Interleukin-1 gene cluster variants and abdominal aortic aneurysms

Rodrig Marculescu; Gottfried Sodeck; Hans Domanovits; Gerhard Hobusch; Markus Exner; Harald Heinzl; Kurt Huber; Christine Mannhalter; Erich Minar; Oswald Wagner; Martin Schillinger

doi:10.1160/TH05-03-0203

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2005; 94(03): 646-650
DOI: 10.1160/TH05-03-0203

Cell Signalling and Vessel Remodelling

Schattauer GmbH

Interleukin-1 gene cluster variants and abdominal aortic aneurysms

A matched case control study

Rodrig Marculescu

¹Departments of Medical and Chemical laboratory Diagnostics

,

Gottfried Sodeck

²Emergency Medicine

,

Hans Domanovits

²Emergency Medicine

,

Gerhard Hobusch

¹Departments of Medical and Chemical laboratory Diagnostics

,

Markus Exner

¹Departments of Medical and Chemical laboratory Diagnostics

,

Harald Heinzl

³Core Unit for Medical Statistics and Informatics

,

Kurt Huber

,

Christine Mannhalter

¹Departments of Medical and Chemical laboratory Diagnostics

,

Erich Minar

¹Departments of Medical and Chemical laboratory Diagnostics

⁵Angiology, Vienna Medical University, Vienna, Austria

,

Oswald Wagner

¹Departments of Medical and Chemical laboratory Diagnostics

,

Martin Schillinger

⁵Angiology, Vienna Medical University, Vienna, Austria

› Author Affiliations

Abstract

Summary

Inflammation is a key factor in the pathogenesis of abdominal aortic aneurysms (AAA). Interleukin 1 (IL-1), a fundamental regulator of the inflammatory cascade, has been shown to be involved in this process. Several functional polymorphisms in the IL-1 gene cluster are known. In this matched case-control study, we investigated a potential association between six genetic variants in IL-1 and IL-1 receptor antagonist (IL-1 RN) withAAA. We enrolled 405 individuals, 135 consecutive patients with AAA were individually age- and sex-matched to 270 patients with coronary artery disease (CAD). Traditional cardiovascular risk factors and IL-1 genotypes were determined, and the distribution of six single nucleotide polymorphisms were compared between patients and controls by multivariable conditional logistic regression analysis: IL-1A (-889) C>T, IL-1A (+4845) G>T, IL-1B (-511) C>T, IL-1B (-31) C>T, IL-1B (+3954) C>T and IL-1RN (+2018) C>T. IL-1A (-889) C>T and IL-1A (+4845) G>T (kappa 0.98, 95% CI 0.96 to 1.00), and IL-1B (-511) C>T and IL-1B (-31) C>T (kappa 0.98, 95% CI 0.96 to 1.00) were closely linked, therefore IL-1A (-889) C>T and IL-1B (-31) C>T were not considered for further analyses. None of the 4 remaining polymorphisms showed a significant association with AAA: IL-1RN (+2018) C>T (p=0.061), IL-1B (+3954) C>T (p=0.51), IL-1B (-511) C>T (p=0.61) and IL-1A (+4845) G>T (p=0.81). No significant first-degree interactions between the genetic variants andAAA were detected. In conclusion, these six genetic variants in the interleukin-1 gene cluster do not seem to play a clinically relevant role in the pathogenesis of AAA, although we cannot rule out the existence of higher degree gene-gene or gene-environment interactions.

Keywords

Abdominal aortic aneurysm - interleukin 1 - inflammation

Full Text

References

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