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Urinary C-peptide creatinine ratio detects absolute insulin deficiency in Type 2 diabetes

机译:尿C肽肌酐比值可检测2型糖尿病患者的绝对胰岛素缺乏

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Aims: To determine the prevalence and clinical characteristics of absolute insulin deficiency in long-standing Type 2 diabetes, using a strategy based on home urinary C-peptide creatinine ratio measurement. Methods: We assessed the urinary C-peptide creatinine ratios, from urine samples taken at home 2 h after the largest meal of the day, in 191 insulin-treated subjects with Type 2 diabetes (diagnosis age ≥45 years, no insulin in the first year). If the initial urinary C-peptide creatinine ratio was ≤0.2 nmol/mmol (representing absolute insulin deficiency), the assessment was repeated. A standardized mixed-meal tolerance test with 90-min stimulated serum C-peptide measurement was performed in nine subjects with a urinary C-peptide creatinine ratio ≤ 0.2 nmol/mmol (and in nine controls with a urinary C-peptide creatinine ratio 0.2 nmol/mmol) to confirm absolute insulin deficiency. Results: A total of 2.7% of participants had absolute insulin deficiency confirmed by a mixed-meal tolerance test. They were identified initially using urinary C-peptide creatinine ratio: 11/191 subjects (5.8%) had two consistent urinary C-peptide creatinine ratios ≤ 0.2 nmol/mmol; 9 of these 11 subjects completed a mixed-meal tolerance test and had a median stimulated serum C-peptide of 0.18 nmol/l. Five of these 9 had stimulated serum C-peptide 0.2 nmol/l and 9/9 subjects with urinary C-peptide creatinine ratio 0.2 had endogenous insulin secretion confirmed by the mixed-meal tolerance test. Compared with subjects with a urinary C-peptide creatinine ratio 0.2 nmol/mmol, those with confirmed absolute insulin deficiency had a shorter time to insulin treatment (median 2.5 vs. 6 years, P=0.005) and lower BMI (25.1 vs. 29.1 kg/m2, P=0.04). Two out of the five patients with absolute insulin deficiency were glutamic acid decarboxylase autoantibody-positive. Conclusions: Absolute insulin deficiency may occur in long-standing Type 2 diabetes, and cannot be reliably predicted by clinical features or autoantibodies. Absolute insulin deficiency in Type 2 diabetes may increase the risk of hypoglycaemia and ketoacidosis, as in Type 1 diabetes. Its recognition should help guide treatment, education and management. The urinary C-peptide creatinine ratio is a practical non-invasive method to aid detection of absolute insulin deficiency, with a urinary C-peptide creatinine ratio 0.2 nmol/mmol being a reliable indicator of retained endogenous insulin secretion.
机译:目的:为了确定长期存在的2型糖尿病中绝对胰岛素缺乏的患病率和临床特征,采用基于家庭尿C-肽肌酐比值测量的策略。方法:我们评估了191位接受胰岛素治疗的2型糖尿病(诊断年龄≥45岁,首次接受胰岛素治疗的患者)在一天的最大一餐后2小时从家中采集的尿液样本中尿C肽肌酐的比率。年)。如果最初的尿C肽肌酐比率≤0.2nmol / mmol(代表绝对胰岛素缺乏),则应重复评估。在9名尿C肽肌酐比值≤0.2 nmol / mmol的受试者中和9名尿C肽肌酐比值> 0.2的对照组中进行了90分钟刺激血清C肽测量的标准混合餐耐受试验(nmol / mmol)确认绝对胰岛素缺乏。结果:混合膳食耐受性测试证实了2.7%的参与者具有绝对胰岛素缺乏症。最初使用尿C肽肌酐比率进行鉴定:11/191名受试者(5.8%)的两个尿C肽肌酐比率一致,≤0.2 nmol / mmol。这11名受试者中有9名完成了混合餐耐受性测试,刺激血清C肽的中位数为0.18 nmol / l。这9名患者中有5名受刺激的血清C肽<0.2 nmol / l,而尿C肽肌酐比> 0.2的9/9名受试者的内源性胰岛素分泌已通过混合餐耐受性试验得以证实。与尿中C肽肌酐比率> 0.2 nmol / mmol的受试者相比,确诊绝对胰岛素缺乏的受试者的胰岛素治疗时间更短(中位2.5 vs. 6岁,P = 0.005)并且BMI较低(25.1 vs. 29.1)。千克/平方米,P = 0.04)。五分之二的绝对胰岛素缺乏患者中,有二位为谷氨酸脱羧酶自身抗体阳性。结论:绝对的胰岛素缺乏症可能发生在长期存在的2型糖尿病中,并且不能通过临床特征或自身抗体可靠地预测。与1型糖尿病一样,2型糖尿病中绝对胰岛素缺乏可能增加低血糖和酮症酸中毒的风险。它的承认应有助于指导治疗,教育和管理。尿C肽肌酐比率是一种实用的非侵入性方法,可帮助检测绝对的胰岛素缺乏,尿C肽肌酐比率> 0.2 nmol / mmol是保留内源性胰岛素分泌的可靠指标。

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