Hong-Ren Yu

Prof. Hong-Ren Yu

Pediatrics, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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1 August 2021 in Journal of Microbiology, Immunology and Infection
Verified
Journal Article
Open access
TTTi-An Tsai
Ti-An Tsai
CTChang-Ku Tsai
Chang-Ku Tsai
KKKuang-Che Kuo
Kuang-Che Kuo
Hong-Ren YuHong-Ren Yu
Hong-Ren Yu
Mycoplasma pneumoniae is a common pathogen that causes community-acquired pneumonia. In the past, M. pneumoniae was sensitive to macrolide antibiotics, and M. pneumoniae pneumonia (MPP) was usually a benign and self-limiting disease. However, despite use of the appropriate antibiotics, persistent fever and clinical deterioration may occur, leading to severe disease. Two major complicated conditions that may be clinically encountered are macrolide-resistant MPP and refractory MPP. Regarding the epidemics in Taiwan, before 2017, the mean rate of macrolide resistance was below 30%. Notably, since 2018, the prevalence of macrolide-resistant MPP in Taiwan has increased rapidly. Macrolide-resistant MPP shows persistent fever and/or no radiological regression to macrolide antibiotics and may even progress to severe and complicated pneumonia. Tetracyclines (doxycycline or minocycline) or fluoroquinolones are alternative treatments for macrolide-resistant MPP. Refractory MPP is characterized by an excessive immune response against the pathogen. In this context, corticosteroids have been suggested as an immunomodulator for downregulating the overactive host immune reaction. Overuse of macrolides may contribute to macrolide resistance, and thereafter, an increase in macrolide-resistant MPP. Delayed effective antimicrobial treatment is associated with prolonged and/or more severe disease. Thus, the appropriate prescription of antibiotics, as well as the rapid and accurate diagnosis of MPP, is important. The exact starting point, dose, and duration of the immunomodulator are yet to be established. We discuss these important issues in this review.

20 June 2007 in Pediatric Allergy and Immunology
Verified
Journal Article
Closed access
PDF file
Ho-Chang KuoHo-Chang Kuo
Ho-Chang Kuo
KYKuender D. Yang
Kuender D. Yang
CLChi‐Di Liang
Chi‐Di Liang
CBChin‐Nam Bong
Chin‐Nam Bong
Hong-Ren YuHong-Ren Yu
Hong-Ren Yu
CWChih‐Lu Wang
Chih‐Lu Wang

21 April 2009 in Pediatric Allergy and Immunology
Verified
Journal Article
Closed access
PDF file
Ho-Chang KuoHo-Chang Kuo
Ho-Chang Kuo
CWChih‐Lu Wang
Chih‐Lu Wang
CLChi‐ Di Liang
Chi‐ Di Liang
Hong-Ren YuHong-Ren Yu
Hong-Ren Yu
CHChien‐Fu Huang
Chien‐Fu Huang
KYKuender D. Yang
Kuender D. Yang

Verified
Journal Article
Open access
PDF file
Hou ChihyaoHou Chihyao
Hou Chihyao
You-Lin TainYou-Lin Tain
You-Lin Tain
Hong-Ren YuHong-Ren Yu
Hong-Ren Yu
Li-Tung HuangLi-Tung Huang
Li-Tung Huang
Resveratrol, also known as 3,5,4′-trihydroxystilbene, is a natural polyphenol that occurs as a phytoalexin. It is produced by plant sources such as grapes, apples, blueberries, plums, peanuts, and other oilseeds. This compound has a variety of effects on human health and diseases. This review summarizes the mounting evidence that resveratrol is helpful in treating metabolic syndrome and related disorders. Resveratrol can be provided either early as a reprogramming agent or later as part of treatment. A few of the main mechanisms underlying the beneficial effects of resveratrol on metabolic syndrome are outlined. This review also discusses the potential of resveratrol derivatives as a complementary or alternative medicine. In conclusion, resveratrol could be a useful regimen for the prevention and treatment of metabolic syndrome and its related conditions.

1 September 2010 in Acta Paediatrica
Verified
Journal Article
Closed access
PDF file
Ho-Chang KuoHo-Chang Kuo
Ho-Chang Kuo
CLChi‐Di Liang
Chi‐Di Liang
CWChih‐Lu Wang
Chih‐Lu Wang
Hong-Ren YuHong-Ren Yu
Hong-Ren Yu
KHKao‐Pin Hwang
Kao‐Pin Hwang
KYKuender D Yang
Kuender D Yang

14 April 2011 in PLOS ONE
Verified
Journal Article
Open access
PDF file
Ho-Chang KuoHo-Chang Kuo
Ho-Chang Kuo
KYKuender D. Yang
Kuender D. Yang
SJSuh-Hang Hank Juo
Suh-Hang Hank Juo
CLChi-Di Liang
Chi-Di Liang
Wei-Chiao ChangWei-Chiao Chang
Wei-Chiao Chang
Wei-Chiao ChangWei-Chiao Chang
Wei-Chiao Chang
Kawasaki disease (KD) is characterized by systemic vasculitis with unknown etiology. Previous studies from Japan indicated that a gene polymorphism of ITPKC (rs28493229) is responsible for susceptibility to KD. We collected DNA samples from 1,531 Taiwanese subjects (341 KD patients and 1,190 controls) for genotyping ITPKC. In this study, no significant association was noted for the ITPKC polymorphism (rs28493229) between the controls and KD patients, although the CC genotype was overrepresented. We further combined our data with previously published case/control KD studies in the Taiwanese population and performed a meta-analysis. A significant association between rs28493229 and KD was found (Odds Ratio:1.36, 95% Confidence Interval 1.12–1.66). Importantly, a significant association was obtained between rs28493229 and KD patients with aneurysm formation (P = 0.001, under the recessive model). Taken together, our results indicated that C-allele of ITPKC SNP rs28493229 is associated with the susceptibility and aneurysm formation in KD patients in a Taiwanese population.