Cavernous Malformation Hemorrhagic Presentation at Diagnosis Associated with Low 25-Hydroxy-Vitamin D Level
Autor: | Shivram Kumar, Giuseppe Lanzino, Ravinder J. Singh, Kelly D. Flemming, Lauren McCreath, Kevin J. Whitehead, Robert D. Brown |
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Rok vydání: | 2020 |
Předmět: |
Adult
Male Hemangioma Cavernous Central Nervous System medicine.medical_specialty Adolescent 030204 cardiovascular system & hematology Risk Assessment Gastroenterology Central Nervous System Neoplasms Angioma Young Adult 03 medical and health sciences 0302 clinical medicine Risk Factors Seizures Internal medicine medicine Vitamin D and neurology Humans Prospective Studies Registries Vitamin D Child Aged medicine.diagnostic_test business.industry Medical record Magnetic resonance imaging Middle Aged Prognosis Vitamin D Deficiency medicine.disease Cavernous malformations Magnetic Resonance Imaging Occult Neurology Female Neurology (clinical) Presentation (obstetrics) Cardiology and Cardiovascular Medicine business Intracranial Hemorrhages Body mass index Biomarkers 030217 neurology & neurosurgery |
Zdroj: | Cerebrovascular Diseases. 49:216-222 |
ISSN: | 1421-9786 1015-9770 |
DOI: | 10.1159/000507789 |
Popis: | Background: Cavernous malformations (CM) are angiographically occult vascular malformations that may be incidental or present with intracerebral or spinal hemorrhage, seizures, or nonhemorrhagic focal neurologic deficit (FND). Recently in vitro data have suggested vitamin D may play a role in stabilizing CCM2 endothelial cells. Little is known about the effect of vitamin D in human CM disease. Methods: Beginning in 2015, consecutive patients at our institution with radiologically confirmed CM were recruited to participate in a prospective clinical registry as well as 25-hydroxy-vitamin D study. A structured interview, survey, and examination were performed at baseline. Medical records and magnetic resonance imaging studies were reviewed and data collected included comorbid conditions, medication use, and location of CM. Standard definition of clinical hemorrhage, FND, and seizures was used. Univariate and multivariate logistic regression models were used, and OR, 95% CIs, and likelihood-ratio p values were calculated to determine the influence of the 25-hydroxy-vitamin D level on clinical presentation with hemorrhage. Results: Of 213 patients enrolled in the clinical registry between January 2015 and October 2018, 70 participated in the vitamin D study (median age: 38.3 years; 51.4% female). Of the 70 participants, 30 (42.9%) presented with hemorrhage. 25-Hydroxy-vitamin D levels were performed within 1 year of symptoms in 64.1% of patients. Patients presenting with hemorrhage had a lower 25-hydroxy-vitamin D level compared to those presenting with seizure without hemorrhage, FND, or as an incidental finding (median 25.5 ng/mL; range 11–59 hemorrhage vs. median 31.0; range 14–60, no hemorrhage; p = 0.04). After adjusting for age, month of blood draw, and body mass index, 25-hydroxy-vitamin D remained a significant predictor of hemorrhagic presentation. Brainstem location also predicted hemorrhage at presentation. Conclusion: Low 25-hydroxy-vitamin D level was more common in patients with CM presenting with hemorrhage. This study supports the potential role of modifiable factor in the initial clinical presentation of CM. Further study is needed to determine the role of vitamin D on prospective hemorrhage risk and whether supplementation may be beneficial. |
Databáze: | OpenAIRE |
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