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Dive into the research topics where Katie M. Williams is active.

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Featured researches published by Katie M. Williams.


Ophthalmology | 2015

Increasing Prevalence of Myopia in Europe and the Impact of Education

Katie M. Williams; Geir Bertelsen; Phillippa M. Cumberland; Christian Wolfram; Virginie J. M. Verhoeven; Eleftherios Anastasopoulos; Gabriëlle H.S. Buitendijk; Audrey Cougnard-Grégoire; Catherine Creuzot-Garcher; Maja G. Erke; Ruth E. Hogg; René Höhn; Pirro G. Hysi; Anthony P. Khawaja; Jean-François Korobelnik; Janina S. Ried; Johannes R. Vingerling; Alain M. Bron; Jean-François Dartigues; Astrid E. Fletcher; Albert Hofman; Robert W. A. M. Kuijpers; Robert Luben; Konrad Oxele; Fotis Topouzis; Therese von Hanno; Alireza Mirshahi; Paul J. Foster; Cornelia M. van Duijn; Norbert Pfeiffer

Purpose To investigate whether myopia is becoming more common across Europe and explore whether increasing education levels, an important environmental risk factor for myopia, might explain any temporal trend. Design Meta-analysis of population-based, cross-sectional studies from the European Eye Epidemiology (E3) Consortium. Participants The E3 Consortium is a collaborative network of epidemiological studies of common eye diseases in adults across Europe. Refractive data were available for 61 946 participants from 15 population-based studies performed between 1990 and 2013; participants had a range of median ages from 44 to 78 years. Methods Noncycloplegic refraction, year of birth, and highest educational level achieved were obtained for all participants. Myopia was defined as a mean spherical equivalent ≤−0.75 diopters. A random-effects meta-analysis of age-specific myopia prevalence was performed, with sequential analyses stratified by year of birth and highest level of educational attainment. Main Outcome Measures Variation in age-specific myopia prevalence for differing years of birth and educational level. Results There was a significant cohort effect for increasing myopia prevalence across more recent birth decades; age-standardized myopia prevalence increased from 17.8% (95% confidence interval [CI], 17.6–18.1) to 23.5% (95% CI, 23.2–23.7) in those born between 1910 and 1939 compared with 1940 and 1979 (P = 0.03). Education was significantly associated with myopia; for those completing primary, secondary, and higher education, the age-standardized prevalences were 25.4% (CI, 25.0–25.8), 29.1% (CI, 28.8–29.5), and 36.6% (CI, 36.1–37.2), respectively. Although more recent birth cohorts were more educated, this did not fully explain the cohort effect. Compared with the reference risk of participants born in the 1920s with only primary education, higher education or being born in the 1960s doubled the myopia prevalence ratio–2.43 (CI, 1.26–4.17) and 2.62 (CI, 1.31–5.00), respectively—whereas individuals born in the 1960s and completing higher education had approximately 4 times the reference risk: a prevalence ratio of 3.76 (CI, 2.21–6.57). Conclusions Myopia is becoming more common in Europe; although education levels have increased and are associated with myopia, higher education seems to be an additive rather than explanatory factor. Increasing levels of myopia carry significant clinical and economic implications, with more people at risk of the sight-threatening complications associated with high myopia.


Experimental Eye Research | 2013

Candidate gene study of macular response to supplemental lutein and zeaxanthin

Ekaterina Yonova-Doing; Pirro G. Hysi; Cristina Venturini; Katie M. Williams; Abhishek Nag; Stephen Beatty; S. H. Melissa Liew; Clare Gilbert; Christopher J. Hammond

Supplementation with carotenoids is proposed to protect against age-related macular degeneration. There is, however, considerable variability in retinal macular pigment response, which may be due to underlying genetic variation. The purpose of this study was to determine whether genetic factors, which have been previously associated with cross-sectional macular pigment levels in the retina or serum lutein, also influence response to supplementation. To this end we conducted an association study in 310 subjects from the TwinsUK cohort between variants in 8 candidate genes and serum lutein and retinal macular pigment optical density (MPOD) levels before and after supplementation. Four variants were associated with MPOD response to supplementation (p < 0.05): rs11057841 (SCARB1), rs4926339 (RPE65), rs1929841 (ABCA1) and rs174534 (FADS1). We also confirmed previous associations between rs6564851 near BMCO1 (p < 0.001) and rs11057841 within SCARB1 (p = 0.01) and baseline measures of serum lutein; while the latter was also associated with MPOD response, none of the BMCO1 variants were. Finally, there was evidence for association between variants near RPE65 and ELOVL2 and changes in lutein concentration after supplementation. This study is the first to show association between genetic variants and response to carotenoids supplementation. Our findings suggest an important link between MP response and the biological processes of carotenoids transport and fatty acid metabolism.


Scientific Reports | 2016

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

Qiao Fan; Xinxing Guo; Jan Willem Lodewijk Tideman; Katie M. Williams; Seyhan Yazar; S.M. Hosseini; Laura D Howe; Beate St Pourcain; David Evans; Nicholas J. Timpson; George McMahon; Pirro G. Hysi; Eva Krapohl; Yonghui Wang; Jost B. Jonas; Paul N. Baird; Jie Jin Wang; Cliff Cheng; Yvonne Teo; Tien Yin Wong; Xiaoyan Ding; Robert Wojciechowski; Terri L. Young; Olavi Pärssinen; Konrad Oexle; Norbert Pfeiffer; Joan E. Bailey-Wilson; Andrew D. Paterson; C. C. W. Klaver; Robert Plomin

Myopia, currently at epidemic levels in East Asia, is a leading cause of untreatable visual impairment. Genome-wide association studies (GWAS) in adults have identified 39 loci associated with refractive error and myopia. Here, the age-of-onset of association between genetic variants at these 39 loci and refractive error was investigated in 5200 children assessed longitudinally across ages 7–15 years, along with gene-environment interactions involving the major environmental risk-factors, nearwork and time outdoors. Specific variants could be categorized as showing evidence of: (a) early-onset effects remaining stable through childhood, (b) early-onset effects that progressed further with increasing age, or (c) onset later in childhood (N = 10, 5 and 11 variants, respectively). A genetic risk score (GRS) for all 39 variants explained 0.6% (P = 6.6E–08) and 2.3% (P = 6.9E–21) of the variance in refractive error at ages 7 and 15, respectively, supporting increased effects from these genetic variants at older ages. Replication in multi-ancestry samples (combined N = 5599) yielded evidence of childhood onset for 6 of 12 variants present in both Asians and Europeans. There was no indication that variant or GRS effects altered depending on time outdoors, however 5 variants showed nominal evidence of interactions with nearwork (top variant, rs7829127 in ZMAT4; P = 6.3E–04).


JAMA Ophthalmology | 2017

Association Between Myopia, Ultraviolet B Radiation Exposure, Serum Vitamin D Concentrations, and Genetic Polymorphisms in Vitamin D Metabolic Pathways in a Multicountry European Study

Katie M. Williams; G.C. Bentham; Ian S. Young; Ann McGinty; Gareth J. McKay; Ruth E. Hogg; Christopher J. Hammond; Usha Chakravarthy; Mati Rahu; Johan H. Seland; G. Soubrane; Laura Tomazzoli; Fotis Topouzis; Astrid E. Fletcher

Importance Myopia is becoming increasingly common globally and is associated with potentially sight-threatening complications. Spending time outdoors is protective, but the mechanism underlying this association is poorly understood. Objective To examine the association of myopia with ultraviolet B radiation (UVB; directly associated with time outdoors and sunlight exposure), serum vitamin D concentrations, and vitamin D pathway genetic variants, adjusting for years in education. Design, Setting, and Participants A cross-sectional, population-based random sample of participants 65 years and older was chosen from 6 study centers from the European Eye Study between November 6, 2000, to November 15, 2002. Of 4187 participants, 4166 attended an eye examination including refraction, gave a blood sample, and were interviewed by trained fieldworkers using a structured questionnaire. Myopia was defined as a mean spherical equivalent of −0.75 diopters or less. Exclusion criteria included aphakia, pseudophakia, late age-related macular degeneration, and vision impairment due to cataract, resulting in 371 participants with myopia and 2797 without. Exposures Exposure to UVB estimated by combining meteorological and questionnaire data at different ages, single-nucleotide polymorphisms in vitamin D metabolic pathway genes, serum vitamin D3 concentrations, and years of education. Main Outcomes and Measures Odds ratios (ORs) of UVB, serum vitamin D3 concentrations, vitamin D single-nucleotide polymorphisms, and myopia estimated from logistic regression. Result Of the included 3168 participants, the mean (SD) age was 72.4 (5) years, and 1456 (46.0%) were male. An SD increase in UVB exposure at age 14 to 19 years (OR, 0.81; 95% CI, 0.71-0.92) and 20 to 39 years (OR, 0.7; 95% CI, 0.62-0.93) was associated with a reduced adjusted OR of myopia; those in the highest tertile of years of education had twice the OR of myopia (OR, 2.08; 95% CI, 1.41-3.06). No independent associations between myopia and serum vitamin D3 concentrations nor variants in genes associated with vitamin D metabolism were found. An unexpected finding was that the highest quintile of plasma lutein concentrations was associated with a reduced OR of myopia (OR, 0.57; 95% CI, 0.46-0.72). Conclusions and Relevance Increased UVB exposure was associated with reduced myopia, particularly in adolescence and young adulthood. The association was not altered by adjusting for education. We found no convincing evidence for a direct role of vitamin D in myopia risk. The relationship between high plasma lutein concentrations and a lower risk of myopia requires replication.


JAMA Ophthalmology | 2014

Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts

Pirro G. Hysi; Omar A. Mahroo; Phillippa M. Cumberland; Robert Wojciechowski; Katie M. Williams; Terri L. Young; David A. Mackey; Jugnoo S. Rahi; Christopher J. Hammond

IMPORTANCE To date, relatively few genes responsible for a fraction of heritability have been identified by means of large genetic association studies of refractive error. OBJECTIVE To explore the genetic mechanisms that lead to refractive error in the general population. DESIGN, SETTING, AND PARTICIPANTS Genome-wide association studies were carried out in 2 British population-based independent cohorts (N = 5928 participants) to identify genes moderately associated with refractive error. MAIN OUTCOMES AND MEASURES Enrichment analyses were used to identify sets of genes overrepresented in both cohorts. Enriched groups of genes were compared between both participating cohorts as a further measure against random noise. RESULTS Groups of genes enriched at highly significant statistical levels were remarkably consistent in both cohorts. In particular, these results indicated that plasma membrane (P = 7.64 × 10⁻³⁰), cell-cell adhesion (P = 2.42 × 10⁻¹⁸), synaptic transmission (P = 2.70 × 10⁻¹⁴), calcium ion binding (P = 3.55 × 10⁻¹⁵), and cation channel activity (P = 2.77 × 10⁻¹⁴) were significantly overrepresented in relation to refractive error. CONCLUSIONS AND RELEVANCE These findings provide evidence that development of refractive error in the general population is related to the intensity of photosignal transduced from the retina, which may have implications for future interventions to minimize this disorder. Pathways connected to the procession of the nerve impulse are major mechanisms involved in the development of refractive error in populations of European origin.


Ophthalmic and Physiological Optics | 2013

Age of myopia onset in a British population‐based twin cohort

Katie M. Williams; Pirro G. Hysi; Abhishek Nag; Ekaterina Yonova-Doing; Cristina Venturini; Christopher J. Hammond

School‐age myopia is becoming more common in Asia and North America; data from the United Kingdom has suggested a significant amount of myopia develops after the age of 17 years. Age of spectacle wear has been used as a proxy of myopia severity in a recent large genome‐wide association study. The purpose of this study was to examine the age of onset of spectacle wear in a large British twin cohort, to examine the reliability and reproducibility of self‐reported age of onset as a proxy measure of myopia severity, and to see if there is evidence in the UK of a rising prevalence of myopia.


Ophthalmology | 2016

Genetic and Dietary Factors Influencing the Progression of Nuclear Cataract.

Ekaterina Yonova-Doing; Zoe A. Forkin; Pirro G. Hysi; Katie M. Williams; Tim D. Spector; Clare Gilbert; Christopher J. Hammond

Purpose To determine the heritability of nuclear cataract progression and to explore prospectively the effect of dietary micronutrients on the progression of nuclear cataract. Design Prospective cohort study. Participants Cross-sectional nuclear cataract and dietary measurements were available for 2054 white female twins from the TwinsUK cohort. Follow-up cataract measurements were available for 324 of the twins (151 monozygotic and 173 dizygotic twins). Methods Nuclear cataract was measured using a quantitative measure of nuclear density obtained from digital Scheimpflug images. Dietary data were available from EPIC food frequency questionnaires. Heritability was modeled using maximum likelihood structural equation twin modeling. Association between nuclear cataract change and micronutrients was investigated using linear and multinomial regression analysis. The mean interval between baseline and follow-up examination was 9.4 years. Main Outcome Measures Nuclear cataract progression. Results The best-fitting model estimated that the heritability of nuclear cataract progression was 35% (95% confidence interval [CI], 13–54), and individual environmental factors explained the remaining 65% (95% CI, 46–87) of variance. Dietary vitamin C was protective against both nuclear cataract at baseline and nuclear cataract progression (β = −0.0002, P = 0.01 and β = −0.001, P = 0.03, respectively), whereas manganese and intake of micronutrient supplements were protective against nuclear cataract at baseline only (β = −0.009, P = 0.03 and β = −0.03, P = 0.01, respectively). Conclusions Genetic factors explained 35% of the variation in progression of nuclear cataract over a 10-year period. Environmental factors accounted for the remaining variance, and in particular, dietary vitamin C protected against cataract progression assessed approximately 10 years after baseline.


Investigative Ophthalmology & Visual Science | 2014

The heritability of the ring-like distribution of macular pigment assessed in a twin study.

Ambreen Tariq; Omar A. Mahroo; Katie M. Williams; S. H. Melissa Liew; Stephen Beatty; Clare Gilbert; Frederik J.G.M. van Kuijk; Christopher J. Hammond

PURPOSE It has been suggested that ring-like patterns of macular pigment, as measured with dual wavelength autofluorescence, are observed less frequently in subjects with age-related maculopathy. We explored relative contributions of genetic and environmental factors in macular pigment optical density (MPOD) distributions using a classic twin study. METHODS As part of a previous nutritional study, 322 healthy Caucasian female twins, aged 16 to 50 (mean 40) years, underwent measurement of MPOD optical density by two-wavelength fundus autofluorescence. In the present study, the right eye MPOD profile was assessed for the presence of a ring-like pattern by two graders independently, using common criteria, with a third grader arbitrating in cases of disagreement. Concordance was calculated as 2C/(2C + D), where C is the number of twin pairs concordant, and D the number discordant, for the ring-like pattern. Also, heritability was calculated using maximum-likelihood structural equation modeling. RESULTS Images and zygosity data were available for 314 twins (88 monozygotic [MZ] and 69 dizygotic [DZ] pairs). The overall prevalence of the ring pattern was 25.8%. Respective concordances for MZ and DZ twins were 0.75 and 0.22. Additive genetic factors were estimated to contribute to 84.0% of the total variance (95% confidence intervals, 63.7%-94.6%). CONCLUSIONS Concordance for MZ twins was over three times that for DZ twins, with heritability estimated at 84%, indicating that genetic factors contribute to the development of the ring structure. Studies have suggested that ring-like patterns of macular pigment can affect risk for age-related maculopathy. In a classic twin study, we found that the presence of such a pattern was highly heritable.


Investigative Ophthalmology & Visual Science | 2014

High Heritability of Posterior Corneal Tomography, as Measured by Scheimpflug Imaging, in a Twin Study

Omar A. Mahroo; Mohammed Oomerjee; Katie M. Williams; David P.S. O'Brart; Christopher J. Hammond

PURPOSE Anterior corneal curvature shows significant heritability. Scheimpflug imaging also permits assessment of posterior tomography. We estimated heritability of posterior and anterior tomographic parameters. METHODS Oculus Pentacam images were obtained in twins from the TwinsUK cohort. Mean anterior and posterior radii of curvature (right cornea) were compared within twin pairs, and heritability calculated (maximum likelihood structural equation modeling, using OpenMx package). Heritability estimates also were calculated for other parameters (anterior and posterior elevation at apex and thinnest point; pachymetry at apex and thinnest point; average pachymetry progression index). RESULTS Images from 138 twins were included (32 monozygotic [MZ] and 37 dizygotic [DZ] twin pairs). Mean (SD) age was 61 (11) years; 91% were female. Coefficients for intrapair correlation for MZ and DZ twins were, respectively, 0.89 and 0.42 for anterior curvature, and 0.93 and 0.46 for posterior curvature (P ≤ 0.0001 for differences between MZ and DZ correlations; Fisher r-to-z transformation). Heritability estimates (95% confidence interval [CI]) for anterior and posterior curvature were 89% (79%-93%) and 90% (83%-94%), respectively. Estimates for all other parameters were 75% or higher, except anterior apical elevation (61%). Point estimates for posterior parameters were consistently higher than anterior parameters, although CIs overlapped. Age-matching yielded similar estimates. Intereye correlations were high; correlations with age were weak (r < 0.30). CONCLUSIONS This is the first study to explore heritability of a number of different parameters of corneal tomography, including posterior curvature. Almost all parameters appeared highly heritable, with a trend toward higher heritability estimates for posterior (versus anterior) parameters.


International Journal of Epidemiology | 2017

Genetically low vitamin D concentrations and myopic refractive error: A Mendelian randomization study

Gabriel Cuellar-Partida; Katie M. Williams; Seyhan Yazar; Jeremy Andrew Guggenheim; Alex W. Hewitt; Cathy Williams; Jie Jin Wang; Pik-Fang Kho; Seang-Mei Saw; Ching-Yu Cheng; Tien Yin Wong; Tin Aung; Terri L. Young; J. Willem L. Tideman; Jost B. Jonas; Paul Mitchell; Robert Wojciechowski; Dwight Stambolian; Pirro G. Hysi; Christopher J. Hammond; David A. Mackey; Robyn M. Lucas; Stuart MacGregor; Myopia (Cream)

Background Myopia prevalence has increased in the past 20 years, with many studies linking the increase to reduced time spent outdoors. A number of recent observational studies have shown an inverse association between vitamin D [25(OH)D] serum levels and myopia. However, in such studies it is difficult to separate the effects of time outdoors and vitamin D levels. In this work we use Mendelian randomization (MR) to assess if genetically determined 25(OH)D levels contribute to the degree of myopia. Methods We performed MR using results from a meta-analysis of refractive error (RE) genome-wide association study (GWAS) that included 37 382 and 8 376 adult participants of European and Asian ancestry, respectively, published by the Consortium for Refractive Error And Myopia (CREAM). We used single nucleotide polymorphisms (SNPs) in the DHCR7, CYP2R1, GC and CYP24A1 genes with known effects on 25(OH)D concentration as instrumental variables (IV). We estimated the effect of 25(OH)D on myopia level using a Wald-type ratio estimator based on the effect estimates from the CREAM GWAS. Results Using the combined effect attributed to the four SNPs, the estimate for the effect of 25(OH)D on refractive error was -0.02 [95% confidence interval (CI) -0.09, 0.04] dioptres (D) per 10 nmol/l increase in 25(OH)D concentration in Caucasians and 0.01 (95% CI -0.17, 0.19) D per 10 nmol/l increase in Asians. Conclusions The tight confidence intervals on our estimates suggest the true contribution of vitamin D levels to degree of myopia is very small and indistinguishable from zero. Previous findings from observational studies linking vitamin D levels to myopia were likely attributable to the effects of confounding by time spent outdoors.

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