APOE ε4 is associated with obstructive sleep apnea/hypopnea -: The Sleep Heart Health Study

被引:138
作者
Gottlieb, DJ
DeStefano, AL
Foley, DJ
Mignot, E
Redline, S
Givelber, RJ
Young, T
机构
[1] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
[2] VA Boston Healthcare Syst, Boston, MA USA
[3] Boston Univ, Sch Publ Hlth, Boston, MA 02215 USA
[4] NIA, Bethesda, MD 20892 USA
[5] Stanford Univ, Stanford, CA 94305 USA
[6] Case Western Reserve Univ, Cleveland, OH 44106 USA
[7] Univ Pittsburgh, Pittsburgh, PA 15260 USA
[8] Univ Wisconsin, Madison, WI USA
关键词
D O I
10.1212/01.WNL.0000134671.99649.32
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Obstructive sleep apnea/hypopnea (OSAH) has a strong heritable component, although its genetic basis remains largely unknown. One epidemiologic study found a significant association between the APOE epsilon4 allele and OSAH in middle-aged adults, a finding that was not replicated in a cohort of elderly adults. The objective of this study was to further examine the association of the APOE epsilon4 allele with OSAH in a community-dwelling cohort, exploring age dependency of the association. Methods: A genetic association study was performed, nested within a prospective cohort study of the cardiovascular consequences of OSAH. Unattended, in-home nocturnal polysomnography was used to measure apnea-hypopnea index (AHI) in 1,775 participants age 40 to 100 years. OSAH was defined as an AHIgreater than or equal to15. The relation of APOE genotype to prevalent OSAH was analyzed using generalized estimating equations to account for non-independent observations of individuals from the same sibship. Results: At least one APOE epsilon4 allele was present in 25% of subjects, with 1.3% epsilon4/epsilon4 homozygotes. The prevalence of OSAH was 19%. After adjustment for age, sex, and BMI, the presence of any APOE epsilon4 allele was associated with increased odds of OSAH (OR 1.41, 95% CI 1.06 to 1.87, p=0.02). The effect was approximately twice as great in subjects <75 (OR 1.61, CI 1.02 to 2.54) as in those >= 75 years old ( OR 1.32, CI 0.91 to 1.90). Exploratory analyses revealed that the strongest effect of APOE epsilon 4 was in subjects age <65 (OR 3.08, CI 1.43 to 6.64), and was stronger in those with hypertension or cardiovascular disease than in those without. Conclusion: The APOE epsilon4 allele is associated with increased risk of OSAH, particularly in individuals under age 65. The mechanisms underlying this association are uncertain. Age-dependency of the APOE-OSAH association may explain previous conflicting results.
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页码:664 / 668
页数:5
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