15 results match your criteria: "GanZhou Women and Children's Health Care Hospital[Affiliation]"

Background: Antiretroviral drugs are essential for preventing mother-to-child transmission (MTCT) of HIV in HIV-infected pregnant women. However, ART treatment for HIV-infected pregnant women with multidrug resistance remains a major challenge. Effective and safe ART regimens for preventing MTCT should be tailored to this special population.

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Article Synopsis
  • The study investigates the genetic relationship between human gut microbiota, osteoarthritis (OA), and the impact of OA-related medications, utilizing bidirectional Mendelian randomization (MR) techniques.
  • By analyzing data from large-scale genome-wide association studies, the research identifies significant genetic associations indicating certain gut microbiota taxa increase or decrease the risk of hip and knee OA.
  • Results demonstrate that the associations remain robust even after adjusting for medication use, suggesting a potential causal link between gut microbiome composition and the risk of developing osteoarthritis.
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Objective: Neonatal sepsis is a serious disease that needs timely and immediate medical attention. So far, there is no specific prognostic biomarkers or model for dependable predict outcomes in neonatal sepsis. The aim of this study was to establish a predictive model based on readily available laboratory data to assess 30-day mortality in neonatal sepsis.

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Breast cancer ranks as the most prevalent cancer globally, surpassing lung cancer, with recurrence/metastasis to be its main account for the cancer-related mortality. MicroRNAs (miRNAs) participate critically in various physiological and pathological processes through posttranscriptional regulation of downstream genes. Our preliminary findings identified miR-338-5p, potentially linked to metastasis in breast cancer, a previously unexplored area.

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Background: Maternal depression may have negative impacts on children's behavior and mental health. Childhood food allergy is a common health issue, yet its relationship with maternal depression remains incompletely understood. This study aimed to analyze the association between children's food allergy symptoms and maternal depression through cross-sectional and cohort studies.

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Objective: To explore the plasma metabolomic characteristics of children with transfusion-dependent thalassemia (TDT), and reveal the changes of metabolic pattern in children with TDT.

Methods: 23 children with TDT who received regular blood transfusion in Ganzhou Women and Children's Health Care Hospital in 2021 were selected, and 11 healthy children who underwent physical examination during the same period were selected as the control group. The routine indexes between children with TDT and the control group were compared, and then the metabolic composition of plasma samples from children with TDT and the control group was detected by liquid chromatography-mass spectrometry.

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Background: Asthma is a common illness with chronic airway inflammation. C1q/tumor necrosis factor (TNF)-related protein 3 (CTRP3) plays a vital role ininflammatory response, but its effect on asthma is imprecise. Herein, we analyzed the functions of CTRP3 in asthma.

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Background: Breast cancer (BC) is the leading cause of cancer-related death among women. One of the hallmarks of cancer is sustained angiogenesis. YAP/STAT3 may promote angiogenesis and driving BC progression.

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Cisplatin (DDP) is widely used in the chemotherapy of cervical cancer (CC), the fourth most common female malignancy worldwide. However, some patients progress to chemotherapy resistance, which leads to chemotherapy failure, tumor recurrence, and poor prognosis. Therefore, strategies to identify the regulatory mechanisms underlying CC development and increase tumor sensitivity to DDP will help improve patient survival.

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Background: Complex febrile seizures are prolonged and can cause neurologic abnormalities, leading to secondary epilepsy and affecting growth and development. At present, the mechanism of secondary epilepsy in children with complex febrile seizures is not clear, and this study aimed to explore the risk factors for secondary epilepsy in children with complex febrile seizures and analyze its effects on the growth and development of children.

Methods: The data of 168 children with complex febrile seizures admitted to the Ganzhou Women and Children's Health Care Hospital between January 2018 and December 2019 were collected retrospectively and divided into a secondary epilepsy group (n=58) and control group (n=110) according to whether the children had secondary epilepsy or not.

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circPLOD2 knockdown suppresses endometriosis progression via the miR-216a-5p/ZEB1 axis.

Reprod Biol

June 2023

Department of Ultrasound, Ganzhou Women and Children's Health Care Hospital, No. 106 Dagong Road, Ganzhou, Jiangxi 341000, China. Electronic address:

The present study aimed to identify the role of circPLOD2 in endometriosis and its underlying mechanisms. We determined circPLOD2 and miR-216a-5p expression in ectopic endometrial (EC) and eutopic endometrial (EU) samples as well as in endometrial samples from uterine fibroids of ectopic patients (EN) and embryonic stem cells (ESCs) using qRT-PCR. The association between circPLOD2 and miR-216a-5p or miR-216a-5p and zinc finger E-box binding homeobox 1 (ZEB1) expression was analyzed using Starbase, TargetScan, and dual-luciferase reporter gene assays.

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Expansion of the mutation spectrum and phenotype of -related neurodevelopmental disorder.

Front Mol Neurosci

November 2022

Department of Medical Genetics, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, People's Hospital of Henan University, Zhengzhou, China.

Article Synopsis
  • - Hao-fountain syndrome (HAFOUS) is a genetic neurodevelopmental disorder marked by severe language and developmental delays, behavioral issues (including autism), and mild intellectual impairment, caused by mutations in the gene located on chromosome 16p13.2.
  • - In this study, researchers described three unrelated patients with novel gene variants identified through trio-whole exome sequencing, which were confirmed via Sanger sequencing. These variants included one frameshift and two missense mutations.
  • - The predominant clinical features among the patients included developmental delays, language impairment, behavioral abnormalities, and various brain imaging anomalies, with facial abnormalities in some cases, expanding the knowledge of HAFOUS and its genetic mutation spectrum.
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GLDC mitigated by miR-30e regulates cell proliferation and tumor immune infiltration in TNBC.

Front Immunol

October 2022

Eye Institute, Eye & Ear, Nose, and Throat (ENT) Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Article Synopsis
  • TNBC (Triple-Negative Breast Cancer) has a poorer prognosis and lacks specific targeted therapies, making it important to identify key regulatory factors for its progression.
  • Analysis of TNBC samples showed that GLDC, an enzyme in the glycine cleavage system, is up-regulated and associated with worse outcomes, with its expression correlating with immune cell types.
  • Modulating GLDC levels affects TNBC cell proliferation, and the microRNA miR-30e inhibits this proliferation by targeting GLDC, suggesting a potential therapeutic pathway for treatment.
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Developmental and epileptic encephalopathies (DEE) caused by heterozygous deleterious variants in Cut Like Homeobox2 () is rare. To the best of our knowledge the only variant associated with a phenotype in this gene is the missense variant c.1768G > A, p.

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