, Dept Neurol, N-9038 Tromso, Norway
关键词
Circulation; Leukoaraiosis; Health survey; Epidemiology;
D O I
10.1016/j.jns.2020.117268
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The Circle of Willis (CoW) is often underdeveloped or incomplete, leading to suboptimal blood supply to the brain. As hypoperfusion is thought to play a role in the aetiology of white matter hyperintensities (WMH), the objective of this study was to assess whether incomplete CoW variants were associated with increased WMH volumes compared to the complete CoW. Methods: In a cross-sectional population sample of 1751 people (age 40-84 years, 46.4% men), we used an automated method to segment WMH using T1-weighted and T2-weighted fluid-attenuated inversion recovery image obtained at 3T. CoW variants were classified from time-of-flight scans, also at 3T. WMH risk factors, including age, sex, smoking and blood pressure, were obtained from questionnaires and clinical examinations. We used linear regression to examine whether people with incomplete CoW variants had greater volumes of deep WMH (DWMH) and periventricular WMH (PWMH) compared to people with the complete CoW, correcting for WMH risk factors. Results: Participants with incomplete CoW variants did not have significantly higher DWMH or PWMH volumes than those with complete CoW when accounting for risk factors. Age, pack-years smoking, and systolic blood pressure were risk factors for increased DWMH and PWMH volume. Diabetes was a unique risk factor for increased PWMH volume. Conclusion: Incomplete CoW variants do not appear to be risk factors for WMH in the general population.
引用
收藏
页数:8
相关论文
共 56 条
  • [1] Brain white matter hyperintensities are associated with carotid intraplaque hemorrhage
    Altaf, Nishath
    Morgan, Paul S.
    Moody, Alan
    MacSweeney, Shane T.
    Gladman, J. R.
    Auer, Dorothee P.
    [J]. RADIOLOGY, 2008, 248 (01) : 202 - 209
  • [2] Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
    Armstrong, Nicola J.
    Mather, Karen A.
    Sargurupremraj, Muralidharan
    Knol, Maria J.
    Malik, Rainer
    Satizabal, Claudia L.
    Yanek, Lisa R.
    Wen, Wei
    Gudnason, Vilmundur G.
    Dueker, Nicole D.
    Elliott, Lloyd T.
    Hofer, Edith
    Bis, Joshua
    Jahanshad, Neda
    Li, Shuo
    Logue, Mark A.
    Luciano, Michelle
    Scholz, Markus
    Smith, Albert V.
    Trompet, Stella
    Vojinovic, Dina
    Xia, Rui
    Alfaro-Almagro, Fidel
    Ames, David
    Amin, Najaf
    Amouyel, Philippe
    Beiser, Alexa S.
    Brodaty, Henry
    Deary, Ian J.
    Fennema-Notestine, Christine
    Gampawar, Piyush G.
    Gottesman, Rebecca
    Griffanti, Ludovica
    Jack, Clifford R., Jr.
    Jenkinson, Mark
    Jiang, Jiyang
    Kral, Brian G.
    Kwok, John B.
    Lampe, Leonie
    Liewald, David C. M.
    Maillard, Pauline
    Marchini, Jonathan
    Bastin, Mark E.
    Mazoyer, Bernard
    Pirpamer, Lukas
    Rafael Romero, Jose
    Roshchupkin, Gennady V.
    Schofield, Peter R.
    Schroeter, Matthias L.
    Stott, David J.
    [J]. STROKE, 2020, 51 (07) : 2111 - 2121
  • [3] Fasting blood glucose levels are associated with white matter hyperintensities' burden in older individuals with and without type 2 diabetes
    Cherbuin, N.
    Wen, W.
    Sachdev, P. S.
    Anstey, K. J.
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 357 : E44 - E44
  • [4] Associations between Circle of Willis Morphology and White Matter Lesion Load in Subjects with Carotid Artery Stenosis
    Chuang, Yu-Ming
    Huang, Kuo-Lun
    Chang, Yeu-Jhy
    Chang, Chien-Hung
    Chang, Ting-Yu
    Wu, Tai-Cheng
    Lin, Ching-Po
    Wong, Ho-Fai
    Liu, Shan-Jin
    Lee, Tsong-Hai
    [J]. EUROPEAN NEUROLOGY, 2011, 66 (03) : 136 - 144
  • [5] Prevalence of cerebral white matter lesions in elderly people: a population based magnetic resonance imaging study. The Rotterdam Scan Study
    de Leeuw, FE
    de Groot, JC
    Achten, E
    Oudkerk, M
    Ramos, LMP
    Heijboer, R
    Hofman, A
    Jolles, J
    van Gijn, J
    Breteler, MMB
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 70 (01) : 9 - 14
  • [6] The clinical importance of white matter hyperintensities on brain magnetic resonance imaging: systematic review and meta-analysis
    Debette, Stephanie
    Markus, H. S.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2010, 341 : 288
  • [7] Variants in the Circle of Willis and White Matter Disease in Ecuadorian Mestizos
    Del Brutto, Oscar H.
    Lama, Julio
    [J]. JOURNAL OF NEUROIMAGING, 2015, 25 (01) : 124 - 126
  • [8] Incompleteness of the Circle of Willis Correlates Poorly with Imaging Evidence of Small Vessel Disease. A Population-based Study in Rural Ecuador (the Atahualpa Project)
    Del Brutto, Oscar H.
    Mera, Robertino M.
    Zambrano, Mauricio
    Lama, Julio
    [J]. JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2015, 24 (01) : 73 - 77
  • [9] Vascular risk factors and progression of white matter hyperintensities in the Lothian Birth Cohort 1936
    Dickie, David Alexander
    Ritchie, Stuart J.
    Cox, Simon R.
    Sakka, Eleni
    Royle, Natalie A.
    Aribisala, Benjamin S.
    Hernandez, Maria del C. Valdes
    Maniega, Susana Munoz
    Pattie, Alison
    Corley, Janie
    Starr, John M.
    Bastin, Mark E.
    Deary, Ian J.
    Wardlaw, Joanna M.
    [J]. NEUROBIOLOGY OF AGING, 2016, 42 : 116 - 123
  • [10] Longitudinal study of blood pressure and white matter hyperintensities -: The EVA MRI cohort
    Dufouil, C
    de Kersaint-Gilly, A
    Besançon, V
    Levy, C
    Auffray, E
    Brunnereau, L
    Alpérovitch, A
    Tzourio, C
    [J]. NEUROLOGY, 2001, 56 (07) : 921 - 926