Thromb Haemost 2005; 93(02): 257-260
DOI: 10.1160/TH04-07-0449
Rapid and Short Communication
Schattauer GmbH

The adaptive immune system and long-term outcome in patients with stable coronary disease

Predictive value of routine laboratory measurements
Alexander Niessner
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
,
Senta Graf
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
,
Mariam Nikfardjam
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
,
Stephan Lehr
2   Department of Medical Computer Sciences, Medical University of Vienna, Vienna, Austria
,
Gerald Maurer
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
,
Johann Wojta
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
,
Kurt Huber
1   Deptartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria
3   Department of Cardiology and Emergency Medicine, Wilhelminen-Hospital, Vienna, Austria
› Author Affiliations
Further Information

Publication History

Received 27 July 2004

Accepted after resubmission 20 January 2004

Publication Date:
11 December 2017 (online)

Summary

Components of the adaptive immune system, in particular lymphocytes and immunoglobulin, play a major role in advanced atherosclerotic lesions. We sought to determine whether routine measurements of the relative number of circulating lymphocytes (%L) and γ -globulin (%G) reflecting immunoglobulin are related to event-free survival in patients with stable coronary artery disease (CAD). We prospectively studied the combined endpoint all-cause mortality, myocardial infarction and coronary revascularization procedures in 141 patients after successful percutaneous coronary intervention during a median follow-up time of 13.2 years. Using Cox regression, we found a significant influence of %L on event-free survival (P = 0.007) with a relative risk of 2.21 comparing third to first tertile. Subjects with higher %G values likewise had a shorter event-free survival (P = 0.008) with a relative risk of 1.67 comparing third to first tertile. The predictive value of %L and %G remained significant after adjustment for demographic data, cardiovascular risk factors, extent of CAD and other inflammatory markers. We conclude that the fraction of γ -globulin and in particular the relative lymphocyte cell count may serve as readily available and reliable prognostic tools for the long-term outcome in patients with stable CAD.

 
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