Fernández-Real José Manuel, Peñarroja Georgina, Castro Antoni, García-Bragado Fernando, Hernández-Aguado Ildefonso, Ricart Wifredo
Unit of Diabetes, Endocrinology and Nutrition, University Hospital of Girona Dr. Josep Trueta, Girona, Spain.
Diabetes. 2002 Apr;51(4):1000-4. doi: 10.2337/diabetes.51.4.1000.
Iron-related insulin-resistance is improved by iron depletion or treatment with iron chelators. The aim of this study was to evaluate insulin sensitivity and insulin secretion after blood letting in patients who had high-ferritin type 2 diabetes and were randomized to blood letting (three phlebotomies [500 ml of blood] at 2-week intervals, group 1) or to observation (group 2). Insulin secretion and sensitivity were tested at baseline and 4 and 12 months thereafter. The two groups were matched for age, BMI, pharmacologic treatment, and chronic diabetic complications. All patients were negative for C282Y mutation of hereditary hemochromatosis. Baseline glycated hemoglobin (6.27 +/- 0.9% vs. 6.39 +/- 1.2%), insulin sensitivity (2.75 +/- 1.8 vs. 3.2 +/- 2.1 mg.dl(-1).min(-1)), and area under the curve for C-peptide (AUC(C-peptide); 38.7 +/- 11.6 vs. 37.6 +/- 14.1 ng.ml(-1).min(-1)) were not significantly different between the two groups of patients. Body weight, blood pressure, blood hematocrit levels, and drug treatment remained essentially unchanged during the study period. As expected, serum ferritin, transferrin saturation index, and blood hemoglobin decreased significantly at 4 months only in patients who received blood letting. In parallel to this changes, blood HbA(1c) decreased significantly only in group 1 subjects (mean differences, -0.61; 95% CI, -0.17 to -1.048; P = 0.01). AUC(C-peptide) decreased by -10.2 +/- 6.3% after blood letting. In contrast, a 10.4 +/- 6.4% increase in AUC(C-peptide) was noted in group 2 subjects at 4 months (P = 0.032). At 12 months, AUC(C-peptide) returned to values not significantly different from baseline in the two groups of subjects. At 4 months, the change in insulin sensitivity from baseline was significantly different between the two groups (80.6 +/- 43.2% vs. -8.6 +/- 9.9% in groups 1 and 2, respectively, P = 0.049). At 12 months, the differences between the two groups were even more marked (55.5 +/- 24.8% vs. -26.8 +/- 9.9%; P = 0.005). When the analysis was restricted to those subjects who completed the follow-up until 12 months, results did not show differences compared with the changes observed at 4 months, except for insulin sensitivity. A statistically significant increase in insulin sensitivity was observed in the blood-letting group (from 2.30 +/- 1.81 to 3.08 +/- 2.55 mg.dl(-1).min(-1) at 4 months, to 3.16 +/- 1.85 mg.dl(-1).min(-1) at 12 months; P = 0,045) in contrast with group 2 subjects (from 3.24 +/- 1.9 to 3.26 +/- 2.05 mg.dl(-1).min(-1) at 4 months, to 2.31 +/- 1.35 mg.dl(-1).min(-1) at 12 months). In summary, blood letting led simultaneously to decreased blood HbA(1c) levels and to changes in insulin secretion and insulin resistance that were significantly different from those observed in a matched observational group of subjects with high-ferritin type 2 diabetes. The mechanisms for improvement in peripheral insulin sensitivity after blood letting should be investigated further.
铁缺乏或使用铁螯合剂治疗可改善与铁相关的胰岛素抵抗。本研究旨在评估对高铁蛋白的2型糖尿病患者进行放血治疗后其胰岛素敏感性和胰岛素分泌情况,这些患者被随机分为放血组(每隔2周进行3次静脉放血[每次放血500毫升],第1组)或观察组(第2组)。在基线时以及之后的4个月和12个月时检测胰岛素分泌和敏感性。两组在年龄、体重指数、药物治疗和慢性糖尿病并发症方面相匹配。所有患者遗传性血色素沉着症的C282Y突变均为阴性。两组患者的基线糖化血红蛋白(6.27±0.9%对6.39±1.2%)、胰岛素敏感性(2.75±1.8对3.2±2.1毫克·分升⁻¹·分钟⁻¹)以及C肽曲线下面积(AUC(C肽);38.7±11.6对37.6±14.1纳克·毫升⁻¹·分钟⁻¹)无显著差异。在研究期间,体重、血压、血细胞比容水平和药物治疗基本保持不变。正如预期的那样,仅在接受放血治疗的患者中,血清铁蛋白、转铁蛋白饱和度指数和血红蛋白在4个月时显著下降。与此变化并行的是,仅第1组受试者的糖化血红蛋白显著下降(平均差异为-0.61;95%可信区间为-0.17至-1.048;P = 0.01)。放血后C肽曲线下面积下降了-10.2±6.3%。相比之下,第2组受试者在4个月时C肽曲线下面积增加了10.4±6.4%(P = 0.032)。在12个月时,两组受试者的C肽曲线下面积恢复到与基线无显著差异的值。在4个月时,两组之间胰岛素敏感性相对于基线的变化有显著差异(第1组和第2组分别为80.6±43.2%对-8.6±9.9%,P = 0.049)。在12个月时,两组之间的差异更为明显(55.5±24.8%对-26.8±9.9%;P = 0.005)。当分析仅限于那些完成12个月随访的受试者时,除胰岛素敏感性外,结果与4个月时观察到的变化相比未显示出差异。在放血组观察到胰岛素敏感性有统计学意义的增加(从4个月时的2.30±1.81毫克·分升⁻¹·分钟⁻¹增加到3.08±2.55毫克·分升⁻¹·分钟⁻¹,12个月时为3.16±1.85毫克·分升⁻¹·分钟⁻¹;P = 0.045),相比之下第2组受试者(从4个月时的3.24±1.9毫克·分升⁻¹·分钟⁻¹增加到3.26±2.05毫克·分升⁻¹·分钟⁻¹,12个月时为2.31±1.35毫克·分升⁻¹·分钟⁻¹)。总之,放血同时导致糖化血红蛋白水平降低以及胰岛素分泌和胰岛素抵抗发生变化,这些变化与在匹配的高铁蛋白2型糖尿病观察组受试者中观察到的情况有显著差异。放血后外周胰岛素敏感性改善的机制应进一步研究。