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dc.contributor.author이한아*
dc.date.accessioned2024-02-15T05:12:03Z-
dc.date.available2024-02-15T05:12:03Z-
dc.date.issued2024*
dc.identifier.issn0269-2813*
dc.identifier.otherOAK-34653*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/267843-
dc.description.abstractBackground: Data on patients switched to tenofovir alafenamide (TAF) from nucleos(t)ide analogues (NUCs) other than tenofovir disoproxil fumarate are limited. Aims: To assess the treatment and renal/bone safety outcomes following the switch to TAF. Methods: We prospectively enrolled adult patients with chronic hepatitis B (CHB) who switched from any NUC to TAF at 14 centres in Japan, Korea, Taiwan and the U.S. Study outcomes were viral suppression (VR; HBV DNA < 20 IU/mL), biochemical response (BR; alanine aminotransferase normalisation), and changes in estimated glomerular filtration rate (eGFR) and T-scores (L-spine) by bone absorptiometry by 24 months after switch to TAF. Results: We enrolled 270 eligible patients. Mean age was 58.1; 58.2% were male; 12.2% had cirrhosis and 73.3% previously received entecavir monotherapy. VR rate increased significantly from 95.2% to 98.8% by 24 months after the switch to TAF (p = 0.014). Between the switch and 24 months later, the mean spine T-score improved significantly from −1.43 ± 1.36 to −1.17 ± 1.38 (p < 0.0001), while there was no significant change in mean eGFR (88.4 ± 16.9–89.5 ± 16.3 mL/min/1.73 m2, p = 0.13). On multivariable analysis adjusted for age, sex, baseline spine T-score and prior TDF or adefovir dipivoxil use, male sex was significantly associated with lower risk of worsening spine T-score (odds ratio: 0.29, p = 0.020), while age was significantly associated with a higher risk of worsening chronic kidney disease stage (OR: 1.07, p = 0.019). Conclusions: At 24 months after the switch to TAF, VR rates and spine bone density improved significantly while renal function remained stable. © 2023 John Wiley & Sons Ltd.*
dc.languageEnglish*
dc.publisherJohn Wiley and Sons Inc*
dc.subjectbone density*
dc.subjectentecavir*
dc.subjecthepatitis B virus*
dc.subjectsequential therapy*
dc.subjecttenofovir alafenamide*
dc.titleIncreased spine bone density in patients with chronic hepatitis B switched to tenofovir alafenamide: A prospective, multinational study*
dc.typeArticle*
dc.relation.issue2*
dc.relation.volume59*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage239*
dc.relation.lastpage248*
dc.relation.journaltitleAlimentary Pharmacology and Therapeutics*
dc.identifier.doi10.1111/apt.17785*
dc.identifier.scopusid2-s2.0-85174800920*
dc.author.googleOgawa*
dc.author.googleEiichi*
dc.author.googleJun*
dc.author.googleDae Won*
dc.author.googleToyoda*
dc.author.googleHidenori*
dc.author.googleHsu*
dc.author.googleYao-Chun*
dc.author.googleYoon*
dc.author.googleEileen L.*
dc.author.googleAhn*
dc.author.googleSang Bong*
dc.author.googleYeh*
dc.author.googleMing-Lun*
dc.author.googleDo*
dc.author.googleSon*
dc.author.googleTrinh*
dc.author.googleHuy N.*
dc.author.googleTakahashi*
dc.author.googleHirokazu*
dc.author.googleEnomoto*
dc.author.googleMasaru*
dc.author.googleKawada*
dc.author.googleNorifumi*
dc.author.googleYasuda*
dc.author.googleSatoshi*
dc.author.googleTseng*
dc.author.googleCheng-Hao*
dc.author.googleKawashima*
dc.author.googleKeigo*
dc.author.googleLee*
dc.author.googleHan Ah*
dc.author.googleInoue*
dc.author.googleKaori*
dc.author.googleHaga*
dc.author.googleHiroaki*
dc.author.googleAi-Thien*
dc.author.googleMaeda*
dc.author.googleMayumi*
dc.author.googleHoang*
dc.author.googleJoseph H.*
dc.author.googleCheung*
dc.author.googleRamsey*
dc.author.googleUeno*
dc.author.googleYoshiyuki*
dc.author.googleEguchi*
dc.author.googleYuichiro*
dc.author.googleFurusyo*
dc.author.googleNorihiro*
dc.author.googleYu*
dc.author.googleMing-Lung*
dc.author.googleTanaka*
dc.author.googleYasuhito*
dc.author.googleNguyen*
dc.author.googleMindie H.*
dc.contributor.scopusid이한아(57190980926;5831162710)*
dc.date.modifydate20240502145036*
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