1.Combined Value of Serum CTRP5,Ficolin-3 and CXCL12 in Predicting Microvascular Lesions in Type 2 Diabetes Mellitus
Yang BAI ; Zhongxiao PING ; Yijun FAN
Acta Medicinae Universitatis Scientiae et Technologiae Huazhong 2025;54(5):720-725
Objective To investigate the relationship between serum levels of tumor necrosis factor-related protein 5(CTRP5),fibronectin-3(Ficolin-3),and CXC chemokine ligand 12(CXCL12)and microvascular lesions in patients with type 2 diabetes mellitus(T2DM).Methods A total of 75 patients with T2DM microangiopathy admitted to the Seventh People's Hos-pital of Zhengzhou from January 2023 to June 2024 were selected as the observation group.At the same time,150 T2DM pa-tients without microangiopathy were included as the control group according to the principle of 1∶2 matching of age,gender and body mass index(BMI).The general information,blood glucose indicators,Homa-insulin resistance(HOMA-IR),and serum CTRP5,Ficolin-3,and CXCL12 levels of the two groups were statistically analyzed by hospital medical staff.The Logistic re-gression equation was used to analyze the influencing factors of the onset of microvascular lesions in T2DM.The relationship be-tween the levels of serum CTRP5,Ficolin-3,and CXCL12 and microvascular lesions in T2DM was analyzed using smooth curve fitting method.The receiver operating characteristic(ROC)curve and area under the curve(AUC)were used to analyze the pre-dictive value of serum CTRP5,Ficolin-3,and CXCL12 for T2DM microvascular lesions.Results There were no significant differences in gender,age,BMI,duration of T2DM,abdominal circumference,DBP,SBP,TC,HDL-C,TG,LDL-C,smoking his-tory and drinking history between the two groups(all P>0.05).FPG,2hPG,HbA1c and HOMA-IR in the observation group were significantly higher than in the control group(all P<0.05).The serum levels of CTRP5,Ficolin-3 and CXCL12 in the ob-servation group were significantly higher than in the control group(all P<0.05).Logistic regression analysis showed that FPG,2hPG,HbA1c,HOMA-IR,CTRP5,Ficolin-3 and CXCL12 were the influencing factors of T2DM microangiopathy(all P<0.05).After adjusting for FPG,2hPG,HbA1c,HOMA-IR and other confounding factors,the relationship between serum Fico-lin-3,CTRP5,CXCL12 and T2DM microangiopathy was analyzed by curve fitting,the results showed that serum Ficolin-3,CTRP5,CXCL12 were linearly positively correlated with T2DM microangiopathy,with the increase of their levels,the risk of T2DM microangiopathy increased.The ROC curve showed that the AUC of serum Ficolin-3,CTRP5 and CXCL12 levels in pre-dicting T2DM microvascular lesions was 0.756,0.761 and 0.791,respectively.The AUC of combined prediction was 0.931,and the sensitivity and specificity were 90.67%and 80.00%,respectively.Delong test showed that the AUC of combined prediction was significantly greater than that of single prediction(Z=32.123,P<0.01).Conclusion The changes in serum levels of CTRP5,Ficolin-3,and CXCL12 are closely related to microvascular lesions in patients with T2DM,providing a reference for ear-ly clinical prediction and evaluation of microvascular lesions in patients with T2DM,as well as for the development of corre-sponding intervention strategies.
2.Combined Value of Serum CTRP5,Ficolin-3 and CXCL12 in Predicting Microvascular Lesions in Type 2 Diabetes Mellitus
Yang BAI ; Zhongxiao PING ; Yijun FAN
Acta Medicinae Universitatis Scientiae et Technologiae Huazhong 2025;54(5):720-725
Objective To investigate the relationship between serum levels of tumor necrosis factor-related protein 5(CTRP5),fibronectin-3(Ficolin-3),and CXC chemokine ligand 12(CXCL12)and microvascular lesions in patients with type 2 diabetes mellitus(T2DM).Methods A total of 75 patients with T2DM microangiopathy admitted to the Seventh People's Hos-pital of Zhengzhou from January 2023 to June 2024 were selected as the observation group.At the same time,150 T2DM pa-tients without microangiopathy were included as the control group according to the principle of 1∶2 matching of age,gender and body mass index(BMI).The general information,blood glucose indicators,Homa-insulin resistance(HOMA-IR),and serum CTRP5,Ficolin-3,and CXCL12 levels of the two groups were statistically analyzed by hospital medical staff.The Logistic re-gression equation was used to analyze the influencing factors of the onset of microvascular lesions in T2DM.The relationship be-tween the levels of serum CTRP5,Ficolin-3,and CXCL12 and microvascular lesions in T2DM was analyzed using smooth curve fitting method.The receiver operating characteristic(ROC)curve and area under the curve(AUC)were used to analyze the pre-dictive value of serum CTRP5,Ficolin-3,and CXCL12 for T2DM microvascular lesions.Results There were no significant differences in gender,age,BMI,duration of T2DM,abdominal circumference,DBP,SBP,TC,HDL-C,TG,LDL-C,smoking his-tory and drinking history between the two groups(all P>0.05).FPG,2hPG,HbA1c and HOMA-IR in the observation group were significantly higher than in the control group(all P<0.05).The serum levels of CTRP5,Ficolin-3 and CXCL12 in the ob-servation group were significantly higher than in the control group(all P<0.05).Logistic regression analysis showed that FPG,2hPG,HbA1c,HOMA-IR,CTRP5,Ficolin-3 and CXCL12 were the influencing factors of T2DM microangiopathy(all P<0.05).After adjusting for FPG,2hPG,HbA1c,HOMA-IR and other confounding factors,the relationship between serum Fico-lin-3,CTRP5,CXCL12 and T2DM microangiopathy was analyzed by curve fitting,the results showed that serum Ficolin-3,CTRP5,CXCL12 were linearly positively correlated with T2DM microangiopathy,with the increase of their levels,the risk of T2DM microangiopathy increased.The ROC curve showed that the AUC of serum Ficolin-3,CTRP5 and CXCL12 levels in pre-dicting T2DM microvascular lesions was 0.756,0.761 and 0.791,respectively.The AUC of combined prediction was 0.931,and the sensitivity and specificity were 90.67%and 80.00%,respectively.Delong test showed that the AUC of combined prediction was significantly greater than that of single prediction(Z=32.123,P<0.01).Conclusion The changes in serum levels of CTRP5,Ficolin-3,and CXCL12 are closely related to microvascular lesions in patients with T2DM,providing a reference for ear-ly clinical prediction and evaluation of microvascular lesions in patients with T2DM,as well as for the development of corre-sponding intervention strategies.
3.Research and Application of Sunshine Medicine Electronic Monitoring Data Analysis System Based on Business Intelligence Technology
Wenge CHEN ; Kang CHEN ; Ting SHU ; Ping QIN ; Zhongxiao LIN ; Dan TANG
China Pharmacy 2016;27(10):1422-1425
OBJECTIVE:To evaluate the research and application situation of Sunshine Medicine Electronic Monitoring Data Analysis System. METHODS:The Sunshine Medicine Electronic Monitoring data Analysis System based on business intelligence technology was introduced in respects of design process,development,implementation and application example. RESULTS:The whole architecture of the system mainly includes hospital business platform,data integration platform,information processing plat-form and application service platform;the functions of the system include medicine homepage show,single species analysis,antimi-crobial agent analysis,national essential medicine analysis,injection analysis and sunshine medicine analysis. It can monitor the drug utilization in multi-angle and multi-level manners by building data center and creating multidimensional models. Besides,the sys-tem could solve thedrugs unified coding and information controlproblems,data collection and information integrationprob-lems in different hospital,andthe efficient calculation and analysis of a large number of drug use data. It can realize drug analy-sis and monitoring in the hospital,analysis and online monitoring of drugs prescribed by the doctor,finding,warning and evaluat-ing abnormal phenomenon of drug use in the medical institutions,so that it is better for the supervisors to monitor the usage of drugs. CONCLUSIONS:The system with easy operation,flexible monitoring,rich chart shows,comprehensive monitor index has a positive effect on rational medication level.

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