1,565 results match your criteria: "Children's hospital of Soochow University[Affiliation]"

Early immune reconstitution, particularly of natural killer (NK) cells with strong graft-versus-leukemia effects, is crucial for the prognosis of patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). This retrospective study examined 122 pediatric patients with acute lymphoblastic leukemia (ALL) or acute myeloid leukemia (AML) who underwent T-cell replete allo-HSCT at the Children's Hospital of Soochow University from 2019 to 2021. Peripheral blood lymphocyte counts on days 30 and 60 post-transplant were analyzed, focusing on NK cell recovery and its impact on overall survival (OS), relapse-free survival (RFS), non-relapse mortality (NRM), relapse, graft-versus-host disease, and CMV reactivation.

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Ultrasonographic characteristics of neonatal appendicitis: a case series.

BMC Pediatr

November 2024

General Surgery Department, Children's Hospital of Soochow University, NO.92, Zhongnan Road, Soochow, 215025, Jiangsu, China.

Background: Neonatal appendicitis is a rare but critical condition that presents diagnostic challenges due to its nonspecific symptoms and clinical manifestations. Early and accurate diagnosis is crucial for reducing the high mortality rates associated with this condition. Abdominal ultrasonography plays a pivotal role in identifying characteristic signs of appendicitis in neonates.

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Introduction: There are few reports of severe hematological involvement in children with neonatal lupus erythematosus (NLE) treated with exchange transfusion. In this case report, we present a female patient with NLE admitted to the Children's Hospital of Soochow University. The main clinical manifestations were pancytopenia and congenital heart block (CHB).

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Background: Correctly diagnosing and accurately distinguishing mycoplasma pneumonia in children has consistently posed a challenge in clinical practice, as it can directly impact the prognosis of affected children. To address this issue, we analyzed chest X-rays (CXR) using various deep learning models to diagnose pediatric mycoplasma pneumonia.

Methods: We collected 578 cases of children with mycoplasma infection and 191 cases of children with virus infection, with available CXR sets.

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Article Synopsis
  • The study explores the role of Manic Fringe (MFNG) in heart valve development, specifically its involvement in the endothelial-to-mesenchymal transition (EndMT) process, which is crucial for forming heart valves.
  • Researchers found that MFNG promotes EndMT by enhancing the Notch signaling pathway, and its loss leads to abnormal heart and valve development in zebrafish models.
  • A mutation in the MFNG gene was identified in patients with congenital heart defects, confirming that MFNG is vital in the development of heart valve malformations and may serve as a target for future diagnosis and treatments.
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Height prediction of individuals with osteogenesis imperfecta by machine learning.

Orphanet J Rare Dis

November 2024

Department of Orthopedics, International Science and Technology Cooperation Base of Spinal Cord Injury, Tianjin Key Laboratory of Spine and Spinal Cord Injury, Tianjin Medical University General Hospital, Tianjin, China.

Background: Osteogenesis imperfecta (OI) is a genetic disorder characterized by low bone mass, bone fragility and short stature. There is a significant gap in knowledge regarding the growth patterns across different types of OI, and the prediction of height in individuals with OI was not adequately addressed. In this study, we described the growth patterns and predicted the height of individuals with OI employing multiple machine learning (ML) models.

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Purpose: Acute lower respiratory tract infections (ALRIs) is a leading cause of child mortality worldwide. Metagenomic next-generation sequencing (mNGS) identifies ALRIs pathogens and explores the lung microbiota's role in disease severity and clinical outcomes. This study examines the association between lung microbiota and ALRIs outcomes in children, exploring its potential as a prognostic biomarker.

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Three-dimensional (3D) organotypic skin in vitro has attracted increasing attention for drug development, cosmetics evaluation, and even clinical applications. However, the severe contraction of these models restricts their application, especially in the analyses based on barrier functions such as percutaneous penetration. For the full-thickness skin equivalents, the mechanical properties of the dermis scaffold plays an important role in the contraction resistance.

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Backgrounds And Aims: Our previous study (CCCG-BNHL-2015) reported the treatment strategies and outcomes of pediatric B-cell non-Hodgkin's lymphoma (B-NHL) in China which showed that children in low-risk groups already have a dramatically favorable prognosis. However, for high-risk groups, the prognosis still needs to be improved. In this study, we aimed to identify the factors influencing prognosis in high-risk groups (stage III and stage IV).

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Despite significant advances in the diagnosis and treatment of colorectal cancer (CRC), the prognosis for late-stage patients remains poor, highlighting the urgent need for new preventive and therapeutic strategies. Recent studies have focused on the ketogenic diet (KD) and its metabolite, β-hydroxybutyrate (BHB), for their tumor-suppressive effects and modulation of inflammatory responses. Using the azoxymethane (AOM) / dextran sulfate sodium (DSS)-induced mouse CRC model, we found that the ketogenic diet and BHB inhibit pro-tumor N2-type tumor-associated neutrophils (TANs) while promoting the polarization of TANs towards the anti-tumor N1 type.

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Introduction: Transforming acidic coiled-coil containing protein 3 (TACC3) exerts a vital role in cancer progression by modulating cell division and facilitating tumor growth. Given the lack of comprehensive research on the pancancer implications of TACC3, our study aimed to analyze the functional role of TACC3 in pancancer and validate it through experimental investigations in lung adenocarcinoma.

Methods: We first employed various bioinformatics techniques to investigate the expression and prognostic significance of TACC3 in pancancer.

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PD-1 immunology in the kidneys: a growing relationship.

Front Immunol

November 2024

Department of Nephrology and Immunology, Children's Hospital of Soochow University, Suzhou, Jiangsu, China.

Article Synopsis
  • Recent advancements in immunotherapy are focusing on the immune regulation of disorders like cancer, with special emphasis on the PD-1 pathway.
  • The PD-1 pathway plays a vital role in maintaining immune tolerance and balance, especially in tumor environments and autoimmune diseases.
  • This review discusses the role of PD-1 immunology in various kidney conditions, including cancer, kidney diseases, and effects related to PD-1 immunotherapy.
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Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in children. Previous studies have shown that children with ADHD have impaired processing of emotional stimuli, but it is unclear whether their ability to integrate multimodal emotional stimuli is impaired and at which processing pathway this impairment exists. The present study investigated the ability of children with ADHD to integrate emotional audiovisual stimuli under different emotional conditions, and the effect of audiovisual integration on IOR to reveal the impaired processing pathway of their emotional audiovisual integration.

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Identifying Typologies of Symptoms and Functional Impairments in Chinese Children With Leukemia and Their Population Characteristics: A Latent Profile Analysis.

Cancer Nurs

November 2024

Author Affiliations: School of Nursing, Naval Medical University (Dr Wang and Mr Bi); School of Nursing, Fudan University (Ms X. Wu and Drs Zhang and Yuan); Department of Nursing, Children's Hospital of Fudan University (Ms Y. W. Wang); and Department of Hematology & Oncology, Children's Hospital of Fudan University (Ms Yu), Shanghai, China; Department of Hematology, Children's Hospital of Soochow University, Suzhou, Jiangsu (Mss H. Wu and Yang); Department of Hematology, Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong (Ms Huang); and Department of Hematology, Children's Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang (Ms Y. Q. Wang), China.

Background: Symptom distress and functional impairments in children with leukemia directly affect their quality of life.

Objectives: To identify subgroups of symptom distress and functional impairments in Chinese children with leukemia and to examine the associations of the latent classes with individual characteristics.

Methods: This multicenter cross-sectional survey study recruited children with leukemia who received chemotherapy in 4 hospitals in Shanghai, Jiangsu, Zhejiang, and Guangdong Province.

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Systemic inflammation markers and the prevalence of hypertension in 8- to 17-year-old children and adolescents: A NHANES cross-sectional study.

Nutr Metab Cardiovasc Dis

September 2024

Department of Pediatrics, The Second Affiliated Hospital of Nantong University, Nantong First People's Hospital, China. Electronic address:

Article Synopsis
  • - This research examined the link between systemic inflammation markers and hypertension in U.S. children and adolescents aged 8 to 17, using data from over 6,000 participants obtained from the NHANES survey between 1999 and 2020.
  • - The study found that higher levels of the systemic immune-inflammation index (SII), neutrophil-to-lymphocyte ratio (NLR), and platelet-to-lymphocyte ratio (PLR) were associated with an increased likelihood of developing hypertension, while the lymphocyte-to-monocyte ratio (LMR) showed a negative correlation.
  • - The findings suggest that systemic inflammatory markers could serve as important risk indicators for hypertension, especially in male youth, indicating a need
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Role of mir-32-3p in the diagnosis and risk assessment of osteoporotic fractures.

J Orthop Surg Res

November 2024

Department of Rehabilitation, The Affiliated Hospital of Youjiang Medical University for Nationalities, No.18, Zhongshan 2nd Road, Baise, Guangxi Zhuang Autonomous Region, 533000, China.

Background: Osteoporotic fractures (OPF) are fractures that occur with low-energy injuries or during daily activities, representing a serious consequence of osteoporosis (OP). With the worsening of population aging, the number of OPF patients continues to expand, causing a significant burden on families and society. Consequently, it is significant to diagnose and analyze OPF at the molecular level.

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Article Synopsis
  • This study explores the trends in respiratory infections among children in Suzhou, China, from 2016 to 2023, focusing on how these trends evolved through different pandemic phases.
  • It analyzed data from over 113,000 patients and found that the positive detection rates of infections dropped during the pandemic but increased significantly afterward, particularly among children aged 6 and older.
  • Genetic testing of pneumonia cases revealed high rates of macrolide resistance, with 97.3% of samples showing mutations, highlighting the need for informed clinical diagnosis and treatment strategies.
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New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.

BMC Med Genomics

October 2024

McKusick-Zhang Center for Genetic Medicine, State Key Laboratory for Complex Severe and Rare Diseases, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing, 100005, China.

Article Synopsis
  • Synpolydactyly (SPD) is primarily linked to mutations in the HOXD13 gene, specifically through polyalanine expansions, and the study aims to clarify the involved cell types and signaling pathways.
  • The research employed weighted gene co-expression network analysis on single-cell RNA sequencing data from limb bud cells in a mouse model harboring HOXD13 mutations.
  • Results indicated that these mutations affect immune response, osteoclast differentiation, and DNA replication, with specific genes (Bmp4, Hand2, Hoxd12, among others) identified as significant contributors to SPD, enhancing our knowledge of limb development.
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[Clinical features and risk factors of cholestasis in small for gestational age preterm infants].

Zhongguo Dang Dai Er Ke Za Zhi

October 2024

Department of Neonatology, Children's Hospital of Soochow University, Suzhou, Jiangsu 215025, China.

Objectives: To investigate the clinical features and risk factors of cholestasis in small for gestational age (SGA) preterm infants.

Methods: This study selected SGA preterm infants born at less than 37 weeks of gestation and admitted to the Department of Neonatology, Children's Hospital of Soochow Universitywithin 24 hours after birth. The infants were divided into two groups: a cholestasis group and a non-cholestasis group.

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Article Synopsis
  • The study aims to create a predictive model using clinical, radiomic, and deep learning features from X-ray and MRI to identify early risk factors for femoral head deformity in Legg-Calvé-Perthes disease (LCPD).
  • Involving 152 patients diagnosed with early unilateral LCPD, various machine learning methods (like XGBoost, which performed best) were used to develop predictive models, with the combined model showing the highest area under the ROC curve (AUC) at 0.853.
  • The results indicate that the integrated Clinic + Rad + DL model could help clinicians better assess the risk of early deformity in LCPD, leading to more personalized treatment strategies.
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Article Synopsis
  • Super enhancers (SEs) are essential for cell identity and can activate oncogenes in cancer, particularly in T-cell acute lymphoblastic leukemia (T-ALL).
  • A new SE has been found in T-ALL that regulates the gene IRF2BP2, influenced by key transcription factors like ERG and ELF1.
  • While IRF2BP2 does not significantly affect normal T cell development, it is vital for T-ALL cell growth and survival, implicating it as a potential target for treatment options.
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The association of enteral micronutrient supplementation and the neurodevelopmental outcomes of preterm or low birth weight (LBW) infants is controversial. This research was prospectively registered (CRD42023454034). We searched MEDLINE, Embase, PsycInfo, ClinicalTrials.

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Walking pace is a protective factor for rheumatoid arthritis: a mendelian randomization study.

Sci Rep

October 2024

Department of Orthopaedics, The Fourth Affiliated Hospital of Soochow University, Suzhou Dushu Lake Hospital, Medical Center of Soochow University, Suzhou, 215000, Jiangsu, P.R. China.

Walking pace is a simple and functional form of exercise and a strong predictor of health, but little is known about its causal association with rheumatoid arthritis. This study aimed to investigate the causal effect of WP on the developing RA using Mendelian randomization analysis. The genetic variation associated with WP was selected as an instrumental variable from the latest genome-wide association studies.

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Neuroblastoma (NB) is a rare and malignant pediatric solid tumor. Due to its heterogeneity, it poses significant challenges for treatment, resulting in a high mortality rate. This study aimed to identify new therapeutic drugs by modeling the TrkB receptor from PDB 4AT5 and conducting virtual screening of compounds from the YaTCM database (containing 47,696 compounds derived from 6220 Traditional Chinese Medicines).

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Article Synopsis
  • KMT2A rearrangements are common in acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL), leading to aggressive forms of leukemia with poor treatment responses.
  • This review consolidates research on KMT2A-r leukemia, covering its genetic traits, cytogenetics, clinical presentation, and potential treatment targets.
  • Future research focuses on understanding the biology of KMT2A-r leukemia and developing personalized, innovative therapies to improve patient outcomes.
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