Guofeng  Wang

Mr. Guofeng Wang


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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8 August 2014 in Obesity Surgery
Verified
Journal Article
Open access
PDF file
GWGuofeng Wang
Guofeng Wang
FHFengxia Huang
Fengxia Huang
NXNing Xu
Ning Xu
DYDong Yin
Dong Yin
YHYuan Hui
Yuan Hui
YCYang Chen
Yang Chen
Background Although a few studies have been reported on predictive factors of postoperative diabetes remission, the conclusions remain inconsistent. This meta-analysis aimed to assess the preoperative clinical factors for type 2 diabetes mellitus (T2DM) remission after bariatric surgery. Methods The Cochrane Library, PubMed, MEDLINE, Embase, and CINAHL databases were searched. All human studies published in English between 1 January 1992 and 1 September 2013 reporting on the parameters of interest were included. Results In total, 15 studies involving 1,753 bariatric surgery patients were selected. Analyses were performed separately for the parameters of interest. T2DM remission was observed to be negatively correlated with age, diabetes duration, insulin use, and HbA1c levels. Baseline body mass index (BMI) and C-peptide levels were positively associated with the remission rate in Asian patients. However, there was no significant association between gender and remission rate. Conclusions Patients with younger age, short diabetes duration, better glucose control, and better β cell function were more likely to achieve T2DM remission after bariatric surgery. However, further randomized controlled trials with uniform remission criteria should be conducted to provide more reliable evidence.

13 January 2019 in Journal of Cellular Physiology
Verified
Journal Article
Closed access
PDF file
GWGuofeng Wang
Guofeng Wang
YYYongxin Yan
Yongxin Yan
NXNing Xu
Ning Xu
YHYuan Hui
Yuan Hui
DYDong Yin
Dong Yin

16 May 2014 in Obesity Surgery
Verified
Journal Article
Closed access
PDF file
YYYon-Xin Yan
Yon-Xin Yan
GWGuofeng Wang
Guofeng Wang
NXNing Xu
Ning Xu
FWFeng-Li Wang
Feng-Li Wang

18 September 2019 in Journal of Cellular Biochemistry
Verified
Journal Article
Closed access
PDF file
GWGuofeng Wang
Guofeng Wang
YYYongxin Yan
Yongxin Yan
NXNing Xu
Ning Xu
DYDong Yin
Dong Yin
YHYuan Hui
Yuan Hui

24 August 2020 in British Journal of Biomedical Science
Verified
Journal Article
Closed access
YYY Yan
Y Yan
FWF Wang
F Wang
HCH Chen
H Chen
XZX Zhao
X Zhao
DYD Yin
D Yin
GWGuofeng Wang
Guofeng Wang
This prospective study compared the efficacy and safety of laparoscopic gastric bypass and laparoscopic sleeve gastrectomy in treating overweight and obese patients with BMI>28 kg/m2 and type-2 dia...

13 March 2020 in Bioscience Reports
Verified
Journal Article
Open access
PDF file
GWGuofeng Wang
Guofeng Wang
YYYongxin Yan
Yongxin Yan
ZZZhichen Zheng
Zhichen Zheng
TZTongyu Zhang
Tongyu Zhang
In the present study, hsa-miR-424-5p mimic plasmid and hsa-mir-424-5p inhibitor plasmid were designed and injected into rats respectively, and miRNA control plasmid was also constructed. Models of Type 1 diabetes (T1D) were built. After successful modeling, the expression of hsa-miR-424-5p in lymphocytes was analyzed by RT-PCR. The expression of protein PD-1, T-bet, CXCR3, STING in Th1 lymphocytes and content of IGF-1 in islet tissue were analyzed by flow analysis. The protein levels of SHP2, Rheb, mTORC1, Rictor and Raptor in islet tissue were analyzed by Western blot. The results showed that hsa-miR-424-5p mimic group had the highest expression of hsa-miR-424-5p in lymphocytes. The expression of PD-1 was in hsa-miR-424-5p inhibitor > miRNA control > hsa-miR-424-5p mimic, while the expression of T-bet, CXCR3 and STING was in hsa-miR-424-5p mimic > miRNA control > hsa-miR-424-5p inhibitor. The expression of IGF-1 protein in hsa-miR-424-5p inhibitor group was the highest (32.08%) and hardly expressed in hsa-miR-424-5p mimic group (2.36%). The expression of SHP2, Rheb, mTORC1, Rictor and Raptor of insulin histoproteins were in hsa-miR-424-5p mimic group > miRNA control of > hsa-miR-424-5p inhibitor group, with statistical differences. It indicates that hsa-miR-424-5p binding PD-1 signaling molecules can stimulate the immune effect through the mTORC signaling pathway and participates in the pathogenesis of T1D.