Insulin secretion, sensitivity, and clearance in normoglycemic Black and White adults with parental type 2 diabetes: association with incident dysglycemia.

IF 3.7 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM BMJ Open Diabetes Research & Care Pub Date : 2024-12-23 DOI:10.1136/bmjdrc-2024-004545
Chimaroke Edeoga, Peace Asuzu, Jim Wan, Samuel Dagogo-Jack
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Abstract

Introduction: Ethnic disparities in the prevalence and pathophysiology of type 2 diabetes are well documented, but prospective data on insulin dynamics vis-à-vis pre-diabetes/early dysglycemia risk in diverse populations are scant.

Research design and methods: We analyzed insulin secretion, sensitivity, and clearance among participants in the Pathobiology of Prediabetes in a Biracial Cohort (POP-ABC) study. The POP-ABC study followed initially normoglycemic offspring of parents with type 2 diabetes for 5.5 years, the primary outcome being incident dysglycemia. Assessments included anthropometry, oral glucose tolerance test, insulin sensitivity (hyperinsulinemic euglycemic clamp, HEC), insulin secretion (intravenous glucose tolerance test, IVGT), and disposition index (DI). Insulin clearance was derived as the molar ratio of plasma C peptide to insulin and by calculating the metabolic clearance rate during HEC.

Results: POP-ABC participants who completed IVGT and HEC at baseline (145 African American, 123 European American; 72% women; mean age 44.6±10.1 years) were included in the present analysis. The baseline fasting plasma glucose was 91.9±6.91 mg/dL (5.11±0.38 mmol/L) and 2-hour plasma glucose was 123±25.1 mg/dL (6.83±1.83 mmol/L). African American offspring of parents with type 2 diabetes had higher insulin secretion and DI, and lower insulin sensitivity and clearance, than their European American counterparts. During 5.5 years of follow-up, 91 of 268 participants developed incident dysglycemia and 177 maintained normoglycemia. In Cox proportional hazards models, insulin secretion (HR 0.997 (95% CI 0.996 to 0.999), p=0.005), insulin sensitivity (HR 0.948 (95% CI 0.913 to 0.984), p=0.005), DI (HR 0.945 (95% CI 0.909 to 0.983), p=0.005) and basal insulin clearance (HR 1.030 (95% CI 1.005 to 1.056), p=0.018) significantly predicted incident dysglycemia.

Conclusions: Insulin sensitivity, secretion, and clearance differ significantly in normoglycemic African American versus European American offspring of parents with type 2 diabetes and are associated with the risk of incident dysglycemia.

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双亲患有2型糖尿病的正常血糖黑人和白人成人的胰岛素分泌、敏感性和清除率:与血糖异常的关系
引言:2型糖尿病患病率和病理生理的种族差异有很好的文献记载,但不同人群中胰岛素动态与-à-vis糖尿病前期/早期血糖异常风险的前瞻性数据很少。研究设计和方法:我们在一项双种族队列(POP-ABC)研究中分析了前驱糖尿病病理生物学参与者的胰岛素分泌、敏感性和清除率。POP-ABC研究对父母患有2型糖尿病的子女进行了为期5.5年的初始血糖正常随访,主要结局是发生血糖异常。评估包括人体测量、口服葡萄糖耐量试验、胰岛素敏感性(高胰岛素正糖钳夹,HEC)、胰岛素分泌(静脉葡萄糖耐量试验,IVGT)和处置指数(DI)。胰岛素清除率由血浆C肽与胰岛素的摩尔比和计算HEC期间的代谢清除率得出。结果:在基线完成IVGT和HEC的POP-ABC参与者(145名非洲裔美国人,123名欧洲裔美国人;72%的女性;平均年龄(44.6±10.1岁)纳入分析。基线空腹血糖为91.9±6.91 mg/dL(5.11±0.38 mmol/L), 2小时血糖为123±25.1 mg/dL(6.83±1.83 mmol/L)。父母患有2型糖尿病的非裔美国人的后代胰岛素分泌和DI较高,胰岛素敏感性和清除率较低。在5.5年的随访中,268名参与者中有91人出现了血糖异常,177人维持了正常血糖。在Cox比例风险模型中,胰岛素分泌(HR 0.997 (95% CI 0.996 ~ 0.999), p=0.005)、胰岛素敏感性(HR 0.948 (95% CI 0.913 ~ 0.984), p=0.005)、DI (HR 0.945 (95% CI 0.909 ~ 0.983), p=0.005)和基础胰岛素清除率(HR 1.030 (95% CI 1.005 ~ 1.056), p=0.018)显著预测了血糖异常的发生。结论:血糖正常的非裔美国人与2型糖尿病父母的欧裔美国人后代的胰岛素敏感性、分泌和清除率存在显著差异,并与发生血糖异常的风险相关。
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来源期刊
BMJ Open Diabetes Research & Care
BMJ Open Diabetes Research & Care Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
9.30
自引率
2.40%
发文量
123
审稿时长
18 weeks
期刊介绍: BMJ Open Diabetes Research & Care is an open access journal committed to publishing high-quality, basic and clinical research articles regarding type 1 and type 2 diabetes, and associated complications. Only original content will be accepted, and submissions are subject to rigorous peer review to ensure the publication of high-quality — and evidence-based — original research articles.
期刊最新文献
Retraction: Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus. Ethnic disparities in HbA1c and hypoglycemia among youth with type 1 diabetes: beyond access to technology, social deprivation and mean blood glucose. Association between use of sodium-glucose co-transporter-2 inhibitor and the risk of incident dementia: a population-based cohort study. Mechanism of TGIF1 on glycolipid metabolism disorders in mice with type 2 diabetes. Risk of renal complications and death in young and middle-aged Swedes with parental type 1 diabetes: a nation-wide, prospective cohort study.
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