Brugts Michael P, Ranke Michael B, Hofland Leo J, van der Wansem Katy, Weber Karin, Frystyk Jan, Lamberts Steven W J, Janssen Joseph A M J L
Department of Internal Medicine, Erasmus MC, Dr. Molewaterplein 50, Rotterdam, The Netherlands.
J Clin Endocrinol Metab. 2008 Jul;93(7):2539-45. doi: 10.1210/jc.2007-2454. Epub 2008 Apr 8.
IGF-I immunoassays are primarily used to estimate IGF-I bioactivity. Recently an IGF-I-specific kinase receptor activation assay (KIRA) has been developed as an alternative method. However, no normative values have been established for the IGF-I KIRA.
The objective of the study was to establish normative values for the IGF-I KIRA in healthy adults.
This was a cross-sectional study in healthy nonfasting blood donors.
Participants included 426 healthy individuals (310 males, 116 females; age range 18-79 yr).
IGF-I bioactivity determined by the KIRA was measured. Results were compared with total IGF-I, measured by five different IGF-I immunoassays.
Mean (+/- sd) IGF-I bioactivity was 423 (+/- 131) pmol/liter and decreased with age (beta = -3.4 pmol/liter.yr, P < 0.001). In subjects younger than 55 yr, mean IGF-I bioactivity was significantly higher in women than men. Above this age this relationship was inverse, suggesting a drop in IGF-I bioactivity after menopause. This drop was not reflected in total IGF-I levels. IGF-I bioactivity was significantly related to total IGF-I (r(s) varied between 0.46 and 0.52; P < 0.001).
We established age-specific normative values for the IGF-I KIRA. We observed a significant drop in IGF-I bioactivity in women between 50 and 60 yr, which was not perceived by IGF-I immunoassays. The IGF-I KIRA, when compared with IGF-I immunoassays, theoretically has the advantage that it measures net effects of IGF-binding proteins on IGF-I receptor activation. However, it has to be proven whether information obtained by the IGF-I KIRA is clinically more relevant than measurements obtained by IGF-I immunoassays.
胰岛素样生长因子-I(IGF-I)免疫测定主要用于评估IGF-I的生物活性。最近,一种IGF-I特异性激酶受体激活测定法(KIRA)已被开发出来作为替代方法。然而,尚未建立IGF-I KIRA的正常参考值。
本研究的目的是建立健康成年人IGF-I KIRA的正常参考值。
这是一项针对健康非空腹献血者的横断面研究。
参与者包括426名健康个体(310名男性,116名女性;年龄范围18 - 79岁)。
测量通过KIRA测定的IGF-I生物活性。将结果与通过五种不同的IGF-I免疫测定法测量的总IGF-I进行比较。
IGF-I生物活性的均值(±标准差)为423(±131)pmol/升,且随年龄下降(β = -3.4 pmol/升·年,P < 0.001)。在55岁以下的受试者中,女性的平均IGF-I生物活性显著高于男性。在这个年龄以上,这种关系相反,表明绝经后IGF-I生物活性下降。这种下降在总IGF-I水平中未得到体现。IGF-I生物活性与总IGF-I显著相关(斯皮尔曼相关系数r(s)在0.46至0.52之间;P < 0.001)。
我们建立了IGF-I KIRA的年龄特异性正常参考值。我们观察到50至60岁女性的IGF-I生物活性显著下降,而IGF-I免疫测定法未察觉到这一点。与IGF-I免疫测定法相比,IGF-I KIRA理论上具有测量IGF结合蛋白对IGF-I受体激活的净效应的优势。然而,IGF-I KIRA获得的信息在临床上是否比IGF-I免疫测定法获得的测量结果更具相关性还有待证实。