Publications by authors named "Yang Yi-Ning"

Metabolic syndrome (MetS) is a collection of metabolic abnormalities including insulin resistance, atherogenic dyslipidemia, central obesity, and hypertension. Recently, long noncoding RNAs (lncRNAs) have emerged as pivotal regulators of metabolic balance, influencing the genes associated with MetS. Although the prevalence of insulin resistance is rising, leading to an increased risk of type 2 diabetes mellitus (T2DM) and its vascular complications, there is still a notable gap in understanding the role of lncRNAs in the context of clinical diabetes.

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Lipid droplets (LDs) serve as crucial hubs for lipid trafficking and metabolic regulation through their numerous interactions with various organelles. While the interplay between LDs and the Golgi apparatus has been recognized, their roles and underlying mechanisms remain poorly understood. Here, we reveal the role of Ras-related protein Rab-2A (Rab2A) in mediating LD-Golgi interactions, thereby contributing to very-low-density lipoprotein (VLDL) lipidation and secretion in hepatocytes.

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Objectives: Aortic valve sclerosis has been proposed to signify greater cardiovascular risk; the correlation between serum trace elements and aortic valve sclerosis has been reported. Therefore, an in-depth exploration of the risk factors for aortic valve sclerosis and early intervention may reduce the risk of cardiovascular disease.

Methods: In this study, Patients with aortic valve sclerosis and non-aortic valve sclerosis who underwent echocardiographic diagnosis in the People's Hospital of Xinjiang Uygur Autonomous Region during the period from 2019 to 2021 were selected for this study.

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Objective: This study aims to investigate the prevalence of dyslipidemia and assess the joint association of physical activity (PA) and diet quality on dyslipidemia risk in urban areas of Xinjiang.

Methods: Conducted from July 2019 to September 2021 in Xinjiang, China, this cross-sectional study involved 11,855 participants (mean age 47.1 ± 9.

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Article Synopsis
  • * Researchers discovered that the low density lipoprotein receptor (LDLR) is crucial for CCHFV entry into cells, as its absence significantly decreases infection rates in various cell types.
  • * Targeting LDLR, either by gene knockout or use of blocking antibodies, shows promise for reducing viral loads and death in mice, suggesting potential strategies for preventing and treating CCHFV infections.
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Background: The impact of left ventricular mechanical dyssynchrony (LVMD) on the long-term prognosis of ST-segment elevation myocardial infarction (STEMI) is unclear.

Hypothesis: MR uniformity ratio estimates (URE) can detect LVMD and assess STEMI prognosis.

Study Type: Retrospective analysis of a prospective multicenter registry (EARLY-MYO trial, NCT03768453).

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Purpose: We investigated the hypothesis that MHR (monocyte-to-high density lipoprotein cholesterol ratio) is related to the severity of coronary artery in ACS (acute coronary syndrome).

Methods: In this case-control study, we recruited 15,853 participants undergoing the first time percutaneous coronary intervention (PCI) including 4093 normal controls, 10,518 chronic coronary artery disease (CAD), and 1242 ACS cases. Examination of demographic clinical data and biochemical profiles, as well as MHR values, were performed before PCI.

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Background: The prognostic role of diastolic dysfunction measured by the circumferential peak early diastolic strain rate (PEDSR) on ST-elevation myocardial infarction (STEMI) is not completely established.

Objectives: We aimed to investigate the prognostic value of diastolic function by measuring PEDSR within 1 week after STEMI.

Methods: The cardiac magnetic resonance (CMR) pictures of 420 subjects from a clinical registry study (NCT03768453) were analyzed and the composite major adverse cardiac events (MACEs) were followed up.

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The introduction of the collectivized school management mode marks a turning point for teacher exchange, however, it also brings numerous challenges. Whether or not breakthroughs can be achieved in teacher exchange hinges on the outcome of stakeholder negotiations. This study employs a qualitative approach through case analysis.

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Background: The prognostic value of coronary artery calcium (CAC) combined with risk factor burdens in middle-aged and elderly patients with symptoms is unclear.

Methods: A cohort study comprising 7432 middle-aged and elderly symptomatic patients (aged above 55 years) was conducted between December 2013 and September 2020. All patients had undergone coronary computed tomography angiography, and the Agatston score were used to measure CAC scores.

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Objective: To investigate the possible association between AT1R gene polymorphisms and major adverse cardiovascular and cerebrovascular events (MACCEs) in hypertension patients combined with or without coronary artery disease (CAD) in Xinjiang.

Methods: 374 CAD patients and 341 non-CAD individuals were enrolled as study participants and all of them have a hypertension diagnosis. AT1R gene polymorphisms were genotyped by SNPscan™ typing assays.

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Objective: The aim of this work was to evaluate the predictive value of FAR combined with CACS for MACCEs.

Background: The fibrinogen-albumin-ratio (FAR), a novel biomarker of inflammation, is associated with the severity of coronary artery disease (CAD). Coronary calcification score (CACS) is associated with the severity of coronary stenosis and is closely related to the prognosis of CAD patients.

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Coronary artery disease (CAD) is a the most common type of heart disease, and is associated with the highest mortality rate. The role of the β-adrenergic receptor gene () in energy homeostasis and lipolysis suggests that it may be associated with obesity, insulin resistance, diabetes, and hypertension. Herein, we sought to examine the relationship between CAD and variants of the gene in individuals with Han and Uygur ethnicities in China.

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Article Synopsis
  • Coronary heart disease is a major health issue in developed countries, with dyslipidemia being a key risk factor linked to genetic regulation of lipid metabolism.
  • This study focuses on the association between DNA methylation levels of specific genes and the risk of dyslipidemia, using samples from hyperlipidemia patients and control groups.
  • Results indicate that higher DNA methylation in certain genes correlates with increased dyslipidemia risk, suggesting that DNA methylation could be a target for future research and potential treatment strategies.
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Background: Diabetes can increase the risk of coronary heart disease, and also increase the mortality rate of coronary heart disease in diabetic patients. Although reperfusion therapy can preserve the viable myocardium, fatal reperfusion injury can also occur. Studies have shown that diabetes can aggravate myocardial ischemia-reperfusion injury, ERK1/2 can reduce myocardial ischemia-reperfusion injury, but its mechanism in hyperglycemic myocardial ischemia-reperfusion injury is unclear.

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Objectives: The aim of this study was to examine the independent and joint associations of baseline coronary artery calcium score (CACS) and cystatin C (Cys-C) with the risk of major adverse cardiac and cerebrovascular events (MACCEs) and all-cause death in symptomatic populations.

Methods: The study included 7140 patients with symptom of chest pain who underwent cardiac computerized tomography examinations to measure CACS. All of them had serum Cys-C results.

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Article Synopsis
  • Endothelial apoptosis is a key factor in atherosclerotic cardiovascular diseases like coronary artery disease (CAD), and understanding its molecular mechanisms is crucial for treatment.
  • The study identifies the -94 ATTG ins/del mutant (rs28362491) as a risk factor for CAD, linking it to higher chances of major adverse cardiac and cerebrovascular events (MACCEs) in patients.
  • Mutant human umbilical vein endothelial cells (DD-mutant HUVECs) showed increased susceptibility to apoptosis and mitochondrial dysfunction, indicating that the DD genotype may lead to worse long-term outcomes for CAD patients.
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  • Metabolic syndrome (MetS) significantly increases the risk of major adverse cardiovascular events (MACCE) in patients who have suffered a ST elevation myocardial infarction (STEMI) and undergone emergency PCI.
  • The study found that higher levels of macrophage migration inhibitory factor (MIF) at admission are associated with a greater incidence of MACCE, particularly in patients with MetS.
  • MIF levels greater than or equal to 143 ng/ml were identified as a strong predictor of long-term adverse outcomes in STEMI patients with MetS, outperforming other traditional risk factors.
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Background: Platelet-related parameters and HDL-C have been regarded as reliable and alternative markers of coronary heart disease (CHD) and the independent predictors of cardiovascular outcomes. PDW is a simple platelet index, which increases during platelet activation. Whether the PDW/HDL-C ratio predicts major adverse cardiovascular and cerebrovascular events (MACCEs) in patients who complained of chest pain and confirmed coronary artery calcification remains to be investigated.

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Background: Several studies have reported that NFKB1 gene rs28362491 polymorphism was associated with susceptibility to coronary heart disease in populations of different genetic backgrounds. To date, there have been no studies on the association between NFKB1 gene rs28362491 polymorphism and the occurrence of major adverse cardiac and cerebrovascular event (MACCE). The present study was to explore the relationship between NFKB1 gene rs28362491 polymorphism and MACCEs to investigate whether identifying NFKB1 gene polymorphism is beneficial to evaluating MACCE risks and patients' prognoses.

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Background: To explore possible associations between glucose transporter 4 (GLUT4) genetic polymorphisms in the patients with coronary heart disease (CHD) in Han and Uygur Chinese populations in Xinjiang, China.

Methods: Two GLUT4 polymorphisms (rs5418 and rs5435) were genotyped in 1262 Han (628 CHD patients and 634 healthy controls) and 896 Uyghur (397 CHD patients and 499 healthy controls) Chinese populations.

Results: In the Han Chinese population, there were no significant differences in allelic or genotypic distribution of rs5418 and rs5435 between the CHD and control groups (all P > 0.

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Article Synopsis
  • The study investigates the relationship between the MALAT1 gene polymorphism (specifically rs3200401) and major adverse cardiac and cerebrovascular events (MACCEs) in myocardial infarction patients.
  • Findings showed that patients with the T allele and CT+TT genotypes had significantly higher occurrences of MACCEs compared to those without, indicating a potential genetic risk factor for these events.
  • However, this association was not present in control participants, suggesting that the relationship may be specific to individuals with conditions like myocardial infarction rather than the general population.
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Article Synopsis
  • Genetic variation in the macrophage migration inhibitory factor gene (specifically, the rs2070766 polymorphism) is linked to an increased risk of acute coronary syndromes (ACS) in a Chinese population.
  • In a study involving 963 ACS patients and 932 controls, individuals with the GG genotype had a 1.7 times higher risk of ACS compared to those with CC or CG genotypes.
  • A nomogram model incorporating genetic variations and clinical factors was developed, showing strong predictive ability for ACS risk and indicating that GG carriers experienced worse clinical outcomes.
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