Publications by authors named "Yeung Hiu-Yan"

Objective: To examine the literature for current evidence on the dietary management of neurogenic bowel in adults with spinal cord injuries (SCIs).

Background: Neurogenic bowel dysfunction presenting as faecal incontinence or constipation is a common occurrence in individuals with SCI. It poses numerous challenges for the management of bowel function and has a significant impact on quality of life following SCI.

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Abnormalities in the melatonin signaling pathway and the involvement of melatonin receptor MT2 have been reported in patients with adolescent idiopathic scoliosis (AIS). Whether these abnormalities were involved in the systemic abnormal skeletal growth in AIS during the peripubertal period remain unknown. In this cross-sectional case-control study, growth plate chondrocytes (GPCs) were cultured from twenty AIS and ten normal control subjects.

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Background Context: Adolescent idiopathic scoliosis (AIS) is associated with low bone mass that could persist into early adulthood and is an important prognostic factor for curve progression. Previous studies were confined to areal bone mineral density measurement that was a two-dimensional investigation for a three-dimensional structure. Evaluation of volumetric BMD (vBMD) and other bone quality parameters are important for gaining in-depth understanding of the etiopathogenesis of AIS.

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Article Synopsis
  • The study investigates the role of melatonin signaling, specifically the MT2 receptor, in adolescent idiopathic scoliosis (AIS).
  • Findings reveal that AIS girls have significantly lower protein and mRNA expression of the MT2 receptor compared to normal controls, while MT1 expression remains unchanged.
  • Lower MT2 expression in AIS girls correlates with longer arm span, suggesting a link between melatonin signaling and abnormal skeletal growth patterns in these individuals.
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Adolescent idiopathic scoliosis (AIS) is prevalent among adolescents and can carry significant morbidities. We evaluated the use of quantitative ultrasound (QUS) for predicting curve progression in patients with AIS. We recruited 294 girls with AIS at a mean age of 13.

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Study Design: A cross-sectional and prospective longitudinal study on the anthropometric parameters and growth pattern of girls with adolescent idiopathic scoliosis (AIS).

Objective: To investigate the growth pattern of girls with AIS with different severities, using cross-sectional and prospective longitudinal data set in comparison with age-matched healthy controls.

Summary Of Background Data: AIS occurs in children during their pubertal growth spurt.

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Article Synopsis
  • Recent studies suggest that adolescent idiopathic scoliosis (AIS) has a multifactorial genetic basis, but the specific heritability has not been thoroughly researched.
  • A genetic epidemiology study involving 415 Chinese female patients and their first-degree relatives found a 17.7% recurrence risk of scoliosis among siblings, with higher rates for female siblings.
  • The study estimated the heritability of AIS to be 87.5%, reinforcing the idea of a strong genetic influence on the condition and marking a significant contribution to understanding its genetic factors in the Asian population.
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Study Design: This was a cross-sectional study.

Objective: The present study aimed to explore the differences in leptin bioavailability between adolescent idiopathic scoliosis (AIS) and healthy age-matched girls in a Chinese Han population.

Summary Of Background Data: AIS is a common spinal deformity mainly occurring in girls during the peripubertal period.

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  • The study investigates the impact of low-intensity pulsed ultrasound (LIPUS) on spinal fusion in rabbits using a bioceramic scaffold and mesenchymal stem cells (MSCs) instead of traditional bone grafts.
  • The experiment revealed that LIPUS significantly improved spinal fusion rates and bone formation, with 86% success in the LIPUS group compared to 0% and 14% in the other groups.
  • Findings suggest LIPUS enhances the integration and amount of new bone formed around the bioceramic implants, highlighting its potential as a beneficial technique in spinal surgery.
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Article Synopsis
  • The study is a case-control analysis that compares bone quality in girls with Adolescent Idiopathic Scoliosis (AIS) to age-matched normal controls using quantitative ultrasound (QUS) and traditional bone mineral density (BMD) measurements.
  • Results indicated that AIS subjects had significantly lower BMD, broadband ultrasound attenuation (BUA), velocity of sound (VOS), and stiffness index (SI) compared to controls, suggesting compromised bone quality in the AIS group.
  • The findings highlight that even after adjusting for factors like maturity and body measurements, AIS girls exhibited notable deficits in bone quality, confirming a potential risk for skeletal issues associated with AIS.
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Background: Despite considerable advances in the past few decades, there is no generally accepted "top theory or theories" of the etiology of adolescent idiopathic scoliosis (AIS). This article aims to provide an overview of the current main hypothetical "concepts" on the etiopathogenesis of AIS.

Methods: An extensive literature review on hypothetical concepts on the etiology and etiopathogenesis of AIS.

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Abnormal anthropometric measurements during the peripubertal growth spurt have been documented in adolescent idiopathic scoliosis (AIS). Magnetic resonance (MR) imaging studies of the spine have suggested a disproportionate endochondral and membranous ossification in AIS. The present study aimed at investigating whether disproportional ossification and skeletal growth occurred in the peripheral bone of AIS patients using the radius as the target bone.

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Objectives: To evaluate and compare thoracic vertebrae morphology between patients with idiopathic and normal adolescents through MRI.

Methods: Two-dimensional sagittal MRI of the spine was performed in 10 normal adolescent, 10 patients with mild idiopathic thoracic scoliosis (Cobb angle 15 degrees - 39 degrees ) and 10 patients with moderate thoracic scoliosis (Cobb angle 40 degrees - 75 degrees ), all of them were female and between 13 - 14 years old. Sagittal imaging was reconstructed on image working station (Easy Vision, Philips Medical Systems, Best, Netherlands).

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Objective: To investigate the microstructure of trabecular bone in adolescent idiopathic scoliosis (AIS) and age-matched congenital scoliosis (CS), and to evaluate the bone mineral status of CS patients compared with normal controls and AIS patients.

Methods: This study included 15 AIS and 16 CS female patients and 35 healthy female adolescents. Corrective surgery was indicated for the AIS and CS patients, from whom iliac crest biopsies were collected during autograft harvesting, and scanned by micro-computer tomography.

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Article Synopsis
  • The study aimed to investigate the association between the MTNR1A gene and adolescent idiopathic scoliosis (AIS) to see if genetic variations affect susceptibility or severity of the condition.
  • Previous research suggested melatonin pathways might play a role in AIS, sparking interest in the MTNR1A gene after findings about the MTNR1B gene's involvement.
  • The results indicated no significant differences in genotype and allele frequencies between AIS patients and controls, suggesting that MTNR1A gene polymorphisms do not impact the occurrence or severity of AIS.
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  • The study aimed to examine the link between the MTNR1A gene promoter polymorphism (rs2119882) and adolescent idiopathic scoliosis (AIS).
  • Researchers analyzed data from 226 AIS patients and 277 control subjects, using PCR-RFLP for genotyping.
  • The findings revealed no significant association between the MTNR1A gene polymorphism and the occurrence or severity of scoliosis in the AIS patients.
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  • The study investigates the connection between polymorphisms in the melatonin receptor 1B (MTNR1B) gene and the predisposition and severity of adolescent idiopathic scoliosis (AIS), using genetic variations identified from the International Hapmap project.
  • A two-stage case-control analysis was conducted, including an initial screening of 472 AIS cases and 304 controls, followed by a replication test with 342 cases and 347 controls, leading to a significant association between the rs4753426 SNP and AIS.
  • Findings indicate that certain MTNR1B gene polymorphisms are linked to AIS risk but do not appear to affect the severity of spinal curvature in affected individuals.
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Although the exact etiology of adolescent idiopathic scoliosis is still undefined, genetic factors play an important role. Some patients have familial genetic disease that appears to have an autosomal dominant pattern. Linkage studies of these families revealed multiple potential genetic loci that may predispose individuals to the condition.

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Although the etiology of scoliosis is multifactorial, genetic factors play an important role. Recent linkage studies on familial idiopathic scoliosis revealed multiple putative predisposition loci. A genetic association study is complementary to linkage studies in defining the genetic basis of complex traits of diseases like idiopathic scoliosis.

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Background: Previous studies have suggested that the relative anterior spinal overgrowth may play an important role in the etiopathogenesis of spinal deformity in adolescent idiopathic scoliosis (AIS). Little is known about the histomorphometry of the anterior and posterior spinal growth plates.

Methods: In the present study, the growth plates from the anterior and posterior column of the spine of the AIS (n = 9) and the congenital scoliosis (CS; n = 9) were harvested intraoperatively.

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Study Design: A genetic association study of estrogen receptor-[alpha] gene (ESR1) with adolescent idiopathic scoliosis (AIS) in Chinese.

Objectives: To investigate whether: 1) PvuII and XbaI polymorphisms in ESR1 are predisposition factor for AIS and 2) these polymorphisms correlate with the severity of curvature in AIS.

Summary Of Background Data: A common single nucleotide polymorphism (SNP) in ESR1 (XbaI) was found to be associated with curve severity in Japanese AIS patients recently.

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Porous bioceramics have been widely investigated in orthopaedic tissue engineering. Attention has been given to manufacturing of a porous bioceramic that mimics the trabecular bone structure for proper bone regeneration. With the advance of biomedical imaging through microcomputed tomography (microCT), this study attempted to quantify the pore structure of different bioceramics.

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Objective: To evaluate the trabecular bone micro-structure from different sites of spine in adolescent idiopathic scoliosis patients. The target site consisted of the bilateral facet joints from apical vertebrae and from end vertebrae.

Methods: Nine AIS patients with mean age 14.

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This study investigated a phytoestrogen-rich herb formula, Xianlinggubao (XLGB) (including genistein 510 microg/g and daidzein 2500 microg/g), concerning prevention of OVX-induced deterioration of musculoskeletal tissues in 11-month-old female Wistar rats, which were randomized into Sham, OVX, and XLGB groups. Daily oral administration of XLGB (250 mg/kg/day) started after OVX for 3 months. mRNA of MHC-I IIa IIb of abductor muscle was determined by RT-PCR.

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