E Ev va al lu ua at ti io on n o of f e en nd do ot th he el li ia al l f fu un nc ct ti io on n a an nd d t th hr ro om mb bo ot ti ic c s sy ys st te em m i in n c ch hi il ld dr re en n w wh ho os se e p pa ar re en nt ts s h ha ad d e ea ar rl ly y o on ns se et t c co or ro on na ar ry y h he ea ar rt t d di is se ea as se e C C. . N Na ac ci i Ö Ön ne er r, , R Ru uk ki iy ye e E Ek ke er r Ö Öm me er ro o¤ ¤l lu u* *, , K Ke em ma al l N Ni ifl fll li i* *, , T Ta an ne er r Y Ya av vu uz z* *, , Ü Üm mi it t T Tü ür rk ko o¤ ¤l lu u* *, , Ü Üm mr ra ah h A Ay yd do o¤ ¤a an n* *, , A Ay yg gü ün n D Di in nd da ar r* *, , T Tü ür rk ka an n E Er rt tu u¤ ¤r ru ul l* * I In nv vi it te ed d A Au ut th ho or r S Su um mm ma ar ry y Aim: Risk of MI in first-degree relatives of patients who had an acute MI prior to age of 55 years is 2-7 fold higher compared to their peers. The aim of this study was to investigate the levels of some haemostatic and inflammatory markers in children whose parents had early onset (<55 years) coronary artery disease (CAD) and whether those markers were effective in indicating the risk for CAD development.
Material and Method:This study was performed in Pediatric Cardiology Division of Istanbul Medical Faculty. Forty-three healthy children whose parents had early onset CAD were matched for age and sex and tissue factor (TF), tissue factor pathway inhibitor (TFPI), fibrinogen, von Willebrand factor (vWF) and highly sensitive CRP (hsCRP) were analyzed in both groups. The study was approved by Istanbul Medical Faculty ethics committee. Data obtained in the study were assessed using SPSS 10.0 program.Results: : The study group had higher vWF than the control group (116.3±52.2 vs. 86.8±41.4 ng/mL), p<0.05). Tissue factor, total and free TFPI, fibrinogen and hsCRP were not statistically different between the two groups.
Conclusions:Although premature CAD is known to have a particularly strong genetic component, this study showed that haemostatic and inflammatory markers except vWF are not independent risk factors for children with a family history of early onset CAD. (Turk Arch Ped 2011; 46: 21-6)