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[胎儿生长受限与胰岛素抵抗。新发现及文献综述]

[Fetal growth restriction and insulin resistance. New findings and review of the literature].

作者信息

Soto I Néstor, Mericq G Verónica

机构信息

Sección de Endocrinología y Diabetes, Hospital Clínico San Borja-Arriarán.

出版信息

Rev Med Chil. 2005 Jan;133(1):97-104. doi: 10.4067/s0034-98872005000100013. Epub 2005 Mar 10.

Abstract

There is a strong association between low birth weight and insulin resistance. The thrifty phenotype hypothesis, which postulates fetal programming for adaptation to an adverse intrauterine environment, resulting in a lower insulin sensitivity in utero, is one of the hypothesis to explain this association. Later in life, syndrome X may develop, featuring hypertension, dyslipidemia, central obesity and type 2 diabetes, associated to an excessive food intake. Our investigation during the first three years of life in a prospective cohort of small (SGA) or appropriate for gestational age newborns, demonstrated that a significant increase of insulin levels is detected in SGA, as early as during the first year of life, but only when catch up growth (CUG) occurs. Orexigenic peptides such as Ghrelin appear to participate in this CUG phenomenon. We also sought to determine whether these associations were observed in individuals born with very low birth weight. We found that in utero as well as postnatal growth rates were independent determinants of insulin sensitivity and secretion. Education about feeding practices and physical activity in SGA children, is a future challenge to prevent the onset of syndrome X in this predisposed population.

摘要

低出生体重与胰岛素抵抗之间存在密切关联。节俭表型假说假定胎儿会进行编程以适应不利的子宫内环境,从而导致子宫内胰岛素敏感性降低,这是解释这种关联的假说之一。在生命后期,可能会出现X综合征,其特征为高血压、血脂异常、中心性肥胖和2型糖尿病,与食物摄入过多有关。我们在前瞻性队列中对小于胎龄儿(SGA)或适于胎龄的新生儿出生后头三年进行的调查表明,早在生命的第一年,就可检测到SGA患儿胰岛素水平显著升高,但仅在出现追赶生长(CUG)时才会如此。诸如胃饥饿素等促食欲肽似乎参与了这种追赶生长现象。我们还试图确定在极低出生体重儿中是否也能观察到这些关联。我们发现,子宫内以及出生后的生长速度是胰岛素敏感性和分泌的独立决定因素。对SGA儿童进行喂养方式和体育活动方面的教育,是预防这一易感人群发生X综合征的未来挑战。

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