• This record comes from PubMed

Replication of SNP associations with keratoconus in a Czech cohort

. 2017 ; 12 (2) : e0172365. [epub] 20170216

Language English Country United States Media electronic-ecollection

Document type Comparative Study, Journal Article

INTRODUCTION: Keratoconus is a relatively frequent disease leading to severe visual impairment. Existing therapies are imperfect and clinical management may benefit from improved understanding of mechanisms leading to this disease. We aim to investigate the replication of 11 single nucleotide polymorphisms (SNPs) with keratoconus. METHODS: SNPs from loci previously found in association with keratoconus were genotyped in 165 keratoconus cases of Caucasian Czech origin (108 males and 57 females) and 193 population and gender-matched controls. They included rs1536482 (COL5A1), rs4839200 (KCND3), rs757219 and rs214884 (IMMP2L), rs1328083 and rs1328089 (DAOA), rs2721051 (FOXO1), rs4894535 (FNDC3B), rs4954218 (MAP3K19, RAB3GAP1), rs9938149 (ZNF469) and rs1324183 (MPDZ). A case-control association analysis was assessed using Fisher's exact tests. RESULTS: The strongest association was found for rs1324183 (allelic test OR = 1.58; 95% CI, 1.10-2.24, p = 0.01). Statistically significant values were also obtained for rs2721051 (allelic test OR = 1.72; 95% CI, 1.07-2.77, p = 0.025) and rs4954218 (allelic test OR = 1.53; 95% CI, 1.01-2.34; p = 0.047) which showed an opposite effect direction compared to previously reported one. CONCLUSION: Independent replication of association between two SNPs and keratoconus supports the association of these loci with the risks for the disease development, while the effect of rs4954218 warrants further investigation. Understanding the role of the genetic factors involved in keratoconus etiopathogenesis may facilitate development of novel therapies and an early detection.

See more in PubMed

Vazirani J, Basu S. Keratoconus: current perspectives. Clin Ophthalmol. 2013;7:2019–2030. 10.2147/OPTH.S50119 PubMed DOI PMC

Kennedy RH, Bourne WM, Dyer JA. A 48-year clinical and epidemiologic study of keratoconus. Am J Ophthalmol. 1986;101:267–273. PubMed

Burdon KP, Vincent AL. Insights into keratoconus from a genetic perspective. Clin Exp Optom. 2013;96:146–154. 10.1111/cxo.12024 PubMed DOI

Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P. Keratoconus in 18 pairs of twins. Acta Ophthalmol. 2012;90:e482–486. 10.1111/j.1755-3768.2012.02448.x PubMed DOI

Davidson AE, Borasio E, Liskova P, Khan AO, Hassan H, Cheetham ME, et al. Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus. Invest Ophthalmol Vis Sci. 2015;56:578–586. 10.1167/iovs.14-15792 PubMed DOI

Burdon KP, Macgregor S, Bykhovskaya Y, Javadiyan S, Li x, Laurie KJ, et al. Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Invest Ophthalmol Vis Sci. 2011;52:8514–8519. 10.1167/iovs.11-8261 PubMed DOI PMC

Li X, Bykhovskaya Y, Haritunians T, Siscovick D, Aldave A, Szczotka-Flynn L, et al. A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Hum Mol Genet. 2012;21:421–429. 10.1093/hmg/ddr460 PubMed DOI PMC

Dudakova L, Palos M, Jirsova K, Stranecky V, Krepelova A, Hysi PG, et al. Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent. Eur J Hum Genet. 2015; 23:1581–3. 10.1038/ejhg.2015.28 PubMed DOI PMC

Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Yang H. Two-stage genome-ewide linkage scan in keratoconus sib pair families. Invest Ophthalmol Vis Sci. 2006;47:3791–3795. 10.1167/iovs.06-0214 PubMed DOI

Lu Y, Vitart V, Burdon KP, Khor CC, Bykhovskaya Y, Mirshahi A, et al. Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet. 2013;45:155–163. 10.1038/ng.2506 PubMed DOI PMC

Li X, Bykhovskaya Y, Canedo AL, Haritunians T, Siscovick D, Aldace AJ, et al. Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. Invest Ophthalmol Vis Sci. 2013;54:2696–2704. 10.1167/iovs.13-11601 PubMed DOI PMC

Sahebjada S, Schache M, Richardson AJ, Snibson G, MacGregor S, Daniell M, et al. Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population. Invest Ophthalmol Vis Sci. 2013;54:8224–8228. 10.1167/iovs.13-12982 PubMed DOI

Kanellopoulos AJ, Asimellis G. Revisiting keratoconus diagnosis and progression classification based on evaluation of corneal asymmetry indices, derived from Scheimpflug imaging in keratoconic and suspect cases. Clin Ophthalmol. 2013;7:1539–1548. 10.2147/OPTH.S44741 PubMed DOI PMC

Bae HA, Mills RA, Lindsay RG, Phillips T, Coster DJ, Mitchell P, et al. Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus. Invest Ophthalmol Vis Sci. 2013;54:5132–5135. 10.1167/iovs.13-12377 PubMed DOI PMC

Smith SM, Maughan PJ. SNP genotyping using KASPar assays. Methods Mol Biol. 2015;1245:243–256. 10.1007/978-1-4939-1966-6_18 PubMed DOI

Lin PI, Vance JM, Pericak-Vance MA, Martin ER. No gene is an island: the flip-flop phenomenon. Am J Hum Genet. 2007;80:531–538. 10.1086/512133 PubMed DOI PMC

Founti P, Haidich AB, Chatzikyriakidou A, Salonikiou A, Anastasopoulos E, Pappas T, et al. Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis. Ann Hum Genet 2015;79:431–450. 10.1111/ahg.12128 PubMed DOI

Karin M. The regulation of AP-1 activity by mitogen-activated protein kinases. J Bio Chem. 1995;270:16483–16486. PubMed

Whitmarsh AJ, Davis RJ. Transcription factor AP-1 regulation by mitogen-activated protein kinase signal transduction pathways. J Mol Med (Berl). 1996;74:589–607. PubMed

Mace M, Galiacy SD, Erraud A, Mejia JE, Etchevers H Allouche M, et al. Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneas. Invest Ophthalmol Vis Sci. 2011;52:6181–619. 10.1167/iovs.10-70981 PubMed DOI

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...