Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage. (31st July 2018)
- Record Type:
- Journal Article
- Title:
- Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage. (31st July 2018)
- Main Title:
- Racial/ethnic variation of APOE alleles for lobar intracerebral hemorrhage
- Authors:
- Sawyer, Russell P.
Sekar, Padmini
Osborne, Jennifer
Kittner, Steven J.
Moomaw, Charles J.
Flaherty, Matthew L.
Langefeld, Carl D.
Anderson, Christopher D.
Rosand, Jonathan
Woo, Daniel - Abstract:
- Abstract : Objective: APOE ε2 and ε4 alleles have been associated with lobar intracerebral hemorrhage (ICH) in predominately white populations; we sought to evaluate whether this held true among black and Hispanic populations. Methods: The Ethnic/Racial Variations of Intracerebral Hemorrhage study is a prospective, multicenter case-control study of ICH among white, black, and Hispanic participants. Controls were recruited to match cases based on age, ethnicity/race, sex, and geographic location. APOE genotyping and ICH location was determined blinded to clinical data. Results: There were 907 cases of lobar ICH and 2, 660 controls with APOE results. Both APOE ε 2 (odds ratio [OR] 1.5, 95% confidence interval [CI] 1.1–2.0, p = 0.01) and APOE ε 4 (OR 2.0, 95% CI 1.5–2.6, p < 1 × 10 −4 ) were associated with lobar ICH among white participants. Among black participants, neither APOE ε 2 (OR 1.0, 95% CI 0.7–1.5, p = 0.97) nor APOE ε 4 (OR 1.0, 95% CI 0.7–1.4, p = 0.90) were independent risk factors for lobar ICH. Similarly, among Hispanic participants, neither APOE ε 2 (OR 1.0, 95% CI 0.6–1.8, p = 0.89) nor APOE ε 4 (OR 1.2, 95% CI 0.8–1.7, p = 0.36) were associated with lobar ICH. Hypertension was a significant risk factor for lobar ICH in all 3 racial/ethnic groups. Conclusion: In contrast to Caucasian patients, in which amyloid risk factors predominate in lobar ICH, we found that hypertension was the predominant risk factor for lobar ICH. While APOE alleles are a risk factorAbstract : Objective: APOE ε2 and ε4 alleles have been associated with lobar intracerebral hemorrhage (ICH) in predominately white populations; we sought to evaluate whether this held true among black and Hispanic populations. Methods: The Ethnic/Racial Variations of Intracerebral Hemorrhage study is a prospective, multicenter case-control study of ICH among white, black, and Hispanic participants. Controls were recruited to match cases based on age, ethnicity/race, sex, and geographic location. APOE genotyping and ICH location was determined blinded to clinical data. Results: There were 907 cases of lobar ICH and 2, 660 controls with APOE results. Both APOE ε 2 (odds ratio [OR] 1.5, 95% confidence interval [CI] 1.1–2.0, p = 0.01) and APOE ε 4 (OR 2.0, 95% CI 1.5–2.6, p < 1 × 10 −4 ) were associated with lobar ICH among white participants. Among black participants, neither APOE ε 2 (OR 1.0, 95% CI 0.7–1.5, p = 0.97) nor APOE ε 4 (OR 1.0, 95% CI 0.7–1.4, p = 0.90) were independent risk factors for lobar ICH. Similarly, among Hispanic participants, neither APOE ε 2 (OR 1.0, 95% CI 0.6–1.8, p = 0.89) nor APOE ε 4 (OR 1.2, 95% CI 0.8–1.7, p = 0.36) were associated with lobar ICH. Hypertension was a significant risk factor for lobar ICH in all 3 racial/ethnic groups. Conclusion: In contrast to Caucasian patients, in which amyloid risk factors predominate in lobar ICH, we found that hypertension was the predominant risk factor for lobar ICH. While APOE alleles are a risk factor for lobar ICH in white patients, they appear to have a much lower effect in lobar ICH in African American and Hispanic American populations. This suggests APOE ε 2 and APOE ε 4 do not affect lobar ICH risk homogeneously across ethnic populations. In addition, hypertension has a prominent role in lobar ICH risk, particularly among minorities. … (more)
- Is Part Of:
- Neurology. Volume 91:Number 5(2018)
- Journal:
- Neurology
- Issue:
- Volume 91:Number 5(2018)
- Issue Display:
- Volume 91, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 91
- Issue:
- 5
- Issue Sort Value:
- 2018-0091-0005-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-07-31
- Subjects:
- Neurology -- Periodicals
Neurology -- Periodicals
Neurologie -- Périodiques
616.8 - Journal URLs:
- http://www.mdconsult.com/public/search?search_type=journal&j_sort=pub_date&j_issn=0028-3878 ↗
http://www.mdconsult.com/about/journallist/192093418-5/about0nz0.html ↗
http://www.neurology.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1212/WNL.0000000000005908 ↗
- Languages:
- English
- ISSNs:
- 0028-3878
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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