The Generation R Study Group and Department of Epidemiology, Erasmus Medical Center, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.
J Clin Endocrinol Metab. 2011 May;96(5):E810-5. doi: 10.1210/jc.2010-2316. Epub 2011 Feb 9.
A recent genome-wide association study identified variants near CCNL1/LEKR1 (rs900400) and in ADCY5 (rs9883204) to be associated with birth weight. We examined the associations of these variants with fetal growth characteristics in different trimesters, with a main interest in the timing of the associations and the affected body proportions.
We used data from two prospective cohort studies from fetal life onward in The Netherlands and Australia. Repeated fetal ultrasound examinations were performed to measure head circumference (HC), abdominal circumference (AC), femur length (FL), and estimated fetal weight (EFW). Analyses were based on a total group of 3909 subjects.
The C-allele of rs900400 was associated in second trimester with smaller fetal HC and FL, and in third trimester with smaller HC, AC, FL, and EFW. For each C-allele, the combined effect estimate for EFW in third trimester was -18.6 g (95% confidence interval, -27.5, -9.7 g; P = 4.2 × 10(-5)). The C-allele of rs9883204 was not associated with fetal growth characteristics in second trimester but was associated with restriction of all growth characteristics, except HC, in third trimester and at birth. For each C-allele, the combined effect estimate was -16.9 g (95% confidence interval, -26.8, -7.0 g; P = 8.4 × 10(-4)) for EFW in third trimester. Both genetic variants were associated with lower birth and placenta weight.
Our results suggest that a genetic variant of rs900400 leads to symmetric growth restriction from early pregnancy onward, whereas a genetic variant of rs9883204 leads to asymmetric growth restriction, characterized by a relatively larger HC, from third trimester.
最近的全基因组关联研究发现,CCNL1/LEKR1(rs900400)附近和 ADCY5(rs9883204)的变异与出生体重相关。我们研究了这些变异与不同孕期胎儿生长特征的关联,主要关注关联的时间和受影响的身体比例。
我们使用了来自荷兰和澳大利亚的两项前瞻性队列研究的数据,这些研究从胎儿期开始一直持续到出生后。通过多次进行胎儿超声检查来测量头围(HC)、腹围(AC)、股骨长(FL)和估计胎儿体重(EFW)。分析基于总共 3909 名受试者的数据。
rs900400 的 C 等位基因与孕中期的胎儿 HC 和 FL 较小以及孕晚期的 HC、AC、FL 和 EFW 较小相关。对于每个 C 等位基因,第三孕期 EFW 的综合效应估计值为-18.6g(95%置信区间,-27.5,-9.7g;P=4.2×10(-5))。rs9883204 的 C 等位基因与孕中期的胎儿生长特征无关,但与第三孕期和出生时所有生长特征的受限相关,除了 HC。对于每个 C 等位基因,第三孕期 EFW 的综合效应估计值为-16.9g(95%置信区间,-26.8,-7.0g;P=8.4×10(-4))。这两种遗传变异均与出生体重和胎盘重量降低有关。
我们的结果表明,rs900400 的遗传变异导致从妊娠早期开始出现对称生长受限,而 rs9883204 的遗传变异导致从第三孕期开始出现不对称生长受限,其特征是 HC 相对较大。