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出生后血清胰岛素样生长因子I缺乏与早产儿视网膜病变及早产的其他并发症相关。

Postnatal serum insulin-like growth factor I deficiency is associated with retinopathy of prematurity and other complications of premature birth.

作者信息

Hellström Ann, Engström Eva, Hård Anna-Lena, Albertsson-Wikland Kerstin, Carlsson Björn, Niklasson Aimon, Löfqvist Chatarina, Svensson Elisabeth, Holm Sture, Ewald Uwe, Holmström Gerd, Smith Lois E H

机构信息

Göteborg Pediatric Growth Research Center, Department of Pediatrics, Institute of the Health of Women and Children, Sweden.

出版信息

Pediatrics. 2003 Nov;112(5):1016-20. doi: 10.1542/peds.112.5.1016.

Abstract

OBJECTIVE

Insulin-like growth factor I (IGF-I) is necessary for normal development of retinal blood vessels in mice and humans. Because retinopathy of prematurity (ROP) is initiated by abnormal postnatal retinal development, we hypothesized that prolonged low IGF-I in premature infants might be a risk factor for ROP.

DESIGN

We conducted a prospective, longitudinal study measuring serum IGF-I concentrations weekly in 84 premature infants from birth (postmenstrual ages: 24-32 weeks) until discharge from the hospital. Infants were evaluated for ROP and other morbidity of prematurity: bronchopulmonary dysplasia (BPD), intraventricular hemorrhage (IVH), and necrotizing enterocolitis (NEC).

RESULTS

Low serum IGF-I values correlated with later development of ROP. The mean IGF-I +/- SEM level during postmenstrual ages 30-33 weeks was lowest with severe ROP (25 +/- 2.41 micro g/L), 29 +/- 1.76 micro g/L with moderate ROP, and 33 +/- 1.72 micro g/L with no ROP. The duration of low IGF-I also correlated strongly with the severity of ROP. The interval from birth until serum IGF-I levels reached >33 micro g/L was 23 +/- 2.6 days for no ROP, 44 +/- 4.8 days for moderate ROP, and 52 +/- 7.5 days for severe ROP. Each adjusted stepwise increase of 5 micro g/L in mean IGF-I during postmenstrual ages 30 to 33 weeks decreased the risk of proliferative ROP by 45%. Other complications (NEC, BPD, IVH) were correlated with ROP and with low IGF-I levels. The relative risk for any morbidity (ROP, BPD, IVH, or NEC) was increased 2.2-fold (95% confidence interval: 1.41-3.43) if IGF-I was <or=33 micro g/L at 33 weeks' postmenstrual age.

CONCLUSIONS

These results indicate that persistent low serum concentrations of IGF-I after premature birth are associated with later development of ROP and other complications of prematurity. IGF-I is at least as strong a determinant of risk for ROP as postmenstrual age at birth and birth weight.

摘要

目的

胰岛素样生长因子I(IGF-I)对小鼠和人类视网膜血管的正常发育至关重要。由于早产儿视网膜病变(ROP)是由出生后视网膜异常发育引发的,我们推测早产儿长期低IGF-I水平可能是ROP的一个危险因素。

设计

我们进行了一项前瞻性纵向研究,从出生(孕龄:24 - 32周)起每周测量84例早产儿的血清IGF-I浓度,直至出院。对婴儿进行ROP及其他早产相关疾病评估:支气管肺发育不良(BPD)、脑室内出血(IVH)和坏死性小肠结肠炎(NEC)。

结果

血清IGF-I水平低与ROP的后期发生相关。孕龄30 - 33周期间,重度ROP患儿的平均IGF-I±SEM水平最低(25±2.41μg/L),中度ROP患儿为29±1.76μg/L,无ROP患儿为33±1.72μg/L。IGF-I水平低的持续时间也与ROP的严重程度密切相关。从出生到血清IGF-I水平达到>33μg/L的间隔时间,无ROP患儿为23±2.6天,中度ROP患儿为44±4.8天,重度ROP患儿为52±7.5天。孕龄30至33周期间,平均IGF-I每调整性逐步升高5μg/L,增殖性ROP的风险降低45%。其他并发症(NEC、BPD、IVH)与ROP及低IGF-I水平相关。如果孕龄33周时IGF-I≤33μg/L,任何疾病(ROP、BPD、IVH或NEC)的相对风险增加2.2倍(95%置信区间:1.41 - 3.43)。

结论

这些结果表明,早产出生后持续低血清IGF-I浓度与ROP及其他早产并发症的后期发生有关。IGF-I至少与出生时的孕龄和出生体重一样,是ROP风险的重要决定因素。

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