Heme oxygenase-1 gene promoter polymorphism is associated with abdominal aortic aneurysm

Objective: Vascular inflammation is a hallmark in the development of abdominal aortic aneurysms (AAA). Heme oxygenase-I (HO-1) is a novel vascular anti-inflammatory factor. A (GT)(n) dinucleotide repeat in the HO-1 gene promoter shows a length polymorphism that modulates the level of gene transcription. Short (<25 GT) repeats are associated with an increased HO-I upregulation in response to inflammatory stimuli than are longer repeats. We hypothesised that patients with AAA had less frequently short repeats in the HO-1 gene promoter compared to patients with coronary (CAD) or peripheral artery disease (PAD), or healthy controls. Methods: 70 consecutive patients with atherosclerotic AAA, each 70 age- and sex-matched patients with CAD and PAD as well as 61 unmatched healthy atherosclerosis-free controls for a total of 271 individuals were studied. The frequency of carriers of short repeats in the HO-1 gene promoter was determined and compared between the groups. Results: In the AAA group, 29 patients (41%) were carriers of short (GT),, repeats compared to 47 patients (67%) in the CAD group, 44 patients (63%) in the PAD group and 35 healthy controls (59%). Patients with AAA were less frequently carriers of short repeats compared to age- and sex-matched patients with CAD (OR=0.38, p=0.006) and PAD (OR=0.35, p=0.01). Healthy controls exhibited short alleles more frequently than patients with AAA (p=0.04), but comparable to CAD (p=0.3) and PAD patients (p=0.7). Conclusion: Patients with AAA were less frequently carriers of short (<25 GT) repeats in the HO-1 gene promoter than patients with atherosclerosis or healthy subjects. This suggests that short alleles, and thus, facilitated upregulation of HO-1, may be a protective anti-inflammatory factor against the development of AAA. (C) 2002 Elsevier Science Ltd. All rights reserved.