Expression analysis of urinary exosome miR-142-3p in type 2 diabetic nephropathy and evaluation of its clinical diagnostic value
1. Preliminary screening of miRNAs: Through GEO database and reading related literature, miRNAs differentially expressed in type 2 diabetes and diabetic nephropathy were selected as potential candidate biomarkers for follow-up verification. 2. Collection and treatment of clinical samples: Urine of diabetic patients was collected from the First Affiliated Hospital of Shandong First Medical University in strict accordance with the drainage standard, and the basic information of patients was registered. Meanwhile, the collected samples were divided into type 2 diabetes group and diabetic nephropathy group according to whether the urine was accompanied by UACR≥30/g. Subsequently, the collected samples were centrifuged and retained for supernatant. 3. Isolation and identification of urinary exosomes: Ultrafast centrifugation method was used to separate the treated urine samples of exosomes, and then identified by transmission electron microscopy, nanoparticle analysis and Western blot respectively. 4. Real-time PCR was used to detect the changes in urinary exosomal miRNA expression levels of the two groups of patients, and statistical analysis and correlation analysis of clinical indicators of the differentially expressed mirnas were performed. Target gene prediction and enrichment pathway analysis of differentially expressed mirnas were performed to screen out pathways that might be related to the occurrence and development of DKD, and then the relevant pathways were verified by immunofluorescence, immunocoprecipitate, Western blot, Real-time PCR and other methods.
Study Type
OBSERVATIONAL
Enrollment
44
The patients were grouped according to the results of previous inpatient tests, and no intervention measures were taken
Qianfoshan Hospital
Jinan, Shandong, China
Preliminary screening of miRNA
Through GEO database and reading related literature, mirnas that are differentially expressed in type 2 diabetes and diabetic nephropathy were selected as potential candidate biomarkers for follow-up verification.
Time frame: 2020-2024
Clinical sample collection and processing
(2) The urine of diabetic patients was collected from the First Affiliated Hospital of Shandong First Medical University in strict accordance with the drainage standard, and the basic information of patients was registered. Meanwhile, the collected samples were divided into type 2 diabetes group and diabetic nephropathy group according to whether the urine was accompanied by UACR≥30/g. Subsequently, the collected samples were centrifuged and retained for supernatant.
Time frame: 2020-2024
Statistical analysis and target gene prediction of misexpressed mirnas and enrichment pathway analysis
Statistical analysis and correlation analysis of clinical indicators of differentially expressed mirnas were performed to further evaluate their clinical diagnostic value. Subsequently, the target genes of the mirnas differentially expressed in urinary exosomes of the two groups were analyzed by miRTarBase database and R software package, and the relevant pathways were screened out through KEGG enrichment pathway analysis. Subsequently, the relevant pathways were verified by immunofluorescence, immunocoprecipitation, Western blot, Real-time PCR and other methods.
Time frame: 2020-2024
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.