Karl J Philip, Alemany Joseph A, Koenig Chad, Kraemer William J, Frystyk Jan, Flyvbjerg Allan, Young Andrew J, Nindl Bradley C
US Army Research Institute of Environmental Medicine, 42 Kansas St., Natick, MA 01760, USA.
Growth Horm IGF Res. 2009 Dec;19(6):491-6. doi: 10.1016/j.ghir.2009.04.001. Epub 2009 May 20.
Insulin-like growth factor I (IGF-I) is a metabolic-regulatory hormone that mediates a variety of physiologic functions. Body composition, fitness status and intake of certain micro- and macronutrients are associated with circulating concentrations of immunoreactive IGF-I. The influence of these factors on IGF-I bioactivity; however, is undetermined. We assessed the relationships between IGF-I bioactivity and lifestyle factors purportedly associated with IGF-I immunoreactivity.
In a cross sectional study, fasted blood samples were obtained from 44 lightly active, college-age (20+/-2 yrs) women. IGF-I bioactivity was estimated by an assay which determines the ability of serum IGFs to phosphorylate IGF-I receptors in cultured cells; free and total IGF-I were measured by immunoassay. Estradiol and progesterone were measured by immunoassay. Body mass index was calculated from measured height and weight, bone mineral density and body fat percentage measured by dual energy X-ray absorptiometry, and peak oxygen consumption (VO(2peak)) determined during a graded treadmill protocol. A food frequency questionnaire measured habitual and a 5-day food record assessed short-term micro- and macronutrient intakes. Associations between bioactive, free and total IGF-I with body composition, sex hormones, VO(2peak), and dietary intake were assessed using univariate and multiple linear regression analyses.
Associations between bioactive IGF-I with age (r=-0.36, P<0.05), body fat percentage (r=-0.32, P<0.05), estradiol (r=0.31, P<0.05) and progesterone (r=0.33, P<0.05) concentrations, habitual alcohol (r=-0.38, P<0.05) and selenium intakes (r=0.41, P<0.01), free IGF-I with age (r=-0.34, P<0.05), estradiol (r=0.48, P<0.01) and progesterone (r=0.52, P<0.001) concentrations, habitual alcohol (r=-0.33, P<0.05) and isoflavone intakes (r=0.30, P<0.05) and total IGF-I with age (r=-0.27, P<0.05) and habitual alcohol intake (r=-0.33, P<0.05) were observed. Habitual alcohol intake was a negative predictor of bioactive, free and total IGF-I in multivariate models.
Of the lifestyle factors measured, the most robust relationship observed was a negative association between habitual alcohol intake and all measures of IGF-I. This finding suggests that alcohol intake may blunt the physiologic actions of the IGF-I axis.
胰岛素样生长因子I(IGF-I)是一种代谢调节激素,介导多种生理功能。身体组成、健康状况以及某些微量和常量营养素的摄入量与免疫反应性IGF-I的循环浓度相关。然而,这些因素对IGF-I生物活性的影响尚不确定。我们评估了IGF-I生物活性与据称与IGF-I免疫反应性相关的生活方式因素之间的关系。
在一项横断面研究中,从44名轻度活跃、大学年龄(20±2岁)的女性中采集空腹血样。通过一种测定血清IGF使培养细胞中的IGF-I受体磷酸化能力的试验来估计IGF-I生物活性;通过免疫测定法测量游离和总IGF-I。通过免疫测定法测量雌二醇和孕酮。根据测量的身高和体重计算体重指数,通过双能X射线吸收法测量骨矿物质密度和体脂百分比,并在分级跑步机试验中测定峰值耗氧量(VO₂峰值)。一份食物频率问卷测量习惯性饮食,一份5天食物记录评估短期微量和常量营养素摄入量。使用单变量和多元线性回归分析评估生物活性、游离和总IGF-I与身体组成、性激素、VO₂峰值和饮食摄入量之间的关联。
观察到生物活性IGF-I与年龄(r = -0.36,P < 0.05)、体脂百分比(r = -0.32,P < 0.05)、雌二醇(r = 0.31,P < 0.05)和孕酮(r = 0.33,P < 0.05)浓度、习惯性酒精摄入量(r = -0.38,P < 0.05)和硒摄入量(r = 0.41,P < 0.01)之间的关联;游离IGF-I与年龄(r = -0.34,P < 0.05)、雌二醇(r = 0.48,P < 0.01)和孕酮(r = 0.52,P < 0.001)浓度、习惯性酒精摄入量(r = -0.33,P < 0.05)和异黄酮摄入量(r = 0.30,P < 0.05)之间的关联;总IGF-I与年龄(r = -0.27,P < 0.05)和习惯性酒精摄入量(r = -0.33,P < 0.05)之间的关联。在多变量模型中,习惯性酒精摄入量是生物活性、游离和总IGF-I的负预测因子。
在所测量的生活方式因素中,观察到的最显著关系是习惯性酒精摄入量与IGF-I的所有测量指标之间的负相关。这一发现表明,酒精摄入可能会削弱IGF-I轴的生理作用。