Publications by authors named "Chris Hammond"

Purpose: Glaucoma is an eye disease that is the most common cause of irreversible blindness worldwide. It has been suggested that gut microbiota can produce reactive oxygen species and pro-inflammatory cytokines that may travel from the gastric mucosa to distal sites, for example, the optic nerve head or trabecular meshwork. There is evidence for a gut-eye axis, as microbial dysbiosis has been associated with retinal diseases.

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Purpose: Genetic variants identified through population-based genome-wide studies are generally of high frequency, exerting their action in the central part of the refractive error spectrum. However, the power to identify associations with variants of lower minor allele frequency is greatly reduced, requiring considerable sample sizes. Here we aim to assess the impact of rare variants on genetic variation of refractive errors in a very large general population cohort.

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Background: To investigate the relationship between dietary intake of niacin (water-soluble form of vitamin B ) and retinal nerve fibre layer (RNFL) thickness in healthy eyes.

Methods: This cross-sectional study examined the association between daily niacin intake and RNFL thickness in three large population-based cohorts with varied age differences. RNFL thickness was extracted from optical coherence tomography data; energy-adjusted niacin intake was estimated from food frequency questionnaires.

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Article Synopsis
  • Refractive errors, especially myopia, are common and can lead to significant visual impairment, with their severity linked to the age of onset.
  • A study using data from the UK Biobank analyzed the age of first spectacle wear (AFSW) to explore genetic factors influencing refractive errors, finding significant associations at 44 genomic loci.
  • Results showed that genes related to AFSW are primarily expressed in central nervous system tissues and are involved in neurogenesis, highlighting the importance of time-to-event analysis in understanding genetic risks for refractive errors.
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Cardiac catheterization associated with central vein cannulation can involve potential thrombotic and infectious complications due to multiple cannulation trials or improper placement. To minimize the risks, medical simulators are used for training. Simulators are also employed to test medical devices such as catheters before performing animal tests because they are more cost-effective and still reveal necessary improvements.

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Optical Coherence Tomography (OCT) enables non-invasive imaging of the retina and is used to diagnose and manage ophthalmic diseases including glaucoma. We present the first large-scale genome-wide association study of inner retinal morphology using phenotypes derived from OCT images of 31,434 UK Biobank participants. We identify 46 loci associated with thickness of the retinal nerve fibre layer or ganglion cell inner plexiform layer.

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Background: Alcohol and cannabis are commonly used by adolescents in the United States. Both alcohol use disorder (AUD) and cannabis use disorder (CUD) have been associated with an increased risk of aggression. One form of aggression seen during retaliation is reactive aggression to social provocation.

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  • * A large-scale study involving nearly 4,700 keratoconus cases and over 116,000 controls identified 36 genomic regions linked to the disease, highlighting issues with collagen integrity and cell differentiation as crucial factors.
  • * The findings reveal shared genetic mechanisms with other corneal diseases and suggest that the identified genetic variants account for 12.5% of keratoconus's genetic risk, paving the way for future diagnostic tests to assess susceptibility.
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  • Primary open-angle glaucoma (POAG) is a heritable eye condition leading to blindness and the study involved a large genetic analysis of over 34,000 patients and nearly 350,000 controls from different ethnic backgrounds.
  • Researchers identified 44 new genetic risk factors for POAG and confirmed 83 previously known ones, finding consistent impacts across various ancestries.
  • The study also suggests that certain genes could play significant roles in the disease's development, indicating potential new drug treatments targeting these genetic risk factors.
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  • The study investigates the links between commonly used medications and refractive errors, especially myopia, in older adults.
  • Results indicate that certain medications, like anti-glaucoma drugs, are linked to increased myopia, while pain-control meds are associated with hyperopia.
  • The findings suggest a potential need for further research on how these medications affect vision and the mechanisms behind these associations.
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  • The study investigates how genetic and early environmental influences, as shown by fetus growth patterns, relate to developing myopia in childhood and adolescence.
  • The research used data from 498 Caucasian participants, tracking fetal growth through ultrasound and analyzing their eye health at a 20-year follow-up.
  • Findings indicate a higher likelihood of myopia in individuals with consistently short or long femur lengths, suggesting that intrauterine growth impacts eye development that continues into adulthood.
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SIX1/SIX6 polymorphism has been shown to be associated with glaucoma. Studies have also found that, in older adults, retinal nerve fibre layer (RNFL) thickness is significantly thinned with each copy of the risk allele in SIX1/SIX6. However, it is not known whether these genetic variants exert their effects in younger individuals.

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Purpose: To describe and compare associations with macular retinal nerve fiber layer (mRNFL), ganglion cell complex (GCC), and ganglion cell-inner plexiform layer (GCIPL) thicknesses in a large cohort.

Design: Cross-sectional study.

Participants: We included 42 044 participants in the UK Biobank.

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  • Keratoconus is a leading cause of vision loss in young adults, with limited understanding of its genetic causes, prompting research into genetic determinants linked to corneal biomechanical properties.
  • A comprehensive genome-wide association study was conducted in two populations, comprising 6645 participants in Stage 1 and 752 keratoconus patients in Stage 2, to identify genetic links between corneal properties and keratoconus.
  • The study identified seven significant genetic loci associated with corneal hysteresis and resistance, which could enhance insights into the etiology of keratoconus.
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Objectives: The aim of this study was to assess the feasibility of quantitative ultrasound imaging (QUI) in assessing the biceps brachii muscle and gastrocnemius muscle in adults with multiple sclerosis (MS).

Methods: From May to October 2018, we prospectively performed B-mode ultrasound imaging and ultrasound strain elastography of the biceps brachii muscle and gastrocnemius muscle in 24 patients with MS and 10 age-matched healthy volunteers. ImageJ (https://imagej.

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Elevated intraocular pressure (IOP) is an important risk factor for glaucoma. Mechanisms involved in its homeostasis are not well understood, but associations between metabolic factors and IOP have been reported. To investigate the relationship between levels of circulating metabolites and IOP, we performed a metabolome-wide association using a machine learning algorithm, and then employing Mendelian Randomization models to further explore the strength and directionality of effect of the metabolites on IOP.

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Glaucoma is the leading cause of irreversible blindness globally . Despite its gravity, the disease is frequently undiagnosed in the community . Raised intraocular pressure (IOP) is the most important risk factor for primary open-angle glaucoma (POAG).

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Lung function measures are used in the diagnosis of chronic obstructive pulmonary disease. In 38,199 European ancestry individuals, we studied genome-wide association of forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC) and FEV1/FVC with 1000 Genomes Project (phase 1)-imputed genotypes and followed up top associations in 54,550 Europeans. We identify 14 novel loci (P<5 × 10(-8)) in or near ENSA, RNU5F-1, KCNS3, AK097794, ASTN2, LHX3, CCDC91, TBX3, TRIP11, RIN3, TEKT5, LTBP4, MN1 and AP1S2, and two novel signals at known loci NPNT and GPR126, providing a basis for new understanding of the genetic determinants of these traits and pulmonary diseases in which they are altered.

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Refractive error (RE) is a complex, multifactorial disorder characterized by a mismatch between the optical power of the eye and its axial length that causes object images to be focused off the retina. The two major subtypes of RE are myopia (nearsightedness) and hyperopia (farsightedness), which represent opposite ends of the distribution of the quantitative measure of spherical refraction. We performed a fixed effects meta-analysis of genome-wide association results of myopia and hyperopia from 9 studies of European-derived populations: AREDS, KORA, FES, OGP-Talana, MESA, RSI, RSII, RSIII and ERF.

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Article Synopsis
  • The introduction of genome-wide association studies (GWAS) has advanced the understanding of the genetic factors contributing to refractive error and myopia.
  • Multiple GWAS across diverse ethnic groups have revealed insights into the genetic structure and underlying causes of refractive error.
  • The review discusses the key findings from existing GWAS and suggests future avenues for further genetic research in myopia and refractive error.
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In October of 2008, an outbreak of trichinellosis occurred in northern California that sickened 30 of 38 attendees of an event at which meat from a black bear was served. Morphologic and molecular testing of muscle from the leftover portion of bear meat revealed that the bear was infected with Trichinella murrelli, a sylvatic species of Trichinella found in temperate North America. Clinical records revealed a high attack rate for this outbreak: 78% for persons consuming any bear meat and 100% for persons consuming raw or undercooked bear meat.

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Platelets are the second most abundant cell type in blood and are essential for maintaining haemostasis. Their count and volume are tightly controlled within narrow physiological ranges, but there is only limited understanding of the molecular processes controlling both traits. Here we carried out a high-powered meta-analysis of genome-wide association studies (GWAS) in up to 66,867 individuals of European ancestry, followed by extensive biological and functional assessment.

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