Publications by authors named "Catherine M Suter"

Measurement of the adverse outcomes of repeated head trauma in athletes is often achieved using tests where the comparator is ‘accuracy’. While it is expected that ex-athletes would perform worse than controls, previous studies have shown inconsistent results. Here we have attempted to address these inconsistencies from a different perspective by quantifying not only accuracy, but also motor response times.

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Chronic traumatic encephalopathy (CTE) is a neuropathological diagnosis defined by a unique pattern of hyperphosphorylated tau (p-tau) accumulation that begins in neocortical regions of the brain. It is associated with a range of neuropsychological symptoms, but a definitive diagnosis can only be made by postmortem brain examination. In 2018, we instituted CTE screening for all autopsy brains as part of our routine departmental protocol by performing p-tau immunohistochemistry on a restricted set of 3 neocortical blocks (frontal, temporal, and parietal).

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Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease associated with a history of repetitive head impacts (RHI). CTE was described in boxers as early as the 1920s and by the 1950s it was widely accepted that hits to the head caused some boxers to become "punch drunk." However, the recent discovery of CTE in American and Australian-rules football, soccer, rugby, ice hockey, and other sports has resulted in renewed debate on whether the relationship between RHI and CTE is causal.

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In this Perspective we explore the evolution of our understanding of chronic traumatic encephalopathy (CTE) and its relationship with repetitive head injury. As with many neurodegenerative conditions, there is an imperfect correspondence between neuropathology and clinical phenotype, but unlike other neurodegenerative diseases, CTE has a discrete and easily modifiable risk factor: exposure to repetitive head injury. Consequently, evaluation of the evidence regarding exposure to repetitive head injury and CTE risk should be undertaken using public or occupational health frameworks of medical knowledge.

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Background: Management of concussion remains a serious issue for professional sports, particularly with the growing knowledge on the consequences of repetitive concussion. One primary concern is the subjective assessment of recovery that dictates the time until a concussed athlete is returned-to-competition. In response to this concern, the Australian Football League (AFL) changed its policy in 2020 such that medical clearance for return-to-competition was extended from 1 day, to a minimum of 5 days, prior to the next scheduled match.

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We and others have previously demonstrated the potential for circulating exosome microRNAs to aid in disease diagnosis. In this study, we sought the possible utility of serum exosome microRNAs as biomarkers for disease activity in multiple sclerosis patients in response to fingolimod therapy. We studied patients with relapsing-remitting multiple sclerosis prior to and 6 months after treatment with fingolimod.

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In the original publication of this article [1] the term 'National Rugby League (NRL)' was used to refer to professional rugby league competition sport in Australia. The term should have read 'professional rugby league' to include the various professional competition nomenclatures over the last fifty years, including but not limited to NRL. In this correction article, the incorrect and correct information are published.

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Article Synopsis
  • Exosomes are tiny vesicles released by cells containing specific molecules, including microRNA, that can cross the blood-brain barrier, particularly relevant in glioblastoma cases.
  • In a pilot study, researchers analyzed serum exosomal microRNAs from glioblastoma patients and found a specific set of 26 differentially expressed microRNAs compared to healthy controls, with seven identified as highly effective classifiers for the disease.
  • The study concluded that serum exosomal microRNA signatures could be a reliable method for diagnosing glioblastoma preoperatively and showed that these signatures differ from those in previous studies involving free-circulating microRNAs.
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Exercise stimulates the release of molecules into the circulation, supporting the concept that inter-tissue signaling proteins are important mediators of adaptations to exercise. Recognizing that many circulating proteins are packaged in extracellular vesicles (EVs), we employed quantitative proteomic techniques to characterize the exercise-induced secretion of EV-contained proteins. Following a 1-hr bout of cycling exercise in healthy humans, we observed an increase in the circulation of over 300 proteins, with a notable enrichment of several classes of proteins that compose exosomes and small vesicles.

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  • - Cytosine methylation is a key epigenetic modification in DNA that influences normal physiology and diseases, but its relationship with sex differences has been underexplored.
  • - Analysis of DNA methylation in various tissues from male and female mice revealed significant sexual dimorphism, with numerous loci exhibiting differences primarily driven by higher methylation levels in females, independent of testosterone in some cases.
  • - The study suggests that sex influences epigenetic states in a tissue-specific manner, which could have important implications for understanding differences in health and disease between genders.
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DNA methylation plays a key role in maintaining transcriptional silence on the inactive X chromosome of eutherian mammals. Beyond eutherians, there are limited genome wide data on DNA methylation from other vertebrates. Previous studies of X borne genes in various marsupial models revealed no differential DNA methylation of promoters between the sexes, leading to the conclusion that CpG methylation plays no role in marsupial X-inactivation.

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  • * Researchers believe that exosomes—tiny particles containing RNA, DNA, and proteins found in the blood—might be useful as biomarkers for detecting and monitoring MS.
  • * The study identified specific exosomal microRNAs in patients with different forms of MS, which could help distinguish between relapsing-remitting and progressive MS with high accuracy, potentially improving diagnosis and treatment monitoring.
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  • ALS is a neurodegenerative disorder that mainly affects people later in life, and while some genetic causes are known, most sporadic cases have unclear origins.
  • Researchers examined the DNA methylation patterns of five pairs of monozygotic twins, where one had ALS and the other did not, and found significant differences in their genetic markers related to neurobiological functions.
  • The study suggests that these differences could lead to potential blood-based biomarkers for ALS, help understand its development, and guide future research in ALS epigenetics.
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Parental health or exposures can affect the lifetime health outcomes of offspring, independently of inherited genotypes. Such 'epigenetic' effects occur over a broad range of environmental stressors, including defects in parental metabolism. Although maternal metabolic effects are well documented, it has only recently been established that that there is also an independent paternal contribution to long-term metabolic health.

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  • - The study investigates whether metabolic traits from obese parents can affect their offspring across generations, even when the later generations aren't directly exposed to obesity.
  • - Researchers found that F1 male mice, whose fathers were obese, showed metabolic issues which they then passed on to their F2 male offspring, despite F2 not being exposed to obesity.
  • - The findings suggest that these inherited traits could be linked to changes in sperm RNA, indicating that non-genetic factors can influence metabolic health for multiple generations.
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  • The study investigates how maternal obesity and Western-style diets impact heart-related microRNAs (miRNAs) in offspring, suggesting a link between these factors and cardiovascular disease risk.
  • Researchers used small RNA sequencing to analyze the heart tissue of young adult mice, discovering that maternal obesity affects 8 specific cardiac miRNAs, but only when paired with a high-fat Western diet.
  • Findings indicate that postnatal diet plays a more significant role in altering miRNA expression than the prenatal programming from maternal obesity, emphasizing how lifestyle choices can influence heart health.
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  • Intersexual genomic conflict in honey bees can cause unequal expression of parental alleles, indicating the presence of genomic imprinting, with DNA methylation potentially playing a key role in this process.
  • A study comparing genome-wide methylation patterns revealed that embryos produced sexually had a higher number of hypermethylated genes compared to embryos produced through asexual reproduction, supporting the theory that paternal genome contributes to increased methylation.
  • Findings indicate that while methylation patterns are influenced by parental origin in general, specific genes like Stan exhibit allele-specific methylation that is not dependent on the parent of origin, highlighting complexities in understanding genomic imprinting and methylation roles.
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Background: Increasing evidence suggests the involvement of epigenetic processes in the development of schizophrenia and bipolar disorder, and recent reviews have focused on findings in post-mortem brain tissue. A systematic review was conducted to synthesise and evaluate the quality of available evidence for epigenetic modifications (specifically DNA methylation) in peripheral blood and saliva samples of schizophrenia and bipolar disorder patients in comparison to healthy controls.

Methods: Original research articles using humans were identified using electronic databases.

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The ability of environmental exposures to induce phenotypic change across multiple generations of offspring has gathered an enormous amount of interest in recent years. There are by now many examples of nongenetic transgenerational effects of environmental exposures, covering a broad range of stressors. Available evidence indicates that epigenetic inheritance may mediate at least some of these transgenerational effects, but how environmental exposures induce changes to the epigenome of the germline is unknown.

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  • The study examines how the number of embryos and maternal undernutrition around conception or before implantation affect liver fat metabolism in sheep fetuses.
  • It reveals that undernutrition leads to decreased expression of key regulators for fat breakdown in both singleton and twin fetuses, but with different protein levels depending on embryo number.
  • The research also highlights changes in microRNA expression, suggesting that both embryo number and timing of maternal undernutrition significantly influence liver fat metabolism mechanisms in developing sheep fetuses.
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