2型糖尿病患者血清chemerin水平与骨密度相关性研究
The relationship between serum chemerin level and bone mineral density in T2DM patients.
  
DOI:10.3969/j.issn.1006.7108.2016.01.014
中文关键词:  2型糖尿病  chemerin  骨质疏松症;骨密度
英文关键词:Type 2 diabetes mellitus  Chemerin  Osteoporosis  Bone mineral density
基金项目:国家自然基金资助项目(81370889);镇江市卫生科技重点项目(SH2013075)
作者单位
施良1 张浩2 李林1 徐萍3 高健青1 周建明1 毛朝明1* 1.江苏大学附属江滨医院核医学科镇江212001 2.江苏大学附属江滨医院急诊内科镇江212001 3.江苏大学附属江滨医院内分泌科镇江212001 
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中文摘要:
      目的 探讨2型糖尿病患者血清chemerin水平与骨密度及相关因素的关系。方法 选取2012年1月?2014年12月本院内分泌科收治的2型糖尿病住院患者,行双能X线骨密度检查,根据WHO骨质疏松诊断标准分为2型糖尿病骨量正常组42例、2型糖尿病骨量减少组50例、2型糖尿病骨质疏松(OP)组58例。记录其身高、体重、病程等临床资料,测定空腹血糖(FBG)、糖化血红蛋白(HbA1C)、血清chemerin、TNF-α及IL4水平。另取30名健康人群作为对照组。结果 糖尿病患者 三组间年龄、身高、体重、病程、糖化血红蛋白无统计学差异。糖尿病骨质疏松组血清chemerin水平高于骨量减少组和骨量正常组(89.7 ±12. 2μg /L;72.5 ±13.6;65. 1 ± 14. 9μg /L),差异均有统计学意义(P <0. 05)。2型糖尿病合并骨质疏松症组血清炎症因子TNF-α和IL-6水平均高于无骨质疏松症组(P<0. 05)。相关性分析结果显示:血清chemerin水平与TNF-α、BMI、 HbA1C、病程相关(r1=0. 52;r2 =0. 76;r3 =0. 63;r4 =0. 59;P 均 <0. 05 ),与腰椎骨密度呈负相关(r= - 0. 67,P < 0. 05 )。结论 chemerin可能通过调控炎症反应参与骨代谢过程,从而促进骨质疏松的发生。
英文摘要:
      Objective To explore the relationship between serum chemerin level and bone mineral density (BMD) in type 2 diabetic patients. Methods The inpatients with type 2 diabetes were chosen from January 2012 to December 2014 in the Department of Endocrinology of our Hospital. BMD were measured with dual energy X-ray absorptiometry. Patients were divided into type 2 diabetic normal bone mass group (n= 42) , type 2 diabetic osteopenia group (n = 50), and type 2 diabetic osteoporosis group (n = 58),according to the WHO diagnostic criteria of osteoporosis. Height, weight, duration of diabetes, and other clinical data were recorded. Fasting blood glucose (FBG), glycosylated hemoglobin (HbA1c) , serum chemerin, TNF-α, and interleukin- 6 (IL-6) were measured. Another 30 cases of normal people were also included in the study as the control group. Results No significant difference of age and sex, height, weight, duration of diabetes,and HbA1c was found in the type 2 diabetic patients among the three groups. Serum chemerin level in type 2 diabetic osteoporosis group was significantly higher than that in type 2 diabetic osteopenia and normal bone mass group (89. 7 ± 12. 2μg /L,72. 5 ± 13. 6,and 65. 1 ± 14.9μg /L,P<0. 05). The TNF-α and IL-6 levels in diabetic osteoporosis group were significantly higher than those in type 2 diabetic normal bone mass group (P < 0. 05). Correlation analysis showed that;serum chemerin level was positively correlated with TNF-α, BMI, HbA1c, and duration of diabetes (r1 =0. 52, r2 = 0. 76, r3 = 0. 63, r4 =0. 59, P <0. 05), but was negatively correlated with BMD of LI-4 (r = -0.67, P < 0. 05 ). Conclusion Chemerin may be involved in the pathogenesis of diabetic osteoporosis by regulating inflammatory reaction, therefore promotes the occurrence of osteoporosis.
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