| Literature DB >> 34569879 |
Ida Rangus1, Lennart S Milles2, Ivana Galinovic3, Kersten Villringer3, Heinrich J Audebert1,3, Jochen B Fiebach3, Christian H Nolte1,3,4.
Abstract
BACKGROUND: Variants of the Circle of Willis (vCoW) may impede correct identification of ischemic lesion patterns and stroke etiology. We assessed reclassifications of ischemic lesion patterns due to vCoW.Entities:
Keywords: Circle of Willis; neuroanatomy; stroke patterns
Mesh:
Year: 2021 PMID: 34569879 PMCID: PMC9358303 DOI: 10.1177/17474930211048381
Source DB: PubMed Journal: Int J Stroke ISSN: 1747-4930 Impact factor: 6.948
Figure 1.Reclassification from more-than-one to one territory stroke pattern.
Example of reclassification from more-than-one to one territory stroke pattern in a patient with ischemic stroke affecting left PCA, ACA (a) and MCA territory (b) in the DWI sequence. Due to fPCA on the left side (indicated with an arrow in figure c), all stroke lesions are located within the arterial supply of the left ICA (anterior territory).
Figure 2.Reclassification from one territory to more-than-one territory stroke pattern.
Example of reclassification from one territory to more-than-one territory stroke pattern in a patient with ischemic stroke in the left thalamus (a) and in the pons and cerebellum (b) in the DWI sequence. MRA revealed fPCA on both sides (indicated with arrows in figure c). Since thalamus arterial supply stems from the fPCA, thalamic lesion is located within the arterial supply of the ICA (anterior territory) while other lesions are located within the territory supplied by the vertebrobasilar system (posterior territory).
Comparison of the demographics and cardiovascular risk factors in patients with posterior vCoW (fPCA) and posterior cCoW (adult PCA). Patients with transitional posterior circulation (n=21) were excluded from this analysis.
| Posterior vCoW (fPCA) n = 330 | Posterior cCoW (adult PCA) n = 640 | p value
| |
|---|---|---|---|
| Age (years); median (IQR) | 74 (66–81) | 74 (66–81) | 0.833 |
| Sex, no. female (%) |
|
|
|
| Arterial hypertension (%) | 284 (86.1) | 552 (86.3) | 1.000 |
| Diabetes mellitus type 2 (%) | 74 (22.4) | 178 (27.8) | 0.076 |
| Hypercholesterinemia (%) | 178 (53.9) | 361 (56.4) | 0.495 |
| Coronary heart disease (%) | 52 (15.8) | 130 (20.3) | 0.099 |
| Atrial fibrillation
| 103 (31.2) | 183 (28.6) | 0.414 |
| Smokers (%) | 61 (18.5) | 133 (20.8) | 0.446 |
| NIHSS on admission; median (IQR) | 4 (2–8) | 4 (2–8) | 0.950 |
| mRS at discharge; median (IQR) | 2 (1–3) | 2 (1–3) | 0.179 |
NIHSS: National Institutes of Health Stroke Scale; mRS: modified Rankin Scale; PCA: posterior cerebral artery; fPCA: fetal posterior cerebral artery; cCoW: complete Circle of Willis; vCoW: Variants of the Circle of Willis.
Mann-Whitney U-test for continuous variables and chi-squared test or Fishers exact test for categorical variables.
Both history of atrial fibrillation and newly diagnosed atrial fibrillation on admission or during hospital stay.
Comparison of the demographics and cardiovascular risk factors in patients with anterior vCoW and anterior cCoW.
| Anterior vCoW n = 67 | Anterior cCoW n = 924 | p value
| |
|---|---|---|---|
| Age, (years); median (IQR) | 75 (69–84) | 74 (65–81) | 0.056 |
| Sex, no. female (%) | 30 (44.8) | 418 (45.2) | 0.942 |
| Arterial hypertension (%) | 60 (89.6) | 794 (85.9) | 0.469 |
| Diabetes mellitus type 2 (%) | 19 (28.4) | 242 (26.2) | 0.774 |
| Hypercholesterinemia (%) | 35 (52.2) | 517 (56.0) | 0.611 |
| Coronary heart disease (%) | 10 (14.9) | 176 (19.0) | 0.427 |
| Atrial fibrillation
| 20 (29.9) | 274 (29.7) | 0.973 |
| Smokers (%) | 10 (14.9) | 189 (20.5) | 0.344 |
| NIHSS on admission; median (IQR) | 5 (2–8) | 4 (2–8) | 0.440 |
| mRS at discharge; median (IQR) | 2 (1–4) | 2 (1–3) | 0.218 |
NIHSS: National Institutes of Health Stroke Scale; mRS: modified Rankin Scale; cCoW: complete Circle of Willis; vCoW: Variants of the Circle of Willis.
Mann-Whitney U-test for continuous variables and chi-squared test or Fishers exact test for categorical variables.
Both history of atrial fibrillation and newly diagnosed atrial fibrillation on admission or during hospital stay.