Pigment epithelium-derived factor is associated with... : Coronary Artery Disease (original) (raw)
Original Research
Pigment epithelium-derived factor is associated with necrotic core progression during statin therapy
Nozue, Tsuyoshi; Yamagishi, Sho-ichi; Hirano, Tsutomu; Yamamoto, Shingo; Tohyama, Shinichi; Fukui, Kazuki; Umezawa, Shigeo; Onishi, Yuko; Kunishima, Tomoyuki; Hibi, Kiyoshi; Terashima, Mitsuyasu; Michishita, Ichiro
aDivision of Cardiology, Department of Internal Medicine, Yokohama Sakae Kyosai Hospital
bDepartment of Cardiology, Tsurumi Nishiguchi Hospital
cDepartment of Cardiology, Yokohama Seamen’s Insurance Hospital
dDepartment of Cardiology, Kanagawa Cardiovascular and Respiratory Center
eDivision of Cardiology, Yokohama City University Medical Center, Yokohama
fDepartment of Pathophysiology and Therapeutic of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume
gFirst Department of Internal Medicine, Showa University School of Medicine, Tokyo
hDepartment of Cardiology, Hiratsuka Kyosai Hospital, Hiratsuka
iFourth Department of Internal Medicine, Mizonokuchi Hospital, Teikyo University School of Medicine, Kawasaki
jCardiovascular Imaging Center, Toyohashi, Japan
Correspondence to Tsuyoshi Nozue, MD, Division of Cardiology, Department of Internal Medicine, Yokohama Sakae Kyosai Hospital, Federation of National Public Service Personnel Mutual Associations, 132 Katsura-cho, Sakae-ku, Yokohama 247-8581, Japan Tel: +81 45 891 2171; fax: +81 45 895 8352; e-mail: [email protected]
Received July 30, 2014
Received in revised form October 1, 2014
Accepted October 2, 2014
Abstract
Objective
Pigment epithelium-derived factor (PEDF) is a potent inhibitor of angiogenesis and an important target molecule for preventing the progression of atherosclerosis. However, the relationship between PEDF and coronary atherosclerosis has not been fully examined. The aim of the present study is to evaluate the effects of statins on serum PEDF levels and the association between PEDF and coronary atherosclerosis.
Patients and methods
Coronary atherosclerosis in nonculprit lesions in the vessel of patients undergoing a percutaneous coronary intervention was evaluated using virtual histology intravascular ultrasound in 99 patients during percutaneous coronary intervention and after 8 months of statin therapy.
Results
Serum PEDF levels at baseline and at the 8-month follow-up did not differ. A significant decrease in the fibro-fatty component (−0.24 mm3/mm, _P_=0.0003) and increases in the necrotic core (0.13 mm3/mm, _P_=0.02) and dense calcium components (0.11 mm3/mm, P<0.0001) were observed during the 8-month statin therapy. On univariate regression analyses, serum PEDF levels (_r_=0.291, _P_=0.004) and unstable angina pectoris (_r_=0.203, _P_=0.04) showed significant positive correlations with the percentage change in necrotic core volume. Multivariate regression analysis showed that serum PEDF level was a significant independent predictor associated with necrotic core progression during statin therapy (_β_=0.218, _P_=0.04).
Conclusion
Statin therapy had no effects on serum PEDF levels. Serum PEDF was a useful biomarker for predicting necrotic core progression during statin therapy, and its levels could be elevated as a counter-regulatory response mechanism to protect against necrotic core progression.
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