Pleiotropic effects of HDL subfractions and HDL-associated enzymes on protection against coronary artery disease
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Erişim
info:eu-repo/semantics/openAccessTarih
2015Yazar
Bostan, MehmetUydu, Hüseyin Avni
Karadağ, Zakir
Atak, Mehtap
Uğurlu, Yavuz
Ergül, Elif
Şatıroğlu, Ömer
Yılmaz, Adnan
Üst veri
Tüm öğe kaydını gösterKünye
Bostan, M., Uydu, H.A., Jaradağ, Z., Atak, M., Uğurlu, Y., Ergül, E., Şatıroğlu, Ö., Yılmaz, Ö. (2013). Pleiotropic effects of HDL subfractions and HDL-associated enzymes on protection against coronary artery disease. Acta Cardiologica, 62(18), C40-C41.Özet
Objective High-density lipoprotein cholesterol (HDL-C) levels are inversely related to the risk of coronary artery disease (CAD). Alterations in HDL-C subclass distribution and HDL-associated enzyme activities may be more important than total HDL levels for the progression of CAD. We intended to investigate the relationship of HDL-C subclass distribution and HDL-associated enzyme activities with CAD. Method and results Our study included 101 patients with stable coronary artery disease, and 64 healthy subjects. Serum levels of HDL lipoprotein-associated-phospholipase A(2) (HDL-LpPLA(2)), paraoxonase 1 (PON1), and HDL subfraction distribution were measured. We found increased small HDL (sHDL) subfractions in patients with one-vessel disease (P < 0.001).We also found a reverse correlation between total HDL-C levels and affected vessel number (P <0.05). Plasma HDL-Lp PLA(2) enzyme level was higher in each vessel disease category compared to the control group (P <0.001). However, PON1 enzyme activity in patients with CAD was not statically significant. Plasma sHDL, HDL-Lp PLA(2) enzyme and Lp(a) were significantly different between subjects with CAD and control participants. Conclusions We demonstrated decreased sHDL particles and a lower cardioprotective HDL-LpPLA(2) enzyme activity in all patient subgroups compared to controls. Measurement of total HDL-C level only may not be sufficient to predict CAD risk.
Kaynak
Acta CardiologicaCilt
68Sayı
18Bağlantı
https://doi.org/10.1080/AC.70.3.3080638https://hdl.handle.net/11436/2813
https://pubmed.ncbi.nlm.nih.gov/26226707/