Merimee T J, Siperstein M D, Hall J D, Fineberg S E
J Clin Invest. 1970 Dec;49(12):2161-4. doi: 10.1172/JCI106434.
A group of 32 sexual ateliotic dwarfs with an isolated deficiency of human growth hormone (HGH) were shown previously to resemble subjects with genetic diabetes mellitus in terms of hyperlipemia, carbohydrate intolerance, and patterns of insulin secretion. 11 of these dwarfs had needle biopsies of the quadriceps femoris carried out and tissue fixed for electron microscopy. Capillary basement membrane thickness was measured and compared with measurements previously obtained in diabetics and normal controls. Measurements were similar in controls and dwarfs (1080 +/-27 A and 1086 +/-90 A, respectively) and significantly less than in diabetics (2403 +/-119 A). Placed in juxtaposition with the absence of retinopathy in dwarfs and the high incidence in the diabetic group (41%), the data support the thesis that these anatomical abnormalities are largely independent of serum lipid and carbohydrate abnormalities. The data are consistent with a supportive, if not causative role of growth hormone in the pathogenesis of these lesions.
先前已表明,一组32例单纯性人类生长激素(HGH)缺乏的性幼稚型侏儒症患者,在高脂血症、碳水化合物不耐受和胰岛素分泌模式方面与遗传性糖尿病患者相似。其中11名侏儒症患者接受了股四头肌的针吸活检,并将组织固定用于电子显微镜检查。测量了毛细血管基底膜厚度,并与先前在糖尿病患者和正常对照中获得的测量结果进行比较。对照组和侏儒症患者的测量结果相似(分别为1080±27 Å和1086±90 Å),且明显低于糖尿病患者(2403±119 Å)。鉴于侏儒症患者无视网膜病变而糖尿病组发病率高(41%),这些数据支持以下论点:这些解剖学异常在很大程度上与血清脂质和碳水化合物异常无关。这些数据与生长激素在这些病变发病机制中起支持作用(即使不是因果作用)是一致的。