Skip to main content
Top
Published in: BMC Medical Genetics 1/2009

Open Access 01-12-2009 | Research article

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

Authors: Christiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, Francesca Pasutto, Eva Reinthal, Bernd Wissinger, Nicole Weisschuh

Published in: BMC Medical Genetics | Issue 1/2009

Login to get access

Abstract

Background

Normal tension glaucoma is a major subtype of glaucoma, associated with intraocular pressures that are within the statistically normal range of the population. Monogenic forms following classical inheritance patterns are rare in this glaucoma subtype. Instead, multigenic inheritance is proposed for the majority of cases. The present study tested common sequence variants in candidate genes for association with normal tension glaucoma in the German population.

Methods

Ninety-eight SNPs were selected to tag the common genetic variation in nine genes, namely OPTN (optineurin), RDX (radixin), SNX16 (sorting nexin 16), OPA1 (optic atrophy 1), MFN1 (mitofusin 1), MFN2 (mitofusin 2), PARL (presenilin associated, rhomboid-like), SOD2 (superoxide dismutase 2, mitochondrial) and CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1). These SNPs were genotyped in 285 cases and 282 fully evaluated matched controls. Statistical analyses comprised single polymorphism association as well as haplogroup based association testing.

Results

Results suggested that genetic variation in five of the candidate genes (RDX, SNX16, OPA1, SOD2 and CYP1B1) is unlikely to confer major risk to develop normal tension glaucoma in the German population. In contrast, we observed a trend towards association of single SNPs in OPTN, MFN1, MFN2 and PARL. The SNPs of OPTN, MFN2 and PARL were further analysed by multimarker haplotype-based association testing. We identified a risk haplotype being more frequent in patients and a vice versa situation for the complementary protective haplotype in each of the three genes.

Conclusion

Common variants of OPTN, PARL, MFN1 and MFN2 should be analysed in other cohorts to confirm their involvement in normal tension glaucoma.
Appendix
Available only for authorised users
Literature
1.
3.
go back to reference Werner EB: Normal tension glaucoma. The Glaucomas. Edited by: Ritch R, Shields MB, Krupin T. 1996, St. Louis: Mosby, 769-797. 2 Werner EB: Normal tension glaucoma. The Glaucomas. Edited by: Ritch R, Shields MB, Krupin T. 1996, St. Louis: Mosby, 769-797. 2
4.
go back to reference Fan BJ, Wang DY, Lam DS, Pang CP: Gene mapping for primary open angle glaucoma. Clin Biochem. 2006, 39: 249-258. 10.1016/j.clinbiochem.2005.11.001.CrossRefPubMed Fan BJ, Wang DY, Lam DS, Pang CP: Gene mapping for primary open angle glaucoma. Clin Biochem. 2006, 39: 249-258. 10.1016/j.clinbiochem.2005.11.001.CrossRefPubMed
5.
go back to reference Allingham RR, Liu Y, Rhee DJ: The genetics of primary open-angle glaucoma: a review. Exp Eye Res. 2009, 88: 837-844. 10.1016/j.exer.2008.11.003.CrossRefPubMed Allingham RR, Liu Y, Rhee DJ: The genetics of primary open-angle glaucoma: a review. Exp Eye Res. 2009, 88: 837-844. 10.1016/j.exer.2008.11.003.CrossRefPubMed
6.
go back to reference Aung T, Ocaka L, Ebenezer ND, Morris AG, Krawczak M, Thiselton DL, Alexander C, Votruba M, Brice G, Child AH, et al: A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene. Hum Genet. 2002, 110 (1): 52-56. 10.1007/s00439-001-0645-7.CrossRefPubMed Aung T, Ocaka L, Ebenezer ND, Morris AG, Krawczak M, Thiselton DL, Alexander C, Votruba M, Brice G, Child AH, et al: A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene. Hum Genet. 2002, 110 (1): 52-56. 10.1007/s00439-001-0645-7.CrossRefPubMed
7.
go back to reference Powell BL, Toomes C, Scott S, Yeung A, Marchbank NJ, Spry PG, Lumb R, Inglehearn CF, Churchill AJ: Polymorphisms in OPA1 are associated with normal tension glaucoma. Mol Vis. 2003, 9: 460-464.PubMed Powell BL, Toomes C, Scott S, Yeung A, Marchbank NJ, Spry PG, Lumb R, Inglehearn CF, Churchill AJ: Polymorphisms in OPA1 are associated with normal tension glaucoma. Mol Vis. 2003, 9: 460-464.PubMed
8.
go back to reference Woo SJ, Kim DM, Kim JY, Park SS, Ko HS, Yoo T: Investigation of the association between OPA1 polymorphisms and normal-tension glaucoma in Korea. J Glaucoma. 2004, 13 (6): 492-495. 10.1097/01.ijg.0000137870.25779.40.CrossRefPubMed Woo SJ, Kim DM, Kim JY, Park SS, Ko HS, Yoo T: Investigation of the association between OPA1 polymorphisms and normal-tension glaucoma in Korea. J Glaucoma. 2004, 13 (6): 492-495. 10.1097/01.ijg.0000137870.25779.40.CrossRefPubMed
9.
go back to reference Yao W, Jiao X, Hejtmancik JF, Leske MC, Hennis A, Nemesure B, Barbados Family Study Group: Evaluation of the association between OPA1 polymorphisms and primary open-angle glaucoma in Barbados families. Mol Vis. 2006, 12: 649-654.PubMed Yao W, Jiao X, Hejtmancik JF, Leske MC, Hennis A, Nemesure B, Barbados Family Study Group: Evaluation of the association between OPA1 polymorphisms and primary open-angle glaucoma in Barbados families. Mol Vis. 2006, 12: 649-654.PubMed
10.
go back to reference Mabuchi F, Tang S, Kashiwagi K, Yamagata Z, Iijima H, Tsukahara S: The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma. Am J Ophthalmol. 2007, 143 (1): 125-130. 10.1016/j.ajo.2006.09.028.CrossRefPubMed Mabuchi F, Tang S, Kashiwagi K, Yamagata Z, Iijima H, Tsukahara S: The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma. Am J Ophthalmol. 2007, 143 (1): 125-130. 10.1016/j.ajo.2006.09.028.CrossRefPubMed
11.
go back to reference Liu Y, Schmidt S, Qin X, Gibson J, Munro D, Wiggs JL, Hauser MA, Allingham RR: No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations. Mol Vis. 2007, 13: 2137-2141.PubMed Liu Y, Schmidt S, Qin X, Gibson J, Munro D, Wiggs JL, Hauser MA, Allingham RR: No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations. Mol Vis. 2007, 13: 2137-2141.PubMed
12.
go back to reference Gong G, Kosoko-Lasaki S, Haynatzki G, Lynch HT, Lynch JA, Wilson MR: Inherited, familial and sporadic primary open-angle glaucoma. J Natl Med Assoc. 2007, 99 (5): 559-563.PubMedPubMedCentral Gong G, Kosoko-Lasaki S, Haynatzki G, Lynch HT, Lynch JA, Wilson MR: Inherited, familial and sporadic primary open-angle glaucoma. J Natl Med Assoc. 2007, 99 (5): 559-563.PubMedPubMedCentral
13.
go back to reference Thorleifsson G, Magnusson KP, Sulem P, Walters GB, Gudbjartsson DF, Stefansson H, Jonsson T, Jonasdottir A, Jonasdottir A, Stefansdottir G, et al: Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007, 317 (5843): 1397-1400. 10.1126/science.1146554.CrossRefPubMed Thorleifsson G, Magnusson KP, Sulem P, Walters GB, Gudbjartsson DF, Stefansson H, Jonsson T, Jonasdottir A, Jonasdottir A, Stefansdottir G, et al: Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007, 317 (5843): 1397-1400. 10.1126/science.1146554.CrossRefPubMed
14.
go back to reference Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, Héon E, Krupin T, Ritch R, Kreutzer D, et al: Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science. 2002, 295 (5557): 1077-1079. 10.1126/science.1066901.CrossRefPubMed Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, Héon E, Krupin T, Ritch R, Kreutzer D, et al: Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science. 2002, 295 (5557): 1077-1079. 10.1126/science.1066901.CrossRefPubMed
15.
go back to reference Forsman E, Lemmelä S, Varilo T, Kristo P, Forsius H, Sankila EM, Järvelä I: The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study. Mol Vis. 2003, 9: 217-222.PubMed Forsman E, Lemmelä S, Varilo T, Kristo P, Forsius H, Sankila EM, Järvelä I: The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study. Mol Vis. 2003, 9: 217-222.PubMed
16.
go back to reference Tang S, Toda Y, Kashiwagi K, Mabuchi F, Iijima H, Tsukahara S, Yamagata Z: The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene. Hum Genet. 2003, 113 (3): 276-279. 10.1007/s00439-003-0964-y.CrossRefPubMed Tang S, Toda Y, Kashiwagi K, Mabuchi F, Iijima H, Tsukahara S, Yamagata Z: The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene. Hum Genet. 2003, 113 (3): 276-279. 10.1007/s00439-003-0964-y.CrossRefPubMed
17.
go back to reference Wiggs JL, Auguste J, Allingham RR, Flor JD, Pericak-Vance MA, Rogers K, LaRocque KR, Graham FL, Broomer B, Del Bono E, et al: Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol. 2003, 121 (8): 1181-1183. 10.1001/archopht.121.8.1181.CrossRefPubMedPubMedCentral Wiggs JL, Auguste J, Allingham RR, Flor JD, Pericak-Vance MA, Rogers K, LaRocque KR, Graham FL, Broomer B, Del Bono E, et al: Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol. 2003, 121 (8): 1181-1183. 10.1001/archopht.121.8.1181.CrossRefPubMedPubMedCentral
18.
go back to reference Weisschuh N, Neumann D, Wolf C, Wissinger B, Gramer E: Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients. Mol Vis. 2005, 11: 284-287.PubMed Weisschuh N, Neumann D, Wolf C, Wissinger B, Gramer E: Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients. Mol Vis. 2005, 11: 284-287.PubMed
19.
go back to reference Weisschuh N, Alavi MV, Bonin M, Wissinger B: Identification of genes that are linked with optineurin expression using a combined RNAi-microarray approach. Exp Eye Res. 2007, 85 (4): 450-461. 10.1016/j.exer.2007.06.012.CrossRefPubMed Weisschuh N, Alavi MV, Bonin M, Wissinger B: Identification of genes that are linked with optineurin expression using a combined RNAi-microarray approach. Exp Eye Res. 2007, 85 (4): 450-461. 10.1016/j.exer.2007.06.012.CrossRefPubMed
20.
go back to reference Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A, Rodriguez M, Kellner U, Leo-Kottler B, Auburger G, et al: OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet. 2000, 26 (2): 211-215. 10.1038/79944.CrossRefPubMed Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A, Rodriguez M, Kellner U, Leo-Kottler B, Auburger G, et al: OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet. 2000, 26 (2): 211-215. 10.1038/79944.CrossRefPubMed
21.
go back to reference Cipolat S, Martins de Brito O, Dal Zilio B, Scorrano L: OPA1 requires mitofusin 1 to promote mitochondrial fusion. Proc Natl Acad Sci USA. 2004, 101 (45): 15927-15932. 10.1073/pnas.0407043101.CrossRefPubMedPubMedCentral Cipolat S, Martins de Brito O, Dal Zilio B, Scorrano L: OPA1 requires mitofusin 1 to promote mitochondrial fusion. Proc Natl Acad Sci USA. 2004, 101 (45): 15927-15932. 10.1073/pnas.0407043101.CrossRefPubMedPubMedCentral
22.
go back to reference Cipolat S, Rudka T, Hartmann D, Costa V, Serneels L, Craessaerts K, Metzger K, Frezza C, Annaert W, D'Adamio L, et al: Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling. Cell. 2006, 126 (1): 163-175. 10.1016/j.cell.2006.06.021.CrossRefPubMed Cipolat S, Rudka T, Hartmann D, Costa V, Serneels L, Craessaerts K, Metzger K, Frezza C, Annaert W, D'Adamio L, et al: Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling. Cell. 2006, 126 (1): 163-175. 10.1016/j.cell.2006.06.021.CrossRefPubMed
23.
go back to reference Duvezin-Caubet S, Koppen M, Wagener J, Zick M, Israel L, Bernacchia A, Jagasia R, Rugarli EI, Imhof A, Neupert W, et al: OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria. Mol Biol Cell. 2007, 18 (9): 3582-3590. 10.1091/mbc.E07-02-0164.CrossRefPubMedPubMedCentral Duvezin-Caubet S, Koppen M, Wagener J, Zick M, Israel L, Bernacchia A, Jagasia R, Rugarli EI, Imhof A, Neupert W, et al: OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria. Mol Biol Cell. 2007, 18 (9): 3582-3590. 10.1091/mbc.E07-02-0164.CrossRefPubMedPubMedCentral
24.
go back to reference Guillery O, Malka F, Landes T, Guillou E, Blackstone C, Lombès A, Belenguer P, Arnoult D, Rojo M: Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential. Biol Cell. 2008, 100 (5): 315-325. 10.1042/BC20070110.CrossRefPubMed Guillery O, Malka F, Landes T, Guillou E, Blackstone C, Lombès A, Belenguer P, Arnoult D, Rojo M: Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential. Biol Cell. 2008, 100 (5): 315-325. 10.1042/BC20070110.CrossRefPubMed
25.
go back to reference Chen H, Detmer SA, Ewald AJ, Griffin EE, Fraser SE, Chan DC: Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development. J Cell Biol. 2003, 160 (2): 189-200. 10.1083/jcb.200211046.CrossRefPubMedPubMedCentral Chen H, Detmer SA, Ewald AJ, Griffin EE, Fraser SE, Chan DC: Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development. J Cell Biol. 2003, 160 (2): 189-200. 10.1083/jcb.200211046.CrossRefPubMedPubMedCentral
26.
go back to reference Tezel G: Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences. Prog Retin Eye Res. 2006, 25 (5): 490-513. 10.1016/j.preteyeres.2006.07.003.CrossRefPubMedPubMedCentral Tezel G: Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences. Prog Retin Eye Res. 2006, 25 (5): 490-513. 10.1016/j.preteyeres.2006.07.003.CrossRefPubMedPubMedCentral
27.
go back to reference Ferreira SM, Lerner SF, Brunzini R, Evelson PA, Llesuy SF: Oxidative stress markers in aqueous humor of glaucoma patients. Am J Ophthalmol. 2004, 137 (1): 62-9. 10.1016/S0002-9394(03)00788-8.CrossRefPubMed Ferreira SM, Lerner SF, Brunzini R, Evelson PA, Llesuy SF: Oxidative stress markers in aqueous humor of glaucoma patients. Am J Ophthalmol. 2004, 137 (1): 62-9. 10.1016/S0002-9394(03)00788-8.CrossRefPubMed
28.
go back to reference Stoilov I, Akarsu AN, Sarfarazi M: Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet. 1997, 6 (4): 641-647. 10.1093/hmg/6.4.641.CrossRefPubMed Stoilov I, Akarsu AN, Sarfarazi M: Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet. 1997, 6 (4): 641-647. 10.1093/hmg/6.4.641.CrossRefPubMed
29.
go back to reference Bhattacharjee A, Banerjee D, Mookherjee S, Acharya M, Banerjee A, Ray A, Sen A, Variation Consortium TI, Ray K: Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis. 2008, 14: 841-850.PubMedPubMedCentral Bhattacharjee A, Banerjee D, Mookherjee S, Acharya M, Banerjee A, Ray A, Sen A, Variation Consortium TI, Ray K: Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis. 2008, 14: 841-850.PubMedPubMedCentral
30.
go back to reference Melki R, Lefort N, Brézin AP, Garchon HJ: Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma. Mol Vis. 2005, 11: 1012-1017.PubMed Melki R, Lefort N, Brézin AP, Garchon HJ: Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma. Mol Vis. 2005, 11: 1012-1017.PubMed
31.
go back to reference Pasutto F, Chavarria-Soley G, Mardin CY, Michels-Rautenstrauss K, Ingelman-Sundberg M, Fernández-Martínez L, Weber BH, Rautenstrauss B, Reis A: Heterozygous loss of function variants in CYP1B1 predispose to primary open angle glaucoma. Invest Ophthalmol Vis Sci. 2009, Pasutto F, Chavarria-Soley G, Mardin CY, Michels-Rautenstrauss K, Ingelman-Sundberg M, Fernández-Martínez L, Weber BH, Rautenstrauss B, Reis A: Heterozygous loss of function variants in CYP1B1 predispose to primary open angle glaucoma. Invest Ophthalmol Vis Sci. 2009,
32.
go back to reference Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, et al: The structure of haplotype blocks in the human genome. Science. 2002, 296 (5576): 2225-2229. 10.1126/science.1069424.CrossRefPubMed Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, et al: The structure of haplotype blocks in the human genome. Science. 2002, 296 (5576): 2225-2229. 10.1126/science.1069424.CrossRefPubMed
33.
go back to reference Barrett JC, Fry B, Maller J, Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005, 21 (2): 263-265. 10.1093/bioinformatics/bth457.CrossRefPubMed Barrett JC, Fry B, Maller J, Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005, 21 (2): 263-265. 10.1093/bioinformatics/bth457.CrossRefPubMed
34.
go back to reference The International HapMap Consortium: The International HapMap Project. Nature. 2003, 426 (6968): 789-796. 10.1038/nature02168.CrossRef The International HapMap Consortium: The International HapMap Project. Nature. 2003, 426 (6968): 789-796. 10.1038/nature02168.CrossRef
35.
go back to reference Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, et al: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81 (3): 559-575. 10.1086/519795.CrossRefPubMedPubMedCentral Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, et al: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81 (3): 559-575. 10.1086/519795.CrossRefPubMedPubMedCentral
36.
go back to reference Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N: Lysyl Oxidase-like 1 Gene Polymorphisms in German Patients With Normal Tension Glaucoma, Pigmentary Glaucoma and Exfoliation Glaucoma. J Glaucoma. 2009, Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N: Lysyl Oxidase-like 1 Gene Polymorphisms in German Patients With Normal Tension Glaucoma, Pigmentary Glaucoma and Exfoliation Glaucoma. J Glaucoma. 2009,
37.
go back to reference Votruba M, Thiselton D, Bhattacharya SS: Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy. Br J Ophthalmol. 2003, 87 (1): 48-53. 10.1136/bjo.87.1.48.CrossRefPubMedPubMedCentral Votruba M, Thiselton D, Bhattacharya SS: Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy. Br J Ophthalmol. 2003, 87 (1): 48-53. 10.1136/bjo.87.1.48.CrossRefPubMedPubMedCentral
38.
go back to reference Fan BJ, Wang DY, Fan DS, Tam PO, Lam DS, Tham CC, Lam CY, Lau TC, Pang CP: SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients. Mol Vis. 2005, 11: 625-631.PubMed Fan BJ, Wang DY, Fan DS, Tam PO, Lam DS, Tham CC, Lam CY, Lau TC, Pang CP: SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients. Mol Vis. 2005, 11: 625-631.PubMed
39.
go back to reference Park BC, Tibudan M, Samaraweera M, Shen X, Yue BY: Interaction between two glaucoma genes, optineurin and myocilin. Genes cells. 2007, 12 (8): 969-979. 10.1111/j.1365-2443.2007.01102.x.CrossRefPubMed Park BC, Tibudan M, Samaraweera M, Shen X, Yue BY: Interaction between two glaucoma genes, optineurin and myocilin. Genes cells. 2007, 12 (8): 969-979. 10.1111/j.1365-2443.2007.01102.x.CrossRefPubMed
40.
go back to reference Jia LY, Tam PO, Chiang SW, Ding N, Chen LJ, Yam GH, Pang CP, Wang NL: Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese. Mol Vis. 2009, 15: 89-98.PubMedPubMedCentral Jia LY, Tam PO, Chiang SW, Ding N, Chen LJ, Yam GH, Pang CP, Wang NL: Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese. Mol Vis. 2009, 15: 89-98.PubMedPubMedCentral
41.
go back to reference Bossy-Wetzel E, Barsoum MJ, Godzik A, Schwarzenbacher R, Lipton SA: Mitochondrial fission in apoptosis, neurodegeneration and aging. Curr Opin Cell Biol. 2003, 15 (6): 706-716. 10.1016/j.ceb.2003.10.015.CrossRefPubMed Bossy-Wetzel E, Barsoum MJ, Godzik A, Schwarzenbacher R, Lipton SA: Mitochondrial fission in apoptosis, neurodegeneration and aging. Curr Opin Cell Biol. 2003, 15 (6): 706-716. 10.1016/j.ceb.2003.10.015.CrossRefPubMed
42.
go back to reference Westermann B: Mitochondrial membrane fusion. Biochim Biophys Acta. 2003, 1641: 195-202. 10.1016/S0167-4889(03)00091-0.CrossRefPubMed Westermann B: Mitochondrial membrane fusion. Biochim Biophys Acta. 2003, 1641: 195-202. 10.1016/S0167-4889(03)00091-0.CrossRefPubMed
43.
go back to reference Pellegrini L, Scorrano L: A cut short to death: Parl and Opa1 in the regulation of mitochondrial morphology and apoptosis. Cell Death Differ. 2007, 14 (7): 1275-1284. 10.1038/sj.cdd.4402145.CrossRefPubMed Pellegrini L, Scorrano L: A cut short to death: Parl and Opa1 in the regulation of mitochondrial morphology and apoptosis. Cell Death Differ. 2007, 14 (7): 1275-1284. 10.1038/sj.cdd.4402145.CrossRefPubMed
44.
go back to reference Abu-Amero KK, Morales J, Bosley TM: Mitochondrial abnormalities in patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci. 2006, 47 (6): 2533-2541. 10.1167/iovs.05-1639.CrossRefPubMed Abu-Amero KK, Morales J, Bosley TM: Mitochondrial abnormalities in patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci. 2006, 47 (6): 2533-2541. 10.1167/iovs.05-1639.CrossRefPubMed
45.
go back to reference Tezel G: Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences. Prog Retin Eye Res. 2006, 25 (5): 490-513. 10.1016/j.preteyeres.2006.07.003.CrossRefPubMedPubMedCentral Tezel G: Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences. Prog Retin Eye Res. 2006, 25 (5): 490-513. 10.1016/j.preteyeres.2006.07.003.CrossRefPubMedPubMedCentral
46.
go back to reference Kong GY, Van Bergen NJ, Trounce IA, Crowston JG: Mitochondrial dysfunction and glaucoma. J Glaucoma. 2009, 18 (2): 93-100. 10.1097/IJG.0b013e318181284f.CrossRefPubMed Kong GY, Van Bergen NJ, Trounce IA, Crowston JG: Mitochondrial dysfunction and glaucoma. J Glaucoma. 2009, 18 (2): 93-100. 10.1097/IJG.0b013e318181284f.CrossRefPubMed
Metadata
Title
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study
Authors
Christiane Wolf
Eugen Gramer
Bertram Müller-Myhsok
Francesca Pasutto
Eva Reinthal
Bernd Wissinger
Nicole Weisschuh
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2009
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-10-91

Other articles of this Issue 1/2009

BMC Medical Genetics 1/2009 Go to the issue