Perseghin G, Lattuada G, De Cobelli F, Esposito A, Costantino F, Canu T, Scifo P, De Taddeo F, Maffi P, Secchi A, Del Maschio A, Luzi L
Internal Medicine Section of Nutrition/Metabolism, via Olgettina 60, 20132, Milan, Italy.
Diabetologia. 2005 Dec;48(12):2615-21. doi: 10.1007/s00125-005-0014-5. Epub 2005 Nov 1.
AIMS/HYPOTHESIS: Insulin resistance may be associated with ectopic fat accumulation potentially determined by reduced lipid oxidation. In patients with type 1 diabetes peripheral insulin resistance is associated with higher intramyocellular lipid content. We assessed whether these patients are also characterised by intrahepatic fat accumulation and abnormal fat oxidation.
Nineteen patients with type 1 diabetes (6 women, 13 men, age 35+/-7 years, BMI 23+/-3 kg/m2), HbA1c 8.7+/-1.4%) and 19 healthy matched individuals were studied by (1) euglycaemic-hyperinsulinaemic clamp combined with [6,6-2H2]glucose infusion to assess whole-body glucose metabolism; (2) indirect calorimetry to assess glucose and lipid oxidation; and (3) localised 1H-magnetic resonance spectroscopy of the liver to assess intrahepatic fat content.
Patients with type 1 diabetes showed a reduced insulin-stimulated metabolic clearance rate of glucose (4.3+/-1.3 ml kg(-1) min(-1)) in comparison with normal subjects (6.0+/-1.6 ml kg(-1) min(-1); p<0.001). Endogenous glucose production was higher in diabetic patients (p=0.001) and its suppression was impaired during insulin administration (66+/-30 vs 92+/-8%; p=0.047) in comparison with normal subjects. Plasma glucagon concentrations were not different between groups. The estimated hepatic insulin concentration was lower in diabetic patients than in normal subjects (p<0.05), as was the intrahepatic fat content (1.5+/-0.7% and 2.2+/-1.0% respectively; p<0.03), the latter in association with a reduced respiratory quotient (0.74+/-0.05 vs 0.84+/-0.06; p=0.01) and increased fasting lipid oxidation (1.5+/-0.5 vs 0.8+/-0.4 mg kg(-1) min(-1); p<0.01).
CONCLUSIONS/INTERPRETATION: In patients with type 1 diabetes, insulin resistance was not associated with increased intrahepatic fat accumulation. In fact, diabetic patients had reduced intrahepatic fat content, which was associated with increased fasting lipid oxidation. The unbalanced hepatic glucagon and insulin concentrations affecting patients with type 1 diabetes may be involved in this abnormality of intrahepatic lipid metabolism.
目的/假设:胰岛素抵抗可能与异位脂肪堆积有关,而异位脂肪堆积可能由脂质氧化减少所决定。在1型糖尿病患者中,外周胰岛素抵抗与细胞内脂质含量升高有关。我们评估了这些患者是否也具有肝内脂肪堆积和脂肪氧化异常的特征。
对19例1型糖尿病患者(6名女性,13名男性,年龄35±7岁,体重指数23±3kg/m²,糖化血红蛋白8.7±1.4%)和19名健康对照个体进行了研究,方法包括:(1)正常血糖-高胰岛素钳夹试验联合[6,6-²H₂]葡萄糖输注以评估全身葡萄糖代谢;(2)间接测热法评估葡萄糖和脂质氧化;(3)肝脏局部¹H磁共振波谱法评估肝内脂肪含量。
与正常受试者相比,1型糖尿病患者胰岛素刺激的葡萄糖代谢清除率降低(4.3±1.3ml·kg⁻¹·min⁻¹)(正常受试者为6.0±1.6ml·kg⁻¹·min⁻¹;p<0.001)。糖尿病患者内源性葡萄糖生成较高(p=0.001),与正常受试者相比,胰岛素输注期间其抑制作用受损(分别为66±30%和92±8%;p=0.047)。两组间血浆胰高血糖素浓度无差异。糖尿病患者的肝脏胰岛素估计浓度低于正常受试者(p<0.05),肝内脂肪含量也较低(分别为1.5±0.7%和2.2±1.0%;p<0.03),后者与呼吸商降低(0.74±0.05对0.84±0.06;p=0.01)和空腹脂质氧化增加(1.5±0.5对0.8±0.4mg·kg⁻¹·min⁻¹;p<0.01)相关。
结论/解读:在1型糖尿病患者中,胰岛素抵抗与肝内脂肪堆积增加无关。事实上,糖尿病患者肝内脂肪含量降低,这与空腹脂质氧化增加有关。影响1型糖尿病患者的肝脏胰高血糖素和胰岛素浓度失衡可能与这种肝内脂质代谢异常有关。