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dc.contributor.author김휘영*
dc.date.accessioned2022-06-02T16:32:28Z-
dc.date.available2022-06-02T16:32:28Z-
dc.date.issued2022*
dc.identifier.issn1542-3565*
dc.identifier.issn1542-7714*
dc.identifier.otherOAK-31532*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/261391-
dc.description.abstractBACKGROUND & AIMS: Antiviral treatment from hepatitis B envelope antigen (HBeAg)-positive status may attenuate the integration of hepatitis B virus DNA into the host genome causing hepatocellular carcinoma (HCC). We investigated the impact of HBeAg status at the onset of antiviral treatment on the risk of HCC. METHODS: The incidence of HCC was evaluated in Korean patients with chronic hepatitis B who started entecavir or tenofovir in either HBeAg-positive or HBeAg-negative phase. The results in the Korean cohort were validated in a Caucasian PAGE-B cohort. RESULTS: A total of 9143 Korean patients (mean age, 49.2 years) were included: 49.1% were HBeAg-positive and 49.2% had cirrhosis. During follow-up (median, 5.1 years), 916 patients (10.0%) developed HCC. Baseline HBeAg positivity was not associated with the risk of HCC in the entire cohort or cirrhotic subcohort. However, in the non-cirrhotic subcohort, HBeAg positivity was independently associated with a lower risk of HCC in multivariable (adjusted hazard ratio [aHR], 0.41; 95% confidence interval [CI], 0.26-0.66), propensity score-matching (aHR, 0.46; 95% CI, 0.28-0.76), and inverse probability weighting analyses (aHR, 0.44; 95% CI, 0.28-0.70). In the Caucasian cohort (n = 719; mean age, 51.8 years; HBeAg-positive, 20.3%; cirrhosis, 34.8%), HBeAg-positivity was not associated with the risk of HCC either in the entire cohort or cirrhotic subcohort. In the non-cirrhotic subcohort, none of the HBeAg-positive group developed HCC, although the difference failed to reach statistical significance (aHR, 0.21; 95% CI, 0.00-1.67). CONCLUSIONS: This multinational cohort study implies that HBeAg positivity at the onset of antiviral treatment seems to be an independent factor associated with a lower risk of HCC in patients with chronic hepatitis B without cirrhosis, but not in those with cirrhosis.*
dc.languageEnglish*
dc.publisherELSEVIER SCIENCE INC*
dc.subjectCumulative Incidence*
dc.subjectDNA*
dc.subjectHepatitis B Virus*
dc.subjectLiver Cancer*
dc.subjectNeoplasm*
dc.titleImpact of HBeAg on Hepatocellular Carcinoma Risk During Oral Antiviral Treatment in Patients With Chronic Hepatitis B*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume20*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1343*
dc.relation.lastpage+*
dc.relation.journaltitleCLINICAL GASTROENTEROLOGY AND HEPATOLOGY*
dc.identifier.doi10.1016/j.cgh.2021.09.001*
dc.identifier.wosidWOS:000832942000021*
dc.identifier.scopusid2-s2.0-85119065401*
dc.author.googleJang, Heejoon*
dc.author.googleYoon, Jun Sik*
dc.author.googlePark, Soo Young*
dc.author.googleLee, Han Ah*
dc.author.googleJang, Myoung-Jin*
dc.author.googleKim, Seung Up*
dc.author.googleSinn, Dong Hyun*
dc.author.googleSeo, Yeon Seok*
dc.author.googleKim, Hwi Young*
dc.author.googleKim, Sung Eun*
dc.author.googleJun, Dae Won*
dc.author.googleYoon, Eileen L.*
dc.author.googleSohn, Joo Hyun*
dc.author.googleAhn, Sang Bong*
dc.author.googleShim, Jae-Jun*
dc.author.googleJeong, Soung Won*
dc.author.googleCho, Yong Kyun*
dc.author.googleKim, Hyoung Su*
dc.author.googleNam, Joon Yeul*
dc.author.googleLee, Yun Bin*
dc.author.googleKim, Yoon Jun*
dc.author.googleYoon, Jung-Hwan*
dc.author.googleZoulim, Fabien*
dc.author.googleLampertico, Pietro*
dc.author.googleDalekos, George N.*
dc.author.googleIdilman, Ramazan*
dc.author.googleSypsa, Vana*
dc.author.googleBerg, Thomas*
dc.author.googleButi, Maria*
dc.author.googleCalleja, Jose Luis*
dc.author.googleGoulis, John*
dc.author.googleManolakopoulos, Spilios*
dc.author.googleLa Janssen, Harry*
dc.author.googlePapatheodoridis, George, V*
dc.author.googleLee, Jeong-Hoon*
dc.contributor.scopusid김휘영(56493773500)*
dc.date.modifydate20240429140130*
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의과대학 > 의학과 > Journal papers
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