Frequency and distribution of corneal astigmatism and keratometry features in adult life: Methodology and findings of the UK Biobank study
Authors:
Nikolas Pontikos aff001; Sharon Chua aff001; Paul J. Foster aff001; Stephen J. Tuft aff001; Alexander C. Day aff001;
Authors place of work:
UCL Institute of Ophthalmology, London, England, United Kingdom
aff001; NIHR Biomedical Research Centre, Moorfields Eye Hospital, London, England, United Kingdom
aff002
Published in the journal:
PLoS ONE 14(9)
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pone.0218144
Summary
Purpose
To describe corneal astigmatism in the UK Biobank population and to look for associations with other biometric variables and socio-demographic factors.
Methods
This analysis included a subsample of 107,452 participants of the UK Biobank study who underwent an enhanced ophthalmic examination including autorefractor keratometry (Tomey RC 5000, Tomey Corp., Nagoya, Japan). Participants were recruited from across the United Kingdom between 2006 and 2010, and all were between 40 to 69 years. After quality control and applying relevant exclusions, data on corneal astigmatism on 83,751 participants were included for analysis. Potential associations were tested through univariable regression and significant parameters carried forward for multivariable analysis.
Results
In univariable analysis, the characteristics significantly associated with higher corneal astigmatism (P<0.001), by order of magnitude were, female gender, white ethnicity, lighter skin colour, use of UV protection, lower alcohol intake, lower corneal-compensated intraocular pressure (ccIOP), older age at completion of education, younger age, higher Townsend deprivation index, lower height and lower systolic blood pressure. After inclusion in the multivariable analysis, gender, skin colour, alcohol intake, age at completion of full-time education, ccIOP, age and Townsend deprivation score remained significant (all P<0.001). Increased corneal astigmatism was also found to be significantly associated with amblyopia or strabismus.
Conclusions
This analysis confirms previous associations with astigmatism such as younger age and female gender, and identified novel risk factors including lighter skin colour, lower alcohol intake, later age having completed full time education later, lower ccIOP and higher Townsend deprivation index. Further research is needed to investigate these novel associations.
Keywords:
Biology and life sciences – Research and analysis methods – People and places – Population groupings – Anatomy – Medicine and health sciences – nutrition – Diet – Alcohol consumption – Head – Age groups – Surgical and invasive medical procedures – ophthalmology – Eye diseases – Eyes – Ocular system – Ocular anatomy – Chemical characterization – Ethnicities – Cornea – Ophthalmic procedures – Cataract surgery – Optical analysis – Refractive index
Introduction
Uncorrected refractive error is the leading cause of moderate to severe visual impairment in all age groups globally [1,2]. Refractive error (ametropia), is a significant public health burden, frequently associated with worse visual acuity and higher risk of amblyopia. The two major components of refractive error in the eye are astigmatism and the spherical refractive error (myopia or hyperopia). Astigmatism is caused by a corneal component and lenticular component. Corneal astigmatism occurs when there are differences in the radius of curvature of the cornea in different meridians such that there is a different focal point for each meridian, with an area of intermediate focus between the two termed the conoid of Sturm[3]. The two meridians are defined as either the steep meridian (also known as the strong meridian) and the flat meridian (also known as the weak meridian). The magnitude of corneal astigmatism has been reported to vary with age [4,5] and there is a shift from the steepest corneal meridian from the vertical (with-the-rule) to the horizontal meridian (against-the-rule)[6–9]. Data on the prevalence and severity of corneal astigmatism is typically obtained from case series of patients undergoing cataract surgery [9–12], with limited data from population based cross-sectional studies or large cohort studies [13]. The UK Biobank (UKBB) studyhttps://paperpile.com/c/PCed6h/ber5o+mNVnR+MTL2y [14–16] recruited over 500,000 men and women aged 40 to 69 years between 2006–2010 from the general population. In 2009 the study protocol was updated to include measurement of ocular data including corneal keratometry, on a subset of these [16]. The aim of our analysis is to describe corneal astigmatism and derived variables in the UKBB population, to look for associations with other biometric variables, socio-demographic factors, and eye conditions.
Materials and methods
UKBB participants
The UKBB participants have previously been described in detail by Allen et al (2012) [16]. In brief, all adults aged between 40 and 69 years old who were registered with the UK National Health Service and living within 25 miles of one of the 22 participating study sites were invited to participate. From a total of 9.2 million postal invitations, 503,325 participants were recruited between 2006 and 2010 (response rate of 5.5%) and after accounting for withdrawals; data on 502,642 participants were available for analysis. All those recruited completed detailed questionnaires on their lifestyle, socioeconomic status, environment and health, and had a number of physiological measures from urine, saliva and blood samples. Further information can be found on the UK Biobank online data showcase (http://biobank.ctsu.ox.ac.uk/crystal/label.cgi).
Ethics
All UK Biobank participants gave written, informed consent. The UK Biobank study was conducted under approval from the NHS National Research Ethics Service (Ref. 11/NW/ 0382), and anonymised data were provided from UK Biobank under application reference 10536.
Eye measurements
Six of the recruiting centres performed an ophthalmic assessment [17] that included LogMAR visual acuity, autorefraction and keratometry (Tomey RC 5000 auto-ref-keratometer Tomey Corp., Nagoya, Japan), intraocular pressure (IOP) (Goldmann-correlated and Corneal-compensated) and corneal biomechanics (both Ocular Response Analyzer, Reichert, Depew, NY, USA). In total, 117,279 (23.3%) of those enrolled had an ophthalmic assessment. The Tomey RC 5000 examination produced autorefraction and keratometric measurements for each eye (http://biobank.ctsu.ox.ac.uk/crystal/label.cgi?id=100014). The Reichert Ocular Response Analyser (Reichert Corp., Philadelphia, PA), measures the biomechanical distortion of the cornea produced by a puff of air for each eye. Measurements included corneal hysteresis, corneal resistance factor and corneal-compensated intraocular pressure (ccIOP) (http://biobank.ctsu.ox.ac.uk/crystal/label.cgi?id=100015). Participants who had eye surgery within the previous 4 weeks or those with possible eye infections did not have IOP measured.
Self-reported eye conditions
The UKBB touchscreen questionnaire allowed participants to report if they had eye disorders or eye diseases, any injury or trauma, which eye was affected and when it was diagnosed. Refractive eye conditions included astigmatism, myopia, hyperopia, presbyopia, strabismus and amblyopia. Eye diseases include diabetic retinopathy, glaucoma, cataract or age-related macular degeneration.
Socio-economic status and ethnicity
The Townsend deprivation index was determined using the participant’s postcodes at recruitment. The Townsend deprivation index has a UK mean of zero, with negative being less deprived and positive being more deprived. Ethnicity choices included white (English/Irish or other white), Asian or British Asian (Indian/Pakistani/Bangladeshi or other Asian), black or black British (Caribbean, African, or other black), Chinese, mixed (white and black Caribbean or African, white and Asian, or other mixed ethnicity), or other ethnic group (not defined).
Lifestyle and environment
The UKBB touchscreen questionnaire also offered questions to participants about their lifestyle, health and environment. In particular, smoking status, alcohol intake frequency, use of sun/UV protection, skin colour without tanning, presence of diabetes. The possible questions/answers and their encoding are explained in more detail in the Table A in S1 File.
Physical measures
Blood pressure and heart rate were measured using the HEM-70151T digital blood pressure monitor (Omron, Hoofddorp, The Netherlands). Weight was measured with the BV-418 MA body composition analyzer (Tanita, Arlington Heights, IL). Height was measured using a Seca 202 height measure (Seca, Birmingham, UK). Body mass index (BMI) was calculated as weight in kg divided by height in m2. Waist circumference at the level of the umbilicus was measured using a Wessex non-stretchable tape measure.
Participant selection
Of the 502,642 participants in UK Biobank, 109,935 had 3mm steep or flat corneal meridian measurement values available for both eyes from which corneal astigmatism measurements could be derived. Participants were excluded if they had any of the following: previous laser refractive eye surgery (n = 7440), previous eye surgery (for cataract, glaucoma or corneal graft) (n = 8051), unreliable 3mm asymmetry index (n = 12,910) or an unreliable keratometry result (n = 6916). This left a total of 83,751 individuals for further analysis.
Corneal astigmatism, mean corneal power and axis of astigmatism
Corneal astigmatism was defined as the 3mm steep meridian minus the 3mm flat meridian. The average of these two values was defined as the mean corneal power. The axis of astigmatism was defined as the angle of the steep meridian. The axis of astigmatism was categorised as with-the-rule if the angle was between 60 and 119 degrees, against-the-rule if the angle was in the intervals 0 to 29 or 150 to 180, otherwise it was categorised as oblique [18].
Statistical methods
We explored the distribution of corneal astigmatism and compared this to previously published studies. We tested the association of mean corneal power and axis of astigmatism with age in both eyes by linear regression. Univariable linear regression and multivariable linear regression statistical analysis models were applied to investigate predictors of corneal astigmatism. Non numeric independent variables were re-coded according to Table A in S1 File. P values for the B coefficients of the linear regressions were derived using a t-test. To account for multiple testing, a Bonferroni corrected P value threshold of < 0.001 was applied to avoid false-positives due to the large number of tests carried out. Only parameters that showed significant association in the univariable analysis were included in the multivariable analysis. Since we found that corneal astigmatism measurements were slightly asymmetric, with left eye having on average higher corneal astigmatism than right eye (Fig A in S1 File) as previously reported by Cumberland et al [17], we repeated statistical analysis in both eyes and only reported parameters which were consistently significantly associated in both eyes. We also repeated the statistical associations with a log-scaled corneal astigmatism variable since the P value derived from a t-test in a linear regression assumes a normally distributed response variable rather than a skewed distribution (Fig B in S1 File). All analyses were performed using R statistical software version 3.2.3. The code is available at https://github.com/pontikos/UKBB/.
Results
Participant selection and distribution of corneal astigmatism
Of the 502,642 UKBB participants who had keratometry measures, after exclusions, 83,751 participants were selected for the purpose of this study. Of these, 36,490 (44%) were male. Ethnicity was 90% white, 3.44% Asian, 3.01% black, 0.89% mixed and 0.41% Chinese (Table 1). In the right eye, 69%, 46%, 29%, 11% and 5% had corneal astigmatism greater than or equal to 0.5, 0.75, 1.0, 1.5 and 2.0 dioptres respectively, and in the left eye, 69%, 46%, 30%, 11% and 5% (Fig 1). After stratification of participants by age group (decade) and gender, corneal astigmatism was found to decrease with age and to be on average higher in females than in males across age groups in the UKBB (Table 2). There was a small but significant difference between corneal astigmatism in left and right eye, with left eye corneal astigmatism higher by on average 0.009 dioptres. A difference between left and right eye corneal astigmatism of less than 1 dioptre was found in 95% of individuals and a difference of more than 2 dioptres (anisometropia) was found in the 0.83% of eyes. This left right asymmetry has previously been reported by Cumberland et al (2015) [17], and is likely due to right eyes always being measured before left eyes according to the UKBB protocol for acquiring keratometry measures (https://biobank.ndph.ox.ac.uk/showcase/showcase/docs/Refraction.pdf, Section 5.1).
Association of mean corneal power and axis of astigmatism with age
Older age was significantly associated with increased mean corneal power in both eyes, with an average increase of 0.15 dioptres per decade (Fig C in S1 File). Axis of astigmatism changed with older age from with-the-rule to against-the-rule (Fig G in S1 File) as reported by Yu et al [19].
Association of amblyopia and strabismus with corneal astigmatism
The number of eyes affected by amblyopia and strabismus in the UKBB are 2483 and 1052 respectively. Corneal astigmatism was highest in eyes affected by amblyopia and strabismus (Fig D in S1 File). This confirms that high corneal astigmatism is a significant risk factor for amblyopia (OR = 1.98 (1.87 to 2.09), P<0.001) and strabismus (OR = 1.73 (1.59 to 1.88), P<0.001) (Fig 4 in S1 File) [20,21].
Univariable and multivariable analysis of corneal astigmatism
Univariable analysis revealed that, by decreasing magnitude of effect size—female gender, white ethnicity, lighter skin colour, use of UV protection, lower alcohol intake, lower ccIOP, older age at completion of education, younger age, higher Townsend deprivation index, lower height and lower systolic blood pressure–were significantly associated with increased corneal astigmatism (Table 3 and Table B in S1 File). After including these variables in the multivariable analysis (Table 4 and Table C in S1 File), the following parameters remained significantly associated with increased corneal astigmatism: female gender, white ethnicity, lighter skin colour, use of UV protection, lower alcohol intake, lower ccIOP, older age at completion of education, younger age and higher Townsend deprivation index.
Discussion
Distribution of corneal astigmatism in the UKBB compared to other cohorts
The distribution of astigmatism in the large population reported in this study supports evidence from previous smaller studies, both in the UK and worldwide, in pre-operative patients [11,12,22–25] and from large consortiums such as CREAM (n = 55,177) [13]. We found that 69%, 29%, 11% and 5% had corneal astigmatism ≥0.5, 1.0, 1.5 and 2.0 dioptres respectively. These are slightly lower than values reported from a recent series of 110,468 cataract pre-operative eyes [25] where 78%, 42%, 21% and 11% having corneal astigmatism ≥0.5, 1.0, 1.5 and 2.0 dioptres respectively. A study of 1,230 eyes undergoing cataract surgery in Wales found corneal astigmatism of >0.5D in 75% in Wales [12] (N = 1,230 eyes). Corneal astigmatism ≥1.0D was found in 36% of eyes with cataract in Germany [26] (N = 15,448 eyes), 47% in China (N = 12,449)[23] and 35% in South Korea [22] (N = 2,847 eyes). Recently, Curragh et al [24] reported that 41% of eyes undergoing cataract surgery (N = 2,080) in Northern Ireland had >1.0D of corneal astigmatism. However, cataract surgery is usually performed in an older age group than those of the participants in the UK Biobank and these pre-operative clinical groups are not necessarily comparable to UKBB participants whose age range is between 40 and 69. A recent CREAM study [27] reported the median corneal astigmatism and median age across 22 studies (8 Asian and 14 European). The median corneal astigmatism was reported in each study and this ranged from 0.539D in the Rotterdam-II European study (N = 3964, mean age = 64.8) [28], to 1.21D in the Asian Singapore Cohort Study of the Risk Factors for Myopia (SCORM) study (N = 1894, mean age = 10.8) [29]. Comparable studies to the UKBB in terms of age and gender demographics of the participants are the Rotterdam-III Study (N = 5850 eyes, mean age = 57)[30], the Singapore Chinese Eye Study (SCES-610K) (N = 1106 eyes, mean age = 57.6)[31], the Gutenberg Health Study (GHS-1) study (N = 4796 eyes, mean age = 55.9)[32] which reported a median corneal astigmatism of 0.618D, 0.703D and 0.65D respectively. This is comparable to the UKBB median corneal astigmatism of 0.71D.
Modelling of corneal astigmatism
In the multivariable analysis, parameters known to be strongly associated with gender, such as height and weight (Table 4), were no longer significantly associated with corneal astigmatism. Variables which remained significantly associated by decreasing order of magnitude were gender, skin colour, alcohol intake, age at completion of full-time education, ccIOP, age and Townsend deprivation score. The adjusted R-squared of the multivariable regression was remarkably low at 0.01 which highlights that there are many other unobserved variables which influence corneal astigmatism.
Gender
Our study confirms, as previously reported by Yuan et al [23], that corneal astigmatism is higher in females than in males even after adjusting for weight and height (Table 4). Females have on average 0.07D more corneal astigmatism in right eye and 0.08D more in left eye (Table 3).
Ethnicity and skin colour
Asian and black ethnicities appear to be significantly protective for corneal astigmatism in both eyes according to the univariable analysis (Table 3 and Table B in S1 File) but are no longer significant in the multivariable analysis (Table 4 and Table 3 in S1 File). However, skin colour remains significantly associated with darker skin being protective (B = -0.032 (-0.042 to -0.024), P<0.001) (Table 4 and Table C in S1 File). This relationship can also be clearly seen independently in males and females (Fig E in S1 File). The link between corneal astigmatism and deficiency in melanin production has been previously reported for albinism [33]. Our data suggests that darker skin and hence possibly increased melanin production appears protective for corneal astigmatism.
Alcohol intake
Alcohol intake is significantly protective for corneal astigmatism according to the univariable and multivariable analysis (B = -0.008, (-0.012 to -0.004), P<0.001). In particular, the group that drinks nearly every day has the lowest average corneal astigmatism at 0.80 dioptres. This is surprising due to the negative consequences of alcohol abuse on eye conditions. However, on closer inspection it appears that the group that drinks nearly every day in the UKBB consists primarily of men in the 65+ age group; 55% of men drink every day in this study vs 44% of women. Alcohol intake effect is difficult to decouple from gender and age due to the three-way interaction between alcohol-intake, age and gender, with “never-drinkers” and “daily drinkers” showing a clear interaction (Fig F in S1 File).
Age completed full-time education
We found a significant positive association between age at which full-time education was completed and corneal astigmatism (B = 0.006 (0.004 to 0.008), P<0.001). As far as we know, this association has not been reported before. This result was consistent with participants with self-reported astigmatism finishing full-time education later than other participants (Fig D in S1 File). Interestingly, this relationship was not observed in individuals with myopia (Fig D in S1 File), which may be supported by recent evidence suggesting that myopia is not linked as much to near work [34], but rather to earlier life exposures [35].
Hysteresis and corneal-compensated intraocular pressure
Of interest, corneal hysteresis, which measures the cornea’s ability to absorb and dissipate energy, was not found to be associated with corneal astigmatism in the univariable nor in the multivariable analysis.
In the univariable analysis (Table 3 and Table B in S1 File), we found a small but significant protective effect of ccIOP on corneal astigmatism in both eyes (B = -0.006 (-0.007 to -0.005), P<0.001), which remained significant in the multivariable analysis (B = -0.005 (-0.006 to -0.004), P<0.001) (Table 4 and Table C in S1 File). As far as we know, the significant association of ccIOP with corneal astigmatism has not been detected before although it has been tested for in a small study [36].
Age
In the age range of the UKBB, from age 40 to 69, corneal astigmatism decreased significantly with age by an average of 0.04 dioptres in both eyes per decade in the univariable and multivariable analysis (Table 4). This result is supported by Yuan et al [23]. However, in a previous UKBB study, Shah et al [37] reported that the level of corneal astigmatism is relatively constant across age groups. However, no linear regression was performed by the authors to support this statement. They did find however that increasing age is associated with higher refractive astigmatism, as derived from cylindrical power, which we have also recapitulated (B = 0.015 (0.014 to 0.016), P<0.001) (Fig C in S1 File). We believe this increase in refractive astigmatism with age is likely driven by increasing lenticular astigmatism, since corneal astigmatism decreases.
Townsend deprivation index
Higher corneal astigmatism is associated with a higher Townsend deprivation index (B = 0.004 (0.002 to 0.006), P<0.001) in the UKBB (Table 4). To our knowledge this association has never been reported before. This association may be partly due to an interaction effect with age since older individuals, hence with lower corneal astigmatism, tend to live in less deprived areas (Fig H in S1 File).
Strengths and limitations of our study
The strength of this study is the large sample size of 83,751 participants and that participants were not pre-operative patients hence more representative of the general population. However due to the limited age range of the participants, between 40 and 69 years, the age distribution is limited to adult life and are results cannot be extrapolated outside that age range. For instance, we cannot confirm whether or not corneal astigmatism increases past the age of 70 [19,23] as none of the UKBB participants had refractometry past the age of 69. Furthermore, due to the voluntary nature of the UKBB study, participants are likely to be a healthier more educated sample of the UK population and not necessarily representative of the general UK population. Regardless, a range of exposures and characteristics are likely to have been captured due to the sample size of the UKBB and so the results can still be applicable to other populations.
Conclusion
This analysis confirms, in a dataset of 83,751 individuals within the 40–69 age range, adverse associations with corneal astigmatism such as younger age and female gender, and identified novel associations including lighter skin colour, lower frequency of alcohol intake, later age having completed full time education, lower ccIOP and higher Townsend deprivation index. Further research and longitudinal data are needed to investigate these novel associations and to infer causality.
Supporting information
S1 File [docx]
Supplementary materials.
Zdroje
1. Bourne RRA, Stevens GA, White RA, Smith JL, Flaxman SR, Price H, et al. Causes of vision loss worldwide, 1990–2010: A systematic analysis. Lancet Glob Heal. 2013;
2. Hashemi H, Fotouhi A, Yekta A, Pakzad R, Ostadimoghaddam H, Khabazkhoob M. Global and regional estimates of prevalence of refractive errors: Systematic review and meta-analysis. Journal of Current Ophthalmology. 2018.
3. Morlet N, Minassian D, Dart J. Astigmatism and the analysis of its surgical correction. The British journal of ophthalmology. 2002.
4. Hirsch MJ. Changes in astigmatism after the age of forty. Optom Vis Sci. 1959;
5. Attebo K, Ivers RQ, Mitchell P. Refractive errors in an older population: The Blue Mountains Eye Study. Ophthalmology. 1999;
6. Hayashi K, Hayashi H, Hayashi F. Topographic Analysis of the Changes in Corneal Shape Due to Aging. Cornea. 1995;
7. Riley AF, Grupcheva CN, Malik TY, Craig JP, McGhee CNJ. The Auckland Cataract Study: Demographic, corneal topographic and ocular biometric parameters. Clin Exp Ophthalmol. 2001;
8. Ho JD, Liou SW, Tsai RJF, Tsai CY. Effects of aging on anterior and posterior corneal astigmatism. Cornea. 2010;
9. Mohammadi M, Naderan M, Pahlevani R, Jahanrad A. Prevalence of corneal astigmatism before cataract surgery. Int Ophthalmol. 2016;
10. Hoffer KJ. Biometry of 7,500 cataractous eyes. Am J Ophthalmol. 1980;
11. Hoffmann PC, Hütz WW. Analysis of biometry and prevalence data for corneal astigmatism in 23 239 eyes. J Cataract Refract Surg. 2010;
12. Khan MI, Muhtaseb M. Prevalence of corneal astigmatism in patients having routine cataract surgery at a teaching hospital in the United Kingdom. J Cataract Refract Surg. 2011;
13. Verhoeven VJM, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, et al. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet. 2012;
14. Ollier W, Sprosen T, Peakman T. UK Biobank: From concept to reality. Pharmacogenomics. 2005;
15. Palmer LJ. UK Biobank: bank on it. Lancet. 2007.
16. Allen N, Sudlow C, Downey P, Peakman T, Danesh J, Elliott P, et al. UK Biobank: Current status and what it means for epidemiology. Heal Policy Technol. 2012;
17. Cumberland PM, Bao Y, Hysi PG, Foster PJ, Hammond CJ, Rahi JS. Frequency and distribution of refractive error in adult life: Methodology and findings of the UK biobank study. PLoS One. 2015;
18. Ueno Y, Hiraoka T, Beheregaray S, Miyazaki M, Ito M, Oshika T. Age-Related Changes in Anterior, Posterior, and Total Corneal Astigmatism. J Refract Surg. 2014;
19. Yu JG, Zhong J, Mei ZM, Zhao F, Tao N, Xiang Y. Evaluation of biometry and corneal astigmatism in cataract surgery patients from Central China. BMC Ophthalmol. 2017;
20. Jonas JB, Kling F, Grundler AE. Optic disc shape, corneal astigmatism, and amblyopia. Ophthalmology. 1997;
21. Harvey EM. Development and treatment of astigmatism-related amblyopia. Optometry and Vision Science. 2009.
22. Oh EH, Kim H, Lee HS, Hwang KY, Joo CK. Analysis of anterior corneal astigmatism before cataract surgery using power vector analysis in eyes of Korean patients Presented in part at the 110th annual meeting of the Korean Ophthalmological Society, Seoul, South Korea, November 2013. J Cataract Refract Surg [Internet]. 2015 Jun [cited 2019 Aug 11];41(6):1256–63. Available from: http://www.ncbi.nlm.nih.gov/pubmed/26189381 doi: 10.1016/j.jcrs.2014.09.043 26189381
23. Yuan X, Song H, Peng G, Hua X, Tang X. Prevalence of corneal astigmatism in patients before cataract surgery in Northern China. J Ophthalmol. 2014;
24. Curragh DS, Hassett P. Prevalence of corneal astigmatism in an NHS cataract surgery practice in Northern Ireland. Ulster Med J. 2017;
25. Day AC, Dhariwal M, Keith MS, Ender F, Perez Vives C, Miglio C, et al. Distribution of preoperative and postoperative astigmatism in a large population of patients undergoing cataract surgery in the UK. Br J Ophthalmol. 2019;
26. Schuster AKG, Pfeiffer N, Schulz A, Hoehn R, Ponto KA, Wild PS, et al. Refractive, corneal and ocular residual astigmatism: distribution in a German population and age-dependency—the Gutenberg health study. Graefe’s Arch Clin Exp Ophthalmol. 2017;
27. Shah RL, Li Q, Zhao W, Tedja MS, Tideman JWL, Khawaja AP, et al. A genome-wide association study of corneal astigmatism: The CREAM Consortium. Mol Vis. 2018;
28. Hofman A, Breteler MMB, Van Duijn CM, Krestin GP, Pols HA, Stricker BHC, et al. The Rotterdam Study: Objectives and design update. Eur J Epidemiol. 2007;
29. Saw SM, Shankar A, Tan SB, Taylor H, Tan DTH, Stone RA, et al. A cohort study of incident myopia in Singaporean children. Investig Ophthalmol Vis Sci. 2006;
30. Hofman A, Brusselle GGO, Murad SD, van Duijn CM, Franco OH, Goedegebure A, et al. The Rotterdam Study: 2016 objectives and design update. Eur J Epidemiol. 2015;
31. R. L, V.S.E. J, Y. Z, P. R, N. C, E.S. T, et al. Methodology of the Singapore Indian Chinese Cohort (SICC) eye study: Quantifying ethnic variations in the epidemiology of eye diseases in Asians. Ophthalmic Epidemiol [Internet]. 2009;16(6):325–36. Available from: http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE=reference&D=emed12&NEWS=N&AN=355791759 doi: 10.3109/09286580903144738 19995197
32. Höhn R, Kottler U, Peto T, Blettner M, Münzel T, Blankenberg S, et al. The ophthalmic branch of the Gutenberg health study: Study design, cohort profile and self-reported diseases. PLoS One. 2015;
33. Schulze Schwering M, Kumar N, Bohrmann D, Msukwa G, Kalua K, Kayange P, et al. Refractive errors, visual impairment, and the use of low-vision devices in albinism in Malawi. Graefe’s Arch Clin Exp Ophthalmol. 2015;
34. Cooper J, Tkatchenko A V. A Review of Current Concepts of the Etiology and Treatment of Myopia. Eye Contact Lens. 2018;
35. Tedja MS, Wojciechowski R, Hysi PG, Eriksson N, Furlotte NA, Verhoeven VJM, et al. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat Genet. 2018;
36. Hagishima M, Kamiya K, Fujimura F, Morita T, Shoji N, Shimizu K. Effect of corneal astigmatism on intraocular pressure measurement using ocular response analyzer and Goldmann applanation tonometer. Graefe’s Arch Clin Exp Ophthalmol. 2010;
37. Shah RL, Guggenheim JA. Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Hum Genet. 2018
Článok vyšiel v časopise
PLOS One
2019 Číslo 9
- Metamizol jako analgetikum první volby: kdy, pro koho, jak a proč?
- Nejasný stín na plicích – kazuistika
- Masturbační chování žen v ČR − dotazníková studie
- Úspěšná resuscitativní thorakotomie v přednemocniční neodkladné péči
- Fixní kombinace paracetamol/kodein nabízí synergické analgetické účinky
Najčítanejšie v tomto čísle
- Graviola (Annona muricata) attenuates behavioural alterations and testicular oxidative stress induced by streptozotocin in diabetic rats
- CH(II), a cerebroprotein hydrolysate, exhibits potential neuro-protective effect on Alzheimer’s disease
- Comparison between Aptima Assays (Hologic) and the Allplex STI Essential Assay (Seegene) for the diagnosis of Sexually transmitted infections
- Assessment of glucose-6-phosphate dehydrogenase activity using CareStart G6PD rapid diagnostic test and associated genetic variants in Plasmodium vivax malaria endemic setting in Mauritania