Honka Miikka-Juhani, Rebelos Eleni, Pekkarinen Laura, Tuomola Nelli, Latva-Rasku Aino, Koukkari Leena, Immonen Heidi, Mari Andrea, Kalliokoski Kari K, Hannukainen Jarna C, Nuutila Pirjo
Turku PET Centre, University of Turku, Turku FI-20520, Finland.
Turku PET Centre, Turku University Hospital, Turku FI-20520, Finland.
J Endocr Soc. 2025 Apr 2;9(5):bvaf054. doi: 10.1210/jendso/bvaf054. eCollection 2025 May.
Postprandial hepatic glycogen synthesis and glycolysis are reduced in hepatic insulin resistance. However, the physiologic interpretation of the reduction in hepatic glucose uptake (GU) during the gold-standard measurement of insulin sensitivity, hyperinsulinemic euglycemic clamp, in insulin resistance is unclear. This is because the peripheral route of glucose and insulin delivery during a clamp study differs greatly from the physiological route.
We hypothesized that hepatic GU during hyperinsulinemic euglycemic clamp would predict glycemia during oral glucose tolerance test (OGTT).
We analyzed cross-sectional data of 120 individuals (70 men and 50 women) who did not have diabetes from the CMgene study cohort. Hepatic GU was measured with [F]fluorodeoxyglucose ([F]FDG) and positron emission tomography.
In a multiple regression analysis, hepatic GU, endogenous glucose production, insulin secretion capacity, and serum triglycerides predicted OGTT glucose area under the curve ( for all <.05), whereas skeletal muscle GU, the antilipolytic insulin index, and insulin clearance were not statistically significant predictors ( > .05).
Hepatic GU measured during hyperinsulinemic euglycemic clamp is an independent predictor of OGTT glucose area under the curves even when accounting for well-known other factors affecting glycemic control. This finding supports the idea that insulin-mediated hepatic GU, and more broadly, first-pass glucose extraction, have a meaningful contribution to glycemic control. Thus, this measurement provides useful information about hepatic insulin sensitivity in the more physiologic conditions of the OGTT which may be useful when studying the pathophysiology of impaired glucose tolerance and when evaluating potential treatments for impaired glycemic control.
在肝脏胰岛素抵抗状态下,餐后肝糖原合成及糖酵解减少。然而,在胰岛素敏感性的金标准测量方法——高胰岛素正常血糖钳夹试验中,肝脏葡萄糖摄取(GU)减少的生理学解释尚不清楚。这是因为钳夹研究中葡萄糖和胰岛素的外周输注途径与生理途径有很大差异。
我们假设高胰岛素正常血糖钳夹试验期间的肝脏GU可预测口服葡萄糖耐量试验(OGTT)期间的血糖水平。
我们分析了CMgene研究队列中120例无糖尿病的个体(70名男性和50名女性)的横断面数据。用[F]氟脱氧葡萄糖([F]FDG)和正电子发射断层扫描测量肝脏GU。
在多元回归分析中,肝脏GU、内源性葡萄糖生成、胰岛素分泌能力和血清甘油三酯可预测OGTT曲线下葡萄糖面积(所有P<0.05),而骨骼肌GU、抗脂解胰岛素指数和胰岛素清除率不是统计学上显著的预测因素(P>0.05)。
即使考虑到其他影响血糖控制的已知因素,高胰岛素正常血糖钳夹试验期间测量的肝脏GU仍是OGTT曲线下葡萄糖面积的独立预测因素。这一发现支持了胰岛素介导的肝脏GU,更广泛地说,首过葡萄糖摄取对血糖控制有重要贡献的观点。因此,这种测量方法在OGTT这种更接近生理状态的条件下提供了有关肝脏胰岛素敏感性的有用信息,这在研究糖耐量受损的病理生理学以及评估血糖控制受损的潜在治疗方法时可能是有用的。