摘要
目的:探讨Ⅱ型糖尿病有无血管病变、患者外周血单核细胞CD36表达和单核细胞-血小板聚集的临床意义。方法:采用流式细胞仪,测定56例糖尿病伴血管病变患者及53例无血管病变患者外周血单核细胞表面CD36平均荧光强度和单核细胞-血小板聚集的百分率,并与56例健康对照组比较。结果:糖尿病伴血管病变患者外周血单核细胞CD36平均荧光强度和单核细胞-血小板聚集的百分率均明显高于无血管病变组和健康对照组(P<0.01);且伴血管病变组外周血单核细胞CD36平均荧光强度与单核细胞-血小板聚集的百分率具有显著的正相关性(r=0.582,P<0.01)。结论:糖尿病患者长期慢性高血糖产生糖基化产物(Advanced Glycation End-product,AGE),可能会促使CD36表达增加,进一步触发单核细胞-血小板聚集体增加,从而加速动脉粥样硬化的发生和发展。
Objective:To study the monocyte CD36 expression and monocyte-platelet aggregates(MPAs) in the type 2 diabetic patients.Methods:The monocyte CD36 expression(Mean fluorescence intensity,MFI) and MPAs percentage were measured in 56 diabetic patients with vascular complications and 53 diabetic patients without vascular complications and control group by FCM.Results:Mean monocyte CD36 expression MFI was higher in the patients with vascular complications(46.2±4.17) than those without vascular complications(22.7±4.65) and control group(27.5±3.01)(P〈0.01).The MPAs formations were also higher in the patients with vascular complications(57.4±12.9%) than without vascular complications(19.6±8.7%) and control group(14.3±6.6%)(P〈0.01).Furthermore,a significant correlation between CD36 MFI and MPAs percentage levels was observed in diabetic patients with vascular complications.Conclusions:The enhanced monocyte CD36 expression and increased MPAs formations play an important role in the development of diabetic angiopatny.They may provide an auto-feed mechanism for accelerating the atherosclerosis in diabetics.
出处
《中国卫生检验杂志》
CAS
2008年第5期864-865,945,共3页
Chinese Journal of Health Laboratory Technology