Bellastella A, Criscuolo T, Iorio S, Parlato F, Sinisi A A, Sinisi A M, Pasquali D, Pisano G
Istituto di Endocrinologia, Facoltà di Medicina e Chirurgia, II Università di Napoli, Italy.
J Endocrinol Invest. 1994 Jan;17(1):37-40. doi: 10.1007/BF03344960.
The aim of this study was to determine if changes in IGF-1 levels and in final stature occur in blind adult subjects. Eighteen subjects (4 females and 14 males) with total blindness (Group 1) and 26 subjects (5 females and 21 males) with only light perception (Group 2), living at an Institute for blind adult subjects in Naples, Italy, were studied. Their height and weight were compared to British standards. Plasma morning IGF-1 levels, measured by IRMA method were compared to those of 18 normal controls (6 females and 12 males) matched for age and weight. A high prevalence of short stature was demonstrated especially in Group 1 (p = 0.00005 by chi-square for trend test) but was also present in Group 2 (p = 0.02). No alterations in weight distribution were observed in both groups. Basal IGF-I levels in both Group 1 and Group 2 were similar to those of controls: IGF-1 (M +/- SE), 30.9 +/- 2.9 nmol/L and 37.9 +/- 2.7 nmol/L, respectively, vs 33.3 +/- 2.9 nmol/L, NS. High prevalence of final short stature in both groups confirms a negative influence of total or partial blindness on growth. These complex mechanisms appear to involve more than alterations in GH and IGF-I secretion.
本研究的目的是确定成年盲人受试者的胰岛素样生长因子-1(IGF-1)水平和最终身高是否发生变化。对居住在意大利那不勒斯一所成年盲人研究所的18名全盲受试者(第1组,4名女性和14名男性)和26名仅存光感的受试者(第2组,5名女性和21名男性)进行了研究。将他们的身高和体重与英国标准进行比较。采用免疫放射分析法(IRMA)测定的血浆早晨IGF-1水平与18名年龄和体重匹配的正常对照者(6名女性和12名男性)的水平进行比较。结果显示,身材矮小的患病率很高,尤其是在第1组(趋势检验的卡方检验p = 0.00005),但在第2组也存在(p = 0.02)。两组均未观察到体重分布的改变。第1组和第2组的基础IGF-1水平与对照组相似:IGF-1(平均值±标准误)分别为30.9±2.9 nmol/L和37.9±2.7 nmol/L,而对照组为33.3±2.9 nmol/L,无显著性差异(NS)。两组最终身材矮小的高患病率证实了全盲或部分失明对生长有负面影响。这些复杂的机制似乎涉及的不仅仅是生长激素(GH)和IGF-1分泌的改变。