Camerini-Davalos R A, Velasco C A, Glasser M, Bloodworth J M
Department of Medicine, New York Medical College, New York.
Diabetes Res Clin Pract. 1988 Jul 13;5(2):113-23. doi: 10.1016/s0168-8227(88)80050-0.
Three muscle biopsies were performed in 53 overt type 2 diabetics over a period of approximately 2 years. At baseline, 21 (40%) had an increased capillary basement membrane width in muscle. Thirty-five patients received glipizide and 18 received placebo. In the patients receiving placebo, the mean of the muscle capillary basement membrane width increased from 158.7 +/- 11.5 nm (SEM) to 170.9 +/- 14.7 nm (P = NS), but in those receiving glipizide the value decreased from 192.9 +/- 13.2 nm to 161.0 +/- 10.2 nm (P = 0.02). Plasma glucose and glycosylated hemoglobin A1 decreased significantly (P less than 0.001) after 2 years in patients receiving glipizide. In 15, mean glycosylated hemoglobin A1 reached a normal range, and mean basement membrane width decreased to a level close to that found in subjects without diabetes (P = NS). These findings are consistent with the hypothesis that effective response to oral medication can decrease the basement membrane thickening, suggesting that diabetic microangiopathy is not necessarily progressive.
在大约两年的时间里,对53名显性2型糖尿病患者进行了三次肌肉活检。基线时,21名(40%)患者的肌肉毛细血管基底膜宽度增加。35名患者接受格列吡嗪治疗,18名患者接受安慰剂治疗。接受安慰剂的患者中,肌肉毛细血管基底膜宽度的平均值从158.7±11.5纳米(标准误)增加到170.9±14.7纳米(P=无显著性差异),但接受格列吡嗪治疗的患者该值从192.9±13.2纳米降至161.0±10.2纳米(P=0.02)。接受格列吡嗪治疗的患者在2年后血浆葡萄糖和糖化血红蛋白A1显著降低(P<0.001)。在15名患者中,糖化血红蛋白A1的平均值达到正常范围,基底膜宽度的平均值降至接近非糖尿病受试者的水平(P=无显著性差异)。这些发现与口服药物有效反应可减少基底膜增厚的假设一致,表明糖尿病微血管病变不一定是进行性的。