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评估细胞因子血浆水平对极低出生体重儿早产儿视网膜病变的检测贡献。

Assessment of the contribution of cytokine plasma levels to detect retinopathy of prematurity in very low birth weight infants.

机构信息

Department of Pediatrics, Newborn Section, Medical School, Federal University of Rio Grande do Sul, and Hospital de Clinicas de Porto Alegre, Porto Alegre RS, Brazil.

出版信息

Invest Ophthalmol Vis Sci. 2011 Mar 10;52(3):1297-301. doi: 10.1167/iovs.10-6279.

Abstract

PURPOSE

To prospectively study the association of high cytokine plasma levels with later development of retinopathy of prematurity (ROP) in preterm infants with early-onset sepsis to assess a laboratory test to detect ROP.

METHODS

A prospective cohort study was conducted of preterm infants with clinical early-onset sepsis whose birth weight (BW) was ≤1500 g and gestational age (GA) was ≤32 weeks. Plasma samples were assayed for cytokines IL-6, IL-8, IL-10, IL-1β, and TNF-α. ROP was diagnosed in screening assessments. For the univariate analysis of the known risk factors for ROP, all infants without ROP were designated as the No ROP group, patients with any stage of ROP formed the ROP group, and all treated patients formed the Severe ROP group. The best cutoff points for all cytokine levels were determined by ROC curves.

RESULTS

Seventy-four patients were enrolled. Mean GA and BW were 29.6 ± 2.1 weeks and 1110.3 ± 232.5 g, respectively; 49 patients (66.2%) had no ROP and 25 (33.8%) had any stage of ROP (17 had stage 1 or 2 ROP and 8 had stage 3 ROP). IL-6 >357 pg/mL, IL-8 >216 pg/mL, and TNF-α >245 pg/mL were significantly associated with treatable ROP.

CONCLUSIONS

There is a relationship between high plasma levels of IL-6, IL-8, and TNF-α in the first days of life with the later development of ROP severe enough to treat in preterm infants with early-onset sepsis. Further epidemiologic studies are needed to explore other possible associations of high serum levels of cytokines with ROP in this population at high risk.

摘要

目的

前瞻性研究早产儿早发性败血症患儿高细胞因子血浆水平与早产儿视网膜病变(ROP)后期发病的关系,评估一种实验室检测ROP 的方法。

方法

对出生体重(BW)≤1500g、胎龄(GA)≤32 周的临床早发性败血症早产儿进行前瞻性队列研究。检测 IL-6、IL-8、IL-10、IL-1β 和 TNF-α 等细胞因子的血浆水平。通过筛查评估诊断 ROP。为了对 ROP 的已知危险因素进行单因素分析,所有无 ROP 的婴儿均被指定为无 ROP 组,任何阶段的 ROP 患者为 ROP 组,所有治疗患者为重度 ROP 组。通过 ROC 曲线确定所有细胞因子水平的最佳截断值。

结果

共纳入 74 例患儿。平均 GA 和 BW 分别为 29.6±2.1 周和 1110.3±232.5g,49 例(66.2%)患儿无 ROP,25 例(33.8%)患儿有任何程度的 ROP(17 例为 1 期或 2 期 ROP,8 例为 3 期 ROP)。IL-6>357pg/mL、IL-8>216pg/mL 和 TNF-α>245pg/mL 与可治疗 ROP 显著相关。

结论

在患有早发性败血症的早产儿中,生命最初几天血浆中高浓度的 IL-6、IL-8 和 TNF-α 与 ROP 后期发展为需要治疗的 ROP 之间存在相关性。需要进一步的流行病学研究来探讨该高危人群中其他高细胞因子血症与 ROP 之间可能存在的关联。

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