AbstractThe aim of the study was to test the correlation of serum levels of
asymmetric dimethylarginine (ADMA), endothelin 1 (ET-1), N-terminal brain
natriuretic pro-peptide (NT-proBNP), and placental growth factor (PIGF-1)
with estimated cardiovascular (CV) risk. The study group was composed of 102
women and 67 men with type 2 diabetes, having their glycemic and metabolic
parameters assessed. All were on oral antidiabetic drugs. Serum levels of
NT-proBNP and PIGF-1 were measured by electro-hemi-luminescence on an
Elecsys 2010 analyzer. Enzymatic immunoassays were used for ADMA and ET-1.
The Framingham Risk Score (FRS), the UKPDS 2.0 and the ADVANCE risk engines
were used to calculate cardiovascular risks while statistical analysis was
performed on SPSS. Levels of PIGF-1 showed no correlation with the
calculated CV risks. The same was true for ADMA, except for a weak
correlation with the UKPDS-based 10-year risk for stroke (Pearsons’s
R=0.167, p=0.039). Plasma levels of ET-1 were correlated
with the UKPDS-based 10-year risk for stroke (R=0.184,
p=0.032) and fatal stroke (R=0.215, p=0.012) only.
NT-proBNP was significantly correlated with all CV risk calculations:
ADVANCE-based 4-yr risk (Spearman’s Rho=0.521,
p<0.001); UKPDS-based 10-year risk for: CHD (Rho=0.209,
p=0.01), fatal CHD (Rho=0.282, p<0.001), stroke
(Rho=0.482, p<0.001), fatal stroke (Rho=0.505,
p<0.001); and 10-year FRS risk (Rho=0.246, p=0.002).
In conclusion, ADMA and PIGF-1 did not seem useful in stratifying CV risk
while ET-1 is linked to the risk of stroke, and NT-proBNP to all CV risk
estimations.