Nyenwe Ebenezer, James Deirdre, Wan Jim, Dagogo-Jack Sam
Department of Medicine, Division of Endocrinology, Diabetes & Metabolism.
Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
J Endocr Soc. 2020 Sep 28;4(11):bvaa137. doi: 10.1210/jendso/bvaa137. eCollection 2020 Nov 1.
Prediabetes, an often unrecognized precursor of type 2 diabetes (T2DM), is associated with cardiometabolic complications. Here, we investigated the utility of dexamethasone challenge in predicting incident prediabetes among normoglycemic subjects with parental T2DM enrolled in the prospective Pathobiology of Prediabetes in a Biracial Cohort study.
After documenting normoglycemic status with an oral glucose tolerance test (OGTT), participants ingested dexamethasone (2 mg) at 10:00 pm, and fasting plasma glucose (FPG-Dex) and cortisol were measured at 8:00 am the next day. Subjects were followed quarterly for 5 years, the primary outcome being incident prediabetes. Serial assessments included body composition, blood chemistry, OGTT, insulin sensitivity, and secretion.
We analyzed data from 190 participants (107 Black, 83 white; mean age 44.7 ± 10.0 years; body mass index [BMI] 29.8 ± 6.8 kg/m; fasting plasma glucose [FPG] 90.9 ± 5.7 mg/dL). Following dexamethasone ingestion, plasma cortisol was < 5 µg/dL; FPG-Dex levels displayed marked variability (81-145 mg/dL) as did delta FPG (-7 to +48 mg/dL). During 5 years of follow-up, 58 of 190 subjects (30.5%) progressed to prediabetes. FPG-Dex (116.8 ± 10.9 vs 106.9 ± 10.8 mg/dL, < 0.0001) and delta FPG (23.4 ± 10.1 vs 17.0 ± 10.2 mg/dL, < 0.0001) were higher in progressors than nonprogressors. FPG-Dex ( = 0.007) was an independent predictor of incident prediabetes in a multivariate model that included age, race, gender, BMI, waist circumference, FPG, insulin sensitivity, and secretion. In further analyses, an FPG-Dex level ≥ 107 mg/dL predicted incident prediabetes with 88% sensitivity and 49% specificity.
The glycemic response to dexamethasone significantly predicted incident prediabetes among offspring of parents with T2DM, and may be a tool for uncovering latent risk of dysglycemia.
糖尿病前期是2型糖尿病(T2DM)常见的未被识别的前驱阶段,与心血管代谢并发症相关。在此,我们在一项双种族队列的糖尿病前期病理生物学前瞻性研究中,调查了地塞米松激发试验在预测有T2DM家族史的血糖正常受试者发生糖尿病前期方面的效用。
通过口服葡萄糖耐量试验(OGTT)记录血糖正常状态后,参与者于晚上10点摄入地塞米松(2毫克),并于次日上午8点测量空腹血糖(FPG-Dex)和皮质醇。对受试者每季度随访5年,主要结局为发生糖尿病前期。系列评估包括身体成分、血液生化、OGTT、胰岛素敏感性和分泌情况。
我们分析了190名参与者的数据(107名黑人,83名白人;平均年龄44.7±10.0岁;体重指数[BMI]29.8±6.8kg/m²;空腹血糖[FPG]90.9±5.7mg/dL)。摄入地塞米松后,血浆皮质醇<5μg/dL;FPG-Dex水平显示出显著变异性(81 - 145mg/dL),FPG变化值(ΔFPG)也是如此(-7至+48mg/dL)。在5年的随访期间,190名受试者中有58名(30.5%)进展为糖尿病前期。进展者的FPG-Dex(116.8±10.9 vs 106.9±10.8mg/dL,P<0.0001)和ΔFPG(23.4±10.1 vs 17.0±10.2mg/dL,P<0.0001)高于未进展者。在包含年龄、种族、性别、BMI、腰围、FPG、胰岛素敏感性和分泌情况的多变量模型中,FPG-Dex(P = 0.007)是发生糖尿病前期的独立预测因素。在进一步分析中,FPG-Dex水平≥107mg/dL预测发生糖尿病前期的敏感性为88%,特异性为49%。
地塞米松激发试验后的血糖反应显著预测了T2DM患者后代发生糖尿病前期的情况,可能是一种发现血糖异常潜在风险的工具。