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Circulating soluble LR11, a novel marker of smooth muscle cell proliferation,is enhanced after coronary stenting in response to vascular injury
Authors:Manabu Ogita  Katsumi Miyauchi  Meizi Jiang  Takatoshi Kasai  Shuta Tsuboi  Ryo Naito  Hirokazu Konishi  Tomotaka Dohi  Takayuki Yokoyama  Shinya Okazaki  Kazunori Shimada  Hideaki Bujo  Hiroyuki Daida
Affiliation:1. Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, Japan;2. Department of Clinical-laboratory and Experimental-Research Medicine, Toho University Sakura Medical Center, Japan
Abstract:

Objective

Restenosis after vascular intervention remains a major clinical problem. Circulating LR11 has been shown a novel marker of intimal smooth muscle cell (SMC) proliferation in human and animal studies. The present study was performed to clarify the clinical significance of circulating LR11 in patients with stable angina pectoris after coronary stenting.

Methods and results

We firstly investigated the circulating sLR11 levels for 28 days after arterial injury in mice, and then assessed time-dependent change in circulating sLR11 level after coronary stenting in a clinical study. Mouse sLR11 levels rapidly increased to 4.0-fold of the control value without cuff placement at postoperative day (POD) 14, and the levels gradually declined to 3.1-fold of the control value until POD 28 in mice. The circulating soluble LR11 levels were measured (before and at 14, 60 and 240 days after coronary stenting in a clinical study of 102 consecutive patients with stable angina pectoris who were treated with percutaneous coronary intervention. Circulating sLR11 levels were significantly increased on days 14 and 60 after the procedure and positively associated with the angiographic late loss index.

Conclusions

Our study suggested that circulating sLR11 levels may be a potential marker for angiographic late loss in patients after coronary stenting. Further mechanistic studies are expected to know the clinical significance of sLR11 as a novel marker for intimal SMC.
Keywords:Percutaneous coronary intervention   Smooth muscle cell   Vascular injury   Restenosis   Biomarker
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