Young, Kim Do
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Young, Kim Do
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Young Kim Do
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Young Kim Do
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Item type:Publication, Prevalence and genotype distribution of hepatitis C virus among apparently healthy individuals in Mongolia: a population‐based nationwide study(Wiley, 2008-11); ; ;Ahn, Sang Hoon ;Nymadawa, PagvajavDahgwahdorj, YagaanbuyantScopus© Citations 31 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Transarterial Chemoembolization in Treatment-Naïve and Recurrent Hepatocellular Carcinoma: A Propensity-Matched Outcome Analysis(Springer Science and Business Media LLC, 2019-12) ;Kim, David Sooik ;Lim, Tae Seop ;Jeon, Mi Young ;Kim, Beom KyungPark, Jun YongOBJECTIVES: Transarterial chemoembolization (TACE) improves the survival of patients with hepatocellular carcinoma (HCC); however, TACE treatment outcomes of patients with treatment-naïve HCC (TN-HCC) and those with recurrent HCC after curative resection (R-HCC) have not yet been compared. METHODS: We recruited 448 patients with TN-HCC, and 275 patients with R-HCC treated with TACE as first-line anti-cancer treatment. RESULTS: At first TACE, patients with TN-HCC showed a significantly lower proportion of male gender (74.9% vs. 84.3%), higher proportion of liver cirrhosis (61.9% vs. 49.3%), higher aspartate aminotransferase (median 48 vs. 31 IU/L), alanine aminotransferase (median 38 vs. 26 IU/L), alpha-fetoprotein (AFP) (median 96.6 vs. 7.7 ng/mL), and total bilirubin (mean 1.0 vs. 0.8 mg/dL) levels, longer prothrombin time (median 1.05 vs. 1.01 international normalized ratio), higher tumor number (mean 2.1 vs. 1.7), larger tumor size (median 3.1 vs. 1.6 cm), and lower proportion of Barcelona Clinic Liver Cancer stage 0-A (55.6% vs. 71.9%) than patients with R-HCC (all P < 0.05). Multivariate analysis showed that TACE for TN-HCC (vs. R-HCC) was an independent predictor of mortality (hazard ratio, 1.328; P = 0.024) with AFP level and tumor number (all P < 0.05). However, treatment outcomes between TN-HCC and R-HCC became statistically similar after propensity score-matched (PSM) analysis using liver cirrhosis, tumor size, and multiple tumors (P < 0.05). CONCLUSIONS: Based on the similar TACE treatment outcomes observed with the PSM analysis, the current TACE treatment guideline for patients with TN-HCC might similarly be applied for patients with R-HCC.Scopus© Citations 9 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Antiviral efficacies of currently available rescue therapies for multidrug-resistant chronic hepatitis B(The Korean Association for the Study of the Liver, 2013) ;Park, Mi Sung ;Kim, Beom Kyung ;Kim, Kyung Sik ;Kim, Ja KyungKim, Seung UpScopus© Citations 10 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Author Correction: Comparison between chronic hepatitis B patients with untreated immune-tolerant phase vs. those with virological response by antivirals(2019-11) ;Lee, Hye Won ;Kim, Seung Up; ;Park, Jun YongAn amendment to this paper has been published and can be accessed via a link at the top of the paper.Scopus© Citations 2 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Lower Incidence of Hepatocellular Carcinoma and Cirrhosis in Hepatitis C Patients with Sustained Virological Response by Pegylated Interferon and Ribavirin(Springer Science and Business Media LLC, 2015-02) ;Moon, Chansoo ;Jung, Kyu Sik; ; Park, Jun YongScopus© Citations 38 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Comparison between chronic hepatitis B patients with untreated immune-tolerant phase vs. those with virological response by antivirals(Springer Science and Business Media LLC, 2019-02) ;Lee, Hye Won ;Kim, Seung Up; ;Park, Jun YongRoutine nucleos(t)ide analogs (NUCs) have not yet been recommended for patients with immune-tolerant (IT) phase in chronic hepatitis B virus (HBV) infection. We aimed to evaluate prognosis of patients in untreated IT-phase (UIT group), compared to those in immune-active phase who achieved virological response by NUCs according to guidelines (VR group). Between 2006 and 2012, patients in UIT or VR groups were included. Cumulative risks of HCC and liver-related events (LREs) development were assessed. Furthermore, propensity-score was calculated based upon age, gender, diabetes and liver stiffness. UIT group (n = 126) showed younger age, lower proportion of male gender and lower LS than VR group (n = 641). UIT group had similar 10-year cumulative risks of HCC (2.7% vs. 2.9%, p = 0.704) and LRE (4.6% vs. 6.1%, p = 0.903) development, compared to VR group. When we re-defined UIT group by the lower ALT cut-offs, 10-year cumulative risks of HCC and LRE development were 2.9% and 4.8%, respectively. Using propensity-score matching and inverse probability treatment weighting analysis, similar results were reproduced. UIT group consistently had similar prognosis compared to VR group. Therefore, further large-scale prospective studies in order to verify rationales of routine NUCs in UIT group are still required.Scopus© Citations 31 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Scopus© Citations 16 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Hepatitis B e antigen‐negative mutations in the precore and core promoter regions in Korean patients(Wiley, 2009-04) ;Choi, Jong Won ;Ahn, Sang Hoon ;Park, Jun Yong ;Chang, Hye YoungKim, Ja KyungScopus© Citations 19 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Prognosis of Untreated Minimally Active Chronic Hepatitis B Patients in Comparison With Virological Responders by Antivirals(Ovid Technologies (Wolters Kluwer Health), 2019-06) ;Lee, Hye Won ;Kim, Seung Up ;Park, Jun Yong; OBJECTIVES: Serum hepatitis B virus (HBV)-DNA > 2,000 IU/mL is associated with higher risk of disease progression. However, without hepatocellular carcinoma (HCC) or cirrhosis, nucleos(t)ide analogs (NUCs) are recommended only for patients with elevated serum HBV-DNA and alanine aminotransferase ≥2 × upper normal limit. METHODS: We evaluated prognosis of untreated minimally active (MA) hepatitis patients (defined as HBV-DNA > 2,000 IU/mL, but never fulfilling current criteria for NUCs during follow-up) (untreated MA group), compared to virological responders by NUCs (NUC-VR group). Eligible patients undergoing transient elastography were consecutively enrolled. Patients with an immune-tolerant or inactive phase and with cirrhosis or HCC at enrollment were excluded. Cumulative risks of disease progression were assessed using the Kaplan-Meier method. RESULTS: The untreated MA group (n = 152) had higher HBV-DNA, alanine aminotransferase, and total bilirubin levels, and lower proportions of male and positive hepatitis B e antigen, compared to the NUC-VR group (n = 641). The untreated MA group had higher risks of HCC (adjusted hazard ratio [HR] 3.485, 95% confidence interval [CI] 1.234-9.846; P = 0.018), but similar risks of cirrhotic complications (adjusted HR 0.649, 95% CI 0.227-1.854; P = 0.420), compared to the NUC-VR group. Inverse probability of treatment weighting analysis using propensity score showed that the untreated MA group had higher risks of HCC (HR 4.464, 95% CI 2.008-9.901; P < 0.001), but similar risks of cirrhotic complications (HR 1.171, 95% CI 0.594-2.309; P = 0.649), compared to the NUC-VR group. DISCUSSION: Through appropriate adjustment of potential prognostic factors, the untreated MA group consistently showed higher risks of HCC, but similar risks of cirrhotic complications, compared to the NUC-VR group. HCC risk might be reduced through earlier NUCs for the untreated MA group.Scopus© Citations 21 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Progression of Untreated Minimally Active Chronic HBV Infection Compared to Inactive Infection(Elsevier BV, 2019-12) ;Lee, Hye Won ;Kim, Seung Up; ;Park, Jun YongNucleos(t)ide analogs (NUCs) are recommended when both are fulfilled in the absence of hepatocellular carcinoma (HCC) or cirrhosis; (1) elevated serum hepatitis B virus (HBV)-DNA (≥20,000 IU/mL for hepatitis B e antigen-positive chronic hepatitis B [CHB] or ≥2000 IU/mL for hepatitis B e antigen-negative CHB) and (2) serum alanine aminotransferase ≥2× upper limit of normal.1 Therefore, many patients still remain untreated. Such untreated patients have so called "minimally active CHB," where serum HBV-DNA is persistently >2000 IU/mL and other parameters for NUCs are below the criteria.2 There have been little data concerning their prognosis.Scopus© Citations 18
