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Genetic Variants and Systemic Complement Activation Levels Are Associated With Serum Lipoprotein Levels in Age-Related Macular Degeneration
Author(s) -
Constantin C. Paun,
Lebriz Ersoy,
Tina Schick,
J.M.M. Groenewoud,
Yara T. E. Lechanteur,
Sascha Fauser,
Carel B. Hoyng,
Eiko K. de Jong,
Anneke I. den Hollander
Publication year - 2015
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.15-17035
Subject(s) - single nucleotide polymorphism , apolipoprotein b , medicine , complement system , lipoprotein , endocrinology , biology , apolipoprotein e , cholesterol , genotype , complement component 3 , genetics , gene , alternative complement pathway , disease , antibody
Genetic variants in genes encoding components of lipid metabolism have been associated with AMD. The aims of this study were to evaluate the relation of these genetic variants with serum lipid levels in AMD in a large case-control cohort (n = 3070) and to test for correlations between lipids and complement activation.

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