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Assessment of the interaction of age and sex on 90-day outcome after intracerebral hemorrhage

  • Michael L. James
  • , Carl D. Langefeld
  • , Padmini Sekar
  • , Charles J. Moomaw
  • , Mitchell S.V. Elkind
  • , Bradford B. Worrall
  • , Kevin N. Sheth
  • , Sharyl R. Martini
  • , Jennifer Osborne
  • , Daniel Woo
  • Duke University
  • Wake Forest University
  • University of Cincinnati
  • Columbia University
  • University of Virginia
  • Yale University
  • Baylor College of Medicine

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Because age affects hormonal production differently in women compared with men, we sought to define sex and age interactions across a multiracial/ethnic population after intracerebral hemorrhage (ICH) to uncover evidence that loss of gonadal hormone production would result in loss of the known neuroprotective effects of gonadal hormones. Methods: Clinical and radiographic data from participants in the Ethnic/Racial Variations of Intracerebral Hemorrhage study and the Genetic and Environmental Risk Factors for Hemorrhagic Stroke study prior to December 2013 were used. Relationships among sex, age, and outcome after ICH in 616 non-Hispanic black, 590 Hispanic, and 868 non-Hispanic white participants were evaluated using multivariable logistic regression analysis. Poor outcome was defined as modified Rankin Scale score ≥3 at 90 days after ICH. Results: Sex differences were found in multiple variables among the racial/ethnic groups, including age at onset, premorbid neurologic status, and neurologic outcome after ICH. Overall, no sex-age interaction effect was found for mortality (p = 0.183) or modified Rankin Scale score (p = 0.378) at 90 days after ICH. In racial/ethnic subgroups, only the non-Hispanic black cohort provided possible evidence of a sex-age interaction on 90-day modified Rankin Scale score (p = 0.003). Conclusion: Unlike in ischemic stroke, there was no evidence that patient sex modified the effect of age on 90-day outcomes after ICH in a large multiracial/ethnic population. Future studies should evaluate biological reasons for these differences between stroke subtypes. Clinicaltrials.gov identifier: NCT01202864.

Original languageEnglish
Pages (from-to)1011-1019
Number of pages9
JournalNeurology
Volume89
Issue number10
DOIs
StatePublished - Sep 5 2017

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