Han Ah Lee

Prof. Han Ah Lee

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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31 October 2023 in Gut
Verified
Journal Article
Closed access
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HLHyeok-Hee Lee
Hyeok-Hee Lee
HLHan Ah Lee
Han Ah Lee
EKEun-Jin Kim
Eun-Jin Kim
HKHwi Young Kim
Hwi Young Kim
HKHyeon Chang Kim
Hyeon Chang Kim
Seung Up KimSeung Up Kim
Seung Up Kim
Objective We explored clinical implications of the new definition of metabolic dysfunction-associated steatotic liver disease (MASLD) by assessing its prevalence and associated cardiovascular disease (CVD) risk. Design From nationwide health screening data, we identified 9 775 066 adults aged 20–79 who underwent health examination in 2009. Participants were categorised into four mutually exclusive groups: (1) MASLD; (2) MASLD with increased alcohol intake (MetALD); (3) MASLD with other combined aetiology (the three collectively referred to as MASLD/related steatotic liver disease (SLD)); and (4) no MASLD/related SLD. SLD was determined by fatty liver index ≥30. The primary outcome was CVD event, defined as a composite of myocardial infarction, ischaemic stroke, heart failure or cardiovascular death. Results The prevalence of MASLD, MetALD and MASLD with other combined aetiology was 27.5%, 4.4% and 1.5%, respectively. A total of 8 808 494 participants without prior CVD were followed up for a median of 12.3 years, during which 272 863 CVD events occurred. The cumulative incidence and multivariable-adjusted risk of CVD were higher in participants with MASLD/related SLD than in those without (HR 1.38 (95% CI 1.37 to 1.39)). Multivariable-adjusted HR (95% CI) of CVD events was 1.39 (1.38 to 1.40) for MASLD, 1.28 (1.26 to 1.30) for MetALD and 1.30 (1.26 to 1.34) for MASLD with other combined aetiology compared to the absence of any of these conditions. CVD risk was also higher in participants with metabolic dysfunction-associated fatty liver disease or non-alcoholic fatty liver disease than in those without the respective condition. Conclusion Over one-third of Korean adults have MASLD/related SLD and bear a high CVD risk.

26 May 2020 in Alimentary Pharmacology & Therapeutics
Verified
Journal Article
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HLHan Ah Lee
Han Ah Lee
HLHYUN WOONG LEE
HYUN WOONG LEE
IKIn-Hee Kim
In-Hee Kim
JPJun Yong Park
Jun Yong Park
DSDong Hyun Sinn
Dong Hyun Sinn
Seung Up KimSeung Up Kim
Seung Up Kim
Summary: Background: Anti‐viral therapy is not indicated for patients with chronic hepatitis B (CHB) in the immune‐tolerant phase.Aims: To investigate the cumulative incidence of phase change and hepatocellular carcinoma (HCC) and independent predictors for phase change in patients with CHB in immune‐tolerant phase.Methods: In total, 946 patients in immune‐tolerant phase, defined as hepatitis B e antigen positivity, HBV‐DNA >20 000 IU/mL and alanine aminotransferase (ALT) ≤40 IU/L, between 1989 and 2017 were enrolled from eight institutes.Results: The mean age of study population (429 men and 517 women) was 36.7 years. The mean ALT and HBV‐DNA levels were 24.6 IU/L and 8.50 log10 IU/mL, respectively. Of the study population, 476 (50.3%) patients remained in immune‐tolerant phase throughout the study period (median: 63.6 months). The cumulative incidence rates of phase change and HCC at 10 years were 70.7% and 1.7%, respectively. Multivariate analyses revealed that HBV‐DNA level >107 IU/mL was associated independently with a reduced risk of phase change (hazard ratio [HR] = 0.734, P = 0.008), whereas a high ALT level, above the cut‐off recommended in the Korean Association for the Study of the Liver guidelines (34 IU/L for men and 30 IU/L for women), was associated independently with a greater risk of phase change (HR = 1.885, P < 0.001).Conclusions: The criterion of HBV‐DNA level > 107 IU/mL may be useful to define immune‐tolerant phase. In addition, an extremely low risk of HCC development was observed in patients with CHB in immune‐tolerant phase.

15 July 2021 in Gut and Liver
Verified
Journal Article
Open access
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HLHan Ah Lee
Han Ah Lee
JJJoon Young Jung
Joon Young Jung
YLYoung-Sun Lee
Young-Sun Lee
YJYoung Kul Jung
Young Kul Jung
JKJi Hoon Kim
Ji Hoon Kim
YSYeon Seok Seo
Yeon Seok Seo
Han Ah Lee, Joon Young Jung, Young-Sun Lee, Young Kul Jung, Ji Hoon Kim, Hyonggin An, Hyung Joon Yim, Yoon Tae Jeen, Jong Eun Yeon, Kwan Soo Byun, Soon Ho Um, and Yeon Seok Seo. Gut and Liver 2021;15:599-605. https://doi.org/10.5009/gnl20171

Verified
Journal Article
Open access
PDF file
HLHan Ah Lee
Han Ah Lee
HKHwi Young Kim
Hwi Young Kim
Nonalcoholic fatty liver disease (NAFLD) can lead to liver fibrosis and cirrhosis. Recently, glucagon-like peptide 1 receptor agonists (GLP-1RAs), a class of drugs used to treat type 2 diabetes and obesity, have shown therapeutic effects against NAFLD. In addition to reducing blood glucose levels and body weight, GLP-1RAs are effective in improving the clinical, biochemical, and histological markers of hepatic steatosis, inflammation, and fibrosis in patients with NAFLD. Additionally, GLP-1RAs have a good safety profile with minor side effects, such as nausea and vomiting. Overall, GLP-1RAs show promise as a potential treatment for NAFLD, and further studies are required to determine their long-term safety and efficacy.

8 June 2023 in Korean Journal of Radiology
Verified
Journal Article
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YCYuri Cho
Yuri Cho
JCJin Woo Choi
Jin Woo Choi
HKHoon Kwon
Hoon Kwon
KKKun Yung Kim
Kun Yung Kim
BLByung Chan Lee
Byung Chan Lee
RAResearch Committee of the Korean Liver Cancer Association
Research Committee of the Korean Liver Cancer Association
Cho Y, et al. Korean J Radiol. 2023 Jun;24:e35. https://doi.org/10.3348/kjr.2023.0385

15 May 2021 in Gut and Liver
Verified
Journal Article
Open access
PDF file
HLHan Ah Lee
Han Ah Lee
YLYoung-Sun Lee
Young-Sun Lee
BKBeom Kyung Kim
Beom Kyung Kim
YJYoung Kul Jung
Young Kul Jung
Seung Up KimSeung Up Kim
Seung Up Kim
YSYeon Seok Seo
Yeon Seok Seo
Han Ah Lee, Young-Sun Lee, Beom Kyung Kim, Young Kul Jung, Seung Up Kim, Jun Yong Park, Ji Hoon Kim, Hyunggin An, Do Young Kim, Hyung Joon Yim, Sang Hoon Ahn, Jong Eun Yeon, Kwan Soo Byun, Kwang-Hyub Han, Soon Ho Um, and Yeon Seok Seo. Gut and Liver 2021;15:420-9. https://doi.org/10.5009/gnl20101