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生化标志物对动脉粥样硬化肥胖患者内皮功能障碍早期预测的敏感性和特异性。

Sensitivity, specificity of biochemical markers for early prediction of endothelial dysfunction in atherosclerotic obese subjects.

机构信息

Biochemistry Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.

Experimental Biochemistry Unit, King Fahd Medical Research Center, KAU.

出版信息

Afr Health Sci. 2022 Jun;22(2):286-294. doi: 10.4314/ahs.v22i2.32.

Abstract

BACKGROUND

The obesity increased incidence of diabetes, hypertension and atherosclerosis and rate of morbidity and mortality. The main cause of atherosclerosis is endothelial dysfunction and formation of foam cells and macrophage that lead to unfavorable complications. This study evaluated specific biomarkers for endothelial dysfunction as sensitive indices for early predication of atherosclerosis in obese subjects.

STUDY DESIGN

One hundred fifty male age and sex matching were included in the current study divided into three groups according to body mass index (BMI): Control (BMI ≤ 22), obese (BMI> 28) and obese with atherosclerosis (BMI> 28). Fasting serum was subjected for determination of adhesion molecules, sICAM-1, sVCAM-1, E-selectin, oxo-LDL and 8-iso-PGF2α by ELISA technique.

RESULTS

Data obtained showed that, a significant elevation of serum inflammatory markers CRP, IL-6 and TNF-α and adhesion molecules sICAM-1 (p<0.001) with sensitivity 96%, sVCAM-1 (p <0.01) with sensitivity 92%, E-selectin (p<0.001) with sensitivity 94%, oxo-LDL (p <0.05) and 8-iso-PGF2α (p < 0.001) with sensitivity 97% in obese with atherosclerosis compared with obese and control.

CONCLUSION

The levels of serum adhesion molecules contributed in the pathogenesis of endothelial dysfunction can be used as sensitive biomarkers for early prediction of atherosclerosis in obese subjects.

摘要

背景

肥胖症会增加糖尿病、高血压和动脉粥样硬化的发病率和死亡率。动脉粥样硬化的主要原因是内皮功能障碍和泡沫细胞及巨噬细胞的形成,导致不良并发症。本研究评估了内皮功能障碍的特定生物标志物,作为肥胖患者早期预测动脉粥样硬化的敏感指标。

研究设计

本研究共纳入 150 名男性,按体重指数(BMI)分为三组:对照组(BMI≤22)、肥胖组(BMI>28)和肥胖合并动脉粥样硬化组(BMI>28)。空腹血清采用 ELISA 技术测定黏附分子、可溶性细胞间黏附分子-1(sICAM-1)、可溶性血管细胞黏附分子-1(sVCAM-1)、E-选择素、氧化型低密度脂蛋白(oxo-LDL)和 8-异前列腺素 F2α(8-iso-PGF2α)。

结果

研究结果显示,与肥胖组和对照组相比,肥胖合并动脉粥样硬化组血清炎症标志物 CRP、IL-6 和 TNF-α以及黏附分子 sICAM-1(p<0.001,灵敏度 96%)、sVCAM-1(p<0.01,灵敏度 92%)、E-选择素(p<0.001,灵敏度 94%)、oxo-LDL(p<0.05)和 8-iso-PGF2α(p<0.001,灵敏度 97%)水平显著升高。

结论

血清黏附分子水平参与了内皮功能障碍的发病机制,可作为肥胖患者早期预测动脉粥样硬化的敏感生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab9/9652627/329cabd116e0/AFHS2202-0286Fig1.jpg

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