Suppr超能文献

可溶性LR11是川崎病后期血管病变的一种新型生物标志物。

Soluble LR11 is a novel biomarker for vascular lesions late after Kawasaki disease.

作者信息

Watanabe Kenichi, Suzuki Hiroshi, Jiang Meizi, Haniu Hisanori, Numano Fujito, Hoshina Satoshi, Saitoh Akihiko, Uchiyama Makoto, Bujo Hideaki

机构信息

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

Atherosclerosis. 2016 Mar;246:94-7. doi: 10.1016/j.atherosclerosis.2015.12.035. Epub 2015 Dec 29.

Abstract

OBJECTIVE

Coronary artery lesions (CALs) and a risk for early onset of atherosclerosis are major concerns following Kawasaki disease (KD). Intimal smooth muscle cells (SMCs) have an important role in vascular lesions in KD. It is known that soluble LR11 (sLR11) is a novel biomarker for vascular lesions and LR11 is markedly expressed in intimal SMCs in atherosclerotic lesions. In this study, we hypothesized that sLR11 reflects the presence of vascular lesions late after KD.

METHODS

Twenty-three age-matched controls (group 1) and 59 patients with a history of KD were enrolled; 36 with KD had normal coronary arteries or regressed aneurysms (group 2), and 23 had CALs (group 3).

RESULTS

Serum sLR11 levels in group 3 (median, interquartile range (IQR): 11.1 ng/mL, 9.3-13.9 ng/mL) were significantly higher than those in groups 1 (8.4 ng/mL, 7.1-10.2 ng/mL, p < 0.001) and 2 (9.0 ng/mL, 7.7-10.1 ng/mL, p < 0.01). Levels of sLR11 were positively correlated with levels of high-sensitivity C-reactive protein (r = 0.480, p < 0.01) and lipoprotein (a) (r = 0.486, p < 0.01).

CONCLUSION

These findings suggest that sLR11 reflects the development of vascular lesions in patients with serious CALs.

摘要

目的

冠状动脉病变(CALs)以及动脉粥样硬化早期发作风险是川崎病(KD)后的主要关注点。内膜平滑肌细胞(SMCs)在KD的血管病变中起重要作用。已知可溶性LR11(sLR11)是血管病变的一种新型生物标志物,且LR11在动脉粥样硬化病变的内膜SMC中显著表达。在本研究中,我们假设sLR11反映KD后晚期血管病变的存在情况。

方法

纳入23名年龄匹配的对照组(第1组)和59名有KD病史的患者;36名KD患者冠状动脉正常或动脉瘤消退(第2组),23名有CALs(第3组)。

结果

第3组血清sLR11水平(中位数,四分位间距(IQR):11.1 ng/mL,9.3 - 13.9 ng/mL)显著高于第1组(8.4 ng/mL,7.1 - 10.2 ng/mL,p < 0.001)和第2组(9.0 ng/mL,7.7 - 10.1 ng/mL,p < 0.01)。sLR11水平与高敏C反应蛋白水平呈正相关(r = 0.480,p < 0.01)以及与脂蛋白(a)水平呈正相关(r = 0.486,p < 0.01)。

结论

这些发现表明sLR11反映了严重CALs患者血管病变的发展情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验