切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2021, Vol. 17 ›› Issue (01) : 37 -45. doi: 10.3877/cma.j.issn.1673-5250.2021.01.006

所属专题: 文献

论著

传统炎性标志物对妊娠期肝内胆汁淤积症的诊断及预后预测价值
田丽莉1,1, 刘婕2,2, 万曼2,2, 谢韵2,2, 吴碧芳2,2, 苏瑞章2,2, 田钊旭3,3, 黄秀敏1,1, 胡益群2,,2()   
  • 收稿日期:2020-09-08 修回日期:2021-01-15 出版日期:2021-02-01
  • 通信作者: 胡益群

Diagnostic and prognostic value of blood routine inflammatory markers in intrahepatic cholestasis of pregnancy

Lili Tian1,1, Jie Liu2,2, Man Wan2,2, Yun Xie2,2, Bifang Wu2,2, Ruizhang Su2,2, Zhaoxu Tian3,3, Xiumin Haung1,1, Yiqun Hu2,2,()   

  • Received:2020-09-08 Revised:2021-01-15 Published:2021-02-01
  • Corresponding author: Yiqun Hu
  • Supported by:
    Medical Innovation Project of Fujian Province(2019-CXB-31)
引用本文:

田丽莉, 刘婕, 万曼, 谢韵, 吴碧芳, 苏瑞章, 田钊旭, 黄秀敏, 胡益群. 传统炎性标志物对妊娠期肝内胆汁淤积症的诊断及预后预测价值[J]. 中华妇幼临床医学杂志(电子版), 2021, 17(01): 37-45.

Lili Tian, Jie Liu, Man Wan, Yun Xie, Bifang Wu, Ruizhang Su, Zhaoxu Tian, Xiumin Haung, Yiqun Hu. Diagnostic and prognostic value of blood routine inflammatory markers in intrahepatic cholestasis of pregnancy[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2021, 17(01): 37-45.

目的

探讨传统炎性标志物对妊娠期肝内胆汁淤积症(ICP)的诊断及预后预测价值。

方法

选择2009年1月至2019年1月,于厦门大学附属中山医院消化内科和妇产科确诊的130例ICP患者为研究对象,并纳入ICP组,其中,初产妇为86例,经产妇为44例。根据ICP严重程度,进一步将其分为重度ICP亚组(n=29)和轻度ICP亚组(n=101)。选择同期在本院就诊的80例健康孕妇纳入对照组。按照86例初产妇的分娩孕龄,进一步分为ICP早产亚组(n=37)和ICP足月亚组(n=49)。采集受试者一般临床资料(年龄、孕龄等),天冬氨酸氨基转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、γ-谷氨酰转肽酶(GGT)、白细胞计数、中性粒细胞计数、淋巴细胞计数、血小板计数、红细胞分布宽度(RDW)、血红蛋白(Hb)、平均血小板体积(MPV)、血细胞比容(HCT)、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)和血清总胆汁酸(sTBA)等。本研究经过厦门大学附属中山医院伦理委员会批准(审批文号:2019076),与所有患者签署临床研究知情同意书。

结果

①ICP组和对照组孕妇年龄、中性粒细胞计数、淋巴细胞计数、血小板计数、MPV、ALP、AST、NLR和sTBA比较,差异均有统计学意义(P<0.05)。2组孕妇孕龄、白细胞计数、HCT、Hb、GGT、ALT和PLR比较,差异无统计学意义(P>0.05)。②轻度ICP亚组患者的孕龄大于重度ICP亚组,而轻度ICP亚组患者sTBA浓度低于重度ICP亚组,2组比较,差异均有统计学意义(P<0.05)。此外,2组患者年龄、白细胞计数、中性粒细胞计数、淋巴细胞计数、MPV、HCT、血小板计数、Hb、GGT、ALP、ALT、AST、NLR和PLR比较,差异均无统计学意义(P>0.05)。③NLR、血小板计数和MPV诊断ICP的受试者工作特征曲线(ROC)分析结果:NLR、血小板计数和MPV诊断ICP的曲线下面积(AUC)分别为0.802(95%CI:0.737~0.867,P<0.001), 0.642(95%CI:0.560~0.724,P<0.001)和0.947(95%CI:0.920~0.974,P<0.001);根据约登指数最大原则,NLR、血小板计数和MPV诊断ICP的最佳临界值分别为2.831、254×109/L和9.662 fL,此时其诊断ICP的敏感度分别为71.4%、64.7%和72.2%,特异度分别为81.3%、71.2%和82.5%。④ICP早产亚组与ICP足月分娩亚组孕妇ALT、AST和sTBA水平比较,差异均有统计学意义(P<0.05);而2组孕妇年龄、白细胞计数、中性粒细胞计数、淋巴细胞计数、血小板计数、MPV、PDW、NLR和PLR比较,差异均无统计学意义(P>0.05)。⑤sTBA、ALT、AST预测ICP所致早产的ROC分析结果:sTBA、ALT和AST预测ICP所致早产的AUC分别为0.634(95%CI:0.513~0.751,P<0.05),0.672(95%CI:0.563~0.784,P<0.001)和0.692(95%CI:0.544~0.793,P<0.001);根据约登指数最大原则,sTBA、ALT和AST预测ICP所致早产的最佳临界值分别为48 μmol/L、56 U/L和37 U/L,此时其预测ICP所致早产的敏感度分别为67.2%、62.2%和63.2%,特异度分别为59.6%、41.3%和49.6%。

结论

传统炎性标志物NLR、血小板计数、MPV对诊断ICP具有良好准确度,而目前发现的传统炎性标志物对ICP严重程度评估均无价值,sTBA、ALT和AST水平可能对ICP所致早产具有一定预测价值。

Objective

To investigate the diagnostic and prognostic value of blood routine inflammatory markers in intrahepatic cholestasis of pregnancy (ICP).

Methods

From January 2009 to January 2019, a total of 130 pregnant women with ICP diagnosed at the Department of Gastroenterology and Department of Obstetrics and Gynecology, Zhongshan Hospital, Affiliated to Xiamen University were selected into this study (ICP group), including 86 primiparae and 44 pluriparae. According to the severity of ICP, they were further divided into severe ICP subgroup (n=29) and mild ICP subgroup (n=101). Meanwhile, another 80 healthy pregnant women who visited the same hospital during same period were included into control group. In addition, those 86 primiparae were further divided into premature subgroup (n=37) and full-term subgroup (n=49).General clinical data (age, gestational age), aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), γ -glutamyltranspeptidase (GGT), leukocyte count, neutrophil count, lymphocyte count, platelet count, red blood cell distribution width (RDW), hemoglobin (Hb), mean platelet volume (MPV), hematocrit (HCT), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and serum total bile acid (sTBA)were collected. This study followed the ethical standards formulated by the Ethics Committee of Zhongshan Hospital, Affiliated to Xiamen University, and was approved (Approval No. 2019076). Informed concent was obtained from each participate.

Results

①There were significant differences between ICP group and control group in age, neutrophil count, lymphocyte count, platelet count, MPV, ALP, AST, NLR and sTBA (P<0.05). There were no significant differences between ICP group and control group in gestational age, white blood cell count, HCT, Hb, GGT, ALT and PLR (P>0.05).②The gestational age in mild ICP subgroup was higher than that in severe ICP subgroup, while the sTBA concentration in mild ICP subgroup was lower than that in severe ICP subgroup, and the differences were statistically significant (P<0.05). In addition, there were no significant differences in age, white blood cell count, neutrophil count, lymphocyte count, MPV, HCT, platelet count, Hb, GGT, ALP, ALT, AST, NLR and PLR between two groups (P>0.05).③Receiver operating characteristic curve (ROC) analysis showed that area under curve (AUC) of NLR, platelet count, MPV for diagnosing ICP were 0.802 (95%CI: 0.737-0.867, P<0.001), 0.642 (95%CI: 0.560-0.724, P<0.001) and 0.947 (95%CI: 0.920-0.974, P<0.001). According to the principle of maximum Youden index, the optimal cut-off value for NLR, platelet count, MPV to diagnose ICP were 2.831, 254×109/L and 9.662 fL, the sensitivity were 71.4%, 64.7% and 72.2%, respectively, and the specificity were 81.3%, 71.2% and 82.5%, respectively.④There were significant differences in ALT, AST and sTBA levels between preterm subgroup and full-term subgroup (P<0.05), but there were no significant differences in age, white blood cell count, neutrophil count, lymphocyte count, platelet count, MPV, PDW, NLR and PLR between two groups (P>0.05).⑤ROC analysis showed that AUC of sTBA, ALT and AST for predicting premature birth caused by ICP were 0.634 (95%CI: 0.513-0.751, P<0.05), 0.672 (95%CI: 0.563-0.784, P<0.001) and 0.692 (95%CI: 0.544-0.793, P<0.001). According to the principle of maximum Youden index, the optimal cut-off value for sTBA, ALT and AST to predicting premature birth caused by ICP were 48 μmol/L, 56 U/L and 37 U/L, the sensitivity were 67.2%, 62.2% and 63.2%, respectively; and the specificity were 59.6%, 41.3% and 49.6%, respectively.

Conclusions

NLR, platelet count and MPV have good accuracy in diagnosis of ICP, but the blood routine inflammatory markers have no value in the evaluation of the severity of ICP, and ALT, AST and sTBA may have certain predictive value in predicting the preterm birth caused by ICP.

表1 ICP组与对照组孕妇相关临床资料与实验室检查结果比较
表2 轻度ICP亚组与重度ICP亚组孕妇相关临床资料与实验室检查结果比较
图1 NLR、血小板计数和MPV诊断ICP的ROC
表3 ICP早产亚组与ICP足月分娩亚组孕妇相关临床资料与实验室检查结果比较
图2 AST、ALT和sTBA对ICP早产预测价值的ROC
[1]
Kremer AE, Wolf K, Ständer S. Intrahepatic cholestasis of pregnancy : rare but important[J]. Hautarzt. 2017, 68(2): 95-102. DOI: 10.1007/s00105-016-3923-y.
[2]
Kulhan M, Kulhan NG, Nayki U, et al. Intrahepatic cholestasis of pregnancy and fetal outcomes. Mini review[J]. Arch Med Sci-Civiliz Dis, 2017,1:85-86. DOI: 10.5114/amscd.2017.67110.
[3]
Diken Z, Usta IM, Nassar AH. A clinical approach to intrahepatic cholestasis of pregnancy[J]. Am J Perinatol, 2014, 31(1):1-8. DOI: 10.1055/s-0033-1333673.
[4]
Rook M, Vargas J, Caughey A, et al. Fetal outcomes in pregnancies complicated by intrahepatic cholestasis of pregnancy in a Northern California cohort[J]. PLoS One, 2012,7(3):e28343. DOI: 10.1371/journal.pone.0028343.
[5]
Puljic A, Kim E, Page J, et al. The risk of infant and fetal death by each additional week of expectant management in intrahepatic cholestasis of pregnancy by gestational age[J]. Am J Obstet Gynecol, 2015, 212(5): 667. e1-e5. DOI: 10.1016/j.ajog.2015.02.012.
[6]
Lee RH, Geenes VL, Williamson C. Primum non nocere: stillbirth rate in intrahepatic cholestasis of pregnancy[J]. Am J Obstet Gynecol, 2015,212(3):414. DOI: 10.1016/j.ajog.2014.11.039.
[7]
Ovadia C, Williamson C. Intrahepatic cholestasis of pregnancy: recent advances[J]. Clin Dermatol, 2016,34(3):327-334. DOI: 10.1016/j.clindermatol.2016.02.004.
[8]
戴钟英. 妊娠期肝内胆汁淤积症时终止妊娠的时机选择[J]. 实用妇产科杂志,2002,18(1):11-12. DOI: 10.3969/j.issn.1003-6946.2002.01.007.
[9]
Arbel Y, Shacham Y, Ziv-Baran T, et al. Higher neutrophil/lymphocyte ratio is related to lower ejection fraction and higher long-term all-cause mortality in ST-elevation myocardial infarction patients[J]. Can J Cardiol, 2014,30(10):1177-1182. DOI: 10.1016/j.cjca.2014.05.010.
[10]
Ethier JL, Desautels D, Templeton A, et al. Prognostic role of neutrophil-to-lymphocyte ratio in breast cancer: a systematic review and Meta-analysis[J]. Breast Cancer Res, 2017,19(1):2. DOI: 10.1186/s13058-016-0794-1.
[11]
Jardak S, Medhioub M, Agar K, et al. P321 ulcerative colitis: role of neutrophil-to-lymphocyte and platelet-to-lymphocyte ratios in predicting disease severity[J]. J Crohn S Colitis,12(suppl 1):S263. DOI: 10.1093/ecco-jcc/jjx180.448.
[12]
Farah R, Samra N. Mean platelets volume and neutrophil to lymphocyte ratio as predictors of stroke[J]. J Clin Lab Anal, 2018, 32(1): e22189. DOI: 10.1002/jcla.22189.
[13]
Turcato G, Campagnaro T, Bonora A, et al. Red blood cell distribution width independently predicts 1-month mortality in acute decompensation of cirrhotic patients admitted to emergency department[J]. Eur J Gastroenterol Hepatol, 2018,30(1):33-38. DOI: 10.1097/MEG.0000000000000993.
[14]
Chen Z, Shen Z, Hu L, et al. Identification of matrix metalloproteinase-2 and 9 as biomarker of intrahepatic cholestasis of pregnancy[J]. Ann Hepatol, 2017,16(2):291-296. DOI: 10.5604/16652681.1231589.
[15]
Jurate K, Rimantas Z, Jolanta S, et al. Sensitivity and specificity of biochemical tests for diagnosis of intrahepatic cholestasis of pregnancy[J]. Ann Hepatol, 2017,16(4):569-573. DOI: 10.5604/01.3001.0010.0294.
[16]
Kremer AE, Bolier R, Dixon PH, et al. Autotaxin activity has a high accuracy to diagnose intrahepatic cholestasis of pregnancy[J]. J Hepatol, 2015,62(4):897-904. DOI: 10.1016/j.jhep.2014.10.041.
[17]
Kremer AE, Wolf K, Ständer S. Intrahepatic cholestasis of pregnancy: rare but important[J]. Hautarzt, 2017, 68(2):95-102. DOI: 10.1007/s00105-016-3923-y.
[18]
Kirbas A, Biberoglu E, Daglar K, et al. Neutrophil-to-lymphocyte ratio as a diagnostic marker of intrahepatic cholestasis of pregnancy[J]. Eur J Obstet Gynecol Reprod Biol, 2014,180:12-15. DOI: 10.1016/j.ejogrb.2014.05.042.
[19]
Yayla AÇ,Vural F, Klçç Ç,et al. Can we predict severity of intrahepatic cholestasis of pregnancy using inflammatory markers?[J]. Turk J Obstet Gynecol, 2017,14(3):160-165. DOI: 10.4274/tjod.67674.
[20]
中华医学会妇产科学分会产科学组. 妊娠期肝内胆汁淤积症诊疗指南(2015)[J].临床肝胆病杂志,2015,31(10):1575-1578. DOI: 10.3969/j.issn.1001-5256.2015.10.003.
[21]
Wood AM, Livingston EG, Hughes BL, et al. Intrahepatic cholestasis of pregnancy: a review of diagnosis and management[J]. Obstet Gynecol Surv, 2018,73(2):103-109. DOI: 10.1097/OGX.0000000000000524.
[22]
Deniz CD, Ozler S, Sayn FK. Association of adverse outcomes of intrahepatic cholestasis of pregnancy with zonulin levels[J]. J Obstet Gynaecol, 2020, 1-6. DOI: 10.1080/01443615.2020.1820463.
[23]
Wang Y, Aoki H, Yang J, et al. The role of sphingosine 1-phosphate receptor 2 in bile-acid-induced cholangiocyte proliferation and cholestasis-induced liver injury in mice[J]. Hepatology, 2017,65(6):2005-2018. DOI: 10.1002/hep.29076.
[24]
Di Mascio D, Quist-Nelson J, Riegel M, et al. Perinatal death by bile acid levels in intrahepatic cholestasis of pregnancy: a systematic review[J]. J Matern Fetal Neonatal Med, 2019:1-9. DOI: 10.1080/14767058.2019.1685965.
[25]
Kate M, O′Brien,Katryn MA, Cheryl ER, et al. IL-17A synergistically enhances bile acid-induced inflammation during obstructive cholestasis[J].Am J Pathol, 2013, 183(5): 1498-1507.DOI: 10.1016/j.ajpath.2013.07.019.
[26]
Silva J, Magenta M, Sisti G, et al. Association between complete blood count components and intrahepatic cholestasis of pregnancy[J]. Cureus, 2020,12(12):e12381. DOI: 10.7759/cureus.12381.
[27]
Ovadia C, Seed PT, Sklavounos A, et al. Association of adverse perinatal outcomes of intrahepatic cholestasis of pregnancy with biochemical markers: results of aggregate and individual patient data Meta-analyses[J]. Lancet, 2019,393(10174):899-909. DOI: 10.1016/S0140-6736(18)31877-4.
[28]
陈昀,邢爱耘,胡雅毅. 糖酵解相关基因在妊娠期肝内胆汁淤积症患者胎盘组织内的变化 [J/CD]. 中华妇幼临床医学杂志(电子版),2017,13(1): 71-77. DOI: 10.3877/cma.j.issn.1673-5250.2017.01.013.
[29]
Oztas E, Erkenekli K, Ozler S, et al. Can routine laboratory parameters predict adverse pregnancy outcomes in intrahepatic cholestasis of pregnancy?[J]. J Perinat Med, 2015, 43(6):667-674. DOI: 10.1515/jpm-2014-0207.
[30]
曲皖君,于婷. 中性粒细胞-淋巴细胞比率和胆酸水平在妊娠期肝内胆汁淤积症中的诊断价值[J].中国临床保健杂志,2015, 18(4):376-379. DOI: 10.3969/J.issn.1672-6790.2015.04.015.
[31]
Jurate K, Rimantas Z, Jolanta S, et al. Sensitivity and specificity of biochemical tests for diagnosis of intrahepatic cholestasis of pregnancy[J]. Ann Hepatol, 2017, 16(4):569-573. DOI: 10.5604/01.3001.0010.0294.
[1] 李圣鹏, 方爱蓝, 刘诗宁, 王丹, 刘湘奇. 下颌阻生第三磨牙拔除难度的预测因素与评估方法[J]. 中华口腔医学研究杂志(电子版), 2023, 17(06): 441-445.
[2] 张俊, 罗再, 段茗玉, 裘正军, 黄陈. 胃癌预后预测模型的研究进展[J]. 中华普通外科学文献(电子版), 2023, 17(06): 456-461.
[3] 王龙彪, 刘洪, 董天雄. 中心体扩增细胞占比和C反应蛋白-白蛋白比值对胃癌根治术治疗预后的预测价值[J]. 中华普通外科学文献(电子版), 2023, 17(05): 352-356.
[4] 李坤河, 寇萌佳, 邝立挺. 肝移植术后二次气管插管的危险因素及预测模型的建立[J]. 中华普通外科学文献(电子版), 2023, 17(05): 366-371.
[5] 唐旭, 韩冰, 刘威, 陈茹星. 结直肠癌根治术后隐匿性肝转移危险因素分析及预测模型构建[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 16-20.
[6] 李建美, 邓静娟, 杨倩. 两种术式联合治疗肝癌合并肝硬化门静脉高压的安全性及随访评价[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 41-44.
[7] 贾成朋, 王代宏, 陈华, 孙备. 可切除性胰腺癌预后术前预测模型的建立及应用[J]. 中华普外科手术学杂志(电子版), 2023, 17(05): 566-570.
[8] 邢晓伟, 刘雨辰, 赵冰, 王明刚. 基于术前腹部CT的卷积神经网络对腹壁切口疝术后复发预测价值[J]. 中华疝和腹壁外科杂志(电子版), 2023, 17(06): 677-681.
[9] 邱朋, 邓正栋, 王剑明. 肝内胆管结石微创治疗策略[J]. 中华肝脏外科手术学电子杂志, 2023, 12(06): 591-596.
[10] 李斌奎. 不可切除肝内胆管细胞癌的转化治疗[J]. 中华肝脏外科手术学电子杂志, 2023, 12(05): 511-516.
[11] 顾睿祈, 方洪生, 蔡国响. 循环肿瘤DNA检测在结直肠癌诊治中的应用与进展[J]. 中华结直肠疾病电子杂志, 2023, 12(06): 453-459.
[12] 秦维, 王丹, 孙玉, 霍玉玲, 祝素平, 郑艳丽, 薛瑞. 血清层粘连蛋白、Ⅳ型胶原蛋白对代偿期肝硬化食管胃静脉曲张出血的预测价值[J]. 中华消化病与影像杂志(电子版), 2023, 13(06): 447-451.
[13] 张郁妍, 胡滨, 张伟红, 徐楣, 朱慧, 羊馨玥, 刘海玲. 妊娠中期心血管超声参数与肝功能的相关性及对不良妊娠结局的预测价值[J]. 中华消化病与影像杂志(电子版), 2023, 13(06): 499-504.
[14] 王小娜, 谭微, 李悦, 姜文艳. 预测性护理对结直肠癌根治术患者围手术期生活质量、情绪及并发症的影响[J]. 中华消化病与影像杂志(电子版), 2023, 13(06): 525-529.
[15] 王亚丹, 吴静, 黄博洋, 王苗苗, 郭春梅, 宿慧, 王沧海, 王静, 丁鹏鹏, 刘红. 白光内镜下结直肠肿瘤性质预测模型的构建与验证[J]. 中华临床医师杂志(电子版), 2023, 17(06): 655-661.
阅读次数
全文


摘要