Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Norwegian National Advisory Unit on Disease-Related Malnutrition, Oslo University Hospital, Oslo, Norway.
Am J Clin Nutr. 2018 Aug 1;108(2):388-397. doi: 10.1093/ajcn/nqy103.
A major pathway through which obesity increases the risk of cardiometabolic diseases and cancer is by inducing hormonal and metabolic abnormalities, including hyperinsulinemia and altered insulin-like growth factor (IGF) signaling. However, little is known about the influence of lifetime adiposity on the relevant biomarkers.
The aim of this study was to examine associations of trajectories of body fatness with plasma biomarker concentrations of the insulin-IGF system in 2 large prospective cohorts of US men and women.
Associations between trajectories of body fatness and concentrations of plasma C-peptide, IGF-I, IGF-binding protein (IGFBP) 1, IGFBP-3, and the IGF-I-to-IGFBP-3 molar ratio was examined in 9386 women of the Nurses' Health Study and 3941 men of the Health Professionals Follow-Up Study. Group-based trajectory modeling was used to create trajectory groups on the basis of self-reported somatotype data at ages 5, 10, 20, 30, and 40 y and body mass index (BMI) at ages 45, 50, 55, and 60 y. We used multivariate linear regression models to examine the associations of trajectories with biomarker concentrations.
Five trajectories of body fatness were identified: "lean-stable," "lean-moderate increase," "lean-marked increase," "medium-stable/increase," and "medium-marked increase." Compared with the lean-stable group, the lean-marked increase and medium-marked increase groups had significantly higher concentrations of C-peptide (percentage difference-women: 44% and 73%; men: 27% and 51%) and lower concentrations of IGFBP-1 (women: -61% and -78%; men: -47% and -65%). Adjustment for current BMI attenuated the association to null for the medium-marked increase group, but the lean-marked increase group still had modestly higher concentrations of C-peptide (women: 10%; men: 6%) and lower concentrations of IGFBP-1 (women: -18%; men: -21%) than the lean-stable group.
Adiposity across the life span was associated with higher C-peptide and lower IGFBP-1 concentrations in adulthood. The associations were largely driven by attained adiposity and, to a lesser extent, weight gain in early-middle adulthood. This trial was registered at www.clinicaltrials.gov as NCT03419455.
肥胖通过诱导激素和代谢异常,包括高胰岛素血症和改变胰岛素样生长因子(IGF)信号,增加患代谢性心血管疾病和癌症的风险,这是一个主要途径。然而,人们对终生肥胖对相关生物标志物的影响知之甚少。
本研究旨在检查美国男性和女性的 2 个大型前瞻性队列中,体脂肪量轨迹与胰岛素-IGF 系统的血浆生物标志物浓度之间的关联。
在护士健康研究中的 9386 名女性和健康专业人员随访研究中的 3941 名男性中,基于 5、10、20、30 和 40 岁时的自报体型数据以及 45、50、55 和 60 岁时的体重指数(BMI),使用基于群组的轨迹建模来创建基于体脂肪量轨迹的群组。我们使用多元线性回归模型来检查轨迹与生物标志物浓度之间的关联。
确定了 5 个体脂肪量轨迹:“瘦稳定”、“瘦适度增加”、“瘦明显增加”、“中稳定/增加”和“中明显增加”。与瘦稳定组相比,瘦明显增加组和中明显增加组的 C 肽浓度明显更高(女性:44%和 73%;男性:27%和 51%),IGFBP-1 浓度更低(女性:-61%和-78%;男性:-47%和-65%)。调整当前 BMI 后,中明显增加组的关联减弱至无统计学意义,但瘦明显增加组的 C 肽浓度仍略高于瘦稳定组(女性:10%;男性:6%),IGFBP-1 浓度也仍低于瘦稳定组(女性:-18%;男性:-21%)。
整个生命过程中的肥胖与成年后更高的 C 肽和更低的 IGFBP-1 浓度有关。这些关联主要由获得的肥胖和一定程度上的成年早期体重增加驱动。该试验在 www.clinicaltrials.gov 上注册为 NCT03419455。