Publications by authors named "Bober M"

Background: Vosoritide is a C-type natriuretic peptide analog that addresses an underlying pathway causing reduced bone growth in achondroplasia. Understanding the vosoritide treatment effect requires evaluation over an extended duration and comparison with outcomes in untreated children.

Methods: After completing ≥6 months of a baseline observational growth study and 52 weeks in a double-blind, placebo-controlled study (ClinicalTrials.

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  • The surgical management of scoliosis in patients with osteogenesis imperfecta (OI) is complicated by factors such as rigid spinal curves, short stature, and fragile bones, prompting a study on various treatment methods.
  • A retrospective review of 30 OI patients (average age 14.1 years) who underwent posterior spinal fusion revealed significant improvements in major curve correction and other spinal parameters after a minimum follow-up of 2 years.
  • Complications were minimal, with only two patients experiencing issues like proximal junctional kyphosis, indicating the approach's effectiveness and safety in addressing severe scoliosis in OI patients.
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  • * Through analysis of fibroblasts and a fruit fly model, we found that these variants resulted in decreased lipid droplet formation and impaired gene expression linked to SREBP, indicating disrupted pathway function.
  • * Our findings suggest that SREBF2 variants hinder the cleavage of S1P targets, causing disease symptoms by negatively affecting SREBP1 and SREBP2 activity.
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Background And Objective: Vosoritide is a recently approved therapy for achondroplasia, the most common form of disproportionate short stature, that has been shown to be well tolerated and effective in increasing linear growth. This study aimed to develop a population pharmacokinetic (PPK) model to characterize pharmacokinetics (PK) of vosoritide and establish a weight-band dosing regimen.

Methods: A PPK model was developed using data from five clinical trials in children with achondroplasia (aged 0.

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  • Osteogenesis imperfecta (OI) is a rare genetic disorder that significantly impacts the quality of life for those affected, leading to increased healthcare needs and economic burdens for individuals, families, and society.
  • The IMPACT survey aimed to gather comprehensive data on various aspects of OI, including the humanistic, clinical, and economic impacts, and included responses from adults, adolescents, caregivers, and close relatives across eight languages.
  • Results revealed that pain was the most common symptom reported, alongside notable issues such as fatigue, scoliosis, and mental health problems, emphasizing the multifaceted challenges faced by individuals with OI.
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  • The skeletal dysplasias are a diverse group of genetic conditions impacting bone and cartilage growth, but the role of cytokines in these disorders is not well understood.
  • A study analyzed cytokine levels in 136 children with skeletal dysplasia compared to 275 healthy controls, focusing on 12 specific cytokines across various dysplasia types.
  • Findings revealed significant differences in cytokine expression, with certain cytokines consistently elevated or decreased across all dysplasia cohorts, highlighting particularly high levels in MOPDII cases.
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Background: Vosoritide is a recombinant C-type natriuretic peptide analogue that increases annualised growth velocity in children with achondroplasia aged 5-18 years. We aimed to assess the safety and efficacy of vosoritide in infants and children younger than 5 years.

Methods: This double-blind, randomised, placebo-controlled, phase 2 trial was done in 16 hospitals across Australia, Japan, the UK, and the USA.

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Hereditary spastic parapareses (HSPs) are clinically heterogeneous motor neuron diseases with variable age of onset and severity. Although variants in dozens of genes are implicated in HSPs, much of the genetic basis for pediatric-onset HSP remains unexplained. Here, we re-analyzed clinical exome-sequencing data from siblings with HSP of unknown genetic etiology and identified an inherited nonsense mutation (c.

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Matrix Gla protein (MGP) is a vitamin K-dependent post-translationally modified protein, highly expressed in vascular and cartilaginous tissues. It is a potent inhibitor of extracellular matrix mineralization. Biallelic loss-of-function variants in the MGP gene cause Keutel syndrome, an autosomal recessive disorder characterized by widespread calcification of various cartilaginous tissues and skeletal and vascular anomalies.

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Scene graph generation is a structured prediction task aiming to explicitly model objects and their relationships via constructing a visually-grounded scene graph for an input image. Currently, the message passing neural network based mean field variational Bayesian methodology is the ubiquitous solution for such a task, in which the variational inference objective is often assumed to be the classical evidence lower bound. However, the variational approximation inferred from such loose objective generally underestimates the underlying posterior, which often leads to inferior generation performance.

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Introduction: Vosoritide is the first precision medical therapy approved to increase growth velocity in children with achondroplasia. Sharing early prescribing experiences across different regions could provide a framework for developing practical guidance for the real-world use of vosoritide.

Methods: Two meetings were held to gather insight and early experience from experts in Europe, the Middle East, and the USA.

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Objective: The objective of this study was to describe the incidence and management of hydrocephalus in patients with achondroplasia over a 60-year period at four skeletal dysplasia centers.

Methods: The Achondroplasia Natural History Study (CLARITY) is a registry for clinical data from achondroplasia patients receiving treatment at four skeletal dysplasia centers in the US from 1957 to 2017. Data were entered and stored in a REDCap database and included surgeries with indications and complications, medical diagnoses, and radiographic information.

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Background: Recently, tracheal narrowing has been recognized as a significant comorbid condition in patients with Morquio A, also known as mucopolysaccharidosis IVA. We studied a large cohort of patients with Morquio A to describe the extent of their tracheal narrowing and its relationship to airway management during anesthesia care.

Methods: This is an observational study, collecting data retrospectively, of a cohort of patients with Morquio A.

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Background: TransCon CNP (navepegritide) is an investigational prodrug of C-type natriuretic peptide (CNP) designed to allow for continuous CNP exposure with once-weekly dosing. This 52-week phase 2 (ACcomplisH) trial assessed the safety and efficacy of TransCon CNP in children with achondroplasia.

Methods: ACcomplisH is a global, randomised, double-blind, placebo-controlled, dose-escalation trial.

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The development of inflammatory bowel diseases (IBD) involves the breakdown of two barriers: the epithelial barrier and the gut-vascular barrier (GVB). The destabilization of each barrier can promote initiation and progression of the disease. Interestingly, first evidence is available that both barriers are communicating through secreted factors that may accordingly serve as targets for therapeutic modulation of barrier functions.

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The air-broadened lines from the oxygen B band were measured for the first time in controlled laboratory conditions with a high signal-to-noise ratio using frequency-stabilized cavity ring-down spectroscopy (FS-CRDS) referenced to the optical frequency comb. Spectra measured at various pressures and temperatures were analyzed with an advanced line-shape model, considering the speed-dependence of collisional broadening and shift, and the effect of velocity-changing collisions. The temperature dependence of collisional broadening and shift is determined, whereas no significant temperature dependence of speed-dependent parameters and Dicke narrowing was observed.

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  • Diastrophic dysplasia (DTD) is caused by mutations in the SLC26A2 gene, affecting sulfate uptake and glycosaminoglycan (GAG) sulfation, and it may benefit from pharmacological treatments as studied in an animal model.
  • In identifying non-invasive biomarkers for DTD, research focused on urinary GAG sulfation and blood levels of collagen X marker (CXM), which are linked to the severity of the condition and growth metrics.
  • Results indicated that DTD patients exhibit undersulfated urinary GAGs and lower than normal CXM levels, suggesting both biomarkers can help evaluate treatment effectiveness and the disorder's metabolism and ossification processes.
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Background: The purpose of this study was to describe the frequency and risk factors for orthopedic surgery in patients with achondroplasia. CLARITY (The Achondroplasia Natural History Study) includes clinical data from achondroplasia patients receiving treatment at four skeletal dysplasia centers in the United States from 1957 to 2018. Data were entered and stored in a Research Electronic Data Capture (REDCap) database.

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As a structured prediction task, scene graph generation aims to build a visually-grounded scene graph to explicitly model objects and their relationships in an input image. Currently, the mean field variational Bayesian framework is the de facto methodology used by the existing methods, in which the unconstrained inference step is often implemented by a message passing neural network. However, such formulation fails to explore other inference strategies, and largely ignores the more general constrained optimization models.

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Unravelling protein distributions within individual cells is vital to understanding their function and state and indispensable to developing new treatments. Here we present the Hybrid subCellular Protein Localiser (HCPL), which learns from weakly labelled data to robustly localise single-cell subcellular protein patterns. It comprises innovative DNN architectures exploiting wavelet filters and learnt parametric activations that successfully tackle drastic cell variability.

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Purpose: Pregnancies affected by maternal or fetal achondroplasia present unique challenges. The optimal route of delivery in fetuses with achondroplasia has not been established. Our objective was to determine whether the route of delivery affects postnatal achondroplasia-related surgical burden.

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Scene graph generation aims to interpret an input image by explicitly modelling the objects contained therein and their relationships. In existing methods the problem is predominantly solved by message passing neural network models. Unfortunately, in such models, the variational distributions generally ignore the structural dependencies among the output variables, and most of the scoring functions only consider pairwise dependencies.

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