Thromb Haemost 2023; 123(03): 326-335
DOI: 10.1055/a-1951-3402
Stroke, Systemic or Venous Thromboembolism

Inflammatory Markers Differentiate Cerebral Venous Sinus Thrombosis from Mimics

Jiayue Ding*
1   Department of Neurology, Tianjin Medical University General Hospital, Tianjin, People's Republic of China
,
Liqun Pan*
2   Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, People's Republic of China
,
Duo Lan*
2   Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, People's Republic of China
,
Zhiying Chen
3   Department of Neurology, Jiujiang University Affiliated Hospital, Jiujiang, Jiangxi, People's Republic of China
,
Zhongao Wang
2   Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, People's Republic of China
,
Ming Zou
1   Department of Neurology, Tianjin Medical University General Hospital, Tianjin, People's Republic of China
,
Ran Meng
2   Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, People's Republic of China
› Author Affiliations
Funding This study was sponsored by the National Key R&D Program of China (2017YFC1308401), the National Natural Science Foundation of China (82171297), the Natural Science Foundation of Beijing Municipality (7212047), the Natural Science Foundation of Tianjin City (19JCYBJC27500), and the Tianjin Key Medical Discipline (Specialty) Construction Project.


Abstract

Imaging tests always misdiagnose anatomical variants of cerebral sinuses as cerebral venous sinus thrombosis (CVST). Anatomical variants of cerebral sinuses are called CVST mimics. This study aimed to identify the role of inflammatory markers in differentiating CVST from mimics. A total of 146 patients diagnosed as CVST and 93 patients with mimics were recruited in this study. Receiver operating characteristic (ROC) analysis was performed to demonstrate the sensitivity and specificity of inflammatory markers for diagnosing CVST. Rank logistic regression analysis was performed to identify the association of markers to CVST severity and prognosis. CVST presented higher inflammatory reactions compared with mimics, demonstrated by the neutrophil count (5.11 [3.97–6.80] vs. 3.06 [2.34–3.86]), interleukin (IL)-6 (7.42 [3.85–14.22] vs. 2.47 [1.50–4.00]), and neutrophil-to-lymphocyte ratio (NLR; 3.19 [2.18–4.62] vs. 1.66 [1.16–2.22]). ROC analysis showed markers with area under the curve (AUC) >0.8, including IL-6 (optimal cutoff: 3.790; kappa value: 0.499), neutrophil count (3.975; 0.522), and NLR (2.070; 0.476). After propensity score matching, only IL-6 had an AUC >0.8, with an optimal cutoff of 3.060 and a kappa value of 0.636. Ranked logistic regression showed that IL-6 (odds ratio, 95% confidence interval: 1.063, 1.026–1.101; 1.029, 1.009–1.050), cerebrospinal fluid (CSF) immunoglobulin (Ig) A (0.279, 0.110–0.706; 0.398, 0.162–0.974), CSF IgM (22.399, 3.004–167.001; 9.545, 1.382–65.928), and CSF IgG (1.287, 1.124–1.473; 1.232, 1.091–1.392) were independently correlated with the baseline and follow-up mRS. In conclusion, inflammatory markers in CVST were different from those in mimics. These markers, especially IL-6, could not only differentiate CVST from its mimics, but also evaluate CVST severity and prognosis.

Author Contributions

J.D., L.P., and R.M. formulated the conception and design of the study, drafted the manuscript, and prepared the figures; L.P., D.L., Z.C., and Z.W. contributed to data acquisition; J.D. and R.M. were responsible for the data interpretation and statistical analysis; M.Z. and R.M. made critical revisions of the manuscript.


* These authors contributed equally to the study.


Supplementary Material



Publication History

Received: 16 July 2022

Accepted: 23 September 2022

Accepted Manuscript online:
27 September 2022

Article published online:
15 December 2022

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