Steno Diabetes Center, 2820 Gentofte, Denmark.
J Clin Endocrinol Metab. 2011 Sep;96(9):2835-43. doi: 10.1210/jc.2011-0577. Epub 2011 Jul 6.
Low birth weight is associated with type 2 diabetes, which to some extent may be mediated via abdominal adiposity and insulin resistance. Fetal growth velocity is high during the third trimester, constituting a potential critical window for organ programming. Intra-pair differences among monozygotic twins are instrumental in determining nongenetic associations between early environment and adult metabolic phenotype.
Our objective was to investigate the relationship between size at birth and third-trimester growth velocity on adult body composition and glucose metabolism using intra-pair differences in young healthy twins.
Fifty-eight healthy twins (42 monozygotic/16 dizygotic) aged 18-24 yr participated. Insulin sensitivity was assessed using hyperinsulinemic-euglycemic clamps. Whole-body fat was assessed by dual-energy x-ray absorptiometry scan, whereas abdominal visceral and sc fat (L1-L4) were assessed by magnetic resonance imaging. Third-trimester growth velocity was determined by repeated ultrasound examinations.
Size at birth was nongenetically inversely associated with adult visceral and sc fat accumulation but unrelated to adult insulin action. In contrast, fetal growth velocity during third trimester was not associated with adult visceral or sc fat accumulation. Interestingly, third-trimester growth was associated with insulin action in a paradoxical inverse manner.
Abdominal adiposity including accumulation of both sc and visceral fat may constitute primary nongenetic factors associated with low birth weight and reduced fetal growth before the third trimester. Reduced fetal growth during vs. before the third trimester may define distinct adult trajectories of metabolic and anthropometric characteristics influencing risk of developing type 2 diabetes.
低出生体重与 2 型糖尿病有关,而 2 型糖尿病在一定程度上可能通过腹部肥胖和胰岛素抵抗来介导。胎儿在妊娠晚期的生长速度较快,这构成了器官编程的潜在关键窗口期。同卵双胞胎之间的个体内差异对于确定早期环境与成人代谢表型之间的非遗传关联至关重要。
本研究旨在使用年轻健康双胞胎的个体内差异,研究出生时的大小和妊娠晚期生长速度与成人身体成分和葡萄糖代谢之间的关系。
本研究共纳入了 58 名年龄在 18-24 岁的健康双胞胎(42 对同卵双胞胎/16 对异卵双胞胎)。使用高胰岛素正葡萄糖钳夹技术评估胰岛素敏感性。通过双能 X 射线吸收仪扫描评估全身脂肪,通过磁共振成像评估腹部内脏和皮下脂肪(L1-L4)。通过重复超声检查确定妊娠晚期的生长速度。
出生时的大小与成人内脏和皮下脂肪积累呈非遗传负相关,但与成人胰岛素作用无关。相比之下,妊娠晚期的胎儿生长速度与成人内脏或皮下脂肪积累无关。有趣的是,妊娠晚期的生长速度与胰岛素作用呈相反的反比关系。
腹部肥胖,包括皮下和内脏脂肪的积累,可能是与低出生体重和妊娠晚期前胎儿生长减少相关的非遗传的主要因素。与妊娠晚期前相比,妊娠晚期胎儿生长减少可能会定义出不同的代谢和人体测量特征的成人轨迹,从而影响 2 型糖尿病的发病风险。