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2型糖尿病患者下肢动脉粥样硬化与骨密度改变的研究

王玲 卜锐 宋滇平 王丹 杨秋萍

昆明医学院学报2012,Vol.33Issue(2):55-59,5.
昆明医学院学报2012,Vol.33Issue(2):55-59,5.

2型糖尿病患者下肢动脉粥样硬化与骨密度改变的研究

The Correlation between Lower Extrimity Atherosclerosis and Bone Mineral Density in Type 2 Diabetes Mellitus Patients

王玲 1卜锐 2宋滇平 3王丹 2杨秋萍3

作者信息

  • 1. 人民医院内分泌科,云南,楚雄,675000
  • 2. 昆明医学院第一附属医院超声科,云南,昆明,650032
  • 3. 昆明医学院第一附属医院糖尿病科,云南,昆明,650032
  • 折叠

摘要

Abstract

Objective To explore the correlation between lower extremity atherosclerosis (LEA) and bone mineral density in type 2 diabetes mellitus (T2-DM) patients. Methods Two hundred and nineteen T2-DM were enrolled in this study. Severity of LEA was examined by Doppler Ultrasound of Aloka -a 10 (Japan). According to severity of LEA score, the subjects were divided into the control (re=65) , mild (n=62) , moderate (n=56) and severe (n=36) groups. The bone mineral density (BMD) in lumbar vertebrate and femoral bone was measured by Dual- energy X- ray absorptiometry (DEXA) made in America. The clinical factors and biochemical parameters of patients in different groups were observed and the correlation between lower extremity atherosclerosis and bone mineral density. Results (1) With the increase in the severity of LEA, the HBAlc, FBG, 2HPBG, TC, TG and LDL were gradually increased , but HDL was decreased in the four groups, there was significant differences (P<0.05). (2) The severity score of LEA was negative correlated with the BMD in lumbar vertebrat and femoral bone. (3) Multivariate Logistic regression analysis showed the change of BMD, HBAlc and TC were major risk factors of LEA T2- DM .Conclusions With the increase in the severity of LEA in T2- DM, the decrease of BMD is more obvious. The decrease of BMD is a risk factor of LEA production and development.

关键词

2型糖尿病/下肢动脉/动脉粥样硬化

Key words

Type 2 diabetes mellitus/ Artery of lower extremity/ Atherosclerosis

分类

医药卫生

引用本文复制引用

王玲,卜锐,宋滇平,王丹,杨秋萍..2型糖尿病患者下肢动脉粥样硬化与骨密度改变的研究[J].昆明医学院学报,2012,33(2):55-59,5.

基金项目

云南省自然科学基金资助项目(2009CD166) (2009CD166)

昆明医学院学报

OACSTPCD

1003-4706

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