Eung Ho Choi

Prof. Eung Ho Choi

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 December 2010 in Hepatology
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Journal Article
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KJKyu Sik Jung
Kyu Sik Jung
Seung Up KimSeung Up Kim
Seung Up Kim
SASang Hoon Ahn
Sang Hoon Ahn
YPYoung Nyun Park
Young Nyun Park
DKDo Young Kim
Do Young Kim
KHKwang-Hyub Han
Kwang-Hyub Han
Liver stiffness measurement (LSM) using FibroScan accurately assesses the degree of liver fibrosis and the risk of hepatocellular carcinoma (HCC) development in patients with chronic hepatitis C. This study investigated the usefulness of LSM as a predictor of HCC development in patients with chronic hepatitis B (CHB). A total of 1,130 patients with non-biopsy–proven CHB who underwent LSM between May 2005 and December 2007 were enrolled in this prospective study. After LSM was performed, patients attended regular follow-up as part of a surveillance program for the detection of HCC. The mean age of the patients (767 men, 363 women) was 50.2 years, and the median LSM was 7.7 kPa. Six hundred seventy-two (59.5%) patients received antiviral treatment before or after enrollment. During the follow-up period (median, 30.7 months; range, 24.0-50.9 months), HCC developed in 57 patients (2.0% per 1 person-year). The 1-, 2-, and 3-year cumulative incidence rates of HCC were 0.80%, 3.26%, and 5.98%, respectively. On multivariate analysis, together with old age, male sex, heavy alcohol consumption (>80 g/day), serum albumin, and hepatitis B e antigen positivity, patients with a higher LSM (>8 kPa) were at a significantly greater risk of HCC development, with the following hazard ratios: 3.07 (95% confidence interval [CI], 1.01-9.31; P = 0.047) for LSM 8.1-13 kPa; 4.68 (95% CI, 1.40-15.64; P = 0.012) for LSM 13.1-18 kPa; 5.55 (95% CI, 1.53–20.04; P = 0.009) for LSM 18.1-23 kPa; and 6.60 (95% CI, 1.83-23.84; P = 0.004) for LSM >23 kPa. Conclusion: Our data suggest that LSM could be a useful predictor of HCC development in patients with CHB. (Hepatology 2011)

25 September 2012 in PLOS ONE
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Journal Article
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YCYoung Eun Chon
Young Eun Chon
ECEung Ho Choi
Eung Ho Choi
KSKi Jun Song
Ki Jun Song
JPJun Yong Park
Jun Yong Park
DKDo Young Kim
Do Young Kim
Seung Up KimSeung Up Kim
Seung Up Kim
Transient elastography (TE), a non-invasive tool that measures liver stiffness, has been evaluated in meta-analyses for effectiveness in assessing liver fibrosis in European populations with chronic hepatitis C (CHC). However, these data cannot be extrapolated to populations in Asian countries, where chronic hepatitis B (CHB) is more prevalent. In this study, we performed a meta-analysis to assess the overall performance of TE for assessing liver fibrosis in patients with CHB. Studies from the literature and international conference abstracts which enrolled only patients with CHB or performed a subgroup analysis of such patients were enrolled. Combined effects were calculated using area under the receiver operating characteristic curves (AUROC) and diagnostic accuracy values of each study. A total of 18 studies comprising 2,772 patients were analyzed. The mean AUROCs for the diagnosis of significant fibrosis (F2), severe fibrosis (F3), and cirrhosis (F4) were 0.859 (95% confidence interval [CI], 0.857–0.860), 0.887 (95% CI, 0.886–0.887), and 0.929 (95% CI, 0.928–0.929), respectively. The estimated cutoff for F2 was 7.9 (range, 6.1–11.8) kPa, with a sensitivity of 74.3% and specificity of 78.3%. For F3, the cutoff value was determined to be 8.8 (range, 8.1–9.7) kPa, with a sensitivity of 74.0% and specificity of 63.8%. The cutoff value for F4 was 11.7 (range, 7.3–17.5) kPa, with a sensitivity of 84.6% and specificity of 81.5%. TE can be performed with good diagnostic accuracy for quantifying liver fibrosis in patients with CHB.

1 March 2010 in Investigative Ophthalmology & Visual Science
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MSMincheol Seong
Mincheol Seong
KSKyung Rim Sung
Kyung Rim Sung
ECEung Ho Choi
Eung Ho Choi
SKSung Yong Kang
Sung Yong Kang
JCJung Woo Cho
Jung Woo Cho
MKMichael S. Kook
Michael S. Kook
Purpose.: To evaluate and compare the glaucoma discrimination ability of macular inner retinal layer (MIRL) thickness with that of peripapillary retinal nerve fiber layer (pRNFL) thickness measured by spectral-domain optical coherence tomography (RTVue-100; Optovue Inc, Fremont, CA) in patients with normal-tension glaucoma (NTG). Methods.: Sixty-five healthy subjects and 102 with NTG were enrolled. MIRL thickness provided by a ganglion cell complex (GCC) scan and two RNFL thicknesses measured by the NHM4 (RNFL1) and RNFL 3.45 (RNFL2) modes of the RTVue-100 system were analyzed. The areas under the receiver operating characteristic curves (AUCs) of MIRL and pRNFL thicknesses for discriminating patients with NTG from control subjects were determined. The AUCs were compared between patients with central visual field (VF) defects (VF; ≤10° of fixation) and peripheral VF defects (>10° from fixation). Results.: The average MIRL thickness showed a strong correlation with both RNFL1 and -2 thicknesses (R 2 = 0.773, 0.774, both P < 0.0001). The AUCs for average MIRL, RNFL1, and RNFL2 thicknesses were not significantly different at 0.945, 0.973, and 0.976, respectively. However, the AUCs of the average and superior MIRL thicknesses were significantly less than that of the pRNFL thickness in eyes with moderate-to-advanced glaucoma and eyes with peripheral VF defects. Conclusions.: The average MIRL thickness showed a strong correlation with pRNFL thickness, because patients with NTG at an early stage showed paracentral VF defects near the fixation point. MIRL thickness showed glaucoma discrimination ability comparable to that of pRNFL thickness in patients with NTG with early VF defects. In eyes with advanced or peripheral VF defect, pRNFL measurement showed a better glaucoma diagnostic ability than did MIRL measurement.

19 June 2013 in Liver International
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YJYoon Ok Jang
Yoon Ok Jang
YKYoung Ju Kim
Young Ju Kim
SBSoon Koo Baik
Soon Koo Baik
MKMoon Young Kim
Moon Young Kim
YEYoung Woo Eom
Young Woo Eom
YKYong Man Kim
Yong Man Kim

1 December 2008 in Journal of Investigative Dermatology
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Journal Article
Closed access
SHSeung P. Hong
Seung P. Hong
MKMin J. Kim
Min J. Kim
MJMin-Young Jung
Min-Young Jung
HJHyerin Jeon
Hyerin Jeon
JGJawoong Goo
Jawoong Goo
ECEung Ho Choi
Eung Ho Choi

16 June 2009 in American Journal of Gastroenterology
Verified
Journal Article
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JCJae Hee Cheon
Jae Hee Cheon
EKEun Soo Kim
Eun Soo Kim
SSSung Jae Shin
Sung Jae Shin
TKTae Il Kim
Tae Il Kim
KLKang Moon Lee
Kang Moon Lee
WKWon Ho Kim
Won Ho Kim
The American Journal of Gastroenterology is published by Nature Publishing Group (NPG) on behalf of the American College of Gastroenterology (ACG). Ranked the #1 clinical journal covering gastroenterology and hepatology*, The American Journal of Gastroenterology (AJG) provides practical and professional support for clinicians dealing with the gastroenterological disorders seen most often in patients. Published with practicing clinicians in mind, the journal aims to be easily accessible, organizing its content by topic, both online and in print. www.amjgastro.com, *2007 Journal Citation Report (Thomson Reuters, 2008)