Chien-Hung Chen

Dr. Chien-Hung Chen

Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

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

Representative Publications

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25 October 2016 in Oncotarget
Verified
Journal Article
Open access
PDF file
KCKuan-Hung Chen
Kuan-Hung Chen
CCChien-Hung Chen
Chien-Hung Chen
CWChristopher Glenn Wallace
Christopher Glenn Wallace
CYChun-Man Yuen
Chun-Man Yuen
GKGour-Shenq Kao
Gour-Shenq Kao
HYHon-Kan Yip
Hon-Kan Yip
Intravenous administration of xenogenic adipose-derived mesenchymal stem cells (ADMSC) and ADMSC-derived exosomes markedly reduced brain infarct volume and preserved neurological function in rat after acute ischemic stroke

1 August 2016 in International Journal of Cardiology
Verified
Journal Article
Closed access
KLKun-Chen Lin
Kun-Chen Lin
HYHon-Kan Yip
Hon-Kan Yip
PSPei-Lin Shao
Pei-Lin Shao
SWShun-Cheng Wu
Shun-Cheng Wu
KCKuan-Hung Chen
Kuan-Hung Chen
MLMel S Lee
Mel S Lee

3 March 2004 in Cancer
Verified
Journal Article
Closed access
PDF file
TCTony Hsiu-Hsi Chen
Tony Hsiu-Hsi Chen
YCYueh‐Hsia Chiu
Yueh‐Hsia Chiu
DLDih‐Ling Luh
Dih‐Ling Luh
MYMing‐Fang Yen
Ming‐Fang Yen
HWHui‐Min Wu
Hui‐Min Wu
CCChien-Hung Chen
Chien-Hung Chen

2 October 2024 in Journal of Microbiology, Immunology and Infection
Verified
Journal Article
Open access
YTYu-Chieh Tsai
Yu-Chieh Tsai
WTWei-Chen Tai
Wei-Chen Tai
CLChih-Ming Liang
Chih-Ming Liang
CWCheng-Kun Wu
Cheng-Kun Wu
MTMing-Chao Tsai
Ming-Chao Tsai
SCSeng-Kee Chuah
Seng-Kee Chuah
The inflammatory bowel disease (IBD), comprising Crohn's disease (CD) and ulcerative colitis (UC) is a complex disease with multifactorial etiology. The intestinal dysbiosis have been investigated to play an important role in IBD pathogenesis and disease activity. The aim of our study was to analyze the intestinal microbiota composition in IBD across different severity levels and the impact of biologic therapy on microbiota modulation. In this study, 27 IBD patients were recruited, including 14 patients undergoing biologic therapy for moderate to severe disease activity and 13 controls with inactive disease. The gut microbial composition was determined by 16 S ribosomal RNA gene sequencing of stool samples. Biologic therapy led to significant clinical improvement in IBD disease activity after 48 weeks. About species richness, community alpha diversity was significant lower in active CD patients and enriched gradually after biologic therapy. The beta-diversity regard to the difference of bacterial community composition showed significant difference between patients in biologic and control group. A decrease in Firmicutes and increase in Bacteroidetes abundance were observed in patients with active disease, both in CD and UC. Biologic treatment induced shifts in gut microbiota, with increased Firmicutes and decreased Bacteroidetes, as well as improved F/B ratio gradually after treatment, correlating with disease activity. Our study suggested that gut microbiota differences changed after biologic therapies among IBD with different disease activity, and a rising Firmicutes/Bacteroidetes ratio could be a potential predictor for disease activity and treatment response monitoring.

19 March 2020 in Nutrients
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Journal Article
Open access
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MTMing-Chao Tsai
Ming-Chao Tsai
YLYu-Yin Liu
Yu-Yin Liu
CLChih‐Che Lin
Chih‐Che Lin
CWChih-Chi Wang
Chih-Chi Wang
YWYi-Ju Wu
Yi-Ju Wu
CCChao-Long Chen
Chao-Long Chen
The gut microbiota plays a role in nonalcoholic fatty liver disease (NAFLD), but data about gut dysbiosis in Asians with NAFLD remains scarce. We analyzed the differences in fecal microbiota between adults with and without NAFLD. This cross-sectional study examined adults with histology-proven NAFLD (25 nonalcoholic fatty liver (NAFL) patients, 25 nonalcoholic steatohepatitis (NASH) patients, and 25 living liver donors (healthy controls)). The taxonomic composition of the gut microbiota was determined by 16S ribosomal RNA gene sequencing of stool samples. The NAFL and NASH groups showed lower total bacterial diversity and richness than the controls. NAFLD patients had higher levels of the phylum Bacteroidetes and lower levels of Firmicutes than controls. The genus Ruminococcaceae UCG-010, family Ruminococcaceae, order Clostridiales, and class Clostridia were less abundant in patients with NAFL or NASH than healthy individuals. The lipopolysaccharide biosynthesis pathway was differentially enriched in the NASH group. This study examined the largest number of Asian patients with biopsy-proven NAFL and NASH in terms of dysbiosis of the gut microbiota in NAFLD patients. NAFLD patients had higher levels of Bacteroidetes and lower levels of Firmicutes. These results are different from research from western countries and could provide different targets for therapies by region.

24 June 2015 in Journal of Pineal Research
Verified
Journal Article
Closed access
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CCChia‐Lo Chang
Chia‐Lo Chang
PSPei-Hsun Sung
Pei-Hsun Sung
Cheuk-Kwan SunCheuk-Kwan Sun
Cheuk-Kwan Sun
CCChien-Hung Chen
Chien-Hung Chen
HCHsin‐Ju Chiang
Hsin‐Ju Chiang
HYHon-Kan Yip
Hon-Kan Yip