Publications by authors named "Lige Xiao"

Article Synopsis
  • - The study focused on understanding risk factors associated with the distal adding-on phenomenon in adolescent idiopathic scoliosis (AIS) patients specifically classified as Lenke 1A/B and 2A/B, and aimed to create a prediction model for this condition.
  • - Researchers analyzed clinical data from 119 AIS patients, assessing radiographic parameters before surgery and at the last follow-up, identifying 39 patients (32.8%) who experienced the adding-on phenomenon.
  • - A logistic regression analysis revealed five significant predictive variables, including the Risser sign, leading to the development of a reliable nomogram that can help predict the occurrence of adding-on and inform better clinical treatment strategies.
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Objectives To find out the prevalence rate of pre-myopia among primary school students in the Mianyang Science City Area, analyze its related risk factors, and thus provide a reference for local authorities to formulate policies on the prevention and control of myopia for primary school students. Methods From September to October 2021, Cluster sampling was adopted by our research group to obtain the vision levels of primary school students employing a diopter test in the Science City Area. In addition, questionnaires were distributed to help us find the risk factors associated with pre-myopia.

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Background: Adolescent idiopathic scoliosis (AIS) is a scoliotic deformity of unknown etiology that occurs during adolescent development. Abnormal bone metabolism is closely related to AIS, but the cause is uncertain. Recent studies have shown that heat shock protein 27 (HSP27) and its phosphorylation (pHSP27) play important roles in bone metabolism.

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Background: Osteopenia has been well documented in adolescent idiopathic scoliosis (AIS). Bone marrow stem cells (BMSCs) are a crucial regulator of bone homeostasis. Our previous study revealed a decreased osteogenic ability of BMSCs in AIS-related osteopenia, but the underlying mechanism of this phenomenon remains unclear.

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Background: Congenital scoliosis (CS) is a congenital deformity of the spine resulting from abnormal and asymmetrical development of vertebral bodies during pregnancy. However, the etiology and mechanism of CS remain unclear. Epigenetics is the study of heritable variations in gene expression outside of changes in nucleotide sequence.

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Background: Autogenous bone grafts, such as iliac bone or rib struts, have been used in the anterior reconstruction of spinal tuberculosis (STB) and have their own benefits and limitations. Here, we introduced a new method, the spinous process (SP), combined with a titanium mesh cage (TMC) as a bone graft in the stability reconstruction of lumbar or lumbosacral STBs. By retrospectively comparing patients who received SP+TMC to traditional TMC bone grafts or allogeneic bone grafts in terms of safety, efficacy and cost-effectiveness, we aimed to evaluate whether SP+TMC could be a possible alternative method.

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Introduction: To evaluate the effectiveness and safety of preoperative halo-femoral traction (HFT) with posterior surgical correction for the treatment of extremely severe rigid congenital scoliosis (>120°).

Methods: We reviewed the records of all patients with extremely severe rigid congenital scoliosis (>120°) treated with preoperative HFT from 2010 through 2018. Radiographic measurements were performed.

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Background: Surgical management of cervical kyphosis in patients with NF-1 is a challenging task. Presently, anterior-only (AO), posterior-only (PO) and combined anterior-posterior (AP) spinal fusion are common surgical strategies. However, the choice of surgical strategy and application of Halo traction remain controversial.

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Objective: Adolescent idiopathic scoliosis (AIS) is a relatively common spinal rotation deformity, and the pathogenesis of AIS is accompanied by metabolic dysfunction and changes in biochemical factors. In this study, plasma metabolite changes in AIS patients were analyzed based on nontargeted metabolomics to provide new insights for clarifying functional metabolic abnormalities in AIS patients.

Methods: Clinical indexes and blood samples were collected from 12 healthy subjects and 16 AIS patients.

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Objectives: To (i) introduce the deformed complex vertebral osteotomy (DCVO) technique for the treatment of severe congenital angular spinal kyphosis; (ii) evaluate the sagittal correction efficacy of the DCVO technique; and (iii) discuss the advantages and limitations of the DCVO technique.

Methods: Multiple malformed vertebrae were considered a malformed complex, and large-range and angle wedge osteotomy was performed within the complex using the DCVO technique. Patients with local kyphosis greater than 80° who were treated with DCVO and did not have tumors, infections, or a history of surgery were included.

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Study Design: Case-control study.

Objective: The aim of this study was to estimate the relationship between circulating cell-free DNA (ccf DNA) and clinical parameters of patients with congenital scoliosis (CS).

Summary Of Background Data: CS is a complex spinal deformity characteristic of congenital vertebral malformations.

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Adolescent idiopathic scoliosis (AIS) is the most common pediatric spine disorder affecting ∼3% of children worldwide. Human genetic studies suggest a complex polygenic disease model for AIS with large genetic and phenotypic heterogeneity. However, the overall genetic etiology of AIS remains poorly understood.

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Adolescent idiopathic scoliosis (AIS) is a common complex disease, and bone homeostasis plays an important role in its pathogenesis. Recent advances in epigenetic research show that dysregulated miRNAs may participate in the development of orthopedic diseases and AIS. The aim of this study was to detect differentially expressed miRNAs in severe AIS and elucidate the mechanism of miRNA deregulation in the pathogenesis of AIS.

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Article Synopsis
  • - The study explores the complex background of congenital scoliosis (CS), focusing on how abnormal DNA methylation impacts spinal development, particularly the KAT6B gene.
  • - Researchers analyzed DNA methylation levels in patients with CS, finding hypermethylation of the KAT6B gene, which correlates with the severity of scoliosis (Cobb angle) and is associated with reduced expression in chondrocytes.
  • - The findings suggest that KAT6B epigenetic modifications could contribute to the development of CS and may serve as potential biomarkers for early detection through maternal blood tests.
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Background: Osteopenia has been well documented in adolescent idiopathic scoliosis (AIS), and ghrelin has been shown to have a positive effect on bone metabolism. However, the circulating level of ghrelin is increased in AIS osteopenia, and the relationship between ghrelin and low bone mass in AIS osteopenia remains unclear.

Method: A total of 563 AIS and 281 age-matched controls were recruited for this study.

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Adolescent idiopathic scoliosis (AIS) is a severe spinal deformity that often occurs during puberty. The occurrence of AIS is suggested to be related to abnormal development of cartilage. Our previous study found increased serum ghrelin levels in AIS patients that may linked to the development of AIS.

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Article Synopsis
  • The study investigates the relationship between adiponectin levels and bone mass in adolescents with idiopathic scoliosis (AIS), finding that AIS patients have lower body mass index (BMI) and higher circulating adiponectin compared to controls.
  • Elevated levels of adiponectin and a specific genetic variant (rs7639352) were significantly linked to osteopenia in AIS patients, suggesting potential genetic and metabolic factors at play.
  • Analysis of bone microstructure revealed that the convex side of the spine in AIS had reduced bone volume and demonstrated different expression levels of bone-related proteins and inflammatory factors compared to the concave side.
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Estrogen receptor plays critical roles in osteogenesis but the underlying mechanism remains unclear. In order to determine the effect of ERα and ERβ on several critical factors in regulating osteogenesis in human osteoblasts. Cell based assy, RT-PCR and immunoblot analyses were used in the research.

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