Bu‐Yuan Hsiao

ORCID: 0009-0000-7822-5937
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About
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Research Areas
  • Pharmaceutical studies and practices
  • Heart Failure Treatment and Management
  • Pharmacogenetics and Drug Metabolism
  • Cardiovascular Function and Risk Factors
  • Pharmacological Effects and Toxicity Studies
  • Electrochemical Analysis and Applications
  • Pharmaceutical Practices and Patient Outcomes
  • Diabetic Foot Ulcer Assessment and Management
  • Zebrafish Biomedical Research Applications
  • Birth, Development, and Health
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Nanoparticles: synthesis and applications
  • Cardiac Ischemia and Reperfusion
  • Cardiac pacing and defibrillation studies
  • Diabetes Treatment and Management
  • BRCA gene mutations in cancer
  • Angiogenesis and VEGF in Cancer
  • Environmental Toxicology and Ecotoxicology
  • Salivary Gland Disorders and Functions
  • Medication Adherence and Compliance
  • Diabetes Management and Research

Taipei Medical University Hospital
2021-2025

Taipei Medical University
2021-2025

Cardiovascular Research Center
2024

In diabetes (DM), elevated blood sugar levels contribute to the overproduction of reactive oxygen species (ROS), leading endothelial progenitor cell (EPC) dysfunction. This study aimed determine potential 2-hydroxy hispolon (2HH), a derivative hispolon, reverse high glucose-induced EPC Under in vitro high-glucose (HG) conditions, we investigated effects 2HH on three types angiogenic cells: outgrowth cells (OECs), circulating (CACs) and (ECs). vivo, high-fat diet streptozotocin-induced...

10.1111/bph.70002 article EN British Journal of Pharmacology 2025-03-04

Sacubitril/valsartan (Entresto) has proven therapeutic effects in heart failure (HF) patients, but its impact on those with advanced chronic kidney disease (CKD) remains unclear, particularly HF patients coexisting end-stage renal (ESRD). This study aims to assess the long-term survival of reduced ejection fraction (HFrEF) and ESRD treated sacubitril/valsartan. A retrospective cohort included 2,860 HFrEF between January 2008 December 2020. After propensity score matching, data from a...

10.1002/cpt.3315 article EN Clinical Pharmacology & Therapeutics 2024-06-16

The aim of this study was to evaluate the potential associations between Sjogren syndrome and outcomes acute myocardial infarction (AMI) hospitalization. This population-based, retrospective observational extracted data from US Nationwide Inpatient Sample 2005 2018. Adults aged 20 years or older hospitalized for AMI were eligible inclusion. Propensity score matching applied balance characteristics comparison groups (ie, with without syndrome). Associations in-hospital determined using...

10.1097/fjc.0000000000001603 article EN Journal of Cardiovascular Pharmacology 2024-06-21

Statins, beta-blockers, and angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers have been advocated by guidelines as secondary prevention medications to improve the long-term outcomes of post-acute myocardial infarction (AMI) patients. However, adequate drug adherence has always challenging, different treatment regimens may lead divergent that remain unclear under current (MI) care standards. This study investigated association between use preventive post-AMI patients'...

10.1097/jcma.0000000000000621 article EN cc-by-nc-nd Journal of the Chinese Medical Association 2021-09-25
Chunyu Wei Ming‐Shien Wen Chih-Kuang Cheng Yi‐Jing Sheen Tsung‐Chieh Yao and 95 more S. Lee Jer-Yuarn Wu Ming-Fang Tsai Ling-Hui Li Chun‐Houh Chen Cathy S.J. Fann Hsin‐Chou Yang Yen‐Tsung Huang Hung‐Hsin Chen Yimin Liu Erh-Chan Yeh Yu‐Ching Peng Shuu‐Jiun Wang Shih‐Pin Chen Ming‐Tsun Tsai Teh‐Ia Huo Chien‐Wei Su Der-Cherng Tarng Chin-Chou Huang Jong‐Ling Fuh Keng‐Hsin Lan Yo-Tsen Liu Ching‐Liang Lu Yi‐Chung Lee Yi-Hsiang Huang Chung‐Pin Li Yen-Feng Wang Yu‐Cheng Hsieh Yi‐Ming Chen Tzu-Hung Hsiao Ching‐Heng Lin Yen‐Ju Chen I‐Chieh Chen Chien-Lin Mao Shu-Jung Chang Yen-Lin Chang Yi-Ju Liao Chih‐Hung Lai Wei‐Ju Lee Hsin Tung Ting‐Ting Yen Hsin-Chien Yen Jer‐Hwa Chang Chun‐Yao Huang Lung Chan Yung-Wei Lin Bu‐Yuan Hsiao Chaur‐Jong Hu Yung‐Kuo Lin Yung‐Feng Lin Tung-Cheng Chang Deng‐Chyang Wu Jung‐Yu Kan Chung‐Yao Hsu Szu‐Chia Chen Ching‐Chia Li Chung‐Feng Huang Chau‐Chyun Sheu Lii-Jia Yang Chung‐Hwan Chen Kang‐Hua Chen Shu-Min Chang Min-Shiuan Liou Shiping Wang Kuan-Ting Lin Hui-Ping Chuang Ying-Ju Chen Joey Sin Ying-Ting Chen Chiung-Chih Chang Chang-Fu Kuo Jing-Chi Lin Ho‐Chang Kuo Tien-Min Chan Chao‐Wei Lee Jenn-Haung Lai Shue‐Fen Luo Hao‐Tsai Cheng Lian‐Yu Lin Li-Chun Chang Chia‐Ti Tsai Hsien‐Li Kao Jian-Jyun Yu Jiann‐Shing Jeng Min‐Chin Chiu Tzu-Chan Hong Shun‐Fa Yang Hsueh‐Ju Lu Sheng‐Chiang Su Pauling Chu Pengfei Li Chia-Lin Tsai Chia‐Kuang Tsai Shih-En Tang Chien‐Ming Lin

ABSTRACT Incorporating pharmacogenetics into clinical practice promises to improve therapeutic outcome by choosing the medication and dosage optimized for a patient based on genetic factors that affect drug response 1 . One of most promising benefits PGx-guided therapy is avoidance adverse reactions 2 To evaluate impact PGx risk variants outcomes, we performed retrospective study analyzed data from largest Han Chinese cohort assembled Taiwan Precision Medicine Initiative. We found nearly all...

10.1101/2024.10.15.24315139 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2024-10-17
Pui–Yan Kwok Ming‐Shien Wen Chih-Kuang Cheng Yi‐Jing Sheen Tsung‐Chieh Yao and 95 more S. Lee Jer-Yuarn Wu Ming-Fang Tsai Ling-Hui Li Chun‐Houh Chen Cathy S.J. Fann Hsin‐Chou Yang Yen‐Tsung Huang Hung‐Hsin Chen Yimin Liu Erh-Chan Yeh Yu‐Ching Peng Shuu‐Jiun Wang Shih‐Pin Chen Ming‐Tsun Tsai Teh–Ia Huo Chien‐Wei Su Der-Cherng Tarng Chin-Chou Huang Jong‐Ling Fuh Keng‐Hsin Lan Yo‐Tsen Liu Ching‐Liang Lu Yi‐Chung Lee Yi-Hsiang Huang Chung‐Pin Li Yen-Feng Wang Yu‐Cheng Hsieh Yi‐Ming Chen Tzu-Hung Hsiao Ching‐Heng Lin Yen‐Ju Chen I‐Chieh Chen Chien-Lin Mao Shu-Jung Chang Yen-Lin Chang Yi‐Ju Liao Chih‐Hung Lai Wei‐Ju Lee Hsin Tung Ting‐Ting Yen Hsin-Chien Yen Jer‐Hwa Chang Chun‐Yao Huang Lung Chan Yung-Wei Lin Bu‐Yuan Hsiao Chaur‐Jong Hu Yung‐Kuo Lin Yung‐Feng Lin Tung-Cheng Chang Deng‐Chyang Wu Jung‐Yu Kan Chung Y. Hsu Szu‐Chia Chen Ching‐Chia Li Chung‐Feng Huang Chau‐Chyun Sheu Lii-Jia Yang Chung‐Hwan Chen Kang‐Hua Chen Shu-Min Chang Min-Shiuan Liou Shiping Wang Kuan-Ting Lin Hui-Ping Chuang Ying-Ju Chen Joey Sin Ying‐Ting Chen Chiung-Chih Chang Chang‐Fu Kuo Jing-Chi Lin Ho‐Chang Kuo Tien-Min Chan Chao‐Wei Lee Jenn-Haung Lai Shue‐Fen Luo Hao‐Tsai Cheng Lian‐Yu Lin Li-Chun Chang Chia‐Ti Tsai Hsien‐Li Kao Jian-Jyun Yu Jiann‐Shing Jeng Min‐Chin Chiu Tzu-Chan Hong Shun‐Fa Yang Hsueh‐Ju Lu Sheng‐Chiang Su Pauling Chu Pengfei Li Chia-Lin Tsai Chia‐Kuang Tsai Shih-En Tang Chien‐Ming Lin

<title>Abstract</title> Incorporating pharmacogenetics into clinical practice promises to improve therapeutic outcome by choosing the medication and dosage optimized for a patient based on genetic factors that affect drug response<sup>1</sup>. One of most promising benefits PGx-guided therapy is avoidance adverse reactions<sup>2</sup>. To evaluate impact PGx risk variants outcomes, we performed retrospective study analyzed data from largest Han Chinese cohort assembled Taiwan Precision...

10.21203/rs.3.rs-5262235/v1 preprint EN 2024-10-30
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