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冠状动脉慢血流现象与血液生化指标的相关性分析

胡贤军 刘宏磊 丁道芳

中国临床医学2017,Vol.24Issue(6):916-919,4.
中国临床医学2017,Vol.24Issue(6):916-919,4.DOI:10.12025/j.issn.1008-6358.2017.20170228

冠状动脉慢血流现象与血液生化指标的相关性分析

Correlation analysis between coronary slow flow phenomenon and blood biochemical indexes

胡贤军 1刘宏磊 2丁道芳3

作者信息

  • 1. 安徽医科大学附属巢湖医院心内科,巢湖238000
  • 2. 上海交通大学医学院附属瑞金医院风湿免疫科,上海200025
  • 3. 上海中医药大学附属曙光医院骨伤科,上海201203
  • 折叠

摘要

Abstract

Objective:To study the correlation between the coronary slow flow phenomenon (CSFP) and blood uric acid (UA),homocysteine (Hcy),hematocrit (Hct) and red blood cell distribution width (RDW).Methods:The data of coronary angiography (CAG) patients with chest distress and chest pain were retrospectively analyzed.121 patients with no obvious epicardial coronary artery stenosis but with coronary slow flow phenomenon were selected as the CSFP group (group SCF).606 patients with completely normal epicardial coronary artery and normal blood flow were set as the normal blood flow group (group NCF).The differences of UA,Hcy,Hct and RDW between the two groups were compared,and the correlation between CSFP and the above indexes,UA and other biochemical indexes was analyzed.Results:The levels of UA,Hcy and Hct in group SCF were higher than those in group NCF (P< 0.001),but there was no significant difference in the level of RDW between the two groups.Conditional Logistic regression analysis showed that UA,Hcy and Hct were all risk factors of CSFP.Spearman correlation and partial correlation analysis showed that UA was positively correlated with Hcy.Conclusions:UA,Hcy and Hct are the risk factors for CSFP,and UA and Hcy may together promote the occurrence and development of CSFP.

关键词

冠状动脉慢血流/血尿酸/红细胞压积/同型半胱氨酸/红细胞分布宽度

Key words

coronary slow flow phenomenon/blood uric acid/hematocrit/homocysteine/red blood cell distribution width

分类

医药卫生

引用本文复制引用

胡贤军,刘宏磊,丁道芳..冠状动脉慢血流现象与血液生化指标的相关性分析[J].中国临床医学,2017,24(6):916-919,4.

基金项目

国家自然科学基金(81502016).Supported by National Natural Science Foundation of China(81502016). (81502016)

中国临床医学

OACSTPCD

1008-6358

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