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Irregularity in the corneal curvature (CC) is highly associated with various eye disorders such as keratoconus and myopia. The sample had limited power to find genomewide significant (5 × 10−8) hits but good power for replication. Thus, an attempt was made to test whether alleles in the FRAP1 and PDGFRA genes, recently found to be associated with CC in Asian populations, also influence CC in Australians of North European ancestry. Results of initial genomewide association studies (GWAS) for CC in Australians were also reported.
Two population-based cohorts of 1788 Australian twins and their families, as well as 1013 individuals from a birth cohort from Western Australia, were genotyped using genomewide arrays. Following separate individual analysis and quality control, the results from each cohort underwent meta-analysis.
Meta-analysis revealed significant replication of association between rs2114039 and corneal curvature (P = 0.0045). The SNP rs2114039 near PDGFRA has been previously implicated in Asians. No SNP at the FRAP1 locus was found to be associated in our Australian samples. No SNP surpassed the genomewide significance threshold of 5 × 10−8. The SNP with strongest association was rs2444240 (P = 3.658 × 10−7), which is 31 kb upstream to the TRIM29 gene.
A significant role of the PDGFRA gene in determining corneal curvature in the Australian population was confirmed in this study, also highlighting the putative association of the TRIM29 locus with CC.
Refraction of light through the cornea is the preliminary step in vision. This bending of light is highly dependent on the curvature of the cornea. Corneal astigmatism or an irregularity in corneal curvature (CC) leads to blurred uncorrected vision. Keratoconus is a disease characterized by a conical-shaped cornea and irregular astigmatism.1 Patients with this corneal condition often experience vision distortion, multiple images, and sensitivity to light. In addition to keratoconus, corneal irregularities are also associated with refractive error2 and Marfan syndrome.3
Variation in corneal curvature is dependent on ethnic background,4,5 geographical as well as environmental conditions,6 age,7 and stature.7 CC is highly heritable,8 with previous studies revealing heritability estimates ranging between 60% and 95%.6,8–11 Improved understanding of the genetic architecture of this biometric trait will aid in determining the molecular mechanisms of blinding eye disorders, and contribute to our ocular development and evolutionary biology knowledge.
Genomewide association studies (GWAS) have been successful in revealing the genetic variants behind various complex traits including age-related macular degeneration, type 2 diabetes as examples.12–15 The only published GWAS for CC is from a Singaporean Asian population, in which the significant associations of single nucleotide polymorphisms (SNPs) in FRAP1 and PDGFRA genes with corneal curvature were reported.6 As is the case with other quantitative traits, CC is likely to be determined by many genes, with ever larger GWASs likely to lead to the identification of additional associated SNPs.16 Furthermore, it is unknown whether genes found to be significantly associated with CC in Asian population would be relevant to other racial groups. In previous studies, ethnic and environmental backgrounds constitute an important determinant of CC.17–19 Thus, we aimed to test whether PDGFRA and FRAP1 genes found to be associated with CC in a Singaporean Asian population also determine the CC in Australians of Northern European ancestry. We also aimed to report initial GWAS on CC in Australians of Northern European ancestry. We conducted two population-based GWASs on 1788 Australian twins and their families,20 as well as 1013 unrelated individuals from a population cohort from Western Australia.
This study was conducted according to the principles expressed in the Declaration of Helsinki. The study was approved by the human research ethics committees of the University of Tasmania, Royal Victorian Eye and Ear Hospital, Queensland Institute of Medical Research, and University of Western Australia. Informed consent was obtained from parents with the child's assent or from adult participants before testing.
In all, 1788 individuals of 857 twin families were recruited from Australia. Recruitment of twins was performed through the Twins Eye Study in Tasmania (TEST) and the Brisbane Adolescent Twin Study (BATS).20 BATS participants ranged in age from 10 to 40 years and TEST participants ranged in age from 5 to 90 years. Corneal curvature was measured using a commercial automatic refractor/keratometer (Humphrey-598 Automatic Refractor/Keratometer; Carl Zeiss Meditec, Inc., Miami, FL). The difference between curvature values of left and right eyes was not significant (t-test, P = 0.24).
Saliva or peripheral blood samples from subjects were used to extract DNA, which was genotyped on the Illumina HumanHap 610W Quad arrays (Illumina, Inc., San Diego, CA). The majority of people from the BATS study were genotyped by deCODE Genetics (Reykjavik, Iceland). TEST participants and a small number of BATS individuals were genotyped by the Centre for Inherited Disease Research (CIDR) (Perth, Australia).
Filtering criteria for genotypic data were: minor allele frequency ≥ 1%, Hardy–Weinberg Equilibrium Test, P ≥ 10−6, SNP call rate > 95% or Illumina Beadstudio GenCall score ≥ 0.7. Quality control of SNPs gave 559,990 SNPs, which then underwent association testing in the twin cohorts.
Ancestral outliers were corrected by principal component analysis (PCA)21 using the “smartpca” program (EIGENSOFT 3.0 software; provided in the public domain, nickp/at/broad.mit.edu). Australian twin data were compared with all populations in HapMap phase 3 and collection of five other GenomEUTWIN populations.22,23 Only PC1 and PC2 with the highest eigenvalues were considered to identify and filter outliers. PC1 reflects the difference between Africans and others, whereas PC2 reflects the difference between East Asian populations with others. As expected, the Australian population clustered with Europeans with some individuals also showing Asian and African ancestry. To remove Australian population outliers like Australians with African or Asian ancestry, the mean and SD of collective European populations, that is, Hapmap CEU (Utah residents with Northern and Western European ancestry from the CEPH collection), TSI (Toscans in Italy), and GenomEUTWIN (European Twin Population), was calculated for reference PC1 and PC2 scores. Any individual that fell away from the mean by >6 times their SD on PC1 and PC2 were removed, with the remainder considered for further analysis.
Using the “MACH v1.0.16b” and “mimimac” packages, imputation of Australian Twin genotyped data was carried out using the 1000 Genomes haplotypes available for 283 European ancestry individuals in the August 2010 release of 1000 Genomes project.24,25 Approximately 482,000 common genotyped markers were used in imputation, which gave 11,914,767 imputed SNPs. Following quality control (R2 > 0.3 for each SNP), 8,016,011 SNPs underwent association analysis. The MERLIN program (Center for Statistical Genetics, Ann Arbor, MI) was used to perform association testing, taking into account relatedness of the twins and their families.26 We used age and sex as covariates.
The 21-year review of the Western Australian Pregnancy Cohort (Raine) Study investigated ophthalmic health and established the Raine Eye Health Study (REHS). The Raine Study is one of the largest ongoing prospective cohort studies of pregnancy, childhood, adolescence, and young adulthood. In 1989, 2900 pregnant women were recruited at 16- to 18-weeks' gestation into a randomized clinical trial at King Edward Memorial Hospital, Perth, Western Australia for investigating effects of intensive ultrasound and Doppler studies in pregnancy outcomes. The cohort has been evaluated in detail during childhood (1, 2, 3, 5, 8, and 10 years) and adolescence (14 and 17 years). Raine participants underwent a comprehensive ocular examination for the first time at the 21-year follow-up. The ocular examination included measurements of visual acuity, cycloplegic auto refraction, as well as several ocular biometric variables and multiple ophthalmic photographs (anterior and posterior segments). A total of 1344 subjects were examined in the 24-month period from March 2010 to February 2012.
Ocular biometric parameters including CC were measured (IOLMaster v.5; Carl Zeiss Meditec AG, Jena, Germany). Three measurements of CC within 0.3D within each meridian with careful alignment and focus were recorded. Complete data were available from 1013 participants for analysis. The average age of the participants was 20.0 (range: 18–22) years. DNA samples from previous assessments and consents for GWAS studies were available for the participants.
Individual genotype data for 1494 participants were extracted from the genomewide array (Illumina 660 Quad Array). Briefly, the genotyping was performed on the Illumina BeadArray Reader at the Centre for Applied Genomics (Toronto, Ontario, Canada) using 250 nanograms of DNA. Any pair of individuals who were related with a π > 0.1875 (in between second- and third-degree relatives; e.g., between half-sibs and cousins) was investigated, and the individual with the higher proportion of missing data was excluded from the “clean” data set (68 individuals excluded). Individuals who had low genotyping success (i.e., missing data) were excluded from the “clean” data set; a threshold of absent data >3% was used for exclusion (16 individuals excluded). Additionally, if they had high levels of heterozygosity then they were also excluded (heterozygosity < 0.30 excluded 3 individuals) because this may indicate sample contamination. In terms of genotyping success rates, we also excluded SNPs that did not satisfy a Hardy–Weinburg equilibrium P value > 5.7 × 10−7 (919 markers), a call rate > 95% (97,718 markers), and a minor allele frequency > 0.01 (1%) (119,246 markers, including CNVs). To account for population stratification, the first five principal components were calculated using a subset of 42,888 SNPS that were not in LD with each other. PCA was conducted using the EIGENSTRAT program (provided in the public domain, aprice/at/hsph.harvard.edu).21
The MACH v1.0.16 (http://www.sph.umich.edu/csg/yli/mach/index.html) software was used for GWAS imputation on the 22 autosomes. Once the data were cleaned, a two-step process was carried out using the CEU samples from HapMap phase2 build 36 release 22 (http://hapmap.ncbi.nlm.nih.gov/index.html.en) as a reference panel.
With PLINK27 as an interface with R (provided in the public domain by the R Foundation for Statistical Computing, Vienna, Austria, available at http://www.r-project.org/), a linear regression model was used to examine the association between SNPs and keratometry adjusted for age, sex, and the first two principal components, which account for population stratification in this cohort.
Meta-analysis increases the power to identify associations by increasing the sample size. The β-coefficients strategy of the program METAL was used to conduct meta-analysis.28
After quality control, the population sizes of the BATS/TEST and Raine studies were 1788 and 1013, respectively. Summary statistics for both the populations under study are shown in Table 1.
With consideration of combined sample size, the GWAS power to detect the variant that could explain at least 1% variation of CC is very low (power = 30%), whereas replication power for significant replication cutoff 0.05/2 is >99%. Thus, our primary emphasis was on replication of FRAP1 and PDGFRA genes, reported genomewide association with CC in Asians, in an Australian population of Northern European ancestry. We tested whether the most significant SNP in each gene was associated in our European ancestry samples. We found that SNP rs2114039 in PDGFRA was associated with corneal curvature (P = 0.0045). Figure 1 shows the recombination profile between the SNPs and PDGFRA locus. The effect size of the trait-increasing allele was 0.02275 mm per copy of the T allele. The effect sizes across different studies are shown in Figure 2A. However, SNP rs6540964 in gene FRAP1 was not associated with curvature (P = 0.2984); effect sizes are shown in Figure 2B.
Although our study does not have enough power to detect a genomewide-associated variant, we report the initial findings. The Independent association test on BATS/TEST and Raine data yielded a best SNP rs4552334 (P = 2.5 × 10−6) and rs11930632 (P = 2.47 × 10−6), respectively. We followed this analysis by meta-analysis of outcomes from the 1,704,858 SNPs common in both studies.
Results from the meta-analysis across the genome are displayed in Figure 3. The 25 most significant SNPs from the meta-analysis are shown in Supplemental Table S1 (see Supplementary Material and Supplementary Table S1, http://www.iovs.org/content/53/11/7131/suppl/DC1).
As expected, meta-analysis did not reveal any genomewide-associated SNPs: the most associated genotyped SNP rs2444240 had a P value of 3.658 × 10−7 at 120.040 Mb (build 37) on chromosome 11. This SNP had a slightly stronger signal in the Raine study, as shown in Table 2. The nearest gene to these SNPs is TRIM29 on the chromosome 11q23.3 region (NCBI build 37), which spans only 26 kb. The recombination profile between the SNPs and TRIM29 locus is shown in Supplemental Figure S1 (see Supplementary Material and Supplemental Fig. S1, http://www.iovs.org/content/53/11/7131/suppl/DC1).
We have conducted a genomewide association study on corneal curvature in an Australian population of Northern European ancestry. Our sample showed that SNPs near PDGFRA, which were very recently shown to play a role in CC in Asians, also play a role in samples of Northern European Ancestry. The allele frequency at rs2114039 is similar (~0.3) across the range of European and Asian ancestry samples in the HapMap3 data. The variance explained by rs2114039 in our European ancestry sample for BATS/TEST and Raine study was 0.6% and 0.1%, respectively, which is somewhat lower than that seen in the Asian studies (1.8%, 11.1%, 4.9%, and 7.5% for SP2, SIMES, SINDI, and SCORM study, respectively). However, the estimates of variance explained in the Asian studies are probably an overestimate of the true effect size due to this SNP being selected as one of the most significant results from a genomewide scan.30 An estimate of the effect size in an independent Asian population would allow us to determine if the effect size at this SNP truly differs in the two populations.
Although our study did not identify any genomewide significant loci, meta-analyzing across two Australian studies led to a more significant top SNP, with rs2444240 in TRIM29 achieving a P value of 3.658 × 10−7. Larger sample sizes are required to unambiguously identify novel loci. With reference to past literature, we found involvement of some of the genes near or within the top 25 SNPs with some related traits.31–34 A gene expression profile of human keratoconus suggests significant expression of the TRIM29 gene.31 This differential expression of the TRIM29 gene could be responsible for the conical shape of the cornea. Apart from this, a linkage study on Ashkenazi Jewish families also supports a possible role of TRIM29 in variation of CC by their report of linkage between 11q23 loci and myopia.32 In addition, a gene expression study on focal loss of retinal ganglion cells suggests significant downregulation of the BCL11B gene.34 Studies on myopia in chicks already established that the flattened cornea is an outcome of ganglion cells' destruction.33 Further study needs to be done to investigate the possible role of TRIM29 and BCL11B genes in determining CC.
In conclusion, our study of CC showed that the SNP in PDGFRA, recently implicated in this trait in Asians, also underlies trait variation in Australians of Northern European ancestry. The other gene reported to be associated with CC in Asian populations, FRAP1, did not show a significant effect in our samples. Although our study was underpowered to detect novel loci, we found some evidence that SNPs near TRIM29 may play a role in determining CC. Our findings of SNPs at TRIM29 and other regions should be replicated in further studies, with meta-analyses likely to prove important in further dissecting this important endophenotype.
The authors of both eye studies thank Camilla Day and staff of the CIDR. The QIMR authors thank the twins eye study participants and their families: Scott D. Gordon, Anjali K. Henders, Sarah E. Medland, Brian McEvoy, Dale R. Nyholt, Margaret J. Wright, Megan J. Campbell, and Anthony Caracella for their assistance in processing the Australian genotyping data; Jane MacKinnon, Shayne Brown, Lisa Kearns, Sandra Staffieri, Olivia Bigault, Colleen Wilkinson, Julie Barbour, Byoung Sung Chu, Jonathan Ruddle Paul Sanfilippo, Cong Sun, Justin Sherwin, Robert Macmillan, Rachael Adams, Robyn Troutbeck, Ya Ling Ma, Christine Chen, and Amy Cohn; and Thanuja Gunasekera, Allison McKenzie, Anne-Louise Ponsonby, Terry Dwyer, James Dilger, Palma Ragno, Jenny Boadle, Kim Dorrell, Shyamali Dharmage, John Hopper, and Jamie Craig for assistance in recruiting twins.
The Raine Eye Health Study authors thank the Raine eye health study participants and their families; the Raine Study team, and ophthalmologists, orthoptists, and medical students at Lions Eye Institute for cohort coordination and data collection, particularly, Hannah Forward, Charlotte McKnight, Alex Tan, Alla Soloshenko, Sandra Oates, and Diane Wood.
Supported by an Australian National Health and Medical Research Council (NHMRC) Enabling Grant 2004–2009 (Australian Twin Registry). Genotyping for part of the Australian sample: NHMRC Medical Genomics Grant; genotyping for the remainder: National Institutes of Health (NIH, Bethesda, Maryland) and Centre for Inherited Disease Research (CIDR) as part of an NIH/National Eye Institute (NEI) Grant 1RO1EY018246; NIH/NEI Grant 1RO1EY018246, and NIH/CIDR genotyping project grant (PI: T. Young). Australian NHMRC Career Development Awards (AWH, SM). Ophthalmic Examination of the Twins: Clifford Craig Medical Research Trust, Ophthalmic Research Institute of Australia (ORIA), American Health Assistance Foundation (AHAF), Peggy and Leslie Cranbourne Foundation, Foundation for Children, National Health and Medical Research Foundation Project Grant 350415 (2005–2007), Jack Brockhoff Foundation, and the Pfizer Australia Senior Research Fellowship (DAM). Core management of the Raine Study: The University of Western Australia (UWA), The Telethon Institute for Child Health Research, Raine Medical Research Foundation, UWA Faculty of Medicine, Dentistry and Health Sciences, Women's and Infant's Research Foundation and Curtin University. Genotyping: NHMRC Project Grant 572613. Raine Eye Health Study: NHMRC Grant 1021105, Lions Eye Institute, the Australian Foundation for the Prevention of Blindness, and Alcon Research Institute.
Disclosure: A. Mishra, None; S. Yazar, None; A.W. Hewitt, None; J.A. Mountain, None; W. Ang, None; C.E. Pennell, None; N.G. Martin, None; G.W. Montgomery, None; C.J. Hammond, None; T.L. Young, None; S. Macgregor, None; D.A. Mackey, None