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Human plasma complement C3 is independently associated with coronary heart disease, but only in heavy smokers (the CODAM study)
Authors:van Greevenbroek Marleen M J  Jacobs Marjon  van der Kallen Carla J H  Blaak Ellen E  Jansen Eugene H J M  Schalkwijk Casper G  Feskens Edith J M  Stehouwer Coen D A
Affiliation:
  • a Laboratory of Metabolism and Vascular Medicine, Cardiovascular Research Institute Maastricht and Department of Internal Medicine, Maastricht University, The Netherlands
  • b Department of Human Biology, Maastricht University, The Netherlands
  • c Laboratory for Health Protection Research, National Institute for Public Health and the Environment, The Netherlands
  • d Division of Human Nutrition, Section Nutrition and Epidemiology, Wageningen University, Wageningen, The Netherlands
  • e Department of Internal Medicine, Maastricht University Medical Center, Maastricht, The Netherlands
  • Abstract:

    Background

    Complement C3 is an emerging risk factor for coronary heart disease (CHD) and is particularly increased in the metabolic syndrome. A direct effect of smoking on structure and function of complement C3 has been suggested.

    Hypothesis

    Smoking behavior may affect the cardiovascular risk that is associated with plasma complement C3.

    Methods

    The association between plasma C3 and CHD was studied in the CODAM (Cohort on Diabetes and Atherosclerosis Maastricht) study population (n = 562, 61% male) with examination of effect modification by smoking.

    Results

    The overall prevalence of CHD was 23.3%. Higher plasma C3 levels were associated with a higher CHD prevalence, and there was a significant interaction with heavy smoking (p = 0.01). In never & light smokers, the univariate OR for CHD per 1 s.d. (0.33 g/L) increase in C3 was 1.09 [95% confidence interval (CI) 0.85-1.41] (p = 0.505) whereas in heavy smokers it was 2.05 [1.43-2.93] (p < 0.001). The association in the group of heavy smokers remained significant (OR 2.38 [1.54-3.68], p < 0.001) after adjustment for traditional risk factors for cardiovascular disease and also after further adjustment for other cardiometabolic risk factors, i.e. the metabolic syndrome, CRP and insulin resistance (HOMA2IR) (OR C3 between 2.16 and 2.29, all p ≤ 0.001).

    Conclusion

    Human plasma complement C3 is associated with prevalent CHD, but only in heavy smokers, and this association is independent of important metabolic cardiovascular risk factors.
    Keywords:Human complement C3   Smoking   Coronary heart disease   Independent cardiovascular risk associate
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