LIFE-Leipzig Research Center for Civilization Diseases, Leipzig University, Leipzig, Germany.
Institute for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics (ILM) Leipzig University, Leipzig, Germany.
J Clin Endocrinol Metab. 2022 Jun 16;107(7):e2991-e3002. doi: 10.1210/clinem/dgac157.
Various clinical factors influencing serum levels of insulin-like growth factor I (IGF-I) and its binding protein 3 (IGFBP-3) are not entirely consistently described.
We asked whether body mass index (BMI), contraceptive drugs (CDs), and hormone replacement therapy (HRT) have potential effects on data for interpreting new age-, sex-, and puberty-adjusted reference ranges for IGF-I and IGFBP-3 serum levels.
Subjects were mainly participants from 2 population-based cohort studies: the LIFE Child study of children and adolescents and the LIFE Adult study.
We investigated 9400 serum samples from more than 7000 healthy and 1278 obese subjects between 3 months and 81 years old.
Associations between IGF-I or IGFBP-3, measured with a new electrochemiluminescence immunoassay, and the predictors BMI and CDs were estimated using hierarchical linear modeling.
During infancy, obese children had up to 1 SD score (SDS) higher mean predicted IGF-I values, converging with levels of normal-weight subjects up to 13 years old. Between 20 and 40 years of age, obesity was related to up to -0.5 lower IGF-I SDS values than the predicted values. Obesity had less impact on IGFBP-3. Estrogen- and progestin-based CDs, but not HRT, decreased IGF-I and increased IGFBP-3 (P < 0.01) in adolescents (β IGF-I = -0.45, β IGFBP-3 = 0.94) and adults (β IGF-I = -0.43, β IGFBP-3 = 1.12). Conversely, progestin-based CDs were significantly positive associated with IGF-I (β IGF-I =0.82).
BMI and CDs must be considered when assessing and interpreting the clinical relevance of IGF-I and IGFBP-3 measurements.
影响胰岛素样生长因子 I(IGF-I)和其结合蛋白 3(IGFBP-3)血清水平的各种临床因素描述并不完全一致。
我们询问了体重指数(BMI)、避孕药(CDs)和激素替代疗法(HRT)是否对解释新的年龄、性别和青春期调整的 IGF-I 和 IGFBP-3 血清水平参考范围的数据有潜在影响。
研究对象主要来自两项基于人群的队列研究:儿童和青少年的 LIFE 研究和成人的 LIFE 研究。
我们调查了 7000 多名健康人和 1278 名肥胖者的 9400 份血清样本,年龄在 3 个月至 81 岁之间。
使用新的电化学发光免疫测定法测量 IGF-I 或 IGFBP-3 与预测因子 BMI 和 CDs 之间的关系,使用分层线性模型进行估计。
在婴儿期,肥胖儿童的 IGF-I 预测值平均高出 1 个标准差(SDS),到 13 岁时与正常体重儿童的水平相吻合。在 20 至 40 岁之间,肥胖与 IGF-I 的 SDS 值比预测值低 0.5 个。肥胖对 IGFBP-3 的影响较小。雌激素和孕激素为基础的 CDs,但不是 HRT,在青少年(β IGF-I = -0.45,β IGFBP-3 = 0.94)和成年人(β IGF-I = -0.43,β IGFBP-3 = 1.12)中降低 IGF-I 并增加 IGFBP-3。相反,孕激素为基础的 CDs 与 IGF-I 呈显著正相关(β IGF-I = 0.82)。
在评估和解释 IGF-I 和 IGFBP-3 测量的临床相关性时,必须考虑 BMI 和 CDs。