Department of General Surgery, School for Nutrition, Toxicology, and Metabolism Research Institute Maastricht, Maastricht University Medical Center, 6200 MD Maastricht, The Netherlands.
J Clin Endocrinol Metab. 2011 Feb;96(2):E379-83. doi: 10.1210/jc.2010-1333. Epub 2010 Nov 17.
Type 2 diabetes mellitus (DM2) is associated with small intestinal hyperplasia and hypertrophy in rodents. Moreover, the small intestine is increasingly acknowledged to play a role in the pathophysiology of DM2.
The objective of the study was to investigate the relation between plasma markers of small intestinal function and chronic hyperglycemia in man.
DESIGN, SETTING, AND PARTICIPANTS: We conducted a cross-sectional observational study of 40 severely obese subjects with chronic hyperglycemia and 30 severely obese subjects without chronic hyperglycemia who were indicated for bariatric surgery.
We assessed plasma levels of citrulline, representing small intestinal enterocyte mass, intestinal fatty acid binding protein (I-FABP), a marker of enterocyte loss, and glucagon-like peptide-2, an intestinotrophic factor, and related them to glycated hemoglobin (HbA(1c)) levels.
Plasma citrulline and I-FABP levels were both significantly elevated in subjects with chronic hyperglycemia (HbA(1c) > 6.0%) compared with subjects with a normal HbA(1c) (≤ 6.0%) (citrulline, 35 ± 2.1 μm vs. 26 ± 1.4 μm, P = 0.001; I-FABP, 140 ± 22 pg/ml vs. 69 ± 14 pg/ml, P = 0.001). Moreover, plasma citrulline and I-FABP levels correlated with HbA(1c) levels (citrulline, r(s) = 0.30, P = 0.02; I-FABP, r(s) = 0.33, P = 0.005). The I-FABP to citrulline ratio was higher in subjects with an elevated HbA(1c) (4.0 vs. 3.1, P = 0.03). Plasma glucagon-like peptide-2 levels were not related to citrulline or I-FABP levels (r(s) = 0.06, P = 0.67; r(s) 0.08, P = 0.54, respectively).
Chronically elevated glucose levels in obese individuals are associated with increased small intestinal enterocyte mass and increased enterocyte loss. These findings argue for the further exploration of the role of the intestine in the pathophysiology of DM2.
2 型糖尿病(DM2)与啮齿动物的小肠增生和肥大有关。此外,小肠在 DM2 的病理生理学中越来越被认为发挥作用。
本研究旨在研究血浆小肠功能标志物与人类慢性高血糖之间的关系。
设计、地点和参与者:我们对 40 名患有慢性高血糖的严重肥胖患者和 30 名因减重手术而患有慢性高血糖的严重肥胖患者进行了横断面观察性研究。
我们评估了血浆瓜氨酸水平,代表小肠肠细胞质量,肠脂肪酸结合蛋白(I-FABP),肠细胞丢失的标志物,和胰高血糖素样肽-2,一种肠营养因子,并将其与糖化血红蛋白(HbA1c)水平相关联。
与 HbA1c 正常(≤6.0%)的患者相比,慢性高血糖(HbA1c>6.0%)患者的血浆瓜氨酸和 I-FABP 水平均显著升高(瓜氨酸,35±2.1 μm vs. 26±1.4 μm,P=0.001;I-FABP,140±22 pg/ml vs. 69±14 pg/ml,P=0.001)。此外,血浆瓜氨酸和 I-FABP 水平与 HbA1c 水平相关(瓜氨酸,r(s)=0.30,P=0.02;I-FABP,r(s)=0.33,P=0.005)。HbA1c 升高的患者 I-FABP 与瓜氨酸的比值更高(4.0 比 3.1,P=0.03)。血浆胰高血糖素样肽-2 水平与瓜氨酸或 I-FABP 水平无关(r(s)=0.06,P=0.67;r(s)0.08,P=0.54)。
肥胖个体慢性高血糖与小肠肠细胞质量增加和肠细胞丢失增加有关。这些发现表明需要进一步探讨肠道在 DM2 病理生理学中的作用。