Literature DB >> 21212179

LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population.

Bao Jian Fan1, Louis R Pasquale, Douglas Rhee, Tiansen Li, Jonathan L Haines, Janey L Wiggs.   

Abstract

PURPOSE: LOXL1 is a major genetic risk factor for exfoliation syndrome (ES) and exfoliation glaucoma (EG). Recent evidence documenting reversal of risk alleles for the disease-associated missense variants R141L and G153D suggests that these variants are not causative and that they may be proxies for other unknown functional LOXL1 variants. The purpose of this study was to investigate the disease association of LOXL1 variants spanning the gene region, including the 5' and 3' regulatory regions, in a U.S. Caucasian case-control sample.
METHODS: Twenty-five LOXL1 single-nucleotide polymorphisms (SNPs), distributed throughout the gene, were genotyped in 196 Caucasian patients with ES/EG and 201 matched controls. Genotype data were analyzed for single SNP associations, SNP interactions, and haplotype associations.
RESULTS: Promoter region haplotypes that included the risk alleles for rs12914489, a SNP located in the distal promoter region and independently associated with ES, and rs16958477, a SNP previously shown to affect gene transcription, were associated with increased disease risk (P=0.0008; odds ratio [OR], 2.34; 95% confidence interval [CI], 1.42-3.85) and with protective effects (P=2.3 × 10(-6); OR, 0.38; 95% CI, 0.25-0.57). Haplotypes containing rs12914489 and rs16958477 risk and protective alleles also significantly influenced the disease risk associated with missense alleles R141L and G153D.
CONCLUSIONS: LOXL1 promoter haplotypes were identified that are significantly associated with ES/EG in a U.S. Caucasian population. These results suggest that promoter region SNPs can influence LOXL1 gene expression, potentially causing a reduction of enzyme activity that may predispose to disease. Copyright 2011 The Association for Research in Vision and Ophthalmology, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21212179      PMCID: PMC3081229          DOI: 10.1167/iovs.10-6268

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  38 in total

1.  LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.

Authors:  John H Fingert; Wallace L M Alward; Young H Kwon; Kai Wang; Luan M Streb; Val C Sheffield; Edwin M Stone
Journal:  Am J Ophthalmol       Date:  2007-12       Impact factor: 5.258

2.  Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Authors:  Francesca Pasutto; Mandy Krumbiegel; Christian Y Mardin; Daniela Paoli; Robert Lämmer; Bernhard H F Weber; Friedrich E Kruse; Ursula Schlötzer-Schrehardt; André Reis
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-04       Impact factor: 4.799

3.  Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population.

Authors:  Hisako Hayashi; Norimoto Gotoh; Yoshiki Ueda; Hideo Nakanishi; Nagahisa Yoshimura
Journal:  Am J Ophthalmol       Date:  2008-01-16       Impact factor: 5.258

4.  Pseudoexfoliation in the Reykjavik Eye Study: prevalence and related ophthalmological variables.

Authors:  Arsaell Arnarsson; Karim F Damji; Thordur Sverrisson; Hiroshi Sasaki; Fridbert Jonasson
Journal:  Acta Ophthalmol Scand       Date:  2007-12

5.  Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

Authors:  Alex W Hewitt; Shiwani Sharma; Kathryn P Burdon; Jie Jin Wang; Paul N Baird; David P Dimasi; David A Mackey; Paul Mitchell; Jamie E Craig
Journal:  Hum Mol Genet       Date:  2007-11-23       Impact factor: 6.150

6.  Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.

Authors:  Gudmar Thorleifsson; Kristinn P Magnusson; Patrick Sulem; G Bragi Walters; Daniel F Gudbjartsson; Hreinn Stefansson; Thorlakur Jonsson; Adalbjorg Jonasdottir; Aslaug Jonasdottir; Gerdur Stefansdottir; Gisli Masson; Gudmundur A Hardarson; Hjorvar Petursson; Arsaell Arnarsson; Mehdi Motallebipour; Ola Wallerman; Claes Wadelius; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Augustine Kong; Fridbert Jonasson; Kari Stefansson
Journal:  Science       Date:  2007-08-09       Impact factor: 47.728

7.  DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity.

Authors:  Bao Jian Fan; Louis Pasquale; Cynthia L Grosskreutz; Douglas Rhee; Teresa Chen; Margaret M DeAngelis; Ivana Kim; Elizabeth del Bono; Joan W Miller; Tiansen Li; Jonathan L Haines; Janey L Wiggs
Journal:  BMC Med Genet       Date:  2008-02-06       Impact factor: 2.103

8.  Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.

Authors:  Vedam Lakshmi Ramprasad; Ronnie George; Nagasamy Soumittra; Ferdinamarie Sharmila; Lingam Vijaya; Govindasamy Kumaramanickavel
Journal:  Mol Vis       Date:  2008-02-09       Impact factor: 2.367

9.  Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma.

Authors:  Pratap Challa; Silke Schmidt; Yutao Liu; Xuejun Qin; Robin R Vann; Pedro Gonzalez; R Rand Allingham; Michael A Hauser
Journal:  Mol Vis       Date:  2008-01-29       Impact factor: 2.367

10.  Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.

Authors:  Jose A Aragon-Martin; Robert Ritch; Jeffrey Liebmann; Colm O'Brien; Karima Blaaow; Franco Mercieca; Anthony Spiteri; Caroline J Cobb; Karim F Damji; Ahti Tarkkanen; Tayebeh Rezaie; Anne H Child; Mansoor Sarfarazi
Journal:  Mol Vis       Date:  2008-03-17       Impact factor: 2.367

View more
  26 in total

Review 1.  Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis.

Authors:  Bao J Fan; Louis R Pasquale; Jae H Kang; Hani Levkovitch-Verbin; Jonathan L Haines; Janey L Wiggs
Journal:  Exp Eye Res       Date:  2015-08-10       Impact factor: 3.467

2.  Genetics, Diagnosis, and Monitoring of Pseudoexfoliation Glaucoma.

Authors:  Niraj Nathan; Rachel W Kuchtey
Journal:  Curr Ophthalmol Rep       Date:  2016-10-11

Review 3.  Genetics of glaucoma.

Authors:  Janey L Wiggs; Louis R Pasquale
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

Review 4.  Is Autophagy Dysfunction a Key to Exfoliation Glaucoma?

Authors:  J Mario Wolosin; Robert Ritch; Audrey M Bernstein
Journal:  J Glaucoma       Date:  2018-03       Impact factor: 2.503

Review 5.  Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome.

Authors:  Janey L Wiggs; Louis R Pasquale
Journal:  J Glaucoma       Date:  2014 Oct-Nov       Impact factor: 2.503

Review 6.  Genetics of Primary Inherited Disorders of the Optic Nerve: Clinical Applications.

Authors:  Keri F Allen; Eric D Gaier; Janey L Wiggs
Journal:  Cold Spring Harb Perspect Med       Date:  2015-07-01       Impact factor: 6.915

7.  Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Authors:  Luis Fernández-Vega Cueto; Tin Aung; Mineo Ozaki; Mei Chin Lee; Ursula Schlötzer-Schrehardt; Gudmar Thorleifsson; Takanori Mizoguchi; Robert P Igo; Aravind Haripriya; Susan E Williams; Yury S Astakhov; Andrew C Orr; Kathryn P Burdon; Satoko Nakano; Kazuhiko Mori; Khaled Abu-Amero; Michael Hauser; Zheng Li; Gopalakrishnan Prakadeeswari; Jessica N Cooke Bailey; Alina Popa Cherecheanu; Jae H Kang; Sarah Nelson; Ken Hayashi; Shin-Ichi Manabe; Shigeyasu Kazama; Tomasz Zarnowski; Kenji Inoue; Murat Irkec; Miguel Coca-Prados; Kazuhisa Sugiyama; Irma Järvelä; Patricio Schlottmann; S Fabian Lerner; Hasnaa Lamari; Yildirim Nilgün; Mukharram Bikbov; Ki Ho Park; Soon Cheol Cha; Kenji Yamashiro; Juan C Zenteno; Jost B Jonas; Rajesh S Kumar; Shamira A Perera; Anita S Y Chan; Nino Kobakhidze; Ronnie George; Lingam Vijaya; Tan Do; Deepak P Edward; Lourdes de Juan Marcos; Mohammad Pakravan; Sasan Moghimi; Ryuichi Ideta; Daniella Bach-Holm; Per Kappelgaard; Barbara Wirostko; Samuel Thomas; Daniel Gaston; Karen Bedard; Wenda L Greer; Zhenglin Yang; Xueyi Chen; Lulin Huang; Jinghong Sang; Hongyan Jia; Liyun Jia; Chunyan Qiao; Hui Zhang; Xuyang Liu; Bowen Zhao; Ya-Xing Wang; Liang Xu; Stéphanie Leruez; Pascal Reynier; George Chichua; Sergo Tabagari; Steffen Uebe; Matthias Zenkel; Daniel Berner; Georg Mossböck; Nicole Weisschuh; Ursula Hoja; Ulrich-Christoph Welge-Luessen; Christian Mardin; Panayiota Founti; Anthi Chatzikyriakidou; Theofanis Pappas; Eleftherios Anastasopoulos; Alexandros Lambropoulos; Arkasubhra Ghosh; Rohit Shetty; Natalia Porporato; Vijayan Saravanan; Rengaraj Venkatesh; Chandrashekaran Shivkumar; Narendran Kalpana; Sripriya Sarangapani; Mozhgan R Kanavi; Afsaneh Naderi Beni; Shahin Yazdani; Alireza Lashay; Homa Naderifar; Nassim Khatibi; Antonio Fea; Carlo Lavia; Laura Dallorto; Teresa Rolle; Paolo Frezzotti; Daniela Paoli; Erika Salvi; Paolo Manunta; Yosai Mori; Kazunori Miyata; Tomomi Higashide; Etsuo Chihara; Satoshi Ishiko; Akitoshi Yoshida; Masahide Yanagi; Yoshiaki Kiuchi; Tsutomu Ohashi; Toshiya Sakurai; Takako Sugimoto; Hideki Chuman; Makoto Aihara; Masaru Inatani; Masahiro Miyake; Norimoto Gotoh; Fumihiko Matsuda; Nagahisa Yoshimura; Yoko Ikeda; Morio Ueno; Chie Sotozono; Jin Wook Jeoung; Min Sagong; Kyu Hyung Park; Jeeyun Ahn; Marisa Cruz-Aguilar; Sidi M Ezzouhairi; Abderrahman Rafei; Yaan Fun Chong; Xiao Yu Ng; Shuang Ru Goh; Yueming Chen; Victor H K Yong; Muhammad Imran Khan; Olusola O Olawoye; Adeyinka O Ashaye; Idakwo Ugbede; Adeola Onakoya; Nkiru Kizor-Akaraiwe; Chaiwat Teekhasaenee; Yanin Suwan; Wasu Supakontanasan; Suhanya Okeke; Nkechi J Uche; Ifeoma Asimadu; Humaira Ayub; Farah Akhtar; Ewa Kosior-Jarecka; Urszula Lukasik; Ignacio Lischinsky; Vania Castro; Rodolfo Perez Grossmann; Gordana Sunaric Megevand; Sylvain Roy; Edward Dervan; Eoin Silke; Aparna Rao; Priti Sahay; Pablo Fornero; Osvaldo Cuello; Delia Sivori; Tamara Zompa; Richard A Mills; Emmanuelle Souzeau; Paul Mitchell; Jie Jin Wang; Alex W Hewitt; Michael Coote; Jonathan G Crowston; Sergei Y Astakhov; Eugeny L Akopov; Anton Emelyanov; Vera Vysochinskaya; Gyulli Kazakbaeva; Rinat Fayzrakhmanov; Saleh A Al-Obeidan; Ohoud Owaidhah; Leyla Ali Aljasim; Balram Chowbay; Jia Nee Foo; Raphael Q Soh; Kar Seng Sim; Zhicheng Xie; Augustine W O Cheong; Shi Qi Mok; Hui Meng Soo; Xiao Yin Chen; Su Qin Peh; Khai Koon Heng; Rahat Husain; Su-Ling Ho; Axel M Hillmer; Ching-Yu Cheng; Francisco A Escudero-Domínguez; Rogelio González-Sarmiento; Frederico Martinon-Torres; Antonio Salas; Kessara Pathanapitoon; Linda Hansapinyo; Boonsong Wanichwecharugruang; Naris Kitnarong; Anavaj Sakuntabhai; Hip X Nguyn; Giang T T Nguyn; Trình V Nguyn; Werner Zenz; Alexander Binder; Daniela S Klobassa; Martin L Hibberd; Sonia Davila; Stefan Herms; Markus M Nöthen; Susanne Moebus; Robyn M Rautenbach; Ari Ziskind; Trevor R Carmichael; Michele Ramsay; Lydia Álvarez; Montserrat García; Héctor González-Iglesias; Pedro P Rodríguez-Calvo; Çilingir Oguz; Nevbahar Tamcelik; Eray Atalay; Bilge Batu; Dilek Aktas; Burcu Kasım; M Roy Wilson; Anne L Coleman; Yutao Liu; Pratap Challa; Leon Herndon; Rachel W Kuchtey; John Kuchtey; Karen Curtin; Craig J Chaya; Alan Crandall; Linda M Zangwill; Tien Yin Wong; Masakazu Nakano; Shigeru Kinoshita; Anneke I den Hollander; Eija Vesti; John H Fingert; Richard K Lee; Arthur J Sit; Bradford J Shingleton; Ningli Wang; Daniele Cusi; Raheel Qamar; Peter Kraft; Margaret A Pericak-Vance; Soumya Raychaudhuri; Steffen Heegaard; Tero Kivelä; André Reis; Friedrich E Kruse; Robert N Weinreb; Louis R Pasquale; Jonathan L Haines; Unnur Thorsteinsdottir; Fridbert Jonasson; R Rand Allingham; Dan Milea; Robert Ritch; Toshiaki Kubota; Kei Tashiro; Eranga N Vithana; Shazia Micheal; Fotis Topouzis; Jamie E Craig; Michael Dubina; Periasamy Sundaresan; Kari Stefansson; Janey L Wiggs; Francesca Pasutto; Chiea Chuen Khor
Journal:  Nat Genet       Date:  2017-05-29       Impact factor: 38.330

8.  Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking lysyl oxidase-like 1 (LOXL1).

Authors:  Janey L Wiggs; Basil Pawlyk; Edward Connolly; Michael Adamian; Joan W Miller; Louis R Pasquale; Ramez I Haddadin; Cynthia L Grosskreutz; Douglas J Rhee; Tiansen Li
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-02-10       Impact factor: 4.799

Review 9.  Genetics of exfoliation syndrome and glaucoma.

Authors:  Inas F Aboobakar; R Rand Allingham
Journal:  Int Ophthalmol Clin       Date:  2014

10.  Review: The role of LOXL1 in exfoliation syndrome/glaucoma.

Authors:  Benjamin T Whigham; R Rand Allingham
Journal:  Saudi J Ophthalmol       Date:  2011-07-27
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.