作为早产儿视网膜病变临床生物标志物的血小板减少症:系统回顾

I. K. Sutyawan, N. M. A. Surasmiati, Putu Anindya Agrasidi, Priscilla Dwianggita, S. Anggara
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引用次数: 0

摘要

研究结果表明,考虑到血小板减少症可以快速、经济、广泛地用于检查,它可以作为筛查早产儿视网膜病变的潜在临床生物标志物。摘要早产儿视网膜病变(ROP)是导致儿童失明的主要原因,发生的原因是早产儿视网膜血管发育不全。血小板对血管生成的调节至关重要。因此,血小板减少可能有助于 ROP 的进展。本系统综述旨在研究血小板减少症与早产儿视网膜病变之间的关系。我们按照《系统综述和元分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)的指南,访问了 PubMed 和 Cochrane 图书馆数据库,纳入了回顾性病例对照和横断面研究。在我们的综述中,共分析了 9 条记录。所有研究都是在 2017 年至 2022 年期间完成的。七项研究报告了早产儿视网膜病变(ROP)婴儿血小板减少症的发病率,从 18.37% 到 71% 不等。在未患早产儿视网膜病变的早产儿中,血小板减少的发生率为 5.71% 至 21%。有七项研究明确指出血小板减少症是导致早产儿视网膜病变的风险因素,血小板减少症的奇数比(OR)从 2.8 到 6.69 不等。因此,可将早产儿血小板减少视为筛查 1 型早产儿视网膜病变的潜在临床生物标志物。此外,这一发现还意味着血小板减少可能是导致早产儿视网膜病变的病理生理学因素之一。关于早产儿视网膜病变中至关重要的血小板计数阈值,还需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thrombocytopenia as a Clinical Biomarker of Retinopathy of Prematurity: A Systematic Review
Highlights: This is the first systematic review investigating thrombocytopenia and its association with retinopathy of prematurity The findings suggest that thrombocytopenia could serve as a potential clinical biomarker for screening ROP, considering its quick, affordable, and widespread availability for examination purposes.   Abstract Retinopathy of prematurity (ROP) is the leading cause of childhood blindness and occurs due to the underdevelopment of retinal blood vessels in premature infants. Platelets are essential in the regulation of angiogenesis. Hence, thrombocytopenia might aid in the progression of ROP. This systematic review aims to look into the relationship between thrombocytopenia and retinopathy of prematurity. The PubMed and Cochrane Library databases were accessed to include retrospective case-control and cross-sectional studies, following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). In our review, 9 records were analyzed. All research was done in the period between 2017 and 2022 . Seven studies have reported the prevalence of thrombocytopenia in infants with retinopathy of prematurity (ROP), ranging from 18.37% to 71%. In preterm children without ROP, the occurrence of thrombocytopenia is between 5.71% and 21%. Seven studies have significantly identified thrombocytopenia as a risk factor for ROP, with the Odd Ratio (OR) for thrombocytopenia ranging from 2.8 to 6.69 . Therefore, thrombocytopenia in premature infants could be thought of as a potential clinical biomarker for Type-1 ROP screening. Additionally, this discovery implied that thrombocytopenia can contribute to the pathophysiology of ROP. The crucial platelet count threshold in ROP requires additional investigations.
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