Plasminogen activator inhibit-I (PAI-I) polymorphisms in patients with obstructive sleep apnoea

Abstract

Cardiovascular diseases are frequent among patients with the obstructive sleep apnoea syndrome (OSAS). The aetiopathogenesis of this association is unclear. Type I plasminogen activator inhibitor (PAI-I) is one of the primary regulators of the fibrinolytic system. A reported association between PAI-I activity and an insertion/deletion polymorphism (4G/SG) in the promoter region of the PAI-I gene suggests a critical role for this genomic region in the pathogenesis of several cardiovascular diseases. In this study, we determined the prevalence of this polymorphism in patients with OSAS and in healthy control subjects. The 4G/5G polymorphism in the promoter region of the PAI-I gene was determined in 78 male patients with severe OSAS (56 ± 2 apnoeas per hour) and in 70 healthy male, non-smoker volunteers of similar age, without personal or familial history of cardiovascular disease. The frequency of the 4G/4G, 4G/5G and 5G/5G genotypes in patients with OSAS (18%, 62%, 19%, respectively) was not significantly different from that seen in healthy subjects (16%, 60%, 24% P=NS). These results show that the distribution of the 4G/5G polymorphism in the promoter region of the PAI-I gene in patients with OSAS is similar to that observed in healthy subjects. This observation suggests that the PAI-I polymorphism has no relationship with the increased risk of cardiovascular diseases seen in patients with OSAS. © 2002 Elsevier Science Ltd.