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临床试验/NCT07835724
NCT07835724招募中不适用

Environmental Determinants of Type 1 Diabetes Risk

Second Xiangya Hospital of Central South University1 个研究点 分布在 1 个国家目标入组 11,240 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
11,240
试验地点
1
主要终点
Change From Baseline in Fasting C-peptide Concentration at 1 Year

研究概览

简要总结

To analyze the environmental risk factors for type 1 diabetes in China.

详细描述

Type 1 diabetes (T1D) is a hyperglycemic disease caused by absolute insulin deficiency. It has an acute and early onset, and patients require lifelong insulin therapy. Global T1D incidence is rising yearly. China has the fourth-largest number of T1D patients and the second-fastest increase in incidence, with a marked rise in adults. T1D results from genetic and environmental factors that cause immune destruction of pancreatic β cells. Genetic risk is relatively clear: HLA DR4-DQ8 and DR3-DQ2 carry the highest risk, and over 70 related loci have been identified. However, environmental factors remain insufficiently characterized. Studies of migrants, socioeconomic differences, and mobile populations suggest that environment and lifestyle have significant effects. Since China's genetic background has not changed substantially while incidence continues to rise, environment-induced immune dysregulation combined with genetic susceptibility may be key. International cohorts such as TEDDY and DAISY confirm that diet, viral infections, and gut microbiota can trigger islet autoimmunity. Among specific factors, high maternal early-pregnancy BMI, rapid childhood growth, and obesity increase risk; vitamin D is protective, and China's north-high/south-low incidence gradient may relate to sunlight and vitamin D. Gluten may trigger islet autoimmune inflammation via gut microbiota and immune activation. Viral infection, pollution, chemical exposure, and socioeconomic status may also contribute. Most evidence comes from European and American populations, while Chinese studies are limited. Therefore, systematically identifying China-specific environmental risk factors has important scientific and public-health value. In summary, genetics determines susceptibility, while modifiable environmental factors are critical in triggering and progression and are key to early prevention and precision management of T1D.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
3 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Individuals with type 1 diabetes (no age restriction):
  • •Clinically diagnosed with T1D by a specialist.
  • •Meeting any one of the following conditions:(1) Age of onset < 15 years;(2) No overweight or obesity at onset;(3) History of ketoacidosis.
  • •Insulin-dependent since disease onset;
  • •Positive for at least one islet autoantibody (GADA, IA-2A, ZnT8A, IAA, ICA);
  • •Disease duration ≤ 3 years.
  • •First-degree relatives:
  • •Parents, siblings, or children of an individual with T1D.
  • •Age ≤ 45 years.

排除标准

  • •Individuals with type 1 diabetes
  • •Gestational diabetes.
  • •Confirmed monogenic diabetes.
  • •Secondary diabetes.
  • •Type 2 diabetes.
  • •Other specific types of diabetes.
  • •First-degree relatives:
  • •Diagnosed with diabetes before screening;
  • •Previous or current use of glucose-lowering drugs.
  • •Common exclusion criteria:
  • •Severe active disease or a condition likely to substantially affect life expectancy, including malignancy or severe cardiac, pulmonary, hepatic, or renal disease.
  • •A condition that may require immunosuppressive therapy during the study period.
  • •Current systemic immunosuppressive therapy.
  • •Current systemic glucocorticoid therapy.
  • •Participation in another drug or medical device trial during recruitment or the study period.
  • •History of major surgery or severe trauma.

研究组 & 干预措施

Controls

Controls matched to the recruited patients.

FDR

First-degree relatives of patients with type 1 diabetes.

T1D

patients with type 1 diabetes

结局指标

主要结局

Change From Baseline in Fasting C-peptide Concentration at 1 Year

时间窗: Baseline to 1 year after enrollment

Fasting C-peptide concentration will be measured at baseline and at 1 year after enrollment. The change from baseline will be calculated as the C-peptide concentration at 1 year minus the baseline concentration and reported in pmol/L.

Change From Baseline in 2-Hour Postprandial C-peptide Concentration at 1 Year

时间窗: Baseline to 1 year after enrollment

Two-hour postprandial C-peptide concentration will be measured at baseline and at 1 year after enrollment. The change from baseline will be calculated as the 2-hour postprandial C-peptide concentration at 1 year minus the baseline concentration and reported in pmol/L.

次要结局

  • Serum Islet Autoantibodies seroconversion.(Baseline to 1 year after enrollment)
  • Change From Baseline in Number of Positive Serum Islet Autoantibodies at 1 Year(Baseline to 1 year after enrollment)

研究者

发起方
Second Xiangya Hospital of Central South University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yang Xiao

Professor; Chief Physician; Vice President, Second Xiangya Hospital of Central South University; Deputy Director, National Clinical Research Center for Endocrine and metabolic Diseases;

Second Xiangya Hospital of Central South University

研究点 (1)

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