In this study, investigators wanted to determine the effect of T2DM susceptibility gene mutations on self-expression. Participants (T2DM patients and controls) were recruited to identify genotypes and detect the levels of T2DM susceptibility genes expression in the fresh peripheral plasma. The normal pancreatic tissues or adjacent tissues of pancreatic cancer were also collected to identify the expression differences of T2DM susceptibility genes under different genotypes.
The primary objective of this study was to investigate the changes of the expression of T2DM susceptible genes (NOS1AP, KCNQ1, TCF7L2, WSF1, GLP-1R, etc.) in participants (newly diagnosed T2DM patients and controls) after gene mutation. Secondly, the expression differences of T2DM susceptible genes in T2DM patients with different genotypes were compared, and the relationship between the expression differences and clinicopathological characteristics of T2DM patients was analyzed. Participants (newly diagnosed T2DM patients and healthy subjects) were screened from the department of endocrinology and health management center, whose fresh peripheral blood were collected. The normal pancreatic tissues or adjacent tissues of pancreatic cancer were collected in the department of general surgery. The DNA genome was extracted for genotyping, and then the expression levels of T2DM related susceptibility genes under different genotypes were detected by ELISA kits, PCR, WB,HE staining, IHC staining, ect. The basic information of T2DM patients was collected, including demographic characteristics, physiological and biochemical data.Then investigators further compared the differences in the expression of susceptible genes between newly diagnosed T2DM patients and controls.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
300
Compared with newly diagnosed T2DM patients, healthy subjects in the control group had normal levels of blood glucose, lipids, glycated hemoglobin levels, etc. Fresh normal pancreatic tissues or adjacent tissues of pancreatic cancer were collected before taking antidiabetic drugs in both groups.
The newly diagnosed T2DM group should not have taken antidiabetic drugs and meet the diagnosis of T2DM. Fresh blood samples were collected before medication for detection. In the control group (healthy subjects), the indicators of physical examination were within the normal range and no hypoglycemic drugs were taken. Similarly, fresh blood samples should be taken for testing.
China, Jiangsu, Department of Endocrinology
Xuzhou, China
RECRUITINGDetection of T2DM susceptibility gene expression in newly diagnosed T2DM patients
To detect the expression levels of susceptible genes in the plasma and the pancreatic tissues of newly diagnosed T2DM patients and compared with those in healthy subjects.
Time frame: 1 month after fresh sample collection
Detection of T2DM susceptibility gene expression in controls
To detect the expression levels of susceptible genes in the plasma and the pancreatic tissues of controls and compared with those in newly diagnosed T2DM patients.
Time frame: 1 month after fresh sample collection
Correlation between T2DM susceptibility gene expression and clinicopathological features
Incidence of clinical pancreatic diseases under expression differences in T2DM susceptibility genes
Time frame: 6 months after obtaining the clinicopathological results
Baseline BMI of newly diagnosed with T2DM patients with different genotypes
Baseline BMI of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline waist hip ratio (WHR) of newly diagnosed with T2DM patients with different genotypes
Baseline WHR of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline fasting plasma glucose (FPG) of newly diagnosed with T2DM patients with different genotypes
Baseline FPG of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline HbA1c of newly diagnosed with T2DM patients with different genotypes
Baseline HbA1c of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline TC of newly diagnosed with T2DM patients with different genotypes
Baseline TC of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline TG of newly diagnosed with T2DM patients with different genotypes
Baseline TG of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline HDL-C of newly diagnosed with T2DM patients with different genotypes
Baseline HDL-C of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline LDL-C of newly diagnosed with T2DM patients with different genotypes
Baseline LDL-C of newly diagnosed with T2DM patients
Time frame: 1 month of completion for individual screening
Baseline BMI of controls with different genotypes
Baseline BMI of controls
Time frame: 1 month of completion for individual screening
Baseline WHR of controls with different genotypes
Baseline WHR of controls
Time frame: 1 month of completion for individual screening
Baseline FPG of controls with different genotypes
Baseline FPG of controls
Time frame: 1 month of completion for individual screening
Baseline HbA1c of controls with different genotypes
Baseline HbA1c of controls
Time frame: 1 month of completion for individual screening
Baseline TC of controls with different genotypes
Baseline TC of controls
Time frame: 1 month of completion for individual screening
Baseline TG of controls with different genotypes
Baseline TG of controls
Time frame: 1 month of completion for individual screening
Baseline HDL-C of controls with different genotypes
Baseline HDL-C of controls
Time frame: 1 month of completion for individual screening
Baseline LDL-C of controls with different genotypes
Baseline LDL-C of controls
Time frame: 1 month of completion for individual screening
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.