期刊文献+

Correlation between COVID-19 and hepatitis B:A systematic review 被引量:2

下载PDF
导出
摘要 BACKGROUND There is growing evidence that patients with coronavirus disease 2019(COVID-19)frequently present with liver impairment.Hepatitis B virus(HBV)remains a major public health threat in current society.Both severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)and HBV can cause liver damage,and current findings on whether HBV infection increases disease severity in COVID-19 patients are inconsistent,and whether SARS-CoV-2 infection accelerates hepatitis B progression or leads to a worse prognosis in hepatitis B patients has not been adequately elucidated.AIM To explore the complex relationship between COVID-19 and hepatitis B in order to inform the research and management of patients co-infected with SARS-CoV-2 and HBV.METHODS An experienced information specialist searched the literature in the following online databases:PubMed,China National Knowledge Infrastructure,Google Scholar,Scopus,Wiley,Web of Science,Cochrane,and ScienceDirect.The literature published from December 2019 to September 1,2022 was included in the search.We also searched medRxiv and bioRxiv for gray literature and manually scanned references of included articles.Articles reporting studies conducted in humans discussing hepatitis B and COVID-19 were included.We excluded duplicate publications.News reports,reports,and other gray literature were included if they contained quantifiable evidence(case reports,findings,and qualitative analysis).Some topics that included HBV or COVID-19 samples but did not have quantitative evidence were excluded from the review.RESULTS A total of 57 studies were eligible and included in this review.They were from 11 countries,of which 33(57.9%)were from China.Forty-two of the 57 studies reported abnormalities in liver enzymes,three mainly reported abnormalities in blood parameters,four indicated no significant liver function alterations,and another eight studies did not provide data on changes in liver function.Fifty-seven studies were retrospective and the total number of co-infections was 1932,the largest sample size was 7723,and the largest number of co-infections was 353.Most of the studies suggested an interaction between hepatitis B and COVID-19,while 12 studies clearly indicated no interaction between hepatitis B and COVID-19.Six of the 57 studies clearly reported HBV activation.Six studies were related to liver transplant patients.CONCLUSION There is some association between COVID-19 and hepatitis B.Future high-quality randomized trials are needed to further elucidate the interaction between COVID-19 and hepatitis B.
出处 《World Journal of Gastroenterology》 SCIE CAS 2022年第46期6599-6618,共20页 世界胃肠病学杂志(英文版)
  • 相关文献

参考文献10

二级参考文献264

  • 1Henry Lik-Yuen Chan,Ambrose Chi-Pong Kwan,Ka-Fai To,Sik-To Lai,Paul Kay-Sheung Chan,Wai-Keung Leung,Nelson Lee,Alan Wu,Joseph Jao-Yiu Sung.Clinical significance of hepatic derangement in severe acute respiratory syndrome[J].World Journal of Gastroenterology,2005,11(14):2148-2153. 被引量:5
  • 2Han DK, Chaudhary PM, Wright ME, et al. MRIT, a noveldeath-effector domain-containing protein, interacts with caspases and BclXL and initiates cell death. Proc Natl Acad Sci U S A 1997; 94:11333-8.
  • 3Inohara N, Koseki T, Hu Y, Chen S, Nunez G. CLARP, a death effector domain-containing protein interacts with caspase8 and regulates apoptosis. Proc Natl Acad Sci U S A 1997; 94:10717-22.
  • 4Rasper DM, Vaillancourt JP, Hadano S, et al. Cell death attenuation by ‘Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex. Cell Death Differ 1998; 5:271-88.
  • 5Thome M, Tschopp J. Regulation of lymphocyte proliferation and death by FLIP. Nat Rev Immunol 2001; 1:50-8.
  • 6Chang DW, Xing Z, Pan Y, et al. c-FLIP(L) is a dual functionregulator for caspase-8 activation and CD95-mediated apoptosis. Embo J 2002; 21:3704-14.
  • 7Yeh WC, Itie A, Elia AJ, et al. Requirement for Casper (c FLIP) in regulation of death receptor-induced apoptosis and embryonic development. Immunity 2000; 12:633-42.
  • 8Hsu H, Huang J, Shu HB, Baichwal V, Goeddel DV. TNF dependent recruitment of the protein kinase RIP to the TNF receptor-1 signaling complex. Immunity 1996; 4:387-96.
  • 9Kelliher MA, Grimm S, Ishida Y, et al. The death domain kinase RIP mediates the TNF-induced NF-kappaB signal. Immunity 1998; 8:297-303.
  • 10Hsu H, Shu HB, Pan MG, Goeddel DV. TRADD-TRAF2 and TRADD-FADD interactions define two distinct TNF receptor 1 signal transduction pathways. Cell 1996; 84:299-308.

共引文献48

同被引文献12

引证文献2

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