Zhan Jianghua,Wang Zhiru.Focusing upon hot issues of diagnosing and treating biliary atresia[J].Journal of Clinical Pediatric Surgery,,22():201-204.[doi:10.3760/cma.j.cn101785-202212026-001]
Click Copy

Focusing upon hot issues of diagnosing and treating biliary atresia

References:

[1] Hartley JL,Davenport M,Kelly DA.Biliary atresia[J].Lancet,2009,374(9702):1704-1713.DOI:10.1016/S0140-6736(09)60946-6.
[2] Bezerra JA,Wells RG,Mack CL,et al.Biliary atresia:clinical and research challenges for the twenty-first century[J].Hepatology,2018,68(3):1163-1173.DOI:10.1002/hep.29905.
[3] Pang SY,Dai YM,Zhang RZ,et al.Autoimmune liver disease-related autoantibodies in patients with biliary atresia[J].World J Gastroenterol,2018,24(3):387-396.DOI:10.3748/wjg.v24.i3.387.
[4] Wang J,Xu YH,Chen ZH,et al.Liver immune profiling reveals pathogenesis and therapeutics for biliary atresia[J].Cell,2020,183(7):1867-1883.e26.DOI:10.1016/j.cell.2020.10.048.
[5] Pal N,Joy PS,Sergi CM.Biliary atresia animal models:is the needle in a haystack?[J].Int J Mol Sci,2022,23(14):7838.DOI:10.3390/ijms23147838.
[6] Kretzschmar K,Clevers H.Organoids:modeling development and the stem cell niche in a dish[J].Dev Cell,2016,38(6):590-600.DOI:10.1016/j.devcel.2016.08.014.
[7] Huch M,Gehart H,van Boxtel R,et al.Long-term culture of genome-stable bipotent stem cells from adult human liver[J].Cell,2015,160(1/2):299-312.DOI:10.1016/j.cell.2014.11.050.
[8] Andersson ER,Chivukula IV,Hankeova S,et al.Mouse model of alagille syndrome and mechanisms of jagged1 missense mutations[J].Gastroenterology,2018,154(4):1080-1095.DOI:10.1053/j.gastro.2017.11.002.
[9] Lorent K,Gong WL,Koo KA,et al.Identification of a plant isoflavonoid that causes biliary atresia[J].Sci Transl Med,2015,7(286):286ra67.DOI:10.1126/scitranslmed.aaa1652.
[10] Cui S,Leyva-Vega M,Tsai EA,et al.Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene[J].Gastroenterology,2013,144(5):1107-1115.e3.DOI:10.1053/j.gastro.2013.01.022.
[11] Chen Y,Gilbert MA,Grochowski CM,et al.A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1[J].PLoS Genet,2018,14(8):e1007532.DOI:10.1371/journal.pgen.1007532.
[12] Ye YQ,Li ZH,Feng Q,et al.Downregulation of microRNA-145 may contribute to liver fibrosis in biliary atresia by targeting ADD3[J].PLoS One,2017,12(9):e0180896.DOI:10.1371/journal.pone.0180896.
[13] Harpavat S,Garcia-Prats JA,Anaya C,et al.Diagnostic yield of newborn screening for biliary atresia using direct or conjugated bilirubin measurements[J].JAMA,2020,323(12):1141-1150.DOI:10.1001/jama.2020.0837.
[14] Chi SQ,Xu PP,Yu P,et al.Dynamic analysis of serum MMP-7 and its relationship with disease progression in biliary atresia:a multicenter prospective study[J].Hepatol Int,2022,16(4):954-963.DOI:10.1007/s12072-022-10322-x.
[15] Zhao JF,Xu XD,Gou QY,et al.TGF-β1-mediated leukocyte cell-derived chemotaxin 2 is associated with liver fibrosis in biliary atresia[J].Front Pediatr,2022,10:901888.DOI:10.3389/fped.2022.901888.
[16] Xu Y,Yu JK,Zhang RZ,et al.The perinatal infection of cytomegalovirus is an important etiology for biliary atresia in China[J].Clin Pediatr (Phila),2012,51(2):109-113.DOI:10.1177/0009922811406264.
[17] Davenport M.Biliary atresia:clinical aspects[J].Semin Pediatr Surg,2012,21(3):175-184.DOI:10.1053/j.sempedsurg.2012.05.010.
[18] Zhao YL,Xu XD,Liu GX,et al.Prognosis of biliary atresia associated with cytomegalovirus:a meta-analysis[J].Front Pediatr,2021,9:710450.DOI:10.3389/fped.2021.710450.
[19] Ginstr?m DA,Hukkinen M,Kivisaari R,et al.Biliary atresia-associated cholangitis:the central role and effective management of bile lakes[J].J Pediatr Gastroenterol Nutr,2019,68(4):488-494.DOI:10.1097/MPG.0000000000002243.
[20] 中华医学会小儿外科学分会肝胆外科学组.胆道闭锁Kasai术后胆管炎诊疗专家共识(2022版)[J].中华小儿外科杂志,2022,43(9):769-774.DOI:10.3760/cma.j.cn421158-20220427-00308. Section of Hepatobiliary Surgery,Branch of Pediatric Surgery,Chinese Medical Association:Expert Consensus on Diagnosing and Treating Cholangitis after Kasai Operation for Biliary Atresia (2022 Edition)[J].Chin J Pediatr Surg,2022,43(9):769-774.DOI:10.3760/cma.j.cn421158-20220427-00308.
[21] Yu P,Li MD,Sun RJ,et al.Primary exploring the value of metagenomic next-generation sequencing in detecting pathogenic bacteria of cholangitis with biliary atresia after Kasai operation[J].Pediatr Surg Int,2022,38(12):1931-1937.DOI:10.1007/s00383-022-05254-4.
[22] 詹江华,王立.胆道闭锁围术期营养状况评价的临床意义[J].天津医药,2019,47(4):342-345.DOI:10.11958/20181411. Zhan JH,Wang L.Clinical significance of evaluating nutrition status in patients with biliary atresia during perioperative period[J].Tianjin Med J,2019,47(4):342-345.DOI:10.11958/20181411.
[23] 詹江华,熊希倩.胆道闭锁Kasai手术加速康复外科理念实施[J].临床小儿外科杂志,2019,18(4):257-260.DOI:10.3969/j.issn.1671-6353.2019.04.002. Zhan JH,Xiong XQ.Conceptual implementation of enhanced recovery after Kasai surgery for biliary atresia[J].J Clin Ped Sur,2019,18(4):257-260.DOI:10.3969/j.issn.1671-6353.2019.04.002.
[24] 张树建,窦然,詹江华.Kasai手术中空肠胆支保留长度与胆管炎发生关系的研究进展[J].临床小儿外科杂志,2020,19(9):851-855.DOI:10.3969/j.issn.1671-6353.2020.09.018. Zhang SJ,Dou R,Zhan JH.Research advances in correlations between Roux-en-Y limb length during Kasai portoenterostomy and cholangitis[J].J Clin Ped Sur,2020,19(9):851-855.DOI:10.3969/j.issn.1671-6353.2020.09.018.
[25] Hinojosa-Gonzalez DE,Bueno LC,Roblesgil-Medrano A,et al.Laparoscopic vs open portoenterostomy in biliary atresia:a systematic review and meta-analysis[J].Pediatr Surg Int,2021,37(11):1477-1487.DOI:10.1007/s00383-021-04964-5.
[26] Dutta S,Woo R,Albanese CT.Minimal access portoenterostomy:advantages and disadvantages of standard laparoscopic and robotic techniques[J].J Laparoendosc Adv Surg Tech A,2007,17(2):258-264.DOI:10.1089/lap.2006.0112.

Memo

收稿日期:2022-12-9。
基金项目:天津市科技局重大专项(21ZXGWSY00070);新疆维吾尔自治区自然科学基金(2022D01A27、2021D01A38);天津大学儿童医院面上项目(Y2020002)
通讯作者:詹江华,Email:zhanjianghuatj@163.com

Last Update: 1900-01-01