Homocysteine has been related to increased risk of CVD. Matrix degradation and
inflammation may be involved in this link between hyperhomocysteinaemia and CVD. Recent studies suggest that
cystatin C can modulate matrix degradation and
inflammation. The present study measured
cystatin C at
protein (plasma) and
mRNA levels (peripheral blood mononuclear cells (PBMC)) in hyperhomocysteinaemic individuals (n 37, female seven and male thirty, aged 20-70 years) before and after
B-vitamin supplementation for 3 months in a randomised, placebo-controlled double-blind trial. In a cross-sectional study, seventeen of the hyperhomocysteinaemic subjects were age- and sex-matched to healthy controls (n 17). Our main findings were: (i) as compared with controls, hyperhomocysteinaemic subjects tended to have higher plasma concentrations of
cystatin C and lower
mRNA levels of
cystatin C in PBMC; (ii) compared with placebo, treatment of hyperhomocysteinaemic individuals with
B-vitamins significantly increased plasma levels of
cystatin C and
mRNA levels of
cystatin C in PBMC; (iii) while plasma levels of
cystatin C were positively correlated with plasma levels of TNF receptor-1,
mRNA levels of
cystatin C in PBMC were inversely correlated with this TNF parameter. Taken together, our findings suggest that disturbed
cystatin C levels may be a characteristic of hyperhomocysteinaemic individuals, potentially related to low-grade systemic
inflammation in hyperhomocysteinaemic subjects, and that
B-vitamins may modulate
cystatin C levels in these individuals.