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转化生长因子-β1 在新生儿坏死性小肠结肠炎诊断中的作用。

Utility of transforming growth factor beta-1 in diagnosis of neonatal necrotizing enterocolitis.

机构信息

Pediatric department, Faculty of Medicine, Benha University, Egypt.

Faculty of Medicine, Benha University, Egypt.

出版信息

J Neonatal Perinatal Med. 2022;15(4):795-801. doi: 10.3233/NPM-210973.

DOI:10.3233/NPM-210973
PMID:35811541
Abstract

Necrotizing enterocolitis (NEC) yet remains a leading cause of morbidity and mortality in premature infants. The developmental deficiency of transforming growth factor-Beta (TGF-β) in the intestine is a risk factor for NEC in premature infants.We aimed to investigate the potential utility of serum TGF-β1 in the early diagnosis and severity assessment of NEC. This prospective case-control study was conducted on 102 VLBW neonates aging less than 32 weeks and weighing less than 1500 gm. They were divided into NEC group of 52 preterm neonates with symptoms and signs of NEC and 50 age and sex-matched neonates without NEC as a control group. All neonates underwent full medical history taking, clinical examination, radiological and laboratory investigations including CBC, CRP, fecal occult blood, and serum TGF-β1. Serum TGF-β1 was tested in NEC patients at the onset of symptoms and signs and 7 days later. Serum TGF-β1 was significantly lower in NEC patients at the onset of symptoms than the control group (P = 0.004) while after 7 days of onset serum TGF-β1 was significantly higher than at the onset of symptoms (P < 0.001). In NEC patients with stage I, TGF-β1 was significantly higher than in NEC patients with stage ≥II (P = 0.027).In conclusion serum TGF-β1 is downregulated in neonatal necrotizing enterocolitis and can be used as a useful biomarker for early diagnosis of NEC and to assess disease severity.

摘要

坏死性小肠结肠炎(NEC)仍然是早产儿发病率和死亡率的主要原因。转化生长因子-β(TGF-β)在肠道中的发育不足是早产儿患 NEC 的一个危险因素。我们旨在研究血清 TGF-β1 在 NEC 的早期诊断和严重程度评估中的潜在应用价值。这项前瞻性病例对照研究纳入了 102 名胎龄小于 32 周、体重小于 1500 克的极低出生体重儿(VLBW)。他们分为 NEC 组(52 例有 NEC 症状和体征的早产儿)和对照组(50 例无 NEC 的年龄和性别匹配的早产儿)。所有新生儿均接受了完整的病史采集、临床检查、影像学和实验室检查,包括全血细胞计数、C 反应蛋白、粪便潜血和血清 TGF-β1。在 NEC 患者出现症状和体征时以及 7 天后检测血清 TGF-β1。NEC 患者在出现症状时的血清 TGF-β1明显低于对照组(P=0.004),而在出现症状后 7 天,血清 TGF-β1明显高于出现症状时(P<0.001)。在 I 期 NEC 患者中,TGF-β1 明显高于≥II 期 NEC 患者(P=0.027)。总之,血清 TGF-β1 在新生儿坏死性小肠结肠炎中下调,可作为早期诊断 NEC 和评估疾病严重程度的有用生物标志物。

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