Inflammatory Markers and Severity of Intracerebral Hemorrhage.

Autor:	Bernstein JE; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA., Savla P; Osteopathy, College of Osteopathic Medicine - Touro University, Vallejo, USA., Dong F; Clinical Research, Western University of Health Sciences, Pomona, USA., Zampella B; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA., Wiginton JG 4th; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA., Miulli DE; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA., Wacker MR; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA., Menoni R; Neurosurgery, Riverside University Health System Medical Center, Moreno Valley, USA.
Jazyk:	angličtina
Zdroj:	Cureus [Cureus] 2018 Oct 31; Vol. 10 (10), pp. e3529. Date of Electronic Publication: 2018 Oct 31.
DOI:	10.7759/cureus.3529
Abstrakt:	Background and purpose The pathogenesis of brain injury after intracerebral hemorrhage is thought to be due to mechanical damage followed by ischemic, cytotoxic, and inflammatory changes in the underlying and surrounding tissue.In recent years, there has been a greater research interest into the various inflammatory biomarkers and growth factors that are secreted during intracerebral hemorrhage. The biomarkers investigated in this study are tumor necrosis factor alpha (TNF alpha), C-reactive protein (CRP), homocysteine (Hcy), and vascular endothelial growth factor (VEGF). The aim of this study was to further investigate the effects of these biomarkers in predicting the acute severity outcome of intracerebral hemorrhage (ICH). Methods We conducted a retrospective chart review of patients with spontaneous ICH with TNF alpha, CRP, VEGF, and Hcy levels drawn on admission. Forty-two patients with spontaneous ICH with at least one of the above labs were included in the study. Primary outcomes included death, Glasgow Coma Scale (GCS) on admission, early neurologic decline (END), and hemorrhage size. Secondary outcomes included GCS on discharge, ICH score, functional outcome risk stratification scale of intracerebral hemorrhage (FUNC score), change in hemorrhage size, need for surgical intervention, and length of intensive care unit (ICU) stay. Results Forty-two patients with spontaneous intracerebral hemorrhage (ICH) were analyzed, 12 patients (28.5%) required surgical intervention, and four patients (9.5%) died. Only low VEGF serum values were found to predict mortality. TNF alpha, CRP, Hcy, and VEGF levels in our patients with ICH were not found to predict early neurologic decline and were not correlated with GCS on admission, initial hemorrhage size, change in hemorrhage size, need for surgical intervention, ICH score, FUNC score, midline shift, and length of ICU stay. CRP and Hcy were elevated in 58% and 31% of patients tested, respectively. GCS on admission and ICH score were significantly associated with mortality. Conclusion After careful statistical review of the data obtained from this patient population, only low VEGF values were found to be a significant predictor of mortality. However, elevated CRP and Hcy levels were associated with a non-significant trend in hemorrhage size and mortality suggesting that CRP and Hcy-lowering therapies may decrease hemorrhagic stroke risk and severity. Competing Interests: The authors have declared that no competing interests exist.
Databáze:	MEDLINE
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