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Reciprocal interactions of obstructive sleep apnea and hypertension associated with ACE I/D polymorphism in males

Authors :
Koyama, Renata G.
Drager, Luciano F.
Lorenzi-Filho, Geraldo
Cintra, Fátima D.
Pereira, Alexandre C.
Poyares, Dalva
Krieger, José Eduardo
Castro, Rosa M.R.P.S.
Tufik, Sérgio
de Mello, Marco Túlio
Pedrazzoli, Mario
Source :
Sleep Medicine. Dec2009, Vol. 10 Issue 10, p1107-1111. 5p.
Publication Year :
2009

Abstract

Abstract: Background: The angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism gene contributes to the genesis of hypertension (HTN) and may help explain the relationship between obstructive sleep apnea (OSA) and HTN. However, ACE is a pleiotropic gene that has several influences, including skeletal muscle and control of ventilation. We therefore tested the hypothesis that ACE polymorphism influences OSA severity. Methods: Male OSA patients (apnea-hypopnea index [AHI]>5 events/h) from 2 university sleep centers were evaluated by polysomnography and ACE I/D polymorphism genotyping. Results: We studied 266 males with OSA (age=48±13y, body mass index=29±5kg/m2, AHI=34±25events/h). HTN was present in 114 patients (43%) who were older (p <0.01), heavier (p <0.05) and had more severe OSA (p <0.01). The I allele was associated with HTN in patients with mild to moderate OSA (p <0.01), but not in those with severe OSA. ACE I/D polymorphism was not associated with apnea severity among normotensive patients. In contrast, the only variables independently associated with OSA severity among patients with hypertension in multivariate analysis were BMI (OR=1.12) and II genotype (OR=0.27). Conclusions: Our results indicate reciprocal interactions between OSA and HTN with ACE I/D polymorphism, suggesting that among hypertensive OSA males, the homozygous ACE I allele protects from severe OSA. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
13899457
Volume :
10
Issue :
10
Database :
Academic Search Index
Journal :
Sleep Medicine
Publication Type :
Academic Journal
Accession number :
45220350
Full Text :
https://doi.org/10.1016/j.sleep.2008.12.012