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Leukocytosis at Presentation Is an Independent Predictor for Hemorrhage in Cerebral Cavernoma
Harun Asoglu1, Tim Lampmann1, Johannes Wach1
1Department of Neurosurgery, University Hospital Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.
Insights
A high white blood cell count (WBC) can help identify acute hemorrhage in cerebral cavernous malformations (CCMs). This finding supports the role of neuroinflammation in CCMs and aids in diagnosing ambiguous cases.
Area of Science:
- Neurology
- Vascular Malformations
- Inflammation Biology
Background:
- Cerebral cavernous malformations (CCMs) often present with hemorrhage, but distinguishing acute from chronic bleeding can be challenging.
- Emerging evidence suggests inflammation plays a key role in CCM pathogenesis.
Purpose of the Study:
- To investigate routine inflammatory parameters for aiding diagnosis in ambiguous cerebral cavernous malformation cases.
- To assess the utility of white blood cell count (WBC) in predicting acute hemorrhage in CCMs.
Main Methods:
- Retrospective analysis of 87 patients who underwent CCM resection.
- Dichotomization into acute hemorrhage and control groups.
- Evaluation of inflammatory markers: C-reactive Protein (CrP), WBC, Red Cell Distribution Width (RDW), and Mean Platelet Volume/Platelet Count Ratio (MPV/PC).
Main Results:
- White blood cell count (WBC) at admission showed moderate diagnostic accuracy (AUC: 0.74) for predicting acute hemorrhage.
- A WBC threshold of ≥6.595 G/L was identified as an independent predictor of acute hemorrhage (aOR: 4.5, p < 0.001).
Conclusions:
- Elevated WBC (>6.595 G/L) is significantly associated with acute hemorrhage in CCMs.
- WBC serves as a practical biomarker for controversial CCM cases, highlighting neuroinflammation's role.
- Further research is needed on inflammation's precise role in CCM pathogenesis and treatment.
Abstract:
Objective: Cerebral cavernous malformations (CCMs) are usually occult but can present with a symptomatic hemorrhage. Treatment recommendations for CCMs are still controversially discussed, as all CCMs have signs of chronic hemorrhage. The distinction of acute hemorrhage can be difficult, especially when patients only present with mild symptoms. Because of emerging evidence supporting inflammatory burden as a main avenue in the disease pathogenesis of CCMs, the aim of the present study was to investigate routine inflammatory parameters to support decision-making in ambiguous cases. Methods: A total of 87 patients who underwent CCM resection at the authors' institution between 2008 and 2021 were included in this study. Data were recorded retrospectively. Patients were dichotomized into two groups: those with acute hemorrhage and those without, as a control group (e.g., resection for seizure control). Inflammatory parameters included C-reactive Protein (CrP), White Blood Cell Count (WBC), Red Cell Distribution Width (RDW), and Mean Platelet Volume/Platelet Count Ratio (MPV/PC). Results: The receiver operating characteristic curve demonstrated moderate diagnostic accuracy for predicting acute hemorrhage from CCM based on WBC at admission (AUC: 0.74, 95%-CI: 0.63-0.84) with a cut-off of ≥6.595 G/L. The multivariable analysis confirmed that having a WBC > 6.595 G/L is an independent predictor for acute hemorrhage of CCM (adjusted odds ratio: 4.5, 95%-CI: 1.8-11.2, p < 0.001). Conclusions: A white blood cell count >6.595 G/L was significantly associated with acute hemorrhage in CCMs and appears to be a quick-to-use biomarker in controversial cases. Moreover, leukocytosis emphasizes the involvement of neuroinflammation in acute hemorrhage of CCM. Further investigations are needed to analyze the precise role of inflammation in CCM pathogenesis and its impact on treatment strategies.
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