武星宇, 张春燕, 田亚平. Citrin缺陷致新生儿肝内胆汁淤积症与胆道闭锁肝功能指标的Meta分析[J]. 解放军医学院学报, 2021, 42(12): 1279-1285. DOI: 10.3969/j.issn.2095-5227.2021.12.010
引用本文: 武星宇, 张春燕, 田亚平. Citrin缺陷致新生儿肝内胆汁淤积症与胆道闭锁肝功能指标的Meta分析[J]. 解放军医学院学报, 2021, 42(12): 1279-1285. DOI: 10.3969/j.issn.2095-5227.2021.12.010
WU Xingyu, ZHANG Chunyan, TIAN Yaping. Comparison of biochemical indicators between neonatal intrahepatic cholestasis caused by Citrin deficiency and biliary atresia: A meta-analysis[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2021, 42(12): 1279-1285. DOI: 10.3969/j.issn.2095-5227.2021.12.010
Citation: WU Xingyu, ZHANG Chunyan, TIAN Yaping. Comparison of biochemical indicators between neonatal intrahepatic cholestasis caused by Citrin deficiency and biliary atresia: A meta-analysis[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2021, 42(12): 1279-1285. DOI: 10.3969/j.issn.2095-5227.2021.12.010

Citrin缺陷致新生儿肝内胆汁淤积症与胆道闭锁肝功能指标的Meta分析

Comparison of biochemical indicators between neonatal intrahepatic cholestasis caused by Citrin deficiency and biliary atresia: A meta-analysis

  • 摘要:
      背景  Citrin缺陷致新生儿肝内胆汁淤积症(neonatal intrahepatic cholestasis caused by citrin deficiency,NICCD)和胆道闭锁(biliary atresia,BA)是两种临床症状相似的疾病,根据临床表现较难区分,所以对两者的鉴别诊断十分有意义。
      目的  探究这两种疾病的总胆红素(total bilirubin,TBIL)、γ-谷氨酰转移酶(γ-glutamyltransferase,GGT)、碱性磷酸酶(alkaline phosphatase,ALP)和总蛋白(total protein,TP) 4种常见肝功能指标的表达差异。
      方法  通过对美国国立医学图书馆PubMed数据库、Web of Science、Embase、中国知网和万方数据库进行文献检索,筛选出截至2021年3月符合要求的文献。按照纽卡斯尔-渥太华量表(Newcastle-Ottawa scale,NOS)对所纳入研究的文献进行质量评价,并提取数据,使用Stata 16.0软件进行Meta分析。
      结果  本项研究最终纳入了2005 - 2019年的英文文献5篇,中文文献4篇,文献NOS评分为5 ~ 8分。其中NICCD组患者189例,BA组患者325例。Meta分析结果显示NICCD组TBIL、GGT、TP水平明显低于BA组(SMD=-0.41,95% CI:-0.75 ~ -0.07;SMD=-1.03,95% CI:-1.23 ~ -0.84;SMD=-1.69,95% CI:-1.99 ~ -1.38。P<0.05),ALP水平高于BA组(SMD=1.37,95% CI:0.52 ~ 2.21,P<0.05)。在对TBIL和ALP进行异质性分析时,显示存在较高的异质性(66.3%,86.4%)。根据样本量之比进行亚组分析,结果表明样本量可能为异质性的来源之一。
      结论  NICCD与BA患者的TBIL、GGT、ALP和TP差异有统计学意义,可为临床早期鉴别诊断BA与NICCD提供参考依据。

     

    Abstract:
      Background  Neonatal intrahepatic cholestasis caused by Citrin deficiency and biliary atresia are two diseases with similar clinical symptoms, which are difficult to distinguish according to clinical manifestations. Therefore, the differential diagnosis of the two diseases is of great significance.
      Objective   To explore the differences in expression levels of total bilirubin (TBIL), γ -glutamyltransferase (GGT), alkaline phosphatase (ALP) and total protein (TP) between the two diseases.
      Methods   Databases including PubMed, Web of science, Embase, CNKI and Wanfang Data were searched systematically. The retrieval time was up to March 2021. The literature quality of the included studies was evaluated according to the NOS (Newcastle-Ottawa scale, NOS) scale. After data extraction, the meta-analysis was performed using Stata 16.0 software.
      Results   Five English and four Chinese literatures were included in this study from 2005 to 2019, with NOS scores ranging from 5-8. There were 189 cases of neonatal intrahepatic cholestasis (NICCD) caused by Citrin deficiency and 325 cases of biliary atresia (BA). Meta-analysis results showed that the levels of TBIL, GGT and TP in NICCD group were significantly lower than those in BA group (SMD=-0.41, 95%CI -0.75, -0.07, SMD=-1.03, 95% CI -1.23, -0.84, SMD=-1.69, 95%CI -1.99, -1.38, all P<0.05), but the level of ALP was higher than that of BA group (SMD=1.37, 95%CI 0.52, 2.21, P<0.05). The heterogeneity analysis of TBIL and ALP showed high heterogeneity (66.3%, 86.4%). Subgroup analysis based on the ratio of sample size indicated that sample size might be one of the sources of heterogeneity.
      Conclusion   The differences of TBil, GGT, ALP and TP in NICCD and BA are statistically significant, which can provide some references for the early clinical differential diagnosis of BA and NICCD.

     

/

返回文章
返回