TY - JOUR
T1 - Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration: Evidence from the EYE-RISK and European Eye Epidemiology Consortia
T2 - Evidence from the EYE-RISK and European Eye Epidemiology Consortia
AU - Colijn, Johanna M.
AU - Verzijden, Timo
AU - Meester-Smoor, Magda A.
AU - Klaver, Caroline C. W.
AU - Colijn, Johanna M.
AU - Demirkan, Ayse
AU - Verzijden, Timo
AU - Meester-Smoor, Magda A.
AU - Ahmad, Shahzad
AU - van Duijn, Cornelia M.
AU - Klaver, Caroline C. W.
AU - den Hollander, Anneke I.
AU - Kersten, Eveline
AU - Hoyng, Carel B.
AU - Klaver, Caroline C. W.
AU - Cougnard-Grégoire, Audrey
AU - Merle, Benedicte M. J.
AU - Korobelnik, Jean-Francois
AU - Delcourt, C. cile
AU - Papageorgiou, Grigorios
AU - Mulder, Monique T.
AU - Costa, Miguel Angelo
AU - Silva, Rufino
AU - Benlian, Pascale
AU - Bertelsen, Geir
AU - Bertelsen, Geir
AU - Bron, Alain M.
AU - Creuzot-Garcher, Catherine
AU - Claes, Birte
AU - Hense, Hans-Werner
AU - Erke, Maja Gran
AU - Fauser, Sascha
AU - Fauser, Sascha
AU - Foster, Paul J.
AU - Khawaja, Anthony P.
AU - Foster, Paul J.
AU - Hammond, Christopher J.
AU - Williams, Katie M.
AU - Hammond, Christopher J.
AU - Williams, Katie M.
AU - Khawaja, Anthony P.
AU - Korobelnik, Jean-Francois
AU - Piermarocchi, Stefano
AU - Segato, Tatiana
AU - Silva, Rufino
AU - European Eye Epidemiology Consortium
AU - Bergen, Arthur
AU - Boon, Camiel
AU - Janssen, Sarah
AU - Verhoeven, Virginie
AU - EYE-RISK Consortium
AU - van Leeuwen, Elisabeth M.
AU - Souied, Eric H
N1 - Copyright © 2018 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Purpose: Genetic and epidemiologic studies have shown that lipid genes and high-density lipoproteins (HDLs) are implicated in age-related macular degeneration (AMD). We studied circulating lipid levels in relationship to AMD in a large European dataset. Design: Pooled analysis of cross-sectional data. Participants: Individuals (N = 30 953) aged 50 years or older participating in the European Eye Epidemiology (E3) consortium and 1530 individuals from the Rotterdam Study with lipid subfraction data. Methods: AMD features were graded on fundus photographs using the Rotterdam classification. Routine blood lipid measurements, genetics, medication, and potential confounders were extracted from the E3 database. In a subgroup of the Rotterdam Study, lipid subfractions were identified by the Nightingale biomarker platform. Random-intercepts mixed-effects models incorporating confounders and study site as a random effect were used to estimate associations. Main Outcome Measures: AMD features and stage; lipid measurements. Results: HDL was associated with an increased risk of AMD (odds ratio [OR], 1.21 per 1-mmol/l increase; 95% confidence interval [CI], 1.14–1.29), whereas triglycerides were associated with a decreased risk (OR, 0.94 per 1-mmol/l increase; 95% CI, 0.91–0.97). Both were associated with drusen size. Higher HDL raised the odds of larger drusen, whereas higher triglycerides decreases the odds. LDL cholesterol reached statistical significance only in the association with early AMD (P = 0.045). Regarding lipid subfractions, the concentration of extra-large HDL particles showed the most prominent association with AMD (OR, 1.24; 95% CI, 1.10–1.40). The cholesteryl ester transfer protein risk variant (rs17231506) for AMD was in line with increased HDL levels (P = 7.7 × 10 –7 ), but lipase C risk variants (rs2043085, rs2070895) were associated in an opposite way (P = 1.0 × 10 –6 and P = 1.6 × 10 –4 ). Conclusions: Our study suggested that HDL cholesterol is associated with increased risk of AMD and that triglycerides are negatively associated. Both show the strongest association with early AMD and drusen. Extra-large HDL subfractions seem to be drivers in the relationship with AMD, and variants in lipid genes play a more ambiguous role in this association. Whether systemic lipids directly influence AMD or represent lipid metabolism in the retina remains to be answered.
AB - Purpose: Genetic and epidemiologic studies have shown that lipid genes and high-density lipoproteins (HDLs) are implicated in age-related macular degeneration (AMD). We studied circulating lipid levels in relationship to AMD in a large European dataset. Design: Pooled analysis of cross-sectional data. Participants: Individuals (N = 30 953) aged 50 years or older participating in the European Eye Epidemiology (E3) consortium and 1530 individuals from the Rotterdam Study with lipid subfraction data. Methods: AMD features were graded on fundus photographs using the Rotterdam classification. Routine blood lipid measurements, genetics, medication, and potential confounders were extracted from the E3 database. In a subgroup of the Rotterdam Study, lipid subfractions were identified by the Nightingale biomarker platform. Random-intercepts mixed-effects models incorporating confounders and study site as a random effect were used to estimate associations. Main Outcome Measures: AMD features and stage; lipid measurements. Results: HDL was associated with an increased risk of AMD (odds ratio [OR], 1.21 per 1-mmol/l increase; 95% confidence interval [CI], 1.14–1.29), whereas triglycerides were associated with a decreased risk (OR, 0.94 per 1-mmol/l increase; 95% CI, 0.91–0.97). Both were associated with drusen size. Higher HDL raised the odds of larger drusen, whereas higher triglycerides decreases the odds. LDL cholesterol reached statistical significance only in the association with early AMD (P = 0.045). Regarding lipid subfractions, the concentration of extra-large HDL particles showed the most prominent association with AMD (OR, 1.24; 95% CI, 1.10–1.40). The cholesteryl ester transfer protein risk variant (rs17231506) for AMD was in line with increased HDL levels (P = 7.7 × 10 –7 ), but lipase C risk variants (rs2043085, rs2070895) were associated in an opposite way (P = 1.0 × 10 –6 and P = 1.6 × 10 –4 ). Conclusions: Our study suggested that HDL cholesterol is associated with increased risk of AMD and that triglycerides are negatively associated. Both show the strongest association with early AMD and drusen. Extra-large HDL subfractions seem to be drivers in the relationship with AMD, and variants in lipid genes play a more ambiguous role in this association. Whether systemic lipids directly influence AMD or represent lipid metabolism in the retina remains to be answered.
KW - Aged
KW - Aged, 80 and over
KW - Cholesterol Ester Transfer Proteins/blood
KW - Cholesterol, HDL/blood
KW - Cholesterol, LDL/blood
KW - Cross-Sectional Studies
KW - European Continental Ancestry Group/statistics & numerical data
KW - European Union
KW - Female
KW - Humans
KW - Lipid Metabolism
KW - Macular Degeneration/blood
KW - Magnetic Resonance Spectroscopy
KW - Male
KW - Metabolomics
KW - Middle Aged
KW - Odds Ratio
KW - Polymorphism, Single Nucleotide
KW - Risk Factors
KW - Triglycerides/blood
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057508316&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/30315903
U2 - https://doi.org/10.1016/j.ophtha.2018.09.045
DO - https://doi.org/10.1016/j.ophtha.2018.09.045
M3 - Article
C2 - 30315903
SN - 0161-6420
VL - 126
SP - 393
EP - 406
JO - Ophthalmology
JF - Ophthalmology
IS - 3
ER -