Kobayashi K, Amemiya S, Kobayashi K, Sawanobori E, Mochizuki M, Ishihara T, Higashida K, Miura M, Nakazawa S
Department of Pediatrics, Yamanashi Medical University, Japan.
Endocr J. 1999 Mar;46 Suppl:S67-9. doi: 10.1507/endocrj.46.suppl_s67.
High GH and low IGF-I are well known in IDDM patients. To delineate this altered GH-IGF-I axis in IDDM, we investigate the role of GH-binding protein (GHBP) in relation to the metabolic and nutritional states.
Forty seven patients with IDDM, mean 13.7 years, were evaluated. Blood samples were obtained before insulin injection and breakfast to test for plasma glucose (PG), IGF-I, IGFBP-1, IGFBP-3, total and complex GHBP (tGHBP and cGHBP), and HbA1c. Urine samples were collected in the morning for urinary GH (uGH). The difference between tGHBP and cGHBP is defined as fGHBP. The levels of PG and HbA1C were not correlated with each level of tGHBP, cGHBP, fGHBP or uGH. The levels of tGHBP, cGHBP and fGHBP were not all correlated with uGH. Both the levels of IGF-I and body mass index (BMI) were positively correlated with fGHBP. The duration of IDDM was negatively correlated with tGHBP, cGHBP and fGHBP.
As the previous report of the relationship between GH binding reserve to GHBP and IGF-I or BMI in non-diabetic subjects, fGHBP again showed statistical links with these parameters in IDDM. We therefore suggest that GHBP, especially its free form, may reflect a malmetabolic state of IDDM liver, resulting in an altered GH-IGF-I axis.
1型糖尿病(IDDM)患者中生长激素(GH)水平高而胰岛素样生长因子-Ⅰ(IGF-Ⅰ)水平低是众所周知的。为了阐明IDDM患者中这种改变的GH-IGF-Ⅰ轴,我们研究了生长激素结合蛋白(GHBP)与代谢和营养状态的关系。
对47例平均年龄13.7岁的IDDM患者进行了评估。在胰岛素注射和早餐前采集血样,检测血浆葡萄糖(PG)、IGF-Ⅰ、胰岛素样生长因子结合蛋白-1(IGFBP-1)、胰岛素样生长因子结合蛋白-3(IGFBP-3)、总生长激素结合蛋白和复合生长激素结合蛋白(tGHBP和cGHBP)以及糖化血红蛋白(HbA1c)。早晨收集尿样检测尿GH(uGH)。tGHBP与cGHBP的差值定义为游离生长激素结合蛋白(fGHBP)。PG和HbA1C水平与tGHBP、cGHBP、fGHBP或uGH的各水平均无相关性。tGHBP、cGHBP和fGHBP水平与uGH并非均相关。IGF-Ⅰ水平和体重指数(BMI)均与fGHBP呈正相关。IDDM病程与tGHBP、cGHBP和fGHBP呈负相关。
正如之前关于非糖尿病受试者中GH与GHBP结合储备与IGF-Ⅰ或BMI关系的报道一样,fGHBP在IDDM中再次显示出与这些参数的统计学联系。因此我们认为,GHBP,尤其是其游离形式,可能反映了IDDM肝脏的代谢不良状态,导致GH-IGF-Ⅰ轴改变。