Publications by authors named "Yupei Shen"

Gestational diabetes mellitus (GDM) poses both short-term and long-term health risks to mothers and infants. This study aims to examine the mechanisms involving insulin resistance mediated by exosomal miRNAs. We enrolled 2284 pregnant women from First People's Hospital of Kunshan, Jiangsu Province in this continuous follow-up study.

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The association between air pollution exposure and gestational diabetes mellitus (GDM) have been studied extensively; however, conclusions regarding the sensitive exposure period and effect of exposure remain inconsistent. We conducted a retrospective cohort study involving 2593 pregnant participants from Kunshan, China. Daily concentrations of particulate matter less than 2.

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This study investigated the association between handgrip strength (HGS) asymmetry and weakness with cognitive function and depressive symptoms among 920 community-dwelling adults aged above 60 years in suburban Shanghai. Participants were selected using a multistage cluster-stratified sampling approach. Assessments included HGS measured with a dynamometer, the Montreal Cognitive Assessment (MoCA) for cognition, and the Geriatric Depression Scale (GDS) for depressive symptoms.

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  • CAPG is a promising target for cancer therapy, especially in uterine corpus endometrial carcinoma (UCEC), but its role in immune response and prognosis requires further study.
  • Research involving public databases showed that higher CAPG expression correlates with poorer survival rates and is linked to immune pathways and tumor microenvironment effects.
  • Experiments revealed CAPG influences cell growth and mobility, affects ferroptosis markers, and its silencing enhances immune-related gene expression; several chemotherapy drugs were found to be effective for UCEC treatment.
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  • Scientists found a specific gene variant called SPRY4 in women who have trouble getting pregnant, which could help explain some cases of infertility.
  • They studied how this gene works in the body and found it's really important for female reproductive health.
  • Before this study, no one had linked this gene to female fertility issues, so their discovery could lead to better understanding and treatments for infertility.
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Aims: 5 mC methylation and hydroxymethylation (5hmC) are associated with Alzheimer's disease (AD). However, previous studies were limited by the absence of a 5hmC calculation. This study aims to find AD associated predictors and potential therapeutic chemicals using bioinformatics approach integrating 5 mC, 5hmC, and expression changes, and an AD mouse model.

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Disruption of iron homeostasis plays a negative role in follicle development. The dynamic changes in follicle growth are dependent on Hippo/YAP signaling and mechanical forces. However, little is known about the liaison between iron overload and the Hippo/YAP signalling pathway in term of folliculogenesis.

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  • The study investigates new plasma biomarkers for predicting gestational diabetes mellitus (GDM) by analyzing protein expression in placental tissues from pregnant women.
  • Researchers identified 123 differentially expressed proteins (DEPs) linked to various biological processes and focused on plasma levels of GAL-3BP, which were significantly higher in women with GDM compared to those with normal glucose tolerance.
  • The combination of GAL-3BP and triglycerides (TG) shows increased predictive power for diagnosing GDM early in pregnancy, with a higher accuracy than either marker alone.
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  • - This study investigates genetic risk factors linked to abnormal uterine bleeding following the insertion of a copper intrauterine device (IUD) using whole-exome sequencing and validation through Sequenom MassARRAY.
  • - Eight genetic variants were identified that could potentially cause clinical issues, with two specific variants (p.Ile971Met and p.Gly365Ser) showing a strong correlation with abnormal uterine bleeding.
  • - The results suggest these genetic variants may influence bleeding by affecting blood clotting and inflammation in the uterine lining, offering a foundation for personalized approaches in IUD implantation.
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Background: Maternal air pollutants exposure is associated with a number of adverse pregnancy outcomes, including recurrent spontaneous abortion (RSA). However, the underlying mechanisms are still unknown. The present study aimed to understand the mechanism of RSA and its relationship with air pollution exposure.

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In this study, we investigated the association between altered methylation in the maternal placenta and hyperglycaemia and explored the epigenetic mechanisms underlying gestational diabetes mellitus (GDM). Reduced representation bisulphite sequencing (RRBS) and RNA sequencing (RNA-seq) were performed on placental tissues obtained from women with GDM and healthy controls. Further, pyrosequencing, correlation analyses, and linear regression analyses were performed to valuate relationships between aberrantly methylated-differentially expressed genes and clinical parameters.

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Introduction: Increasing evidence has shown that circular RNAs (circRNAs) play vital roles in embryonic development. However, the function of circRNAs in recurrent spontaneous abortion (RSA) is largely unknown. This study aimed to investigate the expression profile of human circRNAs and their functional mechanisms in regulating RSA.

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Article Synopsis
  • - The study focused on identifying biomarkers and potential drugs for recurrent spontaneous abortion (RSA) while also examining the role of circular RNAs in RSA regulation.
  • - Researchers analyzed placental and decidual tissue samples from RSA and healthy pregnancies using advanced RNA sequencing to find abnormal gene expressions and validated findings through PCR.
  • - From the analysis, 22 circular RNAs and several other molecules linked to RSA were identified, with one particular circular RNA showing promise as a diagnostic marker and 36 chemicals proposed as potential treatments for RSA.
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Objectives: Venous thromboembolism (VTE) is a common health problem, causing considerable morbidity and mortality. The incidence of VTE is higher in pregnant women than in those who are not pregnant. However, genetic factors for VTE in pregnant women are largely unknown.

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Aim: Intrauterine device (IUD) is a commonly used contraceptive method worldwide. Abnormal uterine bleeding (AUB) is one of the most common side effects of Cu-IUDs. Since AUB varies among Cu-IUD users, changes in the bleeding-related genetic factors may contribute to AUB.

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Article Synopsis
  • Researchers conducted whole-exome sequencing on a cohort of 104 women, split into two groups: 52 controls and 52 with adverse effects from levonorgestrel (LNG) implants.
  • They identified 13 significant single nucleotide variations (SNVs) linked to integrin-mediated signaling and cell proliferation through the MassARRAY platform.
  • Two specific SNVs, rs7255721 and rs1042522, were found to cause changes in protein structure and were significantly different between the two groups, indicating potential pathogenic mutations related to adverse reactions from LNG.
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Objective: To investigate changes in the level of protein in serum and uncover the underlying pathogenesis of abnormal uterine bleeding (AUB) associated with copper intrauterine devices (Cu IUD).

Methods: Protein profiles were investigated via tandem mass tag (TMT)-based quantitative proteomics and bioinformatics technology. Quantification and characterization of candidate proteins were further performed in 33 controls and 45 cases by Luminex assay and enzyme-linked immunosorbent assay.

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This study aimed to identify epigenetic alternations of microRNAs and DNA methylation for gestational diabetes mellitus (GDM) diagnosis and treatment using in silico approach. Data of mRNA and miRNA expression microarray (GSE103552 and GSE104297) and DNA methylation data set (GSE106099) were obtained from the GEO database. Differentially expressed genes (DEGs), differentially expressed miRNAs (DEMs) and differentially methylated genes (DMGs) were obtained by limma package.

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In this study, we examined whether smoking and drinking affect sperm quality and the DNA methylation of the repetitive element , , , , and in sperm. Semen samples were obtained from 143 male residents in a minority-inhabited district of Guizhou province in southwest China. Quantitative DNA methylation analysis of the samples was performed using MassARRAY EpiTYPER assays.

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  • Ischemic stroke is a leading global cause of death and involves genetic and epigenetic factors, but the specific role of epigenetics has not been thoroughly explored.
  • Our study identified over 1,000 differentially methylated CpG sites in genes related to large-artery atherosclerotic stroke through an epigenome-wide association analysis and validated these findings in additional cohorts.
  • The results suggest that methylation changes, particularly in the MTRNR2L8 gene, are significant for stroke diagnostics and could be potential targets for future therapies.
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Purpose: Ischemic stroke (IS) is one of the most common neurologic diseases and is the main cause of death and disability in the Chinese population. This retrospective cohort study was performed to elucidate the relationship between single nucleotide polymorphisms (SNPs) in cytochrome P450 genes and the therapeutic effect of atorvastatin.

Methods: A total of 192 cases of IS were enrolled in the study.

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