Kim Kim

Prof. Dr. Kim Kim

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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1 July 2010 in Digestive and Liver Disease
Verified
Journal Article
Closed access
JLJeong-Hoon Lee
Jeong-Hoon Lee
DKDonghee Kim
Donghee Kim
HKHwa Jung Kim
Hwa Jung Kim
CLChang-Hoon Lee
Chang-Hoon Lee
JYJong In Yang
Jong In Yang
HLHyo-Suk Lee
Hyo-Suk Lee

1 January 2017 in Journal of Hepatology
Verified
Journal Article
Closed access
BKBo Kyung Koo
Bo Kyung Koo
DKDonghee Kim
Donghee Kim
SJSae Kyung Joo
Sae Kyung Joo
JKJung Ho Kim
Jung Ho Kim
MCMee Soo Chang
Mee Soo Chang
KKKim Kim
Kim Kim

5 October 2020 in Nature Communications
Verified
Journal Article
Open access
PDF file
GLGiljae Lee
Giljae Lee
HYHyun Ju You
Hyun Ju You
JBJasmohan Bajaj
Jasmohan Bajaj
SJSae Kyung Joo
Sae Kyung Joo
JYJunsun Yu
Junsun Yu
GKGwangPyo Ko
GwangPyo Ko
Nonalcoholic fatty liver disease (NAFLD) is associated with obesity but also found in non-obese individuals. Gut microbiome profiles of 171 Asians with biopsy-proven NAFLD and 31 non-NAFLD controls are analyzed using 16S rRNA sequencing; an independent Western cohort is used for external validation. Subjects are classified into three subgroups according to histological spectra of NAFLD or fibrosis severity. Significant alterations in microbiome diversity are observed according to fibrosis severity in non-obese, but not obese, subjects. Ruminococcaceae and Veillonellaceae are the main microbiota associated with fibrosis severity in non-obese subjects. Furthermore, stool bile acids and propionate are elevated, especially in non-obese subjects with significant fibrosis. Fibrosis-related Ruminococcaceae and Veillonellaceae species undergo metagenome sequencing, and four representative species are administered in three mouse NAFLD models to evaluate their effects on liver damage. This study provides the evidence for the role of the microbiome in the liver fibrosis pathogenesis, especially in non-obese subjects.

23 January 2012 in Hepatology
Verified
Journal Article
Open access
PDF file
DKDonghee Kim
Donghee Kim
SCSu-Yeon Choi
Su-Yeon Choi
EPEun Ha Park
Eun Ha Park
WLWhal Lee
Whal Lee
JKJin Hwa Kang
Jin Hwa Kang
RKRay W. Kim
Ray W. Kim
Nonalcoholic fatty liver disease (NAFLD) is related to risk factors of coronary artery disease, such as dyslipidemia, diabetes, and metabolic syndrome, which are closely linked with visceral adiposity. The aim of this study was to investigate whether NAFLD was associated with coronary artery calcification (CAC), which is used as a surrogate marker for coronary atherosclerosis independent of computed tomography (CT)-measured visceral adiposity. Out of 5,648 subjects who visited one of our health screening centers between 2003 and 2008, we enrolled 4,023 subjects (mean age, 56.9 ± 9.4 years; 60.7% males) without known liver disease or a history of ischemic heart disease. CAC score was evaluated using the Agatston method. On univariate analysis, the presence of CAC (score >0) was significantly associated with age, sex, body mass index, aspartate aminotransferase, alanine aminotransferase, high-density lipoprotein cholesterol, triglycerides, and increased risk of diabetes, hypertension, smoking, and NAFLD. Increasing CAC scores (0, <10, 10-100, ≥100) were associated with higher prevalence of NAFLD (odds ratio [OR], 1.84; 95% confidence interval [CI], 1.61-2.10; P <0.001). Multivariable ordinal regression analysis was adjusted for traditional risk factors, and CT-measured visceral adipose tissue area in a subgroup of subjects showed that the increased CAC scores were significantly associated with the presence of NAFLD (OR, 1.28, 95% CI, 1.04-1.59; P = 0.023) independent of visceral adiposity. Conclusion: Patients with NAFLD are at increased risk for coronary atherosclerosis independent of classical coronary risk factors, including visceral adiposity. These data suggest that NAFLD might be an independent risk factor for coronary artery disease. (HEPATOLOGY 2012)

1 July 2012 in Journal of Hepatology
Verified
Journal Article
Closed access
GCGoh Eun Chung
Goh Eun Chung
DKDonghee Kim
Donghee Kim
KKKim Kim
Kim Kim
JYJeong Yoon Yim
Jeong Yoon Yim
MPMin Jung Park
Min Jung Park
HLHyo-Suk Lee
Hyo-Suk Lee

1 January 2020 in Cell Host & Microbe
Verified
Journal Article
Closed access
BSBoram Seo
Boram Seo
KJKyungchan Jeon
Kyungchan Jeon
SMSunghyun Moon
Sunghyun Moon
KLKiuk Lee
Kiuk Lee
WKWoon-Ki Kim
Woon-Ki Kim
GKGwangPyo Ko
GwangPyo Ko