Lai Wei

Lai Wei


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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12 November 2017 in Journal of Clinical and Translational Hepatology
Verified
Journal Article
Open access
PDF file
JHJinlin Hou
Jinlin Hou
GWGuiqiang Wang
Guiqiang Wang
FWFusheng Wang
Fusheng Wang
JCJun Cheng
Jun Cheng
HRHong Ren
Hong Ren
LWLai Wei
Lai Wei

16 November 2018 in Journal of Digestive Diseases
Verified
Journal Article
Closed access
PDF file
JFJian-Gao Fan
Jian-Gao Fan
LWLai Wei
Lai Wei
HZHui Zhuang
Hui Zhuang
OAon behalf of the National Workshop on Fatty Liver and Alcoholic Liver Disease, Chinese Society of Hepatology, Chinese Medical Association; Fatty Liver Disease Expert Committee, Chinese Medical Doctor Association
on behalf of the National Workshop on Fatty Liver and Alcoholic Liver Disease, Chinese Society of Hepatology, Chinese Medical Association; Fatty Liver Disease Expert Committee, Chinese Medical Doctor Association

4 February 2022 in Hepatology International
Verified
Journal Article
Open access
PDF file
HYHong You
Hong You
XMXiong Ma
Xiong Ma
CECumali Efe
Cumali Efe
GWGui-Qiang Wang
Gui-Qiang Wang
SJSook-Hyang Jeong
Sook-Hyang Jeong
JJJidong Jia
Jidong Jia

4 November 2024 in Journal of Clinical and Translational Hepatology
Verified
Journal Article
Open access
JFJian-Gao Fan
Jian-Gao Fan
XXXiao-Yuan Xu
Xiao-Yuan Xu
RYRui-Xu Yang
Rui-Xu Yang
YNYuemin Nan
Yuemin Nan
LWLai Wei
Lai Wei
CAChinese Society of Hepatology, Chinese Medical Association,
Chinese Society of Hepatology, Chinese Medical Association,
With the rising epidemic of obesity, metabolic syndrome, and type 2 diabetes mellitus in China, metabolic dysfunction-associated non-alcoholic fatty liver disease has become the most prevalent chronic liver disease. This condition frequently occurs in Chinese patients with alcoholic liver disease and chronic hepatitis B. To address the impending public health crisis of non-alcoholic fatty liver disease and its underlying metabolic issues, the Chinese Society of Hepatology and the Chinese Medical Association convened a panel of clinical experts to revise and update the “Guideline of prevention and treatment of non-alcoholic fatty liver disease (2018, China)”. The new edition, titled “Guideline for the prevention and treatment of metabolic dysfunction-associated fatty liver disease (Version 2024)”, offers comprehensive recommendations on key clinical issues, including screening and monitoring, diagnosis and evaluation, treatment, and follow-up for metabolic dysfunction-associated fatty liver disease and metabolic dysfunction-associated steatotic liver disease. Metabolic dysfunction-associated fatty liver disease is now the preferred English term and is used interchangeably with metabolic dysfunction-associated steatotic liver disease. Additionally, the guideline emphasizes the importance of multidisciplinary collaboration among hepatologists and other specialists to manage cardiometabolic disorders and liver disease effectively.

3 October 2013 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
Open access
PDF file
HRHuiying Rao
Huiying Rao
LWLai Wei
Lai Wei
JLJuan Carlos Lopez‐Talavera
Juan Carlos Lopez‐Talavera
JSJia Shang
Jia Shang
HCHong Chen
Hong Chen
HZHui Zhuang
Hui Zhuang
Background and Aim: Chronic hepatitis C virus (HCV) infection is relatively frequent in China. This study investigated the clinical, demographic, and viral and host genetic characteristics that may influence disease manifestations and clinical management.Methods: In this cross‐sectional observational study, treatment‐naïve Han ethnic adults with recently confirmed chronic HCV infection were enrolled at 28 hospitals across China. HCV genotype and host interleukin 28B (IL28B) genotypes were determined and compared with patient demographic parameters and medical status.Results: Among the 997 HCV‐positive patients analyzed, 56.8% were infected with HCV genotype 1b, followed in prevalence by genotypes 2, 3, and 6, with substantial regional variation. Overall, 84.1% of patients were IL28B genotype CC (rs12979860), with little regional variation. Cirrhosis was reported in 10.1% of patients and was significantly associated with hepatitis B virus coinfection, low HCV viral load, low serum alanine aminotransferase, high serum aspartate aminotransferase, diabetes, and high pickled food consumption. Medical procedures were common transmission risk factors; however, lifestyle‐associated risk factors, including intravenous drug abuse and tattoos or piercings, were more common in patients with HCV genotype 3 or 6.Conclusions: Most HCV‐infected Han Chinese patients were IL28B genotype CC (rs12979860). HCV genotypes varied by geographic region, and disease characteristics differed according to HCV genotype. Relatively frequent detection of advanced liver disease may reflect limitations on access to antiviral therapy, and suggests that greater awareness of factors that influence HCV‐associated disease may help avoid clinical complications and improve patient outcomes.

10 October 2019 in Hepatology
Verified
Journal Article
Closed access
PDF file
FLFeng Liu
Feng Liu
GGGeorge Boon Bee Goh
George Boon Bee Goh
DTDina Tiniakos
Dina Tiniakos
AWAileen Wee
Aileen Wee
WLWei‐Qiang Leow
Wei‐Qiang Leow
LWLai Wei
Lai Wei