Haptoglobin genotype and aneurysmal subarachnoid hemorrhage: Individual patient data analysis.

Journal Article (Journal Article)

OBJECTIVE: To perform an individual patient-level data (IPLD) analysis and to determine the relationship between haptoglobin (HP) genotype and outcomes after aneurysmal subarachnoid hemorrhage (aSAH). METHODS: The primary outcome was favorable outcome on the modified Rankin Scale or Glasgow Outcome Scale up to 12 months after ictus. The secondary outcomes were occurrence of delayed ischemic neurologic deficit, radiologic infarction, angiographic vasospasm, and transcranial Doppler evidence of vasospasm. World Federation of Neurological Surgeons (WFNS) scale, Fisher grade, age, and aneurysmal treatment modality were covariates for both primary and secondary outcomes. As preplanned, a 2-stage IPLD analysis was conducted, followed by these sensitivity analyses: (1) unadjusted; (2) exclusion of unpublished studies; (3) all permutations of HP genotypes; (4) sliding dichotomy; (5) ordinal regression; (6) 1-stage analysis; (7) exclusion of studies not in Hardy-Weinberg equilibrium (HWE); (8) inclusion of studies without the essential covariates; (9) inclusion of additional covariates; and (10) including only covariates significant in univariate analysis. RESULTS: Eleven studies (5 published, 6 unpublished) totaling 939 patients were included. Overall, the study population was in HWE. Follow-up times were 1, 3, and 6 months for 355, 516, and 438 patients. HP genotype was not associated with any primary or secondary outcome. No trends were observed. When taken through the same analysis, higher age and WFNS scale were associated with an unfavorable outcome as expected. CONCLUSION: This comprehensive IPLD analysis, carefully controlling for covariates, refutes previous studies showing that HP1-1 associates with better outcome after aSAH.

Full Text

Duke Authors

Cited Authors

  • Gaastra, B; Ren, D; Alexander, S; Bennett, ER; Bielawski, DM; Blackburn, SL; Borsody, MK; Doré, S; Galea, J; Garland, P; He, T; Iihara, K; Kawamura, Y; Leclerc, JL; Meschia, JF; Pizzi, MA; Tamargo, RJ; Yang, W; Nyquist, PA; Bulters, DO; Galea, I

Published Date

  • April 30, 2019

Published In

Volume / Issue

  • 92 / 18

Start / End Page

  • e2150 - e2164

PubMed ID

  • 30952792

Pubmed Central ID

  • PMC6512887

Electronic International Standard Serial Number (EISSN)

  • 1526-632X

Digital Object Identifier (DOI)

  • 10.1212/WNL.0000000000007397


  • eng

Conference Location

  • United States