Centre for Environmental Sciences, Hasselt University, Diepenbeek, Belgium.
Department of Public Health and Primary Care, Leuven University, Leuven, Belgium.
JAMA Netw Open. 2024 May 1;7(5):e2411246. doi: 10.1001/jamanetworkopen.2024.11246.
The cord blood proteome, a repository of proteins derived from both mother and fetus, might offer valuable insights into the physiological and pathological state of the fetus. However, its association with birth weight and growth trajectories early in life remains unexplored.
To identify cord blood proteins associated with birth weight and the birth weight ratio (BWR) and to evaluate the associations of these cord blood proteins with early growth trajectories.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study included 288 mother-child pairs from the ongoing prospective Environmental Influence on Early Aging birth cohort study. Newborns were recruited from East-Limburg Hospital in Genk, Belgium, between February 2010 and November 2017 and followed up until ages 4 to 6 years. Data were analyzed from February 2022 to September 2023.
The outcome of interest was the associations of 368 inflammatory-related cord blood proteins with birth weight or BWR and with early life growth trajectories (ie, rapid growth at age 12 months and weight, body mass index [BMI] z score, waist circumference, and overweight at age 4-6 years) using multiple linear regression models. The BWR was calculated by dividing the birth weight by the median birth weight of the population-specific reference growth curve, considering parity, sex, and gestational age. Results are presented as estimates or odds ratios (ORs) for each doubling in proteins.
The sample included 288 infants (125 [43.4%] male; mean [SD] gestation age, 277.2 [11.6] days). The mean (SD) age of the child at the follow-up examination was 4.6 (0.4) years old. After multiple testing correction, there were significant associations of birth weight and BWR with 7 proteins: 2 positive associations: afamin (birth weight: coefficient, 341.16 [95% CI, 192.76 to 489.50]) and secreted frizzled-related protein 4 (SFRP4; birth weight: coefficient, 242.60 [95% CI, 142.77 to 342.43]; BWR: coefficient, 0.07 [95% CI, 0.04 to 0.10]) and 5 negative associations: cadherin EGF LAG 7-pass G-type receptor 2 (CELSR2; birth weight: coefficient, -237.52 [95% CI, -343.15 to -131.89]), ephrin type-A receptor 4 (EPHA4; birth weight: coefficient, -342.78 [95% CI, -463.10 to -222.47]; BWR: coefficient, -0.11 [95% CI, -0.14 to -0.07]), SLIT and NTRK-like protein 1 (SLITRK1; birth weight: coefficient, -366.32 [95% CI, -476.66 to -255.97]; BWR: coefficient, -0.11 [95% CI, -0.15 to -0.08]), transcobalamin-1 (TCN1; birth weight: coefficient, -208.75 [95% CI, -305.23 to -112.26]), and unc-5 netrin receptor D (UNC5D; birth weight: coefficient, -209.27 [95% CI, -295.14 to -123.40]; BWR: coefficient, -0.07 [95% CI, -0.09 to -0.04]). Further evaluation showed that 2 proteins were still associated with rapid growth at age 12 months (afamin: OR, 0.32 [95% CI, 0.11-0.88]; TCN1: OR, 2.44 [95% CI, 1.26-4.80]). At age 4 to 6 years, CELSR2, EPHA4, SLITRK1, and UNC5D were negatively associated with weight (coefficients, -1.33 to -0.68 kg) and body mass index z score (coefficients, -0.41 to -0.23), and EPHA4, SLITRK1, and UNC5D were negatively associated with waist circumference (coefficients, -1.98 to -0.87 cm). At ages 4 to 6 years, afamin (OR, 0.19 [95% CI, 0.05-0.70]) and SLITRK1 (OR, 0.32 [95% CI, 0.10-0.99]) were associated with lower odds for overweight.
This cohort study found 7 cord blood proteins associated with birth weight and growth trajectories early in life. Overall, these findings suggest that stressors that could affect the cord blood proteome during pregnancy might have long-lasting associations with weight and body anthropometrics.
脐带血蛋白质组是一种来源于母亲和胎儿的蛋白质库,可能为胎儿的生理和病理状态提供有价值的见解。然而,其与出生体重和生命早期生长轨迹的关系尚未得到探索。
鉴定与出生体重和出生体重比(BWR)相关的脐带血蛋白,并评估这些脐带血蛋白与早期生长轨迹的关联。
设计、地点和参与者:本队列研究纳入了来自正在进行的环境影响早期衰老出生队列研究的 288 对母婴对。新生儿于 2010 年 2 月至 2017 年 11 月期间从比利时根特的东林堡医院招募,并随访至 4 至 6 岁。数据于 2022 年 2 月至 2023 年 9 月进行分析。
本研究的主要结果是,通过多元线性回归模型,研究了 368 种炎症相关脐带血蛋白与出生体重或 BWR 以及与生命早期生长轨迹(即 12 个月时快速生长和体重、体重指数[BMI]z 评分、腰围和 4-6 岁时超重)的关联。BWR 通过将出生体重除以特定人群参考生长曲线的中位数出生体重来计算,考虑到产次、性别和胎龄。结果以每增加一倍蛋白的估计值或比值比(OR)表示。
本研究样本包括 288 名婴儿(125 名[43.4%]为男性;平均[标准差]胎龄为 277.2[11.6]天)。儿童在随访检查时的平均(标准差)年龄为 4.6(0.4)岁。在经过多次测试校正后,有 7 种蛋白质与出生体重和 BWR 存在显著关联:2 种正相关:afamin(出生体重:系数为 341.16[95%置信区间为 192.76 至 489.50])和分泌型卷曲相关蛋白 4(SFRP4;出生体重:系数为 242.60[95%置信区间为 142.77 至 342.43];BWR:系数为 0.07[95%置信区间为 0.04 至 0.10])和 5 种负相关:钙黏蛋白 EGF LAG 7 跨膜 G 型受体 2(CELSR2;出生体重:系数为-237.52[95%置信区间为-343.15 至-131.89])、ephrin 型-A 受体 4(EPHA4;出生体重:系数为-342.78[95%置信区间为-463.10 至-222.47];BWR:系数为-0.11[95%置信区间为-0.14 至-0.07])、SLIT 和 NTRK 样蛋白 1(SLITRK1;出生体重:系数为-366.32[95%置信区间为-476.66 至-255.97];BWR:系数为-0.11[95%置信区间为-0.15 至-0.08])、转钴胺素-1(TCN1;出生体重:系数为-208.75[95%置信区间为-305.23 至-112.26])和 UNC5 神经导向因子 D(UNC5D;出生体重:系数为-209.27[95%置信区间为-295.14 至-123.40];BWR:系数为-0.07[95%置信区间为-0.09 至-0.04])。进一步评估显示,有 2 种蛋白质仍与 12 个月时的快速生长相关(afamin:OR,0.32[95%置信区间为 0.11-0.88];TCN1:OR,2.44[95%置信区间为 1.26-4.80])。在 4 至 6 岁时,CELSR2、EPHA4、SLITRK1 和 UNC5D 与体重(系数为-1.33 至-0.68 千克)和 BMI z 评分(系数为-0.41 至-0.23)呈负相关,EPHA4、SLITRK1 和 UNC5D 与腰围呈负相关(系数为-1.98 至-0.87 厘米)。在 4 至 6 岁时,afamin(OR,0.19[95%置信区间为 0.05-0.70])和 SLITRK1(OR,0.32[95%置信区间为 0.10-0.99])与超重的几率较低相关。
本队列研究发现了 7 种与出生体重和生命早期生长轨迹相关的脐带血蛋白。总体而言,这些发现表明,妊娠期间可能影响脐带血蛋白质组的应激源可能与体重和身体人体测量学有长期关联。