新生儿早期血清脂质结合素的浓度

来源 :世界核心医学期刊文摘(儿科学分册) | 被引量 : 0次 | 上传用户:victor9808
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通过对28例小于胎龄儿(SGA)和34例适于胎龄儿(AGA)的足月儿的血清脂质结合素水平的检测,来了解胎儿的生长与脂质结合素水平有何种关系。生后第1 个24 h内采集测定脂质结合素的血液样本。以上新生儿(SGA和AGA)的血清脂质结合素水平显著高于正常孩子(28.7±17.0 mg/L t vs 9.3±6.1 mg/L,P< 0.01)。在SGA和AGA之间,脂质结合素水平也有显著性差异(23.2±14.8 mg/L vs 33.2±17.5 mg/L,P =0.02)。所有新生儿的血清脂质结合素水平与出生体重和头围呈正相关,分别为(r=0.27,P<0.05)和(r=0.30,P<0.05)。血清脂质结合素水平与胎龄、出生身长、血糖水平、生后采集血液样本的时间无关。所有新生儿脂质结合素水平在男婴和女婴的浓度分别为30.0±19.7 mg/L vs 28.0±15.5 mg/L,无性别差异。结果表明:血清脂质结合素水平与出生体重的正相关关系和高脂血症不能仅凭机体脂肪的低百分数解释。SGA比AGA的脂质结合素水平更低,并不表示宫内发育迟缓的婴儿在生后早期有胰岛素抵抗,但可能成为将来发展成胰岛素抵抗或者2型糖尿病的因素。 To understand fetal growth and lipid binding levels by measuring serum levels of lipid-binding proteins in 28 infants of less than gestational age (SGA) and 34 infants of age eligible for gestational age (AGA) relationship. Blood samples for the determination of lipidin were collected within the first 24 hours after birth. Serum lipid-binding protein levels were significantly higher in neonates (SGA and AGA) than in normal children (28.7 ± 17.0 mg / L t vs 9.3 ± 6.1 mg / L, P <0.01). There was also a significant difference in lipid-binding protein levels between SGA and AGA (23.2 ± 14.8 mg / L vs 33.2 ± 17.5 mg / L, P = 0.02). Serum lipid-binding protein levels in all newborns were positively correlated with birth weight and head circumference (r = 0.27, P <0.05) and (r = 0.30, P <0.05), respectively. Serum lipid-binding protein levels were independent of the gestational age, length of birth, blood glucose level, and time spent collecting blood samples after birth. All neonatal lipid-binding protein levels in male and female infants were 30.0 ± 19.7 mg / L vs 28.0 ± 15.5 mg / L, respectively, with no gender differences. The results showed that the positive correlation between serum lipid levels and birth weight and hyperlipidemia can not be explained solely by the low percentage of body fat. SGA has lower levels of lipid-binding proteins than AGA and does not imply that infants with intrauterine growth retardation have insulin resistance early in life, but may be a factor in the future development of insulin resistance or type 2 diabetes.
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