Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults

被引:28
作者
Bjornsson, Eythor [1 ,2 ,3 ]
Thorleifsson, Gudmar [1 ]
Helgadottir, Anna [1 ]
Gudnason, Thorarinn [3 ]
Gudbjartsson, Tomas [2 ,4 ]
Andersen, Karl [2 ,3 ]
Gretarsdottir, Solveig [1 ]
Olafsson, Isleifur [5 ]
Tragante, Vinicius [1 ,6 ]
Olafsson, Olafur Hreidar [1 ,2 ]
Jonsdottir, Birna [7 ]
Eyjolfsson, Gudmundur I. [8 ]
Sigurdardottir, Oloef [9 ]
Thorgeirsson, Gudmundur [1 ,2 ,3 ]
Gudbjartsson, Daniel F. [1 ,10 ]
Thorsteinsdottir, Unnur [1 ,2 ]
Holm, Hilma [1 ]
Stefansson, Kari [1 ,2 ]
机构
[1] Amgen Inc, deCODE Genet, Sturlugata 8, IS-101 Reykjavik, Iceland
[2] Univ Iceland, Fac Med, Reykjavik, Iceland
[3] Landspitali Natl Univ Hosp Iceland, Div Cardiol, Reykjavik, Iceland
[4] Landspitali Natl Univ Hosp Iceland, Div Cardiothorac Surg, Reykjavik, Iceland
[5] Landspitali Natl Univ Hosp Iceland, Dept Clin Biochem, Reykjavik, Iceland
[6] Univ Utrecht, Univ Med Ctr Utrecht, Dept Cardiol, Div Heart & Lungs, Utrecht, Netherlands
[7] Rontgen Domus, Reykjavik, Iceland
[8] Lab Mjodd, Reykjavik, Iceland
[9] Akureyri Hosp, Dept Clin Biochem, Akureyri, Iceland
[10] Univ Iceland, Sch Engn & Nat Sci, Reykjavik, Iceland
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; OF-FUNCTION MUTATIONS; NON-HDL CHOLESTEROL; APOLIPOPROTEIN-B; ARTERY CALCIUM; HEART-DISEASE; LONG-TERM; RISK; TRIGLYCERIDES; VARIANTS;
D O I
10.1001/jamacardio.2019.2946
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Question Are genetically predicted lipid levels associated with the extent of coronary atherosclerosis? Findings This study found that a genetic score for non-high-density lipoprotein cholesterol was significantly associated with the extent of coronary atherosclerosis, as estimated by coronary angiography or coronary calcium scanning in Icelandic adults. The association persists after accounting for low-density lipoprotein cholesterol. Meaning Elevated non-high-density lipoprotein cholesterol is associated with the development of coronary atherosclerosis and may be a better marker for atherogenic lipoproteins than low-density lipoprotein cholesterol. This genetic study uses data from Icelandic adults who have been genotyped to estimate the contributions of genetically predicted blood lipid levels on the extent of coronary atherosclerosis. Importance Genetic studies have evaluated the influence of blood lipid levels on the risk of coronary artery disease (CAD), but less is known about how they are associated with the extent of coronary atherosclerosis. Objective To estimate the contributions of genetically predicted blood lipid levels on the extent of coronary atherosclerosis. Design, Setting, and Participants This genetic study included Icelandic adults who had undergone coronary angiography or assessment of coronary artery calcium using cardiac computed tomography. The study incorporates data collected from January 1987 to December 2017 in Iceland in the Swedish Coronary Angiography and Angioplasty Registry and 2 registries of individuals who had undergone percutaneous coronary interventions and coronary artery bypass grafting. For each participant, genetic scores were calculated for levels of non-high-density lipoprotein cholesterol (non-HDL-C), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides, based on reported effect sizes of 345 independent, lipid-associated variants. The genetic scores' predictive ability for lipid levels was assessed in more than 87000 Icelandic adults. A mendelian randomization approach was used to estimate the contribution of each lipid trait. Exposures Genetic scores for levels of non-HDL-C, LDL-C, HDL-C, and triglycerides. Main Outcomes and Measures The extent of angiographic CAD and coronary artery calcium quantity. Results A total of 12460 adults (mean [SD] age, 65.1 [10.7] years; 8383 men [67.3%]) underwent coronary angiography, and 4837 had coronary artery calcium assessed by computed tomography. A genetically predicted increase in non-HDL-C levels by 1 SD (38 mg/dL [to convert to millimoles per liter, multiply by 0.0259]) was associated with greater odds of obstructive CAD (odds ratio [OR], 1.83 [95% CI, 1.63-2.07]; P = 2.8 x 10(-23)). Among patients with obstructive CAD, there were significant associations with multivessel disease (OR, 1.26 [95% CI, 1.11-1.44]; P = 4.1 x 10(-4)) and 3-vessel disease (OR, 1.47 [95% CI, 1.26-1.72]; P = 9.2 x 10(-7)). There were also significant associations with the presence of coronary artery calcium (OR, 2.04 [95% CI, 1.70-2.44]; P = 5.3 x 10(-15)) and log(e)-transformed coronary artery calcium (effect, 0.70 [95% CI, 0.53-0.87]; P = 1.0 x 10(-15)). Genetically predicted levels of non-HDL-C remained associated with obstructive CAD and coronary artery calcium extent even after accounting for the association with LDL-C. Genetically predicted levels of HDL-C and triglycerides were associated individually with the extent of coronary atherosclerosis, but not after accounting for the association with non-HDL cholesterol. Conclusions and Relevance In this study, genetically predicted levels of non-HDL-C were associated with the extent of coronary atherosclerosis as estimated by 2 different methods. The association was stronger than for genetically predicted levels of LDL-C. These findings further support the notion that non-HDL-C may be a better marker of the overall burden of atherogenic lipoproteins than LDL-C.
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页码:13 / 20
页数:8
相关论文
共 44 条
  • [1] QUANTIFICATION OF CORONARY-ARTERY CALCIUM USING ULTRAFAST COMPUTED-TOMOGRAPHY
    AGATSTON, AS
    JANOWITZ, WR
    HILDNER, FJ
    ZUSMER, NR
    VIAMONTE, M
    DETRANO, R
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 15 (04) : 827 - 832
  • [2] Beyond Low-Density Lipoprotein Cholesterol
    Arsenault, Benoit J.
    Rana, Jamal S.
    Stroes, Erik S. G.
    Despres, Jean-Pierre
    Shah, Prediman K.
    Kastelein, John J. P.
    Wareham, Nicholas J.
    Boekholdt, S. Matthijs
    Khaw, Kay-Tee
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 55 (01) : 35 - 41
  • [3] Common Sequence Variants Associated With Coronary Artery Disease Correlate With the Extent of Coronary Atherosclerosis
    Bjornsson, Eythor
    Gudbjartsson, Daniel F.
    Helgadottir, Anna
    Gudnason, Thorarinn
    Gudbjartsson, Tomas
    Eyjolfsson, Kristjan
    Patel, Riyaz S.
    Ghasemzadeh, Nima
    Thorleifsson, Gudmar
    Quyyumi, Arshed A.
    Thorsteinsdottir, Unnur
    Thorgeirsson, Gudmundur
    Stefansson, Kari
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2015, 35 (06) : 1526 - 1531
  • [4] Association of LDL Cholesterol, Non-HDL Cholesterol, and Apolipoprotein B Levels With Risk of Cardiovascular Events Among Patients Treated With Statins A Meta-analysis
    Boekholdt, S. Matthijs
    Arsenault, Benoit J.
    Mora, Samia
    Pedersen, Terje R.
    LaRosa, John C.
    Nestel, Paul J.
    Simes, R. John
    Durrington, Paul
    Hitman, Graham A.
    Welch, K. M. A.
    DeMicco, David A.
    Zwinderman, Aeilko H.
    Clearfield, Michael B.
    Downs, John R.
    Tonkin, Andrew M.
    Colhoun, Helen M.
    Gotto, Antonio M., Jr.
    Ridker, Paul M.
    Kastelein, John J. P.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2012, 307 (12): : 1302 - 1309
  • [5] Coronary Calcium Predicts Events Better With Absolute Calcium Scores Than Age-Sex-Race/Ethnicity Percentiles MESA (Multi-Ethnic Study of Atherosclerosis)
    Budoff, Matthew J.
    Nasir, Khurram
    McClelland, Robyn L.
    Detrano, Robert
    Wong, Nathan
    Blumenthal, Roger S.
    Kondos, George
    Kronmal, Richard A.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 53 (04) : 345 - 352
  • [6] Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
    Crosby, Jacy
    Peloso, Gina M.
    Auer, Paul L.
    Crosslin, David R.
    Stitziel, Nathan O.
    Lange, Leslie A.
    Lu, Yingchang
    Tang, Zheng-zheng
    Zhang, He
    Hindy, George
    Masca, Nicholas
    Stirrups, Kathleen
    Kanoni, Stavroula
    Do, Ron
    Jun, Goo
    Hu, Youna
    Kang, Hyun Min
    Xue, Chenyi
    Goel, Anuj
    Farrall, Martin
    Duga, Stefano
    Merlini, Pier Angelica
    Asselta, Rosanna
    Girelli, Domenico
    Olivieri, Oliviero
    Martinelli, Nicola
    Yin, Wu
    Reilly, Dermot
    Speliotes, Elizabeth
    Fox, Caroline S.
    Hveem, Kristian
    Holmen, Oddgeir L.
    Nikpay, Majid
    Farlow, Deborah N.
    Assimes, Themistocles L.
    Franceschini, Nora
    Robinson, Jennifer
    North, Kari E.
    Martin, Lisa W.
    DePristo, Mark
    Gupta, Namrata
    Escher, Stefan A.
    Jansson, Jan-Hakan
    Van Zuydam, Natalie
    Palmer, Colin N. A.
    Wareham, Nicholas
    Koch, Werner
    Meitinger, Thomas
    Peters, Annette
    Lieb, Wolfgang
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (01) : 22 - 31
  • [7] Mendelian randomization: genetic anchors for causal inference in epidemiological studies
    Davey Smith, George
    Hemani, Gibran
    [J]. HUMAN MOLECULAR GENETICS, 2014, 23 : R89 - R98
  • [8] Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
    Dewey, Frederick F.
    Gusarova, Viktoria
    O'Dushlaine, Colm
    Gottesman, Omri
    Trejos, Jesus
    Hunt, Charleen
    Van Hout, Cristopher V.
    Habegger, Lukas
    Buckler, David
    Lai, Ka-Man V.
    Leader, Joseph B.
    Murray, Michael F.
    Ritchie, Marylyn D.
    Kirchner, H. Lester
    Ledbetter, David H.
    Penn, John
    Lopez, Alexander
    Borecki, Ingrid B.
    Overton, John D.
    Reid, Jeffrey G.
    Carey, David J.
    Murphy, Andrew J.
    Yancopoulos, George D.
    Baras, Aris
    Gromada, Jesper
    Shuldiner, Alan R.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (12) : 1123 - 1133
  • [9] Di Angelantonio E, 2009, JAMA-J AM MED ASSOC, V302, P1993, DOI 10.1001/jama.2009.1619
  • [10] Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
    Do, Ron
    Stitziel, Nathan O.
    Won, Hong-Hee
    Jorgensen, Anders Berg
    Duga, Stefano
    Merlini, Pier Angelica
    Kiezun, Adam
    Farrall, Martin
    Goel, Anuj
    Zuk, Or
    Guella, Illaria
    Asselta, Rosanna
    Lange, Leslie A.
    Peloso, Gina M.
    Auer, Paul L.
    Girelli, Domenico
    Martinelli, Nicola
    Farlow, Deborah N.
    DePristo, Mark A.
    Roberts, Robert
    Stewart, Alexander F. R.
    Saleheen, Danish
    Danesh, John
    Epstein, Stephen E.
    Sivapalaratnam, Suthesh
    Hovingh, G. Kees
    Kastelein, John J.
    Samani, Nilesh J.
    Schunkert, Heribert
    Erdmann, Jeanette
    Shah, Svati H.
    Kraus, William E.
    Davies, Robert
    Nikpay, Majid
    Johansen, Christopher T.
    Wang, Jian
    Hegele, Robert A.
    Hechter, Eliana
    Marz, Winfried
    Kleber, Marcus E.
    Huang, Jie
    Johnson, Andrew D.
    Li, Mingyao
    Burke, Greg L.
    Gross, Myron
    Liu, Yongmei
    Assimes, Themistocles L.
    Heiss, Gerardo
    Lange, Ethan M.
    Folsom, Aaron R.
    [J]. NATURE, 2015, 518 (7537) : 102 - +