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Pretreatment gamma-glutamyl transferase predicts mortality in patients with chronic hepatitis B treated with nucleotide/nucleoside analogs
DC Field | Value | Language |
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dc.contributor.author | 정장한 | - |
dc.date.accessioned | 2025-03-13T16:56:24Z | - |
dc.date.available | 2025-03-13T16:56:24Z | - |
dc.date.issued | 2024-02 | - |
dc.identifier.issn | 1607-551X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/204226 | - |
dc.description.abstract | Elevated serum gamma-glutamyl transferase (GGT) levels are associated with chronic hepatitis B (CHB)-related hepatocellular carcinoma. However, their role in predicting mortality in patients with CHB treated with nucleotide/nucleoside analogs (NAs) remains elusive. Altogether, 2843 patients with CHB treated with NAs were recruited from a multinational cohort. Serum GGT levels before and 6 months (Month-6) after initiating NAs were measured to explore their association with all-cause, liver-related, and non-liver-related mortality. The annual incidence of all-cause mortality was 0.9/100 person-years over a follow-up period of 17,436.3 person-years. Compared with patients who survived, those who died had a significantly higher pretreatment (89.3 vs. 67.4 U/L, p = 0.002) and Month-6-GGT levels (62.1 vs. 38.4 U/L, p < 0.001). The factors associated with all-cause mortality included cirrhosis (hazard ratio [HR]/95% confidence interval [CI]: 2.66/1.92-3.70, p < 0.001), pretreatment GGT levels (HR/CI: 1.004/1.003-1.006, p < 0.001), alanine aminotransferase level (HR/CI: 0.996/0.994-0.998, p = 0.001), and age (HR/CI: 1.06/1.04-1.07, p < 0.001). Regarding liver-related mortality, the independent factors included cirrhosis (HR/CI: 4.36/2.79-6.89, p < 0.001), pretreatment GGT levels (HR/CI: 1.006/1.004-1.008, p < 0.001), alanine aminotransferase level (HR/CI: 0.993/0.990-0.997, p = 0.001), age (HR/CI: 1.03/1.01-1.05, p < 0.001), and fatty liver disease (HR/CI: 0.30/0.15-0.59, p = 0.001). Pretreatment GGT levels were also independently predictive of non-liver-related mortality (HR/CI: 1.003/1.000-1.005, p = 0.03). The results remained consistent after excluding the patients with a history of alcohol use. A dose-dependent manner of <25, 25-75, and >75 percentile of pretreatment GGT levels was observed with respect to the all-cause mortality (trend p < 0.001). Pretreatment serum GGT levels predicted all-cause, liver-related, and non-liver-related mortality in patients with CHB treated with NAs. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English, Chinese | - |
dc.publisher | Kaohsiung Medical College | - |
dc.relation.isPartOf | KAOHSIUNG JOURNAL OF MEDICAL SCIENCES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Alanine Transaminase | - |
dc.subject.MESH | Hepatitis B, Chronic* / drug therapy | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Cirrhosis | - |
dc.subject.MESH | Liver Neoplasms* | - |
dc.subject.MESH | Nucleosides | - |
dc.subject.MESH | Nucleotides | - |
dc.subject.MESH | gamma-Glutamyltransferase | - |
dc.title | Pretreatment gamma-glutamyl transferase predicts mortality in patients with chronic hepatitis B treated with nucleotide/nucleoside analogs | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Tyng-Yuan Jang | - |
dc.contributor.googleauthor | Po-Cheng Liang | - |
dc.contributor.googleauthor | Dae Won Jun | - |
dc.contributor.googleauthor | Jang Han Jung | - |
dc.contributor.googleauthor | Hidenori Toyoda | - |
dc.contributor.googleauthor | Chih-Wen Wang | - |
dc.contributor.googleauthor | Man-Fung Yuen | - |
dc.contributor.googleauthor | Ka Shing Cheung | - |
dc.contributor.googleauthor | Satoshi Yasuda | - |
dc.contributor.googleauthor | Sung Eun Kim | - |
dc.contributor.googleauthor | Eileen L Yoon | - |
dc.contributor.googleauthor | Jihyun An | - |
dc.contributor.googleauthor | Masaru Enomoto | - |
dc.contributor.googleauthor | Ritsuzo Kozuka | - |
dc.contributor.googleauthor | Makoto Chuma | - |
dc.contributor.googleauthor | Akito Nozaki | - |
dc.contributor.googleauthor | Toru Ishikawa | - |
dc.contributor.googleauthor | Tsunamasa Watanabe | - |
dc.contributor.googleauthor | Masanori Atsukawa | - |
dc.contributor.googleauthor | Taeang Arai | - |
dc.contributor.googleauthor | Korenobu Hayama | - |
dc.contributor.googleauthor | Masatoshi Ishigami | - |
dc.contributor.googleauthor | Yong Kyun Cho | - |
dc.contributor.googleauthor | Eiichi Ogawa | - |
dc.contributor.googleauthor | Hyoung Su Kim | - |
dc.contributor.googleauthor | Jae-Jun Shim | - |
dc.contributor.googleauthor | Haruki Uojima | - |
dc.contributor.googleauthor | Soung Won Jeong | - |
dc.contributor.googleauthor | Sang Bong Ahn | - |
dc.contributor.googleauthor | Koichi Takaguchi | - |
dc.contributor.googleauthor | Tomonori Senoh | - |
dc.contributor.googleauthor | Maria Buti | - |
dc.contributor.googleauthor | Elena Vargas-Accarino | - |
dc.contributor.googleauthor | Hiroshi Abe | - |
dc.contributor.googleauthor | Hirokazu Takahashi | - |
dc.contributor.googleauthor | Kaori Inoue | - |
dc.contributor.googleauthor | Jee-Fu Huang | - |
dc.contributor.googleauthor | Wan-Long Chuang | - |
dc.contributor.googleauthor | Ming-Lun Yeh | - |
dc.contributor.googleauthor | Chia-Yen Dai | - |
dc.contributor.googleauthor | Chung-Feng Huang | - |
dc.contributor.googleauthor | Mindie H Nguyen | - |
dc.contributor.googleauthor | Ming-Lung Yu | - |
dc.identifier.doi | 10.1002/kjm2.12771 | - |
dc.contributor.localId | A05182 | - |
dc.relation.journalcode | J04702 | - |
dc.identifier.eissn | 2410-8650 | - |
dc.identifier.pmid | 37885338 | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1002/kjm2.12771 | - |
dc.subject.keyword | GGT | - |
dc.subject.keyword | HBV | - |
dc.subject.keyword | NA | - |
dc.subject.keyword | mortality | - |
dc.subject.keyword | treatment | - |
dc.contributor.alternativeName | Jung, Jang Han | - |
dc.contributor.affiliatedAuthor | 정장한 | - |
dc.citation.volume | 40 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 188 | - |
dc.citation.endPage | 197 | - |
dc.identifier.bibliographicCitation | KAOHSIUNG JOURNAL OF MEDICAL SCIENCES, Vol.40(2) : 188-197, 2024-02 | - |
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