Wenjin Shang

Dr. Wenjin Shang

First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China
orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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1 August 2019 in American Journal of Neuroradiology
Verified
Journal Article
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WSWenjin Shang
Wenjin Shang
HCH.B. Chen
H.B. Chen
LSL.M. Shu
L.M. Shu
HLH.Q. Liao
H.Q. Liao
XHX.Y. Huang
X.Y. Huang
HHHua Hong
Hua Hong
BACKGROUND AND PURPOSE: FLAIR vascular hyperintensity has been recognized as a marker of collaterals in ischemic stroke, but the impact on outcome is still controversial. We hypothesized that the association between FLAIR vascular hyperintensity and outcome varies with time. MATERIALS AND METHODS: We included 459 consecutive patients with middle cerebral artery stroke and divided them into 3 groups by symptom-to-MR imaging time (group 1, ≤7 days; group 2, 8–14 days; group 3, ≥15 days). The FLAIR vascular hyperintensity score, ranging from 0 to 3 points, was based on territory distributions of different MCA segments. The associations between FLAIR vascular hyperintensity and outcome with time were analyzed qualitatively and quantitatively. RESULTS: No patients underwent MR imaging within 6 hours of onset. The proportion of FLAIR vascular hyperintensity (+) and severe stenosis or occlusion of MCA was not significantly dependent on time. In groups 1 and 2, FLAIR vascular hyperintensity (+) was significantly associated with larger lesions, the prevalence of flow injury, and unfavorable outcome (mRS ≥ 2). There were no such associations in group 3. Multiple logistic regressions demonstrated that FLAIR vascular hyperintensity (+) was an independent risk factor for unfavorable outcome in group 2. Infarction volume tended to increase with the increase of the distal FLAIR vascular hyperintensity score in groups 1 and 2, while declining in group 3. CONCLUSIONS: FLAIR vascular hyperintensity is associated with unfavorable outcome within 6 hours to 14 days of onset, while the wider distribution of distal FLAIR vascular hyperintensity may be favorable beyond 14 days of onset in MCA infarction. Symptom-to-MR imaging time should be considered when assessing the prognostic value of FLAIR vascular hyperintensity.

6 September 2017 in Metabolic Brain Disease
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Journal Article
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WSWenjin Shang
Wenjin Shang
XCXiuhui Chen
Xiuhui Chen
XLXunhua Li
Xunhua Li
HCHongbing Chen
Hongbing Chen
STShujin Tang
Shujin Tang
HHHua Hong
Hua Hong

6 May 2020 in Neurological Sciences
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Journal Article
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WSWenjin Shang
Wenjin Shang
LSLiming Shu
Liming Shu
XZX. Zhou
X. Zhou
HLH. Q. Liao
H. Q. Liao
XCX. H. Chen
X. H. Chen
HCH. B. Chen
H. B. Chen

1 January 2021 in Acta Neurologica Scandinavica
Verified
Journal Article
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JCJiaxin Chen
Jiaxin Chen
WSWenjin Shang
Wenjin Shang
YCYin Chen
Yin Chen
YLYan Li
Yan Li
XHXin Huang
Xin Huang
HFHuiyu Feng
Huiyu Feng
Objectives To summarize the clinical features of thymomatous myasthenia gravis (T-MG), examine the association between MG and thymoma, and identify the related factors or predictors for long-term prognosis of T-MG. Methods A retrospective, observational study was conducted on 100 patients with T-MG and 96 patients with non-T-MG (NT-MG) between January 1, 2009 and December 31, 2019. The baseline characteristics were recorded for each patient. Logistic regression was used to measure the association between all clinical variables and T-MG prognosis. Results Between the T-MG and NT-MG groups, age at onset (45.66 +/- 11.53 years vs 39.06 +/- 14.39 years); age >40 years (72.0% vs. 40.6%); AChR-Ab positive rate (100.0% vs. 83.3%); Myasthenia Gravis Foundation of America (MGFA) classification at the worst condition (>= grade III, 61.0% vs. 33.0%); thyroid dysfunction (7.0% vs. 20.8%); and outcome (complete stable remission + pharmacologic remission + improvement, 74.0% vs. 93.7%) were statistically significant (P < .05). Presence of thymoma (OR = 0.196, 95%CI = 0.076-0.511,P = .001) was a risk factor for MG. Male sex, post-operative complications, higher grade of MGFA classification, and thymoma Masaoka-Koga pathological stage were risk predictors for long-term prognosis of T-MG (P < .1). Use of preoperative anticholinesterase drugs (OR = 5.504, 95%CI = 1.424-21.284,P = .013) was identified as an independent predictor for T-MG. Conclusion T-MG is clinically different from NT-MG, and thymoma is considered a risk factor for MG. Preoperative anticholinesterase drug use is a protective factor for long-term prognosis of T-MG. A comprehensive understanding of the characteristics of T-MG will likely help improve its prognosis.

6 April 2023 in Neuroradiology
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WSWenjin Shang
Wenjin Shang
KZKaiyi Zhong
Kaiyi Zhong
LSLiming Shu
Liming Shu
ZLZhuhao Li
Zhuhao Li
HHHua Hong
Hua Hong

23 December 2022 in Brain Sciences
Verified
Journal Article
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WSWenjin Shang
Wenjin Shang
KZKaiyi Zhong
Kaiyi Zhong
LSLiming Shu
Liming Shu
ZLZhuhao Li
Zhuhao Li
HHHua Hong
Hua Hong
Many patients show poor outcomes following endovascular reperfusion therapy (ERT), and poor cortical venous outflow is a risk factor for these poor outcomes. We investigated the association between the outflow of the internal jugular vein (IJV) and baseline cortical venous outflow and the outcomes after ERT. We retrospectively enrolled 78 patients diagnosed with an acute anterior circulation stroke and successful ERT. Poor IJV outflow on the affected side was defined as stenosis ≥50% or occlusion of ipsilateral IJV, and poor outflow of bilateral IJVs was defined as stenosis ≥50% or occlusion of both IJVs. Poor cortical venous outflow was defined as a cortical vein opacification score (COVES) of 0 on admission. Multivariate analysis showed that poor outflow of IJV on the affected side was an independent predictor for hemorrhagic transformation. The poor outflow of bilateral IJVs was an independent risk factor for poor clinical outcomes. These patients also had numerical trends of a higher incidence of symptomatic intracranial hemorrhage, midline shift >10 mm, and in-hospital mortality; however, statistical significance was not observed. Additionally, poor IJV outflow was an independent determinant of poor cortical venous outflow. For acute large vessel occlusion patients, poor IJV outflow is associated with poor baseline cortical venous outflow and outcomes after successful ERT.