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"Byung Ik Kim"

Case Report

Hepatic neoplasm

Complete cure of advanced hepatocellular carcinoma with right adrenal gland metastasis and portal vein thrombosis by multiple applications of an interdisciplinary therapy: case report with 8-year follow up
Hojung Jung, Byung Ik Kim, Yong Kyun Cho, Woo Kyu Jeon, Hong Joo Kim, Hyun Pyo Hong
Clin Mol Hepatol 2018;24(4):424-429.
Published online November 14, 2017
DOI: https://doi.org/10.3350/cmh.2017.0032
Hepatocellular carcinoma (HCC) is the sixth most common cause of death worldwide and the main cause of primary liver cancer. The principle problem of HCC is the poor prognosis, since advanced HCC reportedly has a median survival of only 9 months. The standard therapies are sorafenib and regorafenib, but the outcomes remain unclear. We report a 60-year-old man with advanced HCC with right adrenal gland metastasis and portal vein tumor thrombosis, who showed a complete response to multiple applications of an interdisciplinary therapy.

Citations

Citations to this article as recorded by  Crossref logo
  • Long-term sustained complete response with off-therapy to sorafenib in advanced hepatocellular carcinoma: a case report
    Takeshi Koujima, Yoshikatsu Endo, Takeharu Yamamoto, Toshifumi Tada, Kazuhiko Morii, Shinichiro Nakamura, Kyohei Kai
    Kanzo.2020; 61(5): 255.     CrossRef
  • 13,627 View
  • 183 Download
  • 1 Web of Science
  • Crossref

Original Articles

Viral hepatitis

Clinical characteristics of patients with chronic hepatitis B who developed genotypic resistance to entecavir: Real-life experience
Hong Joo Kim, Yong Kyun Cho, Woo Kyu Jeon, Byung Ik Kim
Clin Mol Hepatol 2017;23(4):323-330.
Published online September 5, 2017
DOI: https://doi.org/10.3350/cmh.2017.0005
Background/Aims
Clinical characteristics of patients with chronic hepatitis B (CHB) who developed genotypic resistance to entecavir (ETV) were compared to those without resistance.
Methods
Two hundred fifty eight CHB patients who underwent ETV treatment in our institution from July 2007 to May 2013 were included.
Results
Eight (3.1%) patients developed genotypic resistance to ETV during the follow-up period. The patterns of genotypic resistance to ETV were as follows: L180M + M204V + S202G (n=3); M204I + V173M (n=1); I169V + V173M (n=1); L180M + M204V + V173L (n=1); L180M + M204V + V173L + M250V (n=1); M204I + V214A + P237H (n=1). The cumulative occurrence rates of genotypic resistance to ETV were not significantly different between CHB patients with prior nucleos(t)tide analogues (NA) exposure (NA experienced, n=56) and NA naïve patients (n=202, P=0.823 by log rank comparison). Older age, higher baseline log10hepatitis B virus-deoxynucleic acid (log10HBV-DNA), higher log10HBV-DNA at 3, 6, 12 and 24 months after baseline, and complete virologic response (CVR, undetectable serum HBV-DNA by polymerase chain reaction 6 months after ETV treatment) were significant contributors to the development of genotypic resistance to ETV. Multivariate analyses showed higher log10HBV-DNA 6 months after baseline and absence of CVR were independent and significant contributors to the development of ETV resistance.
Conclusions
Clinical characteristics of patients who developed ETV resistance were higher log10HBV-DNA 6 months after baseline and absence of CVR during the ETV treatment.

Citations

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  • Specific association and independent predictive value of HBV RNA in the disease progression of hepatitis B with low-level viremia
    Liang Xu, Bin Yin, Dandan Chen, Xia Xiong, Yongfeng Yang, Xuping Wu
    Clinics and Research in Hepatology and Gastroenterology.2025; 49(7): 102648.     CrossRef
  • Risk factors related to low-level viraemia in chronic hepatitis B patients receiving entecavir treatment
    Zhong-Bin Li, Dan-Dan Chen, Yun-Fei Jia, Qing-Juan He, Li Cui, Feng-Xia Du, Yao-Jie Kang, Xin Feng, Mengwen He, Xue-Yuan Jin, Jing Chen, Yudong Wang, Dong Ji, George Lau, Shu-Gao Wu
    Frontiers in Cellular and Infection Microbiology.2024;[Epub]     CrossRef
  • Risk factors of low‐level viremia in chronic hepatitis B patients receiving Entecavir monotherapy: a retrospective cohort study
    He Chen, Juan‐Juan Fu, Li Li, Xia Wang, Xiu‐Cheng Pan
    Journal of Gastroenterology and Hepatology.2024; 39(1): 180.     CrossRef
  • A systematic review and meta-analysis of the risk of hepatitis B virus (HBV) resistance in people treated with entecavir or tenofovir
    Sheila F. Lumley, Marion Delphin, Jolynne F. Mokaya, Cedric C.S. Tan, Emily Martyn, Motswedi Anderson, Ka Chun Li, Elizabeth Waddilove, Gloria Sukali, Louise O. Downs, Khadija Said, Dorcas Okanda, Cori Campbell, Eli Harriss, Yusuke Shimakawa, Philippa C.
    Journal of Clinical Virology.2024; 174: 105711.     CrossRef
  • The urgency to expand the antiviral indications of general chronic hepatitis B patients
    Ping Fan, Lan-Qing Li, En-Qiang Chen
    Frontiers in Medicine.2023;[Epub]     CrossRef
  • Research Progress of Low-Level Viraemia in Patients with Chronic Hepatitis B
    祥运 张
    Advances in Clinical Medicine.2023; 13(12): 20083.     CrossRef
  • The association of the heterogeneity of HBV reverse transcriptase quasispecies with antiviral efficacy after treatment with nucleos(t)ide analogues for 10 years
    Tai-Cheng Zhou, Feng-Wei Liu, Jing-Hua Fan, Si-Hang Zhang, Song-Qin Lv, Zhi-Yong Yu, Yan-Mei Zhang, Liang Zhang, Jia Wei
    Infection, Genetics and Evolution.2021; 89: 104706.     CrossRef
  • Detection of Hepatitis B Virus M204V Mutation Quantitatively via Real-time PCR
    Jingjing Liang, Xinmiao Liang, Hong Ma, Leng Nie, Ying Tian, Guang Chen, Yu Wang
    Journal of Clinical and Translational Hepatology.2021; 000(000): 000.     CrossRef
  • Hepatitis B virus resistance to tenofovir: fact or fiction? A systematic literature review and structural analysis of drug resistance mechanisms
    Jolynne Mokaya, Anna L. McNaughton, Phillip A Bester, Dominique Goedhals, Eleanor Barnes, Brian D Marsden, Philippa C. Matthews
    Wellcome Open Research.2020; 5: 151.     CrossRef
  • Current state-of-the-art pharmacotherapy for the management of hepatitis B infection
    Hans L. Tillmann, Gbeminiyi Samuel
    Expert Opinion on Pharmacotherapy.2019; 20(7): 873.     CrossRef
  • Entecavir

    Reactions Weekly.2018; 1688(1): 98.     CrossRef
  • Is it possible to predict the development of an entecavir resistance mutation in patients with chronic hepatitis B in clinical practice?
    Joon Yeul Nam, Jeong-Hoon Lee
    Clinical and Molecular Hepatology.2017; 23(4): 311.     CrossRef
  • 9,953 View
  • 185 Download
  • 9 Web of Science
  • Crossref

Viral hepatitis

Comparison of the clinical outcomes between antiviral-naïve patients treated with entecavir and lamivudine-resistant patients receiving adefovir add-on lamivudine combination treatment
Hong Joo Kim, Soo Kyung Park, Hyo Joon Yang, Yoon Suk Jung, Jung Ho Park, Dong Il Park, Yong Kyun Cho, Chong Il Sohn, Woo Kyu Jeon, Byung Ik Kim, Kyu Yong Choi
Clin Mol Hepatol 2016;22(3):350-358.
Published online September 25, 2016
DOI: https://doi.org/10.3350/cmh.2016.0019
Background/Aims
To analyze the effects of preexisting lamivudine (LAM) resistance and applying antiviral treatment (adefovir [ADV] add-on LAM combination treatment) on long-term treatment outcomes, and comparing the clinical outcomes of antiviral-naïve chronic hepatitis B patients receiving entecavir (ETV) monotherapy.
Methods
This study enrolled 73 antiviral-naïve patients who received 0.5-mg ETV as an initial therapy and 54 patients who received ADV add-on LAM combination treatment as a rescue therapy from July 2006 to July 2010.
Results
During 24-month treatments, the decreases in serum log10HBV-DNA values (copies/mL) were significantly greater in the antiviral-naïve patients treated with ETV than the patients receiving ADV add-on LAM combination treatment. The biochemical response rates for alanine aminotransferase normalization at 6 months (ETV) and 12 months (ADV add-on LAM) were 90.4% (66/73) and 77.8% (42/54), respectively (P=0.048). A Kaplan-Meier analysis indicated that the rates of serologic response, viral breakthrough, and emergence of genotypic resistance did not differ significantly between the two patient groups. There were also no significant intergroup differences in the rates of disease progression (PD) and new development of hepatocellular carcinoma (HCC).
Conclusions
The long-term clinical outcomes of antiviral-naïve patients treated with ETV and LAM-resistant patients receiving ADV add-on LAM combination treatment were comparable in terms of the emergence of HCC and disease progression.

Citations

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  • Efficacy and cost-effectiveness of antiviral regimens for entecavir-resistant hepatitis B: A systematic review and network meta-analysis
    Si-Si Yang, Cheng-Wei Cai, Xue-Qing Ma, Jia Xu, Cheng-Bo Yu
    Hepatobiliary & Pancreatic Diseases International.2020; 19(6): 507.     CrossRef
  • 11,250 View
  • 142 Download
  • 1 Web of Science
  • Crossref

Case Report

Hepatic neoplasm

Primary squamous cell carcinoma of the liver: a case report
Tae Kyung Yoo, Byung Ik Kim, Eun Na Han, Dong Hyung Kim, Jung Hee Yoo, Seung Jae Lee, Yong Kyun Cho, Hong Joo Kim
Clin Mol Hepatol 2016;22(1):177-182.
Published online March 28, 2016
DOI: https://doi.org/10.3350/cmh.2016.22.1.177
Primary squamous cell carcinoma (SCC) of the liver is very rare, and few cases have been reported in Korea. Primary SCC of the liver is known to be associated with hepatic cysts and intrahepatic stones. A 71-year-old male was admitted to our hospital, and a abdominal computed tomography scan revealed a 10 × 6 cm mass in the liver. Analysis of a biopsy sample suggested SCC, and so our team performed a thorough workup to find the primary lesion, which was revealed hepatoma as a pure primary SCC of the liver with multiple distant metastases. The patient was treated with one cycle of radiotherapy, transferred to another hospital for hospice care, and then died 1 month after discharge.

Citations

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  • Clinical Outcomes of Hepatic Squamous Cell Carcinoma With Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation: A Case Report
    Ryogo Minami, Masamichi Kimura, Koji Nishikawa, Jun Imamura, Kiminori Kimura
    Cureus.2025;[Epub]     CrossRef
  • Immunotherapy for primary squamous cell carcinoma of the liver: A case report
    Jian Jiang, Guomin Dong, Suoni Li, Jiequn Ma, Jie Bai, Jinzi Hui, Hongbian Gao, Zheng Zhao
    Oncology Letters.2025; 29(6): 1.     CrossRef
  • Primary hepatic squamous cell carcinoma with pseudoachalasia treated with TACE: Case report and literature review
    Yang He, Hang Du, An Tianzhi
    Radiology Case Reports.2025; 20(10): 4906.     CrossRef
  • Primary Hepatic Squamous Cell Carcinoma: A Case Report
    Manal Lyagoubi, Chourouq Mehdaoui, Anass Haloui, Nassira Karish, Zahi Ismaili, Amal Bennani
    Cureus.2024;[Epub]     CrossRef
  • A case report of primary intrahepatic adeno squamous cell cholangiocarcinoma
    Fionn Woulfe, Michael Devine, Brian Hayes, Rory Crotty, Adrian O'Sullivan
    International Journal of Surgery Case Reports.2024; 124: 110366.     CrossRef
  • Diagnostic value of imaging modalities in primary squamous cell carcinoma of the liver
    Yuxuan Song, Jiahong Shi, Xiujuan Zhang, Meng Qiao, Zhixia Sun, Siyu Tian
    Journal of Clinical Ultrasound.2023; 51(5): 887.     CrossRef
  • Immunotherapy as adjuvant therapy for a patient with adenosquamous carcinoma of the intrahepatic bile duct: A case report and literature review
    Jun Feng, Aimaiti Yasen, Tianxing Dai, Runbin Liang, Zhihong Liao, Ping He, Zhihong Lin, Guoying Wang
    Liver Research.2023; 7(2): 156.     CrossRef
  • Unusual Case of Primary Hepatic Squamous Carcinoma on 18F-FDG PET/CT
    Wei Li, Zhidong Liu, Rusen Zhang
    Clinical Nuclear Medicine.2023; 48(12): e596.     CrossRef
  • Primary hepatic squamous cell carcinoma: case report and systematic review of the literature
    Lin Zhao, Yan Zhou, Jianmin Ding, Zhengyi Qin, Hongyu Zhou, Xiang Jing
    Frontiers in Oncology.2023;[Epub]     CrossRef
  • Primary squamous cell carcinoma of the liver: A case report
    Li-Min Kang, Di-Ping Yu, Yong Zheng, Ya-Hao Zhou
    World Journal of Clinical Cases.2022; 10(19): 6744.     CrossRef
  • Primary squamous cell carcinoma of liver. First case report from Pakistan and South Asia
    Muhammad Atiq, Ahmed Siddique Ammar, Rabia Mahmood Ali, Siraj Haider, Imran Ahmed, Faisal Saud Dar
    International Journal of Surgery Case Reports.2022; 99: 107655.     CrossRef
  • Primary Squamous Cell Carcinoma of the Liver with Good Response to Carboplatin and 5-Flurouracil: A Case Report
    Hsu-Lin Lee, Chun-Kai Fu, Liang-Yu Chien, Li-Mien Chen
    Medicina.2022; 58(12): 1864.     CrossRef
  • Primary squamous cell carcinoma of the liver: a case report
    Yu Sun, Guangyu Jin
    Journal of International Medical Research.2021;[Epub]     CrossRef
  • Primary intrahepatic squamous cell carcinoma in a sika deer
    Kazuya MATSUDA, Junji YAMADA, Shun KOGAME, Ryo MURATA, Yuto SANO
    Journal of Veterinary Medical Science.2020; 82(2): 135.     CrossRef
  • Primary squamous cell carcinoma of the liver: an unexpected pathological finding
    Fabio Tuminello, Davide Castiglione, Giuseppe Broggi, Giada Maria Vecchio, Antonio Basile, Stefano Puleo, Antonio Pesce
    Egyptian Liver Journal.2020;[Epub]     CrossRef
  • Primary hepatic squamous cell carcinoma with abdominal incision metastasis after hepatectomy
    Jia-Xi Mao, Fei Teng, Hang Yuan, Cong Liu, Hong Fu, Ke-Yan Sun, Guo-Shan Ding, Wen-Yuan Guo
    Hepatobiliary & Pancreatic Diseases International.2019; 18(2): 194.     CrossRef
  • 14,170 View
  • 140 Download
  • 17 Web of Science
  • Crossref
Original Articles

Rescue therapy with adefovir in decompensated liver cirrhosis patients with lamivudine-resistant hepatitis B virus
Hyun Young Woo, Jong Young Choi, Seung Kew Yoon, Dong Jin Suh, Seung Woon Paik, Kwang Hyub Han, Soon Ho Um, Byung Ik Kim, Heon Ju Lee, Mong Cho, Chun Kyon Lee, Dong Joon Kim, Jae Seok Hwang
Clin Mol Hepatol 2014;20(2):168-176.
Published online June 30, 2014
DOI: https://doi.org/10.3350/cmh.2014.20.2.168
Background/Aims

Adefovir dipivoxil (ADV) is a nucleotide analogue that is effective against lamivudine-resistant hepatitis B virus (HBV). The aim of this study was to determine the long-term clinical outcomes after ADV rescue therapy in decompensated patients infected with lamivudine-resistant HBV.

Methods

In total, 128 patients with a decompensated state and lamivudine-resistant HBV were treated with ADV at a dosage of 10 mg/day for a median of 33 months in this multicenter cohort study.

Results

Following ADV treatment, 86 (72.3%) of 119 patients experienced a decrease in Child-Pugh score of at least 2 points, and the overall end-stage liver disease score decreased from 16±5 to 14±10 (mean ± SD, P<0.001) during the follow-up period. With ADV treatment, 67 patients (56.3%) had undetectable serum HBV DNA (detection limit, 0.5 pg/mL). Virologic breakthrough occurred in 38 patients (36.1%) and 9 patients had a suboptimal ADV response. The overall survival rate was 89.9% (107/119), and a suboptimal response to ADV treatment was associated with both no improvement in Child-Pugh score (≥2 points; P=0.001) and high mortality following ADV rescue therapy (P=0.012).

Conclusions

Three years of ADV treatment was effective and safe in decompensated patients with lamivudine-resistant HBV.

Citations

Citations to this article as recorded by  Crossref logo
  • Targeting hepatitis B virus-associated nephropathy: efficacy and challenges of current antiviral treatments
    Yongzheng Hu, Yue Zhang, Wei Jiang
    Clinical and Experimental Medicine.2025;[Epub]     CrossRef
  • Autologous bone marrow cell transplantation in the treatment of HIV patients with compensated cirrhosis
    Baochi Liu, Mingrong Cheng, Xiaodong Chen, Lei Li, Yanhui Si, Shijia Wang, Ying Wang, Yufang Shi
    Bioscience Reports.2020;[Epub]     CrossRef
  • Analysis of the prevalence of drug-resistant hepatitis B virus in patients with antiviral therapy failure in a Chinese tertiary referral liver centre (2010–2014)
    Tian Meng, Xiaofeng Shi, Xuyang Gong, Haijun Deng, Yao Huang, Xuefeng Shan, Youlan Shan, Ailong Huang, Quanxin Long
    Journal of Global Antimicrobial Resistance.2017; 8: 74.     CrossRef
  • 10,994 View
  • 65 Download
  • 5 Web of Science
  • Crossref

Steatotic liver disease

Elevated red cell distribution width is associated with advanced fibrosis in NAFLD
Hwa Mok Kim, Bum Soo Kim, Yong Kyun Cho, Byung Ik Kim, Chong Il Sohn, Woo Kyu Jeon, Hong Joo Kim, Dong Il Park, Jung Ho Park, Kwan Joong Joo, Chang Joon Kim, Yong Sung Kim, Woon Je Heo, Won Seok Choi
Clin Mol Hepatol 2013;19(3):258-265.
Published online September 30, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.3.258
Background/Aims

The red-blood-cell distribution width (RDW) is a newly recognized risk marker in patients with cardiovascular disease, but its role in nonalcoholic fatty liver disease (NAFLD) has not been well defined. The aim of the present study was to determine the association between RDW values and the level of fibrosis in NAFLD according to BARD and FIB-4 scores.

Methods

This study included 24,547 subjects who had been diagnosed with NAFLD based on abdominal ultrasonography and questionnaires about alcohol consumption. The degree of liver fibrosis was determined according to BARD and FIB-4 scores. The association between RDW values and the degree of fibrosis in NAFLD was analyzed retrospectively.

Results

After adjusting for age, hemoglobin level, mean corpuscular volume, history of hypertension, history of diabetes, and high-sensitivity C-reactive protein, the RDW values were 12.61±0.41% (mean±SD), 12.70±0.70%, 12.77±0.62%, 12.87±0.82%, and 13.25±0.90% for those with BARD scores of 0, 1, 2, 3, and 4, respectively, and 12.71±0.72%, 12.79±0.66%, and 13.23±1.52% for those with FIB-4 scores of <1.30, 1.31-2.66, and ≥2.67, respectively (P<0.05). The prevalence of advanced fibrosis (BARD score of 24 and FIB-4 score of ≥1.3) increased with the RDW [BARD score: 51.1% in quartile 1 (Q1) vs. 63.6% in Q4; FIB-4 score: 6.9% in Q1 vs. 10.5% in Q4; P<0.001]. After adjustments, the odds ratio of having advanced fibrosis for those in Q4 compared to Q1 were 1.76 (95%CI=1.55-2.00, P<0.001) relative to BARD score and 1.69 (95%CI=1.52-1.98, P<0.001) relative to FIB-4 score.

Conclusions

Elevated RDW is independently associated with advanced fibrosis in NAFLD.

Citations

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    Hepatology.2025; 81(3): E99.     CrossRef
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    Frontiers in Medicine.2025;[Epub]     CrossRef
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    BMC Gastroenterology.2025;[Epub]     CrossRef
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    Scientific Reports.2025;[Epub]     CrossRef
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    Elżbieta Supruniuk, Kamil Grubczak, Anna Parfieniuk-Kowerda, Robert Flisiak, Marcin Moniuszko, Jerzy Jaroszewicz, Adrian Chabowski, Magdalena Świderska
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    Current Pulmonology Reports.2025;[Epub]     CrossRef
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    Meltem GÜMÜŞ, Alaaddin YORULMAZ, Hakan CANDAN, Mehmet ÖZTÜRK, Fuat BUĞRUL, Halil Haldun EMİROĞLU
    Journal of Contemporary Medicine.2023; 13(5): 1024.     CrossRef
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    Journal of Clinical Medicine.2023; 12(24): 7760.     CrossRef
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    Medicine.2021; 100(6): e24723.     CrossRef
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    European Journal of Gastroenterology & Hepatology.2019; 31(12): 1527.     CrossRef
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    Jian Yang, Bin Yan, Lihong Yang, Huimin Li, Yajuan Fan, Feng Zhu, Jie Zheng, Xiancang Ma
    BMC Gastroenterology.2018;[Epub]     CrossRef
  • The role of red cell distribution width as a noninvasive index for predicting liver cell failure and portal hypertension in cirrhotic patients
    Howaida A. Nafady, Tarek A. Hassan, Lobna A. Ahmed, Marina A. Waheeb
    The Egyptian Journal of Internal Medicine.2018; 30(4): 255.     CrossRef
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Viral hepatitis

Efficacy and safety of entecavir plus carnitine complex (GODEX®) compared to entecavir monotherapy in patient with ALT elevated chronic hepatitis B: randomized, multicenter open-label trials. The GOAL study
Dae Won Jun, Byung Ik Kim, Yong Kyun Cho, Hong Ju Kim, Young Oh Kwon, Soo Young Park, Sang Young Han, Yang Hyun Baek, Yong Jin Jung, Hwi Young Kim, Won Kim, Jeong Heo, Hyun Young Woo, Seong Gyu Hwang, Kyu Sung Rim, Jong Young Choi, Si Hyun Bae, Young Sang Lee, Young Suck Lim, Jae Youn Cheong, Sung Won Cho, Byung Seok Lee, Seok Hyun Kim, Joo Hyun Sohn, Tae Yeob Kim, Yong Han Paik, Ja Kyung Kim, Kwan Sik Lee
Clin Mol Hepatol 2013;19(2):165-172.
Published online June 27, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.2.165
Background/Aims

Carnitine and vitamin complex (Godex®) is widely used in patients with chronic liver disease who show elevated liver enzyme in South Korea. The purpose of this study is to identify the efficacy and safety of carnitine from entecavir combination therapy in Alanine aminotransferase (ALT) elevated Chronic Hepatitis B (CHB) patients.

Methods

130 treatment-naïve patients with CHB were enrolled from 13 sites. The patients were randomly selected to the entecavir and the complex of entecavir and carnitine. The primary endpoint of the study is ALT normalization level after 12 months.

Results

Among the 130 patients, 119 patients completed the study treatment. The ALT normalization at 3 months was 58.9% for the monotherapy and 95.2% for the combination therapy (P<0.0001). ALT normalization rate at 12 months was 85.7% for the monotherapy and 100% for the combination group (P=0.0019). The rate of less than HBV DNA 300 copies/mL at 12 months was not statistically significant (P=0.5318) 75.9% for the monotherapy, 70.7% for the combination and it was. Quantification of HBsAg level was not different from the monotherapy to combination at 12 months. Changes of ELISPOT value to evaluate the INF-γ secretion by HBsAg showed the increasing trend of combination therapy compare to mono-treatment.

Conclusions

ALT normalization rate was higher in carnitine complex combination group than entecavir group in CHB. Combination group was faster than entecavir mono-treatment group on ALT normalization rate. HBV DNA normalization rate and the serum HBV-DNA level were not changed by carnitine complex treatment.

Citations

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Steatotic liver disease

The influence of waist circumference on insulin resistance and nonalcoholic fatty liver disease in apparently healthy Korean adults
Deok Yun Ju, Young Gil Choe, Yong Kyun Cho, Dong Suk Shin, Su Hyeon Yoo, Seo Hyoung Yim, Ji Yong Lee, Jung Ho Park, Hong Joo Kim, Dong Il Park, Chong Il Sohn, Woo Kyu Jeon, Byung Ik Kim
Clin Mol Hepatol 2013;19(2):140-147.
Published online June 27, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.2.140
Background/Aims

Waist circumference (WC) is a risk factor for metabolic syndrome and is related to insulin resistance (IR) and nonalcoholic fatty liver disease (NAFLD). The purpose of this study was to determine the association between WC and IR and NAFLD in apparently healthy Korean adults.

Methods

The volunteers included in this cross-sectional study comprised 9,159 adults (5,052 men, 4,107 women) who participated in a comprehensive health checkup program. IR was evaluated by the homeostasis model assessment of IR (HOMA-IR) and was considered to be present when the HOMA-IR score was >2. NAFLD was evaluated by ultrasound examination. Elevated alanine aminotransferase (ALT) was defined as >40 IU/L in men and >35 IU/L in women. Logistic regression was performed to determine the odds ratios (ORs) and 95% confidence intervals (95% CIs) for NAFLD, IR, and ALT according to categorized levels of WC.

Results

NAFLD was found in 2,553 (27.9%) of the participants (82.6% men, 17.4% women), while IR and elevated ALT were found in 17.2% (68.1% men, 31.9% women) and 10% (83% men, 17% women), respectively. After adjusting for confounding factors, the prevalence of NAFLD, IR, and elevated ALT was significantly associated with increases in WC quartile: highest quartile for NAFLD in men, OR=15.539, 95% CI=12.687-19.033; highest quartile for NAFLD in women, OR=48.732, 95% CI=23.918-99.288 (P<0.001); and highest quartile for IR in men, OR=17.576, 95% CI=13.283-23.255; highest quartile for IR in women, OR=11.078, 95% CI=7.813-15.708 (P<0.001); highest quartile for elevated ALT in men, OR=7.952, 95% CI=6.046-10.459; and highest quartile for elevated ALT in women, OR=8.487, 95% CI=4.679-15.395 (P<0.001).

Conclusions

WC contributes to IR and NAFLD in apparently healthy Korean adults, and thus may be an important factor in the development of IR and NAFLD.

Citations

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Liver fibrosis, cirrhosis, and portal hypertension

Is there any vindication for low dose nonselective β-blocker medication in patients with liver cirrhosis?
Tae Wan Kim, Hong Joo Kim, Chang Uk Chon, Hyun Sun Won, Jung Ho Park, Dong Il Park, Yong Kyun Cho, Chong Il Sohn, Woo Kyu Jeon, Byung Ik Kim
Korean J Hepatol 2012;18(2):203-212.
Published online June 26, 2012
DOI: https://doi.org/10.3350/cmh.2012.18.2.203
Background/Aims

Nonselective β-blockers (NSBBs), such as propranolol, reportedly exert a pleiotropic effect in liver cirrhosis. A previous report suggested that survival was higher in patients receiving adjusted doses of NSBBs than in ligation patients. This study investigated whether low-dose NSBB medication has beneficial effects in patients with liver cirrhosis, especially in terms of overall survival.

Methods

We retrospectively studied 273 cirrhotic patients (199 males; age 53.6±10.2 years, mean±SD) who visited our institution between March 2003 and December 2007; follow-up data were collected until June 2011. Among them, 138 patients were given a low-dose NSBB (BB group: propranolol, 20-60 mg/day), and the remaining 135 patients were not given an NSBB (NBB group). Both groups were stratified randomly according to Child-Turcotte-Pugh (CTP) classification and age.

Results

The causes of liver cirrhosis were alcohol (n=109, 39.9%), hepatitis B virus (n=125, 45.8%), hepatitis C virus (n=20, 7.3%), and cryptogenic (n=19, 7.0%). The CTP classes were distributed as follows: A, n=116, 42.5%; B, n=126, 46.2%; and C, n=31, 11.4%. Neither the overall survival (P=0.133) nor the hepatocellular carcinoma (HCC)-free survival (P=0.910) differed significantly between the BB and NBB groups [probability of overall survival at 4 years: 75.1% (95% CI=67.7-82.5%) and 81.2% (95% CI=74.4-88.0%), respectively; P=0.236]. In addition, the delta CTP score did not differ significantly between the two groups.

Conclusions

Use of low-dose NSBB medication in patients with liver cirrhosis is not indicated in terms of overall and HCC-free survival.

Citations

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    Xinyi He, Zimo Zhao, Xi Jiang, Yan Sun
    Frontiers in Pharmacology.2023;[Epub]     CrossRef
  • Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
    He-Yun Cheng, Hsiu C. Lin, Hsiu L. Lin, Yow S. Uang, Joseph J. Keller, Li H. Wang
    Frontiers in Pharmacology.2022;[Epub]     CrossRef
  • Antitumor Effects and Mechanisms of Metabolic Syndrome Medications on Hepatocellular Carcinoma
    Kyoko Oura, Asahiro Morishita, Joji Tani, Tsutomu Masaki
    Journal of Hepatocellular Carcinoma.2022; Volume 9: 1279.     CrossRef
  • Low dose of propranolol treatment is associated with better survival in cirrhotic patients with hepatic encephalopathy
    Pei-Chang Lee, Yu-Ju Chen, Yueh-Ching Chou, Kuei-Chuan Lee, Ping-Hsien Chen, Wei-Yu Kao, Yi-Hsiang Huang, Teh-Ia Huo, Han-Chieh Lin, Ming-Chih Hou, Fa-Yauh Lee, Jaw-Ching Wu, Chien-Wei Su
    European Journal of Gastroenterology & Hepatology.2020; 32(3): 365.     CrossRef
  • Propranolol Is Associated with Lower Risk of Incidence of Hepatocellular Carcinoma in Patients with Alcoholic Cirrhosis: A Tertiary-Center Study and Indirect Comparison with Meta-Analysis
    Tzu-Hao Li, Yu-Lien Tsai, Chien-Fu Hsu, Chih-Wei Liu, Chia-Chang Huang, Ying-Ying Yang, Hung-Cheng Tsai, Shiang-Fen Huang, Yun-Cheng Hsieh, Hsuan-Miao Liu, Tzung-Yan Lee, Ming-Chih Hou, Chang-Youh Tsai, Han-Chieh Lin
    Gastroenterology Research and Practice.2020; 2020: 1.     CrossRef
  • Effect of Propranolol Treatment on the Incidence of Hepatocellular Carcinoma in Patients Waiting for Liver Transplant With Cirrhosis: A Retrospective, Surveillance Study in a Tertiary Center
    Nuretdin Suna, Diğdem Özer Etik, Serkan Öcal, Haldun Selçuk
    Experimental and Clinical Transplantation.2019; 17(5): 632.     CrossRef
  • Does Angiotensin‐Converting Enzyme Inhibitor and β‐Blocker Use Reduce the Risk of Primary Liver Cancer? A Case–Control Study Using the UK Clinical Practice Research Datalink
    Katrina Wilcox Hagberg, Vikrant V. Sahasrabuddhe, Katherine A. McGlynn, Susan S. Jick
    Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy.2016; 36(2): 187.     CrossRef
  • The use of β-blockers is associated with a lower risk of developing hepatocellular carcinoma in patients with cirrhosis
    Iván Herrera, Sonia Pascual, Pedro Zapater, Fernando Carnicer, Pablo Bellot, José María Palazón
    European Journal of Gastroenterology & Hepatology.2016; 28(10): 1194.     CrossRef
  • Non‐selective beta‐blockers may reduce risk of hepatocellular carcinoma: a meta‐analysis of randomized trials
    Maja Thiele, Agustín Albillos, Rozeta Abazi, Reiner Wiest, Lise L. Gluud, Aleksander Krag
    Liver International.2015; 35(8): 2009.     CrossRef
  • Management of Hepatocellular Carcinoma in Cirrhotic Patients with Portal Hypertension: Relevance of Hagen-Poiseuille's Law
    Gerond Lake-Bakaar, Muneeb Ahmed, Amy Evenson, Alan Bonder, Salomao Faintuch, Vinay Sundaram
    Liver Cancer.2014; 3(3-4): 428.     CrossRef
  • Can non-selective beta-blockers prevent hepatocellular carcinoma in patients with cirrhosis?
    Maja Thiele, Reiner Wiest, Lise Lotte Gluud, Agustín Albillos, Aleksander Krag
    Medical Hypotheses.2013; 81(5): 871.     CrossRef
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Viral hepatitis

Clinical impacts of hazardous alcohol use and obesity on the outcome of entecavir therapy in treatment-naïve patients with chronic hepatitis B infection
Won Gil Chung, Hong Joo Kim, Young Gil Choe, Hyo Sun Seok, Chang Wook Chon, Yong Kyun Cho, Byung Ik Kim, Young Yool Koh
Korean J Hepatol 2012;18(2):195-202.
Published online June 26, 2012
DOI: https://doi.org/10.3350/cmh.2012.18.2.195
Background/Aims

The aim of this study was to analyze the clinical impacts of obesity and hazardous alcohol use on the outcome of entecavir (ETV) therapy in chronic hepatitis B (CHB) patients.

Methods

The medical records of 88 treatment-naïve patients who were diagnosed with CHB and received ETV between March 2007 and September 2009 were analyzed retrospectively. Body mass index (BMI) values and Alcohol Use Disorders Identification Test (AUDIT) scores were obtained at 6 months after the initiation of ETV (0.5 mg daily) treatment.

Results

A BMI of 25 kg/m2 or more was recognized as an indicator of obesity, and a total AUDIT score of 8 or more was recognized as an indicator of hazardous alcohol use. Of the cohort, 24 patients (27.3%) were obese and 17 (19.3%) were hazardous alcohol users. The rate of seroconversion, alanine aminotransferase (ALT) normalization, and hepatitis B virus (HBV)-DNA negativity (<300 copies/mL) at 3, 6, and 12 months of treatment did not differ significantly between the normal-BMI and high-BMI groups. Moreover, the rate of seroconversion and HBV-DNA negativity at 3, 6, and 12 months of treatment did not differ significantly between the nonhazardous and hazardous alcohol users. However, the frequency of ALT normalization at 12 months was significantly lower among hazardous alcohol users (91.5% vs. 70.6%; P=0.033).

Conclusions

Obesity and hazardous alcohol drinking have no significant impact on the outcome of ETV treatment. However, the ALT normalization rate at 12 months after initiation of ETV treatment was significantly lower among the hazardous alcohol users.

Citations

Citations to this article as recorded by  Crossref logo
  • Impact of Alcohol Use on Nonalcohol-Related Liver Diseases
    Hanna Blaney, Ade Waterman, Alyson Kaplan
    Clinics in Liver Disease.2026; 30(1): 147.     CrossRef
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    Fangfang Duan, Shanshan Song, Hang Zhai, Yazhi Wang, Jun Cheng, Song Yang
    Health Science Reports.2025;[Epub]     CrossRef
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    Amedeo Lonardo, Ralf Weiskirchen
    Exploration of Medicine.2025;[Epub]     CrossRef
  • The co-existence of NAFLD and CHB is associated with suboptimal viral and biochemical response to CHB antiviral therapy: a systematic review and meta-analysis
    Georgia Zeng, Benjamin R. Holmes, Saleh A. Alqahtani, Upkar S. Gill, Patrick T. F. Kennedy
    Frontiers in Gastroenterology.2024;[Epub]     CrossRef
  • KASL clinical practice guidelines for management of chronic hepatitis B

    Clinical and Molecular Hepatology.2022; 28(2): 276.     CrossRef
  • Alcohol Intake and Mortality in Patients With Chronic Viral Hepatitis: A Nationwide Cohort Study
    Dong Hyun Sinn, Danbee Kang, Eliseo Guallar, Yoosoo Chang, Seungho Ryu, Di Zhao, Yun Soo Hong, Juhee Cho, Geum-Youn Gwak
    American Journal of Gastroenterology.2021; 116(2): 329.     CrossRef
  • Optimal drug administration manner would rescue partial virological response in chronic hepatitis B patients with entecavir or tenofovir treatment
    Ya‐Chao Tao, Meng‐Lan Wang, Dong‐Mei Zhang, Dong‐Bo Wu, Yong‐Hong Wang, Juan Liao, Hong Tang, En‐Qiang Chen
    Journal of Viral Hepatitis.2020; 27(7): 731.     CrossRef
  • Impact of hepatic steatosis on treatment response in nuclesos(t)ide analogue-treated HBeAg-positive chronic hepatitis B: a retrospective study
    Yi-Cheng Chen, Wen-Juei Jeng, Chao-Wei Hsu, Chun-Yen Lin
    BMC Gastroenterology.2020;[Epub]     CrossRef
  • KASL clinical practice guidelines for management of chronic hepatitis B

    Clinical and Molecular Hepatology.2019; 25(2): 93.     CrossRef
  • Natural History and Treatment Indications of Chronic Hepatitis B
    Dong Hyun Sinn
    The Korean Journal of Gastroenterology.2019; 74(5): 245.     CrossRef
  • Effect of Metabolic Syndrome on the Clinical Outcomes of Chronic Hepatitis B Patients with Nucleos(t)ide Analogues Treatment
    Nam Hee Kim, Yong Kyun Cho, Byung Ik Kim, Hong Joo Kim
    Digestive Diseases and Sciences.2018; 63(10): 2792.     CrossRef
  • Hepatitis B virus infection and alcohol consumption
    Ayako Iida-Ueno, Masaru Enomoto, Akihiro Tamori, Norifumi Kawada
    World Journal of Gastroenterology.2017; 23(15): 2651.     CrossRef
  • Emerging concepts in alcoholic hepatitis
    Phoenix Fung, Nikolaos Pyrsopoulos
    World Journal of Hepatology.2017; 9(12): 567.     CrossRef
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    N. V. Dhurandhar, D. Bailey, D. Thomas
    Obesity Reviews.2015; 16(12): 1017.     CrossRef
  • Metabolic syndrome delays HBeAg seroclearance in Chinese patients with hepatitis B
    J. C. Hsiang, G. L.‐H. Wong, H. L.‐Y. Chan, A. W.‐H. Chan, A. M.‐L. Chim, V. W.‐S. Wong
    Alimentary Pharmacology & Therapeutics.2014; 40(6): 716.     CrossRef
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Chemical pleurodesis for the management of refractory hepatic hydrothorax in patients with decompensated liver cirrhosis
Woo Jin Lee, Hong Joo Kim, Jung Ho Park, Dong Il Park, Yong Kyun Cho, Chong Il Sohn, Woo Kyu Jeon, Byung Ik Kim
Korean J Hepatol 2011;17(4):292-298.
Published online December 26, 2011
DOI: https://doi.org/10.3350/kjhep.2011.17.4.292
Background/Aims

Hepatic hydrothorax in patients with decompensated liver cirrhosis is a challenging problem. Treatment with diuretics and intermittent thoracentesis can be effective in selected patients. However, there are few effective therapeutic options in patients who are intolerant of these therapies. This study investigated the clinical usefulness of chemical pleurodesis with or without video-assisted thoracoscopic surgery (VATS) for patients with refractory hepatic hydrothorax.

Methods

Eleven consecutive patients with refractory hepatic hydrothorax who underwent chemical pleurodesis with or without VATS between July 2007 and February 2011 were enrolled in this study. The medical records and radiologic imagings of these patients were thoroughly reviewed.

Results

The median number of chemical pleurodesis sessions performed was 3 (range: 2-10). Successful pleurodesis was achieved in 8 of the 11 patients (72.7%), 5 (62.5%) of whom remained asymptomatic and hydrothorax free for a median follow-up of 16 weeks (range: 2-52 weeks). Complications were low-grade fever/leukocytosis (n=11, 100%), pneumonia (n=1, 9.1%), pneumothorax (n=4, 36.4%), azotemia/acute renal failure (n=6, 54.6%), and hepatic encephalopathy (n=4, 36.4%). Five patients were suspected as having procedure-related mortality (45.5%) due to the occurrence of acute renal failure with hepatic failure. The overall survival was significantly longer in the success group than in the non-success group.

Conclusions

Although chemical pleurodesis may improve the clinical symptoms and the radiologic findings in as many as 72.7% of patients with refractory hepatic hydrothorax, a significantly high prevalence of procedure-related morbidity and mortality hinders the routine application of this procedure for such patients.

Citations

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    Shuya Hashimoto, Toyoshi Yanagihara, Natsumi Kushima, Rei Sanai, Takato Ikeda, Naoki Hamada, Masaki Fujita
    Cureus.2025;[Epub]     CrossRef
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    Brandon-Joe Cilia, James Haridy, Ashok Raj, Nicholas Hannah
    World Journal of Hepatology.2025;[Epub]     CrossRef
  • Effectiveness of Chemical Pleurodesis Using Doxycycline in Malignant and Nonmalignant Pleural Disorders: A Retrospective Study from Rural South India
    Bimal Raj Rajalingam, Priya R Panicker, Archana L Peethambaran, Alexander Jenish Babu, Ravichandran Vijayakumar
    Indian Journal of Respiratory Care.2024; 12(4): 299.     CrossRef
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    Khaled Alshabani, Estefania Rivera, Alichia Paton, Juan Camilo Lara, Sebastian Fernandez-Bussy, Adnan Majid
    Annals of the American Thoracic Society.2024; 21(5): 823.     CrossRef
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    Y. Rahim, R.V. Reddy, M. Naeem, G. Tsaknis
    Respiratory Medicine Case Reports.2024; 50: 102039.     CrossRef
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    Anand Sundaralingam, Elzbieta M. Grabczak, Patrizia Burra, M. Inês Costa, Vineeth George, Eli Harriss, Ewa A. Jankowska, Julius P. Janssen, Georgia Karpathiou, Christian B. Laursen, Kornelija Maceviciute, Nick Maskell, Federico Mei, Blin Nagavci, Vasiliki
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    World Journal of Clinical Cases.2022; 10(17): 5531.     CrossRef
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    Mohammed F. Abdelghany, Khaled Essmat, Atef Farouk El-Karn, Sahar Farghly Youssif
    The Egyptian Journal of Chest Diseases and Tuberculosis.2022; 71(2): 248.     CrossRef
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    Daniela Matei, Rares Craciun, Dana Crisan, Bogdan Procopet, Tudor Mocan, Sergiu Pasca, Roxana Zaharie, Bogdan Popovici, Zeno Sparchez
    Journal of Clinical Medicine.2021; 10(16): 3688.     CrossRef
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    Bubu A. Banini, Yahya Alwatari, Madeline Stovall, Nathan Ogden, Evgeni Gershman, Rachit D. Shah, Brian J. Strife, Samira Shojaee, Richard K. Sterling
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    O. J. Bintcliffe, D. T. Arnold, N. A. Maskell
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