期刊文献+

尿S-100B蛋白动态变化对早产儿脑损伤的诊断价值 被引量:10

Diagnostic value of urine S-100B protein levels in brain injury in premature infants
下载PDF
导出
摘要 目的探讨尿S-100B蛋白水平动态变化在早期诊断早产儿脑损伤中的价值。方法选择2012年1月至12月住院的胎龄<35周的早产儿76例,分别留取生后24、72、120 h尿液,应用化学发光法检测S-100B蛋白含量。根据颅脑超声及磁共振成像(MRI)检查结果,将其分为脑室周围白质软化(PVL)组(16例)、脑室周围及脑室内出血(PVH-IVH)组(20例)及无脑损伤组(40例),比较各组间S-100B的变化。结果在生后24、72、120 h各时间点,无脑损伤组、PVL组和PVH-IVH组三组间尿S100B蛋白水平差异有统计学意义(P均<0.01);在各时间点,均以无脑损伤组最低,PVL组最高,差异有统计学意义(P均<0.01)。PVL组和PVH-IVH组尿S100B蛋白水平随时间点推移的差异有统计学意义(P均<0.01);均在72 h达到高峰,120 h时有所下降。结论尿S100-B蛋白水平可作为早期预测脑损伤的敏感标志物,动态监测有助于判断疾病严重程度及评估患儿预后。 Objective To investigate the diagnostic value of urine S-100B protein levels in brain injury in premature infants. Methods A total of 76 premature infants with gestational age less than 35 weeks were selected from January to December 2012. Urine samples were obtained at 24 h, 72 h and 120 h after birth, and S-100B protein levels in urine were detected by chemiluminescence. According to the results of cranial ultrasound and MRI, all infants were divided into periventricular leukomalacia (PVL) group (n=16), periventricular-intraventricular haemorrhage (PVH-IVH) group (n=20) and no brain injury group (control group) (n=40). Urine S-100B protein levels were compared among groups. Results There was significant difference in Urine S-100B protein levels among PVL, PVH-IVH and control groups at 24 h, 72 h and 120 h after birth (P〈0.01). At each time point, the urine S-100B protein levels were highest in PVL group and lowest in control group, and the differences were signiifcant (P〈0.01). The urine S-100B protein levels were signiifcantly different among different time points in PVL and PVH-IVH groups (P〈0.01), reaching a peak at 72 h and starting to decrease at 120 h. Conclusions Urine S-100B protein can be used as a sensitive indicator of brain injury in judging disease severity and assessing prognosis.
出处 《临床儿科杂志》 CAS CSCD 北大核心 2015年第1期44-47,共4页 Journal of Clinical Pediatrics
关键词 脑室周围-脑室内出血 脑室周围白质软化 S-100B蛋白 早产儿 periventricular-intraventricular haemorrhage periventricular leukomalacia S-100B protein premature infant
  • 相关文献

参考文献12

  • 1周丛乐.早产儿脑损伤的诊治进展[J].中国实用儿科杂志,2006,21(9):650-653. 被引量:28
  • 2张素娥,薛辛东,富建华.早产儿脑白质损伤的影像学研究进展[J].中国新生儿科杂志,2011,26(5):350-352. 被引量:24
  • 3Elovitz MA, Mrinalini C, Sammel MD. Elucidating theearly signal transduction pathways leading to fetal brain in-jury in preterm birth [J]. Pediatr Res, 2006, 59(1): 50-55.
  • 4Ravasi T, Has K, GoyetteJ, et al. Probing the S-100protein family through genomic and functional analysis [J].Genomics, 2004, 84(1): 10-22.
  • 5Streitbiirger DP, Arelin K,Kratesch J, et al Validatingserum S100B and neurom-specific enolase as biomarkers forthe human brain -- a combined serum, gene expression andMRI study [J]. PloS One, 2012, 7(8): e43284.
  • 6Bouvier D, Castellani C, Fournier M,et al. Referenceranges fur serum S100B protein during the first three yearsof life [J]. Clin Biochem, 2011, 44(10-11): 927-929.
  • 7谢爱兰,陈尚勤,林益怡,王玉环.脐血S100B蛋白在早产儿脑损伤中的临床意义及预测价值[J].现代实用医学,2010,22(1):20-22. 被引量:7
  • 8Gazzolo D, Abella R, Frigiola A, et al. Neuromarkersand unconventional biological fluids [J]. J Matern FetalNeonatl Med, 2010, 23(Suppl 3): 66-69.
  • 9Risso FM, Serpero LD, Zimmermann LJ, et al Perinatalasphyxia : kidney failure does not affect S100B urine con-centrations [J]. Clin Chim Acta, 2012, 413(1-2): 150-153.
  • 10Hayakata T, Shiozaki T, TasakiO, et al Changes in CSFS100B and eytokine concentrations in early-pphase severetraumatic brain injury [J]. Shock, 2004, 22(2) : 102-107.

二级参考文献40

  • 1王庆红,宋健辉,王霞,刘沉涛,毕丹东.血清S100B蛋白在新生儿窒息后脑损伤中的临床意义[J].中国当代儿科杂志,2005,7(4):318-320. 被引量:13
  • 2侯新琳,周丛乐,黄岚,丁海曙,王红梅.早产儿脑反应性及其神经发育的近红外光谱评价研究[J].中华儿科杂志,2006,44(6):445-449. 被引量:10
  • 3Gazzolo D, Bruschettini M, Lituania M, et al, Increased urinary S 100B protein as an Early indicator of intraventricular Hemerrhage in Pretemn infants: correlation with the Grade of Hemorrhage[J].Clin Chem, 2001, 47(10): 1836-1838.
  • 4Michetti F, Gazzolo D. S 100B Protein in Biological Fluids: A Tool for Perinatal Medicine[J]. Clinical Chemistry, 2002,48(12): 2097-2104.
  • 5Nagdyman N, Komen W, Ko HK, et al. Early biochemical indicators of hypoxic-ischemic eneephalopathy after birth asphyxia [J].Pediatr Res, 2001, 49(4): 502-504.
  • 6Murase M, Ishida A. Early hypocarbia of preterm infants: its relationship to periventricular leukomalacia and cerebral palsy, and its perinatal risk factors[J]. Acta Paediatr, 2005, 94(1):85-91.
  • 7Volpe JJ. Cerebral white matter injury of the premature infant- more common than you think. Pediatrics, 2003, 112:176-180.
  • 8McQuillen PS, Ferreiro DM. Perinatal subplate neuron injury: implications fnr cortical development and plasticity. Brain Pathol, 2005, 15:250-260.
  • 9Rutherford MA, Supramaniam V, Ederies A, et al. Magnetic resonance imaging of white matter diseases of" prematurity. Neuroradiology, 2010, 52:505-521.
  • 10Counsell SJ,Allsop JM, Harrison MC, et al. Diffusion-weighted imaging of the brain in I?reterm infants with focal anti diffuse white matter abnormality. Pediatrics, 2003, 112 : 1-7.

共引文献49

同被引文献63

引证文献10

二级引证文献65

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部