Association of LIPC and advanced age-related macular degeneration

Purpose To determine whether there is an association between hepatic lipase ( LIPC ) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. Methods A discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150...

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Published in:Eye (London) Vol. 27; no. 2; pp. 265 - 271
Main Authors: Lee, J, Zeng, J, Hughes, G, Chen, Y, Grob, S, Zhao, L, Lee, C, Krupa, M, Quach, J, Luo, J, Wei, X, Zhang, X, Zhu, J, Duan, Y, Ferreyra, H, Goldbaum, M, Haw, W, Shaw, P X, Tang, L, Zhang, K
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Published: London Nature Publishing Group UK 01-02-2013
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Abstract Purpose To determine whether there is an association between hepatic lipase ( LIPC ) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. Methods A discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150 controls were genotyped for two single-nucleotide polymorphisms (SNPs) in the promoter region of LIPC . The associations between the SNPs and AMD were examined by χ 2 tests. Results In the discovery cohort, rs493258 and rs10468017 were both associated with advanced AMD ( P =9.63E−3 and P =0.048, respectively). The association was corroborated in the replication cohort ( P =4.48E−03 for rs493258 and P =0.015 for rs10468017). Combined analysis resulted in even more significant associations ( P =1.21E−04 for rs493258 and P =1.67E−03 for rs10468017). Conclusion The LIPC promoter variants rs493258 and rs10468017 were associated with advanced AMD in two independent Caucasian populations, confirming that LIPC polymorphisms may be a genetic risk factor for AMD in the Caucasian population.
AbstractList Purpose To determine whether there is an association between hepatic lipase ( LIPC ) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. Methods A discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150 controls were genotyped for two single-nucleotide polymorphisms (SNPs) in the promoter region of LIPC . The associations between the SNPs and AMD were examined by χ 2 tests. Results In the discovery cohort, rs493258 and rs10468017 were both associated with advanced AMD ( P =9.63E−3 and P =0.048, respectively). The association was corroborated in the replication cohort ( P =4.48E−03 for rs493258 and P =0.015 for rs10468017). Combined analysis resulted in even more significant associations ( P =1.21E−04 for rs493258 and P =1.67E−03 for rs10468017). Conclusion The LIPC promoter variants rs493258 and rs10468017 were associated with advanced AMD in two independent Caucasian populations, confirming that LIPC polymorphisms may be a genetic risk factor for AMD in the Caucasian population.
PURPOSETo determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. METHODSA discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150 controls were genotyped for two single-nucleotide polymorphisms (SNPs) in the promoter region of LIPC. The associations between the SNPs and AMD were examined by χ(2) tests. RESULTSIn the discovery cohort, rs493258 and rs10468017 were both associated with advanced AMD (P=9.63E-3 and P=0.048, respectively). The association was corroborated in the replication cohort (P=4.48E-03 for rs493258 and P=0.015 for rs10468017). Combined analysis resulted in even more significant associations (P=1.21E-04 for rs493258 and P=1.67E-03 for rs10468017). CONCLUSIONThe LIPC promoter variants rs493258 and rs10468017 were associated with advanced AMD in two independent Caucasian populations, confirming that LIPC polymorphisms may be a genetic risk factor for AMD in the Caucasian population.
To determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. A discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150 controls were genotyped for two single-nucleotide polymorphisms (SNPs) in the promoter region of LIPC. The associations between the SNPs and AMD were examined by χ(2) tests. In the discovery cohort, rs493258 and rs10468017 were both associated with advanced AMD (P=9.63E-3 and P=0.048, respectively). The association was corroborated in the replication cohort (P=4.48E-03 for rs493258 and P=0.015 for rs10468017). Combined analysis resulted in even more significant associations (P=1.21E-04 for rs493258 and P=1.67E-03 for rs10468017). The LIPC promoter variants rs493258 and rs10468017 were associated with advanced AMD in two independent Caucasian populations, confirming that LIPC polymorphisms may be a genetic risk factor for AMD in the Caucasian population.
To determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. A discovery cohort of 1626 patients with advanced AMD and 859 normal controls and a replication cohort of 2159 cases and 1150 controls were genotyped for two single-nucleotide polymorphisms (SNPs) in the promoter region of LIPC. The associations between the SNPs and AMD were examined by χ(2) tests. In the discovery cohort, rs493258 and rs10468017 were both associated with advanced AMD (P=9.63E-3 and P=0.048, respectively). The association was corroborated in the replication cohort (P=4.48E-03 for rs493258 and P=0.015 for rs10468017). Combined analysis resulted in even more significant associations (P=1.21E-04 for rs493258 and P=1.67E-03 for rs10468017). The LIPC promoter variants rs493258 and rs10468017 were associated with advanced AMD in two independent Caucasian populations, confirming that LIPC polymorphisms may be a genetic risk factor for AMD in the Caucasian population.
Author Lee, J
Luo, J
Krupa, M
Goldbaum, M
Chen, Y
Zhu, J
Grob, S
Lee, C
Zhang, X
Zhao, L
Haw, W
Hughes, G
Zeng, J
Quach, J
Ferreyra, H
Shaw, P X
Wei, X
Tang, L
Zhang, K
Duan, Y
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  organization: Department of Ophthalmology and Shiley Eye Center and Institute for Genomic Medicine, University of California, San Diego, Department of Ophthalmology, Second Xiangya Hospital, Central South University, Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine
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  surname: Chen
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  organization: Department of Ophthalmology and Shiley Eye Center and Institute for Genomic Medicine, University of California, San Diego, Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Department of Ophthalmology and Vision Science, Eye and ENT Hospital, Shanghai Medical School, Fudan University
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  surname: Zhu
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  organization: Department of Ophthalmology and Shiley Eye Center and Institute for Genomic Medicine, University of California, San Diego, Department of Ophthalmology, Second Xiangya Hospital, Central South University, Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Department of Ophthalmology and Vision Science, Eye and ENT Hospital, Shanghai Medical School, Fudan University
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  email: kangzhang@ucsd.edu
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/23348725$$D View this record in MEDLINE/PubMed
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Keywords advanced age-related macular degeneration
genetics
hepatic lipase
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Snippet Purpose To determine whether there is an association between hepatic lipase ( LIPC ) and age-related macular degeneration (AMD) in two independent Caucasian...
To determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. A...
To determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian cohorts. A...
PURPOSETo determine whether there is an association between hepatic lipase (LIPC) and age-related macular degeneration (AMD) in two independent Caucasian...
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StartPage 265
SubjectTerms 631/208/205
631/208/726/649
631/378/1689/1626
692/499
Aged
Aged, 80 and over
Alleles
Cohort Studies
Female
Gene Frequency
Genetic Predisposition to Disease
Humans
Laboratory Medicine
Laboratory Study
Lipase - genetics
Macular Degeneration - genetics
Male
Medicine
Medicine & Public Health
Middle Aged
Ophthalmology
Pharmaceutical Sciences/Technology
Polymorphism, Single Nucleotide
Promoter Regions, Genetic - genetics
Surgery
Surgical Oncology
Title Association of LIPC and advanced age-related macular degeneration
URI https://link.springer.com/article/10.1038/eye.2012.276
https://www.ncbi.nlm.nih.gov/pubmed/23348725
https://www.proquest.com/docview/1287506692
https://search.proquest.com/docview/1288313229
https://pubmed.ncbi.nlm.nih.gov/PMC3574263
Volume 27
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