Publications by authors named "Elizabeth Terhune"

Objectives: To systematically evaluate definitions of "racial health equity" (RHE) and related terms within health-related academic literature.

Study Design And Setting: We systematically evaluated definitions of RHE and related terms within health-related academic articles. Articles published in English were included, and no date restrictions were imposed.

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Article Synopsis
  • - The study aimed to find evidence syntheses of health interventions that focus on racial health equity, examining the use of equity-focused frameworks and logic models.
  • - Researchers conducted a search across multiple sources, including bibliographic databases and interviews, to identify effective frameworks, finding only two out of 153 reviews used logic models to explain interventions.
  • - The results indicated a scarcity of logic models and frameworks in these studies, highlighting an urgent need for more comprehensive frameworks to better guide the research and interpretation of findings in racial health equity.
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Objectives: Systematic reviews hold immense promise as tools to highlight evidence-based practices that can reduce or aim to eliminate racial health disparities. Currently, consensus on centering racial health equity in systematic reviews and other evidence synthesis products is lacking. Centering racial health equity implies concentrating or focusing attention on health equity in ways that bring attention to the perspectives or needs of groups that are typically marginalized.

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Article Synopsis
  • The study evaluated systematic reviews of interventions aimed at improving racial health equity among racialized populations, particularly those published between January 2020 and January 2023.
  • Analysis of 157 reviews revealed that only 14% addressed the role of racism in health disparities, and 67% merely summarized studies without proper synthesis, with many using biased methods for effect sizes.
  • The findings highlight a need for better research quality, comprehensive examination of racism, and a focus on structural interventions to enhance opportunities for racialized groups in addressing health inequities.
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  • The study aims to explore how health-related syntheses address racial health equity and how they engage diverse interest holders in the process.
  • Out of the 157 syntheses reviewed, only 29 (18%) reported engaging stakeholders, often lacking detailed methods or outcomes of the engagement, particularly for racially diverse groups.
  • The review highlights significant gaps in the understanding of effective engagement strategies for promoting racial health equity and calls for more specific guidance on involving diverse populations in health research.
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Article Synopsis
  • - The USA faces significant health disparities among racial and ethnic groups, prompting the term "racial health equity" (RHE) to gain traction, though no clear definition currently exists.
  • - A scoping review aims to explore how RHE is defined and what gaps exist in its research and understanding, using data from health organizations, published articles, and synthesis studies.
  • - The ultimate goal of this review is to clarify the definitions and concepts surrounding RHE, promoting a unified approach to addressing racial health equity in the healthcare system.
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Background: Adolescent idiopathic scoliosis (AIS) is a structural lateral spinal curvature of ≥10° with rotation. Approximately 2%-3% of children across populations are affected with AIS, and this condition is responsible for ~$3 billion in costs within the USA. Although AIS is believed to have a strong genetic contribution, clinical translation of identified genetic variants has stalled.

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Idiopathic scoliosis (IS) is a three-dimensional rotation of the spine >10 degrees with an unknown etiology. Our laboratory established a late-onset IS model in zebrafish () containing a deletion in . A total of 25% of zebrafish develop spinal curvatures and are otherwise developmentally normal, although the molecular mechanisms underlying the scoliosis are unknown.

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Vertigo due to vestibular dysfunction is rare in children. The elucidation of its etiology will improve clinical management and the quality of life of patients. Genes for vestibular dysfunction were previously identified in patients with both hearing loss and vertigo.

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Medial collateral ligament (MCL) injuries are typically managed non-operatively, with high rates of clinical success. However, patients who present with medial knee laxity with valgus stress testing of a fully extended knee, anteromedial rotatory instability, associated tibial plateau fracture, or multiligament injury or those who continue to be symptomatic after non-operative treatment may benefit from surgical intervention. Patients with a history of total knee arthroplasty who suffer MCL and posterior oblique ligament (POL) injuries represent a challenging patient population and often require surgical attention.

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Article Synopsis
  • Adolescent idiopathic scoliosis (AIS) affects 2-3% of children, causing significant healthcare costs, primarily due to limited treatment options like bracing and surgery.
  • The study plans to review various databases for genetic evidence linked to AIS, focusing on factors like curve severity and genetic variants.
  • The goal of the systematic review is to enhance understanding of genetic causes of AIS to improve diagnosis and patient care quality, registered under PROSPERO CRD42021243253.*
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Article Synopsis
  • Idiopathic scoliosis (IS) is a common spinal deformity in children, characterized by a curvature of at least 10°, and has a significant genetic influence, although its exact causes remain unclear.
  • This review discusses the use of genetic animal models to study IS, highlighting challenges in replicating the condition due to its complex genetic and biomechanical nature.
  • The authors stress the importance of choosing appropriate animal models for research and suggest future studies should incorporate multiple genetic and environmental factors to better mimic the human condition.
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Epigenetic mechanisms may contribute to idiopathic scoliosis (IS). We identified 8 monozygotic twin pairs with IS, 6 discordant (Cobb angle difference > 10°) and 2 concordant (Cobb angle difference ≤ 2°). Genome-wide methylation in blood was measured with the Infinium HumanMethylation EPIC Beadchip.

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Article Synopsis
  • Adolescent idiopathic scoliosis (AIS) is a condition affecting 2-3% of children, characterized by a spinal curvature greater than 10° and has a significant genetic basis, but its exact cause is largely unknown.
  • The study involved exome sequencing in 23 multigenerational families to identify rare genetic variants that might cause AIS, resulting in 1448 variants across 1160 genes, with a focus on variants related to cytoskeletal and extracellular matrix functions.
  • Findings indicate that AIS is a polygenic disorder with limited shared genetic factors among affected families, providing a valuable resource for future genetic studies on familial AIS.
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Idiopathic scoliosis (IS) is a spinal disorder affecting up to 3% of otherwise healthy children. IS has a strong familial genetic component and is believed to be genetically complex due to significant variability in phenotype and heritability. Previous studies identified putative loci and variants possibly contributing to IS susceptibility, including within extracellular matrix, cilia, and actin networks, but the genetic architecture and underlying mechanisms remain unresolved.

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Negative pressure wound therapy is becoming more commonly used to prevent wound complications in joint arthroplasty, although few studies have assessed its outcomes compared with those of a traditional dry sterile dressing. This retrospective study assessed complications that required return to the operating room in a cohort of patients who received a dry sterile dressing (n=159) vs negative pressure wound therapy (n=32). There were significantly more overall complications (P=.

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Idiopathic scoliosis (IS) is a structural lateral spinal curvature of ≥10° that affects up to 3% of otherwise healthy children and can lead to life-long problems in severe cases. It is well-established that IS is a genetic disorder. Previous studies have identified genes that may contribute to the IS phenotype, but the overall genetic etiology of IS is not well understood.

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Purpose: To investigate the relation of the at-risk structures (distal femoral physis, lateral collateral ligament, anterolateral ligament, popliteus, and articular cartilage) during all-epiphyseal femoral tunnel drilling. A second purpose was 2-fold: (1) to develop recommendations for tunnel placement and orientation that anatomically reconstruct the anterior cruciate ligament (ACL) while minimizing the risk of injury to these at-risk structures, and (2) to allow for maximal tunnel length to increase the amount of graft in the socket to facilitate healing.

Methods: Three-dimensional models of 6 skeletally immature knees (aged 7-11 years) were reconstructed from computed tomography and used to simulate all-epiphyseal femoral tunnels.

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Diabetes is a disease with wide-ranging personal and societal impacts that has been managed medicinally for over half a century. Since the discovery of stem cells, pancreatic islet regeneration has become a central target for clinical application that has the potential to decrease or eliminate the need for insulin administration and adjunctive medications. The discovery of alternative routes to pluripotency that bypass the ethical implications of embryonic stem cells has significantly expanded the horizons of stem cell based therapy.

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Background: Anterior cruciate ligament (ACL) reconstruction failure rates are highest in youth athletes. The role of the anterolateral ligament in rotational knee stability is of increasing interest, and several centers are exploring combined ACL and anterolateral ligament reconstruction for these young patients. Literature on the anterolateral ligament of the knee is sparse in regard to the pediatric population.

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Bats are the only mammals capable of powered flight, but little is known about the genetic determinants that shape their wings. Here we generated a genome for Miniopterus natalensis and performed RNA-seq and ChIP-seq (H3K27ac and H3K27me3) analyses on its developing forelimb and hindlimb autopods at sequential embryonic stages to decipher the molecular events that underlie bat wing development. Over 7,000 genes and several long noncoding RNAs, including Tbx5-as1 and Hottip, were differentially expressed between forelimb and hindlimb, and across different stages.

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Purpose: Adolescent athletes undergo preparticipation screening for long QT syndrome. Medications that are associated with QT interval prolongation are increasingly being prescribed to precollege students. The side effect profile of these medications during exercise is unknown.

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Gibbons are small arboreal apes that display an accelerated rate of evolutionary chromosomal rearrangement and occupy a key node in the primate phylogeny between Old World monkeys and great apes. Here we present the assembly and analysis of a northern white-cheeked gibbon (Nomascus leucogenys) genome. We describe the propensity for a gibbon-specific retrotransposon (LAVA) to insert into chromosome segregation genes and alter transcription by providing a premature termination site, suggesting a possible molecular mechanism for the genome plasticity of the gibbon lineage.

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Background: A delay in pediatric and adolescent anterior cruciate ligament (ACL) reconstruction is associated with an increase in the number of concomitant meniscal and chondral injuries. Factors that contribute to this delay have not been well described.

Hypothesis: Socioeconomic and demographic factors are related to ACL surgery timing.

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