Type 1 diabetes (T1D) is characterized by absolute insulin deficiency. Although the discovery and application of exogenous insulin has prolonged the lifespan of T1D patients, the chronic diabetic complications caused by long-term poor glycemic control will still reduce patients' quality of life and the overall life expectancy. According to the studies focused on long-term T1D, part of the patients with long disease duration showed resistance to microvascular complications, and several protective factors have been identified. The prevalence of T1D in China is extremely low compared to that in the western world, and little is known about the characteristics of patients with long-term T1D in China. Therefore, this study is designed to collect variable clinical and laboratory features of patients with long-term T1D, explore the risk and protective factors for the development of microvascular complications, and provide reference for the prediction and prevention of these complications.
This is a single-center, prospective, observational study. The investigators propose to enroll 400 patients with type 1 diabetes (T1D) ≥10 years. The patients will be followed up annually for 3 years. In order to ensure high quality data, two staff are responsible for the input of original data into the database to check and confirm the accuracy. When the data entered by two people is inconsistent, the auxiliary staff decides which data to use. Missing data will be filled in with the multiple imputation method. The regression analysis will be used to explore the risk and protective factors for the development and progression of microvascular complications.
Study Type
OBSERVATIONAL
Enrollment
400
For each follow-up, the glycated albumin(GA) reflecting glycemic control of the past 2-3 weeks, the glycated hemoglobin(HbA1c) reflecting glycemic control of the past 2-3 months, and the advanced glycation end products(AGEs) will be measured.
For each follow-up, fasting and stimulated C-peptide levels will be measured.
Genetic variations of interest will be detected with the blood sample collected at baseline.
For each follow-up, the dietary constitutes for the past 3 days will be recorded.
For each follow-up, the fecal and oral samples will be collected for measurement.
For each follow-up, the serum and urine samples will be collected for measurement.
For each follow-up, the peripheral blood mononuclear cells will be collected for measurement.
Institute of Metabolism and Endocrinology, Second Xiangya Hospital, Central South University
Changsha, Hunan, China
RECRUITINGthe development or progression of diabetic nephropathy
measured by urine microalbumin/creatinine
Time frame: from May 2022 to December 2025
the development or progression of diabetic retinopathy
diagnosed by an ophthalmologist based on fundus photography
Time frame: from May 2022 to December 2025
the changes of memory function
measured by the Auditory Verbal Learning Test (AVLT)
Time frame: from May 2022 to December 2025
the changes of executive function
measured by the Shape Trail Test (STT)
Time frame: from May 2022 to December 2025
the changes of language function
measured by the Boston Naming Test (BNT)
Time frame: from May 2022 to December 2025
the changes on magnetic resonance imaging(MRI)
the MRI reflects the changes of cerebral structure and functional connectivity
Time frame: from May 2022 to December 2025
the changes of bone mineral density(BMD)
measured by dual x-ray absorbtiometry(DXA), indicating bone density
Time frame: from May 2022 to December 2025
the changes of brachial-ankle pulse wave velocity(baPWV)
measured by ultrasound, indicating large artery stiffness
Time frame: from May 2022 to December 2025
the changes of carotid intima-media thickness(IMT)
measured by ultrasound, indicating the form of carotid atherosclerotic plaque
Time frame: from May 2022 to December 2025
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