Summary
Moderate hyperhomocysteinaemia is considered as an independent risk marker for cardiovascular
disease and stroke. Earlier, increased homocysteine production was detected in stimulated
immunocompetent cells in vitro, and several markers of inflammation like neopterin
or C-reactive protein (CRP) were demonstrated as significant indicators of cardiovascular
risk. The relationship between coronary artery disease (CAD), homocysteine metabolism
and markers of immune activation and inflammation was investigated in a population
of 1717 patients undergoing coronary angiography, recruited as participants of the
LUdwigshafen RIsk and Cardiovascular Health (LURIC) study. 1325 patients (77.2%) suffered
from coronary artery disease (CAD), which was was defined as the occurrence of a visible
luminal narrowing (≥20% stenosis) in at least 1 of 15 coronary segments according
to the classification of the American Heart Association, the remaining 392 individuals
of the study population served as controls. Significant differences regarding systolic
blood pressure, homocysteine, neopterin and folic acid concentrations were observed
between patients and controls. Older age, decreased creatinine-clearance and higher
concentrations of homocysteine and CRP were indicative for CAD. Low B-vitamin availability,
therapy and the extent of immune activation strongly influenced homocysteine concentrations.
Homocysteine concentrations were correlated with neopterin levels (rs =0.325, p<0.001), and hyperhomocysteinaemic patients also presented with significantly
higher CRP concentrations. Homocysteine accumulation coincided with impaired renal
and heart function (as reflected by ProBNP[Brain natriuretic peptide]-concentrations).
We conclude that homocysteine accumulation could result from B-vitamin deficiency
which is related to chronic immune activation.
Keywords
Homocysteine - coronary artery disease - inflammation - neopterin - CRP