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细胞因子水平及产后因素与早产儿视网膜病变的关联

The association of cytokine levels and postnatal factors with retinopathy of prematurity.

作者信息

Yazib Syatirah Abu, Choo May May, Khaliddin Nurliza, Ong Christine Py, Choo Yao Mun, Kamar Azanna Ahmad, Lingam Gopal G, Kamalden Tengku A

机构信息

Department of Ophthalmology, UM Eye Research Centre, Faculty of Medicine, Universiti Malaya, Malaysia.

Department of Ophthalmology, Central Clinical School, Faculty of Medicine, University of Sydney, Australia.

出版信息

Indian J Ophthalmol. 2025 Jan 1;73(Suppl 1):S139-S143. doi: 10.4103/IJO.IJO_515_24. Epub 2024 Oct 25.

Abstract

PURPOSE

Prematurity has been known to trigger several cellular pathways, leading to the clinical occurrence of retinopathy of prematurity (ROP). This study compared the levels of a panel of serum cytokines in premature infants with and without ROP.

METHODS

This is a prospective observational study. Premature infants at 36-38 weeks' gestational age were recruited, their clinical data recorded, and serum samples collected and assayed for 18 cytokines. Based on follow-up examinations, patients were divided into two groups: No ROP and ROP. The ROP group was further divided into two subgroups: non-vision-threatening ROP (non-VTROP), and vision-threatening ROP (VTROP).

RESULTS

On univariate analysis, among the clinical parameters, gestation age, birth weight, duration of invasive ventilation, and duration of stay in neonatal intensive care unit (NICU) were found to be significant. The univariate analysis also showed an association between raised levels of VEGF-D and IL-8 in the VTROP group. Multiple logistic regression indicated that gestation age was a significant risk factor across all subgroups. Additionally, VEGF-D levels were found to be significantly associated with VTROP.

CONCLUSION

Higher VEGF-D levels are associated with an increased risk of severe ROP that requires treatment and could potentially be used as a biomarker.

摘要

目的

早产已知会触发多种细胞通路,导致早产儿视网膜病变(ROP)的临床发生。本研究比较了患有和未患ROP的早产儿血清中一组细胞因子的水平。

方法

这是一项前瞻性观察性研究。招募了孕龄为36 - 38周的早产儿,记录其临床数据,并采集血清样本检测18种细胞因子。根据随访检查,将患者分为两组:无ROP组和ROP组。ROP组进一步分为两个亚组:非威胁视力性ROP(非VTROP)和威胁视力性ROP(VTROP)。

结果

单因素分析显示,在临床参数中,孕龄、出生体重、有创通气时间和新生儿重症监护病房(NICU)住院时间具有显著意义。单因素分析还表明,VTROP组中VEGF - D和IL - 8水平升高之间存在关联。多因素逻辑回归表明,孕龄是所有亚组中的一个显著危险因素。此外,发现VEGF - D水平与VTROP显著相关。

结论

较高的VEGF - D水平与需要治疗的严重ROP风险增加相关,并且有可能用作生物标志物。

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