Min Yang

Prof. Dr. Min Yang

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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30 January 2020 in Journal of Neurogastroenterology and Motility
Verified
Journal Article
Open access
PDF file
YWYan-Jun Wang
Yan-Jun Wang
XLXiu-Qiong Lang
Xiu-Qiong Lang
DWDan Wu
Dan Wu
YHYu-Qin He
Yu-Qin He
CLChun-Hui Lan
Chun-Hui Lan
MYMin Yang
Min Yang
Yan-Jun Wang, Xiu-Qiong Lang, Dan Wu, Yu-Qin He, Chun-Hui Lan, Xiao-Xiao, Bin Wang, Duo-Wu Zou, Ji-Min Wu, Yong-Bin Zhao, Peter W Dettmar, Dong-Feng Chen,and Min Yang. J Neurogastroenterol Motil 1999;0:. https://doi.org/10.5056/jnm19032

29 December 2016 in Chinese Journal of Integrative Medicine
Verified
Journal Article
Closed access
PDF file
MYMin Yang
Min Yang
MGMing-Yang Guo
Ming-Yang Guo
YLYong Luo
Yong Luo
MYMing-Dong Yun
Ming-Dong Yun
JYJiao Yan
Jiao Yan
CXChanghong Xiao
Changhong Xiao

25 October 2016 in Neurogastroenterology & Motility
Verified
Journal Article
Closed access
PDF file
YHY-Q He
Y-Q He
XLX-Q Lang
X-Q Lang
LLL Lin
L Lin
LJL Ji
L Ji
XYX-Y Yuan
X-Y Yuan
MYMin Yang
Min Yang

1 February 2024 in Case Studies in Construction Materials
Verified
Journal Article
Open access
MYMin Yang
Min Yang
Chao LiChao Li
Chao Li
HLHao Liu
Hao Liu
LHLongfei Huo
Longfei Huo
Xiaofei YaoXiaofei Yao
Xiaofei Yao
XDXiaojun Ding
Xiaojun Ding

11 February 2026 in Clinical Nuclear Medicine
Verified
Journal Article
Closed access
WLWenbo Mm Li
Wenbo Mm Li
WSWen Mm Shi
Wen Mm Shi
XLXiang Mm Li
Xiang Mm Li
JSJinju Mm Sun
Jinju Mm Sun
ZLZhixue Mm Liu
Zhixue Mm Liu
KLKaijun Liu
Kaijun Liu
Purpose: Accurate evaluation of intestinal lesions and severity assessment of ulcerative colitis (UC) are crucial for therapeutic strategies and prognosis. This study aims to compare the efficacy of 18 F-FAPI and 18 F-FDG PET/CT in the evaluation of intestinal lesions and disease activity assessment of UC. Methods: This is a prospective cohort study, and patients with newly diagnosed or relapsed UC were enrolled. All participants underwent 18 F-FAPI PET/CT, 18 F-FDG PET/CT, abdominal contrast-enhanced CT, and colonoscopy within 1 week. Mayo Endoscopic Subscore (MES) was used as the reference standard for identification and severity assessment of intestinal lesions. Target-to-background ratio (TBR) of each segment in 18 F-FAPI/ 18 F-FDG PET/CT and global 18 F-FAPI/ 18 F-FDG PET/CT score were computed to represent the activity of independent segments and all segments, respectively. Before examinations, partial Mayo score was calculated based on clinical manifestations of patients, and levels of C-reactive protein, interleukin-6, erythrocyte sedimentation rate, platelet, and hemoglobin were determined. Finally, all data were analyzed to compare the efficacy of 18 F-FAPI and 18 F-FDG PET/CT in the evaluation of intestinal lesions and disease activity in UC. Results: A total of 113 intestinal segments (including 90 lesion segments) were evaluated among 23 participants. Through receiver operating characteristic (ROC) analysis, 18 F-FAPI PET/CT showed significantly superior performance in detecting intestinal lesions compared with 18 F-FDG PET/CT ( P = 0.046) and abdominal contrast-enhanced CT ( P = 0.007). The correlations between FAPI-TBR and MES ( R 2 = 0.75) and abdominal contrast-enhanced CT score ( R 2 = 0.55) were stronger than those of FDG-TBR. 18 F-FAPI PET/CT showed superior discriminative capacity across different disease activity levels at both segmental ( P < 0.001) and patient-level ( P < 0.05) in intergroup comparison. The global 18 F-FAPI PET/CT score was significantly correlated with other activity indicators ( r = 0.49–0.76). Moreover, 18 F-FAPI PET/CT was also significantly superior to 18 F-FDG PET/CT ( P < 0.001) and abdominal contrast-enhanced CT ( P = 0.001) in detecting active lesions according to ROC analysis. Conclusions: The efficacy of 18 F-FAPI PET/CT in the evaluation of intestinal lesions and disease activity assessment of UC was superior to that of 18 F-FDG PET/CT. 18 F-FAPI PET/CT also correlated well with endoscopy, abdominal contrast-enhanced CT, clinical manifestations, and biomarkers. Therefore, 18 F-FAPI PET/CT may be a promising method for noninvasive assessment of disease activity of UC.

7 April 2026 in BMJ Open Gastroenterology
Verified
Journal Article
Open access
PDF file
WLWenbo Li
Wenbo Li
MHMingyang Hou
Mingyang Hou
YLYi Li
Yi Li
HYHoude Yu
Houde Yu
YHYuqin He
Yuqin He
MYMin Yang
Min Yang
Objective: Obstructed defecation syndrome (ODS) is a chronic constipation subtype. Conventional tests are limited by non-physiological conditions and poor correlation with symptoms. This study investigated anorectal dynamics and dyssynergia phenotypes in patients with ODS using Fecobionics. Methods: This study was designed as a prospective observational study including 10 control subjects and 25 patients with ODS. All measurements were performed according to a predefined protocol. All patients with ODS underwent clinical evaluation, anorectal manometry (ARM) and defecography. Fecobionics recorded anorectal pressures, sensation and expulsion performance. Expulsion dynamics were further analysed using preload–afterload diagrams to characterise dyssynergia subtypes. Results: Compared with the control group, the ODS group showed prolonged expulsion time (76 (23–120) vs 18.7 s (10.6–34), p<0.01), reduced effective propulsive force (P_delta) (26.2 (8.6–35.9) vs 48.2 cmH₂O (32.5–88.0), p<0.01), increased number of contractions (7 (4–14) vs 2.5 (1.3–3.8), p<0.01) and higher paradoxical contraction rates (71% (50–100) vs 0% (0–44), p<0.01). ARM during attempted evacuation (push) demonstrated lower anal relaxation rates in the ODS group (16% (12–37) vs 36% (27–44), p<0.03). Correlation analyses demonstrated that impaired Fecobionics metrics were associated with greater symptom burden. Three dyssynergia phenotypes were identified: multiple simultaneous contractions, insufficient or delayed anal relaxation and persistently elevated outlet pressure. Conclusion: Fecobionics enables integrated and physiologically relevant assessment of anorectal function and identifies distinct dyssynergia phenotypes in ODS, reflecting heterogeneous mechanisms of outlet obstruction with implications for individualised management. Study registration: ChiCTR2300078807.