Key result
Early elevated TNF-α is linked to poor 3-month outcome after SAH without predicting vasospasm.
Why the study?
Inflammation may mediate poor outcome in subarachnoid hemorrhage, but the association of serum TNF-α and IL-6 with vasospasm and outcome is unclear.
Is early elevation of serum TNF-α and IL-6 associated with vasospasm and poor outcome in patients with subarachnoid hemorrhage?
Cohort (n=52)
Is early elevation of serum TNF-α and IL-6 associated with vasospasm and poor outcome in patients with subarachnoid hemorrhage?
p-value: p=0.0004
Early and global elevation of serum TNF-α is associated with poor clinical outcomes at 3 months in patients with subarachnoid hemorrhage, suggesting a role for inflammation in SAH-related brain injury.
Early TNF-α elevation should not yet guide SAH care; hypothesis-generating for inflammation-targeted trials independent of vasospasm.
OBJECTIVE: Subarachnoid hemorrhage (SAH) is associated with inflammation that may mediate poor outcome in SAH. We hypothesize that elevated serum tumor necrosis factor α (TNF-α) and interleukin 6 (IL-6) are associated with vasospasm and poor outcome in SAH. METHODS: In 52 consecutive SAH subjects, we compared TNF-α and IL-6 levels on post-SAH days 0 to 1, 2 to 3, 4 to 5, 6 to 8, and 10 to 14 with respect to vasospasm and to poor outcome at 3 and 6 months. Vasospasm was defined as more than 50% reduction in vessel caliber on angiography. Poor outcome was defined as modified Rankin score greater than 2. RESULTS: Elevated TNF-α on post-SAH days 2 to 3 was associated with poor 3-month outcome (P = 0.0004). Global elevation of TNF-α over time (post-SAH days 0-14) was independently associated with poor 3-month outcome after adjusting for Hunt-and-Hess grade and age (P = 0.02). Neither cross-sectional nor IL-6 levels over time were associated with outcome. Neither TNF-α nor IL-6 levels were associated with vasospasm. CONCLUSIONS: Elevation in serum TNF-α on post-SAH days 2 to 3 and global elevation of TNF-α over time are associated with poor outcome but not with angiographic vasospasm in this small cohort. Future studies are needed to define the role of TNF-α in SAH-related brain injury and its potential as a SAH outcome biomarker.
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Chou et al. (2012) conducted a cohort in Subarachnoid hemorrhage (n=52). Elevated serum tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) vs. Non-elevated levels was evaluated on Poor outcome (modified Rankin score > 2) at 3 months (p=0.0004). Elevated serum TNF-α on post-SAH days 2 to 3 was associated with poor 3-month outcome (P=0.0004), but neither TNF-α nor IL-6 levels were associated with angiographic vasospasm.
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