河北医学
河北醫學
하북의학
HEBEI MEDICINE
2014年
10期
1619-1621
,共3页
2型糖尿病%炎症因子%胰岛素抵抗
2型糖尿病%炎癥因子%胰島素牴抗
2형당뇨병%염증인자%이도소저항
Type 2 diabetes%Inflammatory cytokines%Insulin resistance
目的:探讨初诊2型糖尿病患者血清超敏C反应蛋白水平及相关因素。方法:选择50例初诊2型糖尿病患者及50例健康体检者作为研究对象,比较两组患者血清hs-CRP 水平,并分析2型糖尿病患者hs-CRP相关因素。结果:初诊2型糖尿病患者BMI、腰围、SBP、DBP、TC、TG及hs-CRP水平均明显高于健康对照组,差异有统计学意义( P<0.05);2型糖尿病患者BMI、腰围、FBG、HOMA-IR与血清CRP 水平呈正相关性(P<0.05),HOMA-B与血清CRP 水平呈负相关性(P<0.05)。结论:血清hs-CRP 水平在初诊2型糖尿病患者明显升高,可能与超重或肥胖及胰岛素抵抗、胰岛β细胞功能衰退相关。
目的:探討初診2型糖尿病患者血清超敏C反應蛋白水平及相關因素。方法:選擇50例初診2型糖尿病患者及50例健康體檢者作為研究對象,比較兩組患者血清hs-CRP 水平,併分析2型糖尿病患者hs-CRP相關因素。結果:初診2型糖尿病患者BMI、腰圍、SBP、DBP、TC、TG及hs-CRP水平均明顯高于健康對照組,差異有統計學意義( P<0.05);2型糖尿病患者BMI、腰圍、FBG、HOMA-IR與血清CRP 水平呈正相關性(P<0.05),HOMA-B與血清CRP 水平呈負相關性(P<0.05)。結論:血清hs-CRP 水平在初診2型糖尿病患者明顯升高,可能與超重或肥胖及胰島素牴抗、胰島β細胞功能衰退相關。
목적:탐토초진2형당뇨병환자혈청초민C반응단백수평급상관인소。방법:선택50례초진2형당뇨병환자급50례건강체검자작위연구대상,비교량조환자혈청hs-CRP 수평,병분석2형당뇨병환자hs-CRP상관인소。결과:초진2형당뇨병환자BMI、요위、SBP、DBP、TC、TG급hs-CRP수평균명현고우건강대조조,차이유통계학의의( P<0.05);2형당뇨병환자BMI、요위、FBG、HOMA-IR여혈청CRP 수평정정상관성(P<0.05),HOMA-B여혈청CRP 수평정부상관성(P<0.05)。결론:혈청hs-CRP 수평재초진2형당뇨병환자명현승고,가능여초중혹비반급이도소저항、이도β세포공능쇠퇴상관。
Objective:To investigate levels and related factors of serum high sensitivity C-reactive pro-tein(hs-CRP) in newly diagnosed type 2 diabetic patients.Method:50 cases of newly diagnosed type 2 di-abetic patients and 50 healthy volunteers were included in this study , the serum hs-CRP levels in two groups and hs-CRP relevant factors in type 2 diabetes were analyzed.Result:The BMI, waist circumference ,SBP, DBP,TC,TG and hs-CRP in patients with type 2 diabetes were significantly higher than those in control group, the difference was statistically significant ( P<0.05); In type 2 diabetes patients ,the BMI, waist circumference , FBG, HOMA-IR and serum CRP levels were of positively connection ( P<0.05) , HOMA-B and serum CRP levels was of negatively connection ( P <0.05) .Conclusion:The serum hs-CRP levels are significantly elevated in patients with newly diagnosed type 2 diabetes , and may be associated with over-weight or obesity and insuLin resistance , pancreatic B-cell function decline .