4.5 Article

Role of Apolipoprotein E Genotypes in Aneurysmal Subarachnoid Hemorrhage: Susceptibility, Complications, and Prognosis

Journal

WORLD NEUROSURGERY
Volume 118, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.wneu.2018.07.019

Keywords

Aneurysmal subarachnoid hemorrhage; Apolipoprotein E; Complications; Prognosis; Susceptibility

Funding

  1. National Natural Science Foundation of China [81601155, 81701292]

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BACKGROUND: Aneurysmal subarachnoid hemorrhage (aSAH) is a devastating disease. Emerging evidence has indicated that the apolipoprotein E (ApoE) genotype might be associated with the risk of aSAH as well as complications and outcomes after aSAH, although the results remain controversial. METHODS: We searched published literature on PuhMed, Embase, China National Knowledge Infrastructure, and VVanfang database to identify studies involving the ApoE genotype and aSAH. A meta -analysis wag performed to summarize the relationship between ApoE genotype and aSAH, including susceptibility, complications, and prognosis. RESULTS: Eighteen studies were considered eligible for inclusion. Generally,.4 carriers had increased risk of aSAH (odds ratio [OR] 1,23, 95% confidence interval [CO 1.01-1,49). White patients with the c2.42 genotype had a greater risk of aSAH (OR 3.38, 95% CI 1.13 10.11). The patients with aSAH carrying the e 4 allele had an increased risk of poor outcome (OR 2,21, 95% CI 1.21-4.05) compared with non -r4 carriers, especially in Asian patients (OR 4.99, 95% CI 1.73-14.40). ApoE e 4 carriers have increased risk of delayed ischemic neurologic deficit compared with non -r'4 carriers in the overall population. No significant difference vvas detected regarding the effect of certain ApoE genotypes aan aSAH admission severity, rebleeding, or cerebral vasospasm after aSAH. CONCLUSIONS: We found that the ApoE genotype was significantly associated with aSAH risk, whereas its effect on certain ethnic populations differs. Patient carrying the r4 allele might have a worse outcome, whereas current evidence was insufficient to prove the association between ApoE genotypes and post-SAH complications.

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