[1]郑 红,李 磊,张文杰,等.新生儿支气管肺发育不良患者血清miR-382-5p、miR-203a-3p水平表达及临床意义[J].现代检验医学杂志,2026,41(02):117-121.[doi:10.3969/j.issn.1671-7414.2026.02.020]
 ZHENG Hong,LI Lei,ZHANG Wenjie,et al.Serum miR-382-5p and miR-203a-3p Levels and Their Clinical Significance in Patients with Neonatal Bronchopulmonary Dysplasia[J].Journal of Modern Laboratory Medicine,2026,41(02):117-121.[doi:10.3969/j.issn.1671-7414.2026.02.020]
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新生儿支气管肺发育不良患者血清miR-382-5p、miR-203a-3p水平表达及临床意义()

《现代检验医学杂志》[ISSN:/CN:]

卷:
第41卷
期数:
2026年02期
页码:
117-121
栏目:
论著
出版日期:
2026-03-15

文章信息/Info

Title:
Serum miR-382-5p and miR-203a-3p Levels and Their Clinical Significance in Patients with Neonatal Bronchopulmonary Dysplasia
文章编号:
1671-7414(2026)02-117-05
作者:
郑 红李 磊张文杰张婷婷
淮安市妇幼保健院新生儿科,江苏淮安 223002
Author(s):
ZHENG HongLI LeiZHANG WenjieZHANG Tingting
Department of Neonatology, Huai’an Maternal and Child Health Hospital, Jiangsu Huai’an 223002, China
关键词:
新生儿支气管肺发育不良微小核糖核酸-382-5p微小核糖核酸-203a-3p
分类号:
R722.1;R392.11
DOI:
10.3969/j.issn.1671-7414.2026.02.020
文献标志码:
A
摘要:
目的探究新生儿支气管肺发育不良(BPD)患儿血清微小RNA(miR)-382-5p、miR-203a-3p水平变化及意义。方法选取2021年1月~2024年1月在淮安市妇幼保健院出生的BPD患儿130例作为研究对象纳入观察组,另选取同期足月伴有呼吸障碍新生儿125例作为对照组。实时荧光定量PCR(RT-qPCR)法检测所有新生儿血清miR-382-5p、miR-203a-3p水平,采用Pearson法分析BPD患儿血清miR-382-5p、miR-203a-3p表达水平的相关性,采用Logistic回归分析新生儿患BPD的相关因素,采用受试者操作特征(ROC)曲线分析血清miR-382-5p、miR-203a-3p水平对BPD发生的预测价值。结果观察组患儿出现新生儿窒息、需要机械通气人数占比、氧疗时间、呼出气一氧化氮(FeNO)、血清miR-203a-3p水平显著高于对照组(t/χ2=9.046~23.234),血清miR-382-5p水平显著低于对照组(t=8.785),差异具有统计学意义(均P<0.05)。血清miR-382-5p与miR-203a-3p表达水平呈负相关(r=-0.404,P<0.001);高水平血清miR-382-5p是患BDP的独立保护因素,高水平血清miR-203a-3p是患BDP的独立危险因素(Waldχ2=7.101、7.858,均P<0.05);患儿血清miR-382-5p、miR-203a-3p二者联合预测BDP发生的曲线下面积(AUC)优于miR-382-5p、miR-203a-3p单独预测,差异具有统计学意义(Z=2.023、2.119,均P<0.05)。结论BDP患儿血清miR-382-5p水平降低,miR-203a-3p水平升高,二者联合检测可有效预测新生儿BPD的发生。
Abstract:
Objective To investigate the changes and clinical significance of serum miR-382-5p and miR-203a-3p levels in patients with neonatal bronchopulmonary dysplasia (BPD). Methods A total of 130 neonates with BPD born at Huai’an Maternal and Child Health Hospital between January 2021 and January 2024 were enrolled as the study subjects and labeled as observation group. An additional 125 full-term neonates with respiratory distress born during the same period were labeled as control group. Using U6 as an internal reference gene, fluorescence quantitative PCR (RT-qPCR) was used to detect the levels of miR-382-5p and miR-203a-3p in the serum of all neonates. Pearson correlation analysis was performed to assess the correlation between serum miR-382-5p and miR-203a-3p expression levels in BPD neonates. Logistic regression analysis identified factors associated with BPD development. In addition, receiver operating characteristic (ROC) curve was used to analyze the predictive value of serum miR-382-5p and miR-203a-3p for the occurrence of BPD. Results The incidence of neonatal asphyxia and proportions requiring mechanical ventilation, duration of oxygen therapy, exhaled nitric oxide (FeNO),and serum miR-203a-3p in the observation group were significantly higher than those of control group (t/χ2=9.046~23.234), while serum miR-382-5p levels were significantly lower than those in the control group (t=8.785), and the differences were statistically significant (all P<0.05). The expression levels of serum miR-382-5p and miR-203a-3p in neonates with BDP were negatively correlated (r=-0.404, P<0.001). Elevated serum miR-382-5p was an independent protective factor against BDP (P<0.05), while elevated serum miR-203a-3p acted as an independent risk factor for BDP (Wald χ2=7.101, 7.858, all P<0.05). The combined prediction of BPD using serum miR-382-5p and miR-203a-3p demonstrated superior area under the curve (AUC) compared to prediction with either miR-382-5p or miR-203a-3p alone, with statistically significant differenc-es (Z=2.023, 2.119, all P<0.05). Conclusions Compared with healthy neonates, the serum miR-382-5p is reduced and miR-203a-3p is increased in neonates with BPD. The changes in both levels can effectively predict the occurrence of neonatal BPD.

参考文献/References:

[1] 张磊,王海萍,李静,等.早产儿血清miR-125b,ln-cRNA MALAT1表达水平与支气管肺发育不良的相关性研究 [J].现代检验医学杂志, 2023, 38(6):81-86. ZHANG L, WANG H P, LI J, et al. Correlation between the expression of serum miR-125b, lncRNA MALAT1 and bronchopulmonary dysplasia in premature in-fants[J]. Journal of Modern Laboratory Medicine, 2023, 38(6): 81-86.
[2] SCHMIDT A R, RAMAMOORTHY C. Bronchopul-monary dysplasia[J]. Clinics in Perinatology, 1992, 19(3): 174-180.
[3] ALONSO-OJEMBARRENA A, ALDECOA-BILBAO V, DE LUCA D N E. Imaging of bronchopulmonary dysplasia[J]. Seminars in Perinatology, 2023, 47(6):151812.
[4] SHUKLA V V, AMBALAVANAN N. Recent advances in bronchopulmonary dysplasia[J]. Indian Journal of Pediatrics, 2021, 88(7): 690-695.
[5] MOSCHINO L, BONADIES L, BARALDI E. Lung growth and pulmonary function after prematurity and bronchopulmonary dysplasia[J]. Pediatric Pulmonolo-gy, 2021, 56(11): 3499-3508.
[6] 伍倩茹,舒畅.儿童支气管肺发育不良与成年期慢性肺部疾病关系研究进展[J].临床医学进展, 2024, 14(4): 1330-1336. WU Q R, SHU C. Research progress on the relation-ship between bronchopulmonary dysplasia in children and chronic lung diseases in adulthood[J]. Advances in Clinical Medicine, 2024, 14(4): 1330-1336.
[7] 孙祎璠,马俐,龚小慧,等.基于生物信息学分析microR-NA-495-5p在早产儿支气管肺发育不良中的表达及其临床意义[J].中国当代儿科杂志, 2020, 22(1):24-30. SUN Y F, MA L, GONG X H, et al. Expression of microRNA-495-5p in preterm infants with bronchopul-monary dysplasia: a bioinformatics analysis[J]. Chinese Journal of Contemporary Pediatrics, 2020, 22(1): 24-30.
[8] L? Y Y, LI Y, WANG J Y, et al. MiR-382-5p suppress-es M1 macrophage polarization and inflammatory response in response to bronchopulmonary dysplasia through targeting CDK8: involving inhibition of STAT1 pathway[J]. Genes to Cells, 2021, 26(10): 772-781.
[9] CHENG H R, CHEN L, WEI Y L, et al. Knockdown of miR-203a-3p alleviates the development of bron-chopulmonary dysplasia partly via the up-regulation of vascular endothelial growth factor A[J]. Journal of Bioenergetics and Biomembranes, 2021, 53(1): 13-23.
[10] 中国医药教育协会儿科专业委员会,中华医学会儿科学分会呼吸学组,中华医学会儿科学分会新生儿学组,等.支气管肺发育不良的儿童期管理专家共识[J].中华实用儿科临床杂志,2022,37(20):1527-1538. China Medicine Education Association Committee on Pediatrics, the Subspecialty Group of Respiratory, the Society of Pediatrics, Chinese Medical Association, the Subspecialty Group of Neonatology, the Society of Pediatrics, Chinese Medical Association, et al. Expert consensus on childhood management of bronchopulmo-nary dysplasia [J]. Chinese Journal of Applied Clinical Pediatrics, 2022, 37(20): 1527-1538.
[11] 秦欣,赵小朋,张华岩.重度支气管肺发育不良患儿内源性呼气末正压测定及其临床结局[J].中国当代儿科杂志,2024,26(10):1034-1039. QIN X, ZHAO X P, ZHANG H Y. Measurement of intrinsic positive end-expiratory pressure and clinical outcomes of infants with severe bronchopulmonary dysplasia[J]. Chinese Journal of Contemporary Pediat-rics, 2024, 26(10): 1034-1039.
[12] 陈慧娟,孙文强,李梦曌,等.血清吲哚胺2,3-双加氧酶和犬尿喹啉酸在支气管肺发育不良早产儿中的变化[J].中华围产医学杂志,2024,27(3):215-219. CHEN H J, SUN W Q, LI M Z, et al. Changes in serum indoleamine 2, 3-dioxygenase and kynurenic acid levels in preterm infants with bronchopulmonary dysplasia[J]. Chi-nese Journal of Perinatal Medicine, 2024, 27(3): 215-219.
[13] CHEN H J, SUN W Q, LI M Z, et al. Changes in serum indoleamine 2, 3-dioxygenase and kynurenic acid levels in preterm infants with bronchopulmonary dysplasia[J]. Chi-nese Journal of Perinatal Medicine, 2024, 27(3): 215-219.
[14] 樊雨薇,张伊佳,温和梅,等.双胎早产儿支气管肺发育不良危险因素分析:一项多中心研究[J].中国当代儿科杂志, 2024, 26(6):611-618. FAN Y W, ZHANG Y J, WEN H M, et al. Risk fac-tors for bronchopulmonary dysplasia in twin preterm infants:a multicenter study[J]. Chinese Journal of Con-temporary Pediatrics, 2024, 26(6): 611-618.
[15] 李红亚,吕园园,张丛敏,等.miR-382-5p、PCT、SAA、CRP与早产儿肺部疾病相关性研究[J].中国妇幼健康研究,2023,34(9):62-67. LI H Y, LYU Y Y, ZHANG C M, et al. Correlation be-tween miR-382-5p,PCT,SAA,CRP and pulmonary dis-eases in preterm infants[J]. Chinese Journal of Woman and Child Health Research, 2023, 34(9): 62-67.
[16] 刘博,胡金霞,胡阳.环状RNA circSATB2通过调控miR-382-5p对肺癌细胞增殖、迁移、侵袭的机制研究[J].临床肺科杂志, 2022,27(7): 1080-1085. LIU B, HU J X, HU Y. The mechanism of circRNA circ-SATB2 regulates the proliferation,migration,and invasion of lung cancer cells by targeting miR-382-5p[J]. Journal of Clinical Pulmonary Medicine, 2022, 27(7): 1080-1085.
[17] 吕园园.miR-382-5p靶向CDK8抑制支气管肺发育不良M1型巨噬细胞极化及杨梅素治疗作用的初步探讨[D].石家庄:河北医科大学,2022. LYU Y Y. MiR-382-5p targets CDK8 to inhibit the polar-ization of M1 macrophages in bronchopulmonary dysplasia andpreliminary study on the therapeutic effect of myricet-in[D].Shijiazhuang: Hebei Medical University, 2022.
[18] 吴慧.MiR-203a-3p转染脂肪干细胞后条件培养基对小鼠IPF上皮间质转化的影响研究[D].唐山:华北理工大学, 2022. WU H. Effect of conditioned medium obtained from miR-203a-3p transfected adipose stem cells on epithelial-mes-enchymal transitions of IPF in mice[D].Tangshan: North China University of Science and Technology, 2022.
[19] FAN Q, JIAN Y. MiR-203a-3p regulates TGF-β1-induced epithelial-mesenchymal transition (EMT) in asthma by regulating Smad3 pathway through SIX1[J]. Bioscience Reports, 2020, 40(2): BSR20192645.
[20] 陈姿坛,富建华.氧化应激损伤与支气管肺发育不良关系的研究进展[J].中华新生儿科杂志(中英文), 2023, 38(5): 312-316 CHEN Z T ,FU J H .Research progress of the relation-ship between oxidative stress injury and bronchopul-monary dysplasia [J]. Chinese Journal of Neonatology, 2023, 38(5): 312-316.
[21] 李超,王吉,顾海红,等.早产儿机械通气时间对呼吸功能及支气管肺发育的影响[J].现代实用医学, 2023, 35(11): 1497-1501. LI C, WANG J, GU H H, et al. Effect of mechanical ventilation duration on respiratory function and bron-chopulmonary development in preterm infants[J]. Mod-ern Practical Medicine, 2023, 35(11): 1497-1501.

备注/Memo

备注/Memo:
基金项目:江苏省卫生健康委员会科研项目(编号:H1018009)。
作者简介:郑红(1989-),女,硕士研究生,主治医师,研究方向:支气管肺发育不良,E-mail:1160209164@qq.com。
通讯作者:张婷婷(1990-),女,硕士研究生,主治医师,研究方向:支气管肺发育不良,E-mail:1047718202@qq.com。
更新日期/Last Update: 2026-03-15