Xiaoyu Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Xiaoyu Liu has a total of 34 co-authors. Here are the top co-authors by number of shared publications:
- Yuhua Jia
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong Province 510515, China
4 shared publications Peikun He
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China
3 shared publicationsYao Jin
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China
3 shared publicationsYaxin Zhang
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China
3 shared publicationsZhaoyong Li
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China
3 shared publications- Fenghua Zhou
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China
2 shared publications
Latest Publications
- Open Access
- 1 April 2026
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 15 (7) , 2676
Prognostic Impact of Renin–Angiotensin System Inhibitors in Revascularized Patients with Acute Myocardial Infarction and Preserved or Mildly Reduced Ejection Fraction: A Retrospective Cohort Study
Background: The prognostic value of discharge renin–angiotensin–aldosterone system inhibitor (RASi) therapy in contemporary PCI-treated acute myocardial infarction (AMI) survivors with preserved or mildly reduced left ventricular ejection fraction (LVEF) remains uncertain. Methods: A retrospective cohort study of 2530 AMI patients (2019–2022) stratified by RASi use. Exclusion criteria were in-hospital mortality, LVEF < 40%, contraindications to the use of RASis or no percutaneous coronary intervention (PCI). Primary endpoints included heart failure (HF) events, recurrent acute coronary syndrome (ACS), and all-cause mortality. Kaplan–Meier analyses and inverse probability of treatment weighting (IPTW)-weighted Cox models were applied. Results: Over a mean follow-up of 49 months, discharge RASi therapy was not associated with all-cause mortality overall, but was associated with fewer HF rehospitalizations (HR 0.62, 95% CI 0.40–0.95; p = 0.03). Mortality associations differed by AMI type and hypertension status, particularly for NSTEMI (HR 0.36, 95% CI 0.14–0.91; p = 0.03; p for interaction = 0.02) and hypertension (HR 0.36, 95% CI 0.15–0.84; p = 0.02; p for interaction = 0.04). Conclusions: In this single-center observational cohort of PCI-treated AMI survivors with LVEF ≥ 40%, discharge RASi therapy was associated with fewer HF rehospitalizations but not with lower overall mortality. Exploratory subgroup analyses suggested potential heterogeneity according to NSTEMI status and hypertension, but these findings should be considered hypothesis-generating and require confirmation.
- 1 April 2026
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 15 (7) , 2676
Open AccessPrognostic Impact of Renin–Angiotensin System Inhibitors in Revascularized Patients with Acute Myocardial Infarction and Preserved or Mildly Reduced Ejection Fraction: A Retrospective Cohort Study
Background: The prognostic value of discharge renin–angiotensin–aldosterone system inhibitor (RASi) therapy in contemporary PCI-treated acute myocardial infarction (AMI) survivors with preserved or mildly reduced left ventricular ejection fraction (LVEF) remains uncertain. Methods: A retrospective cohort study of 2530 AMI patients (2019–2022) stratified by RASi use. Exclusion criteria were in-hospital mortality, LVEF < 40%, contraindications to the use of RASis or no percutaneous coronary intervention (PCI). Primary endpoints included heart failure (HF) events, recurrent acute coronary syndrome (ACS), and all-cause mortality. Kaplan–Meier analyses and inverse probability of treatment weighting (IPTW)-weighted Cox models were applied. Results: Over a mean follow-up of 49 months, discharge RASi therapy was not associated with all-cause mortality overall, but was associated with fewer HF rehospitalizations (HR 0.62, 95% CI 0.40–0.95; p = 0.03). Mortality associations differed by AMI type and hypertension status, particularly for NSTEMI (HR 0.36, 95% CI 0.14–0.91; p = 0.03; p for interaction = 0.02) and hypertension (HR 0.36, 95% CI 0.15–0.84; p = 0.02; p for interaction = 0.04). Conclusions: In this single-center observational cohort of PCI-treated AMI survivors with LVEF ≥ 40%, discharge RASi therapy was associated with fewer HF rehospitalizations but not with lower overall mortality. Exploratory subgroup analyses suggested potential heterogeneity according to NSTEMI status and hypertension, but these findings should be considered hypothesis-generating and require confirmation.
- 6 February 2026
- Published by Elsevier in Phytomedicine
- Vol. 153, 157924
Dingxin recipe Ⅲ ameliorates atherosclerosis through stard4-mediated regulation of hepatic lipid metabolism
- 6 February 2026
- Published by Elsevier in Phytomedicine
- Vol. 153, 157924
Dingxin recipe Ⅲ ameliorates atherosclerosis through stard4-mediated regulation of hepatic lipid metabolism
- Open Access
- 2 September 2025
- Published by Elsevier in Journal of Ethnopharmacology
- Vol. 354, 120525
Dingxin recipe III ameliorates endothelial cell senescence in atherosclerosis by activating the FOXO3a/PINK1/Parkin axis
- 2 September 2025
- Published by Elsevier in Journal of Ethnopharmacology
- Vol. 354, 120525
Open AccessDingxin recipe III ameliorates endothelial cell senescence in atherosclerosis by activating the FOXO3a/PINK1/Parkin axis
- Open Access
- 4 May 2023
- Published by Elsevier in Journal of Ethnopharmacology
- Vol. 314, 116532
Geniposide ameliorates atherosclerosis by regulating macrophage polarization via perivascular adipocyte-derived CXCL14
- 4 May 2023
- Published by Elsevier in Journal of Ethnopharmacology
- Vol. 314, 116532
Open AccessGeniposide ameliorates atherosclerosis by regulating macrophage polarization via perivascular adipocyte-derived CXCL14
- Open Access
- 1 March 2019
- Published by Elsevier in Immunobiology
- Vol. 224 (2) , 296-306
Geniposide regulates the miR-101/MKP-1/p38 pathway and alleviates atherosclerosis inflammatory injury in ApoE-/- mice
- 1 March 2019
- Published by Elsevier in Immunobiology
- Vol. 224 (2) , 296-306
Open AccessGeniposide regulates the miR-101/MKP-1/p38 pathway and alleviates atherosclerosis inflammatory injury in ApoE-/- mice