Genetic Risk Analysis of Coronary Artery Disease in a Population-based Study in Portugal, Using a Genetic Risk Score of 31 Variants

被引:9
|
作者
Pereira, Andreia [1 ]
Mendonca, Maria Isabel [1 ]
Borges, Sofia [1 ]
Freitas, Sonia [1 ]
Kdriques, Eva, I [1 ]
Rodrigues, Mariana [1 ]
Freitas, Ana Isabel [2 ]
Sousa, Ana Celia [1 ]
Brehm, Antonio [2 ]
dos Reis, Roberto Palma [3 ]
机构
[1] Hosp Dr Nelio Mendonca, Unidade Invest, Funchal, Portugal
[2] Univ Madeira, Lab Genet Humana, Funchal, Portugal
[3] Univ Nova Lisboa, Fac Ciencias Med, Lisbon, Portugal
关键词
Coronary Artery Disease / history; Coronary Artery Disease / morbidity; Mortality; Polymorphism; Genetic; Epidemiology; Risk Factors; GENOME-WIDE ASSOCIATION; HEART-DISEASE; CONSENSUS;
D O I
10.5935/abc.20180107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Genetic risk score can quantify individual's predisposition to coronary artery disease; however, its usefulness as an independent risk predictor remains inconclusive. Objective: To evaluate the incremental predictive value of a genetic risk score to traditional risk factors associated with coronary disease. Methods: Thirty-three genetic variants previously associated with coronary disease were analyzed in a case-control population with 2,888 individuals. A multiplicative genetic risk score was calculated and then divided into quartiles, with the 1st quartile as the reference class. Coronary risk was determined by logistic regression analysis. Then, a second logistic regression was performed with traditional risk factors and the last quartile of the genetic risk score. Based on this model, two ROC curves were constructed with and without the genetic score and compared by the Delong test. Statistical significance was considered when p values were less than 0.05. Results: The last quartile of the multiplicative genetic risk score revealed a s ign ificant increase in coronary artery disease risk (OR = 2.588; 95% CI: 2.090-3.204; p < 0.0001). The ROC curve based on traditional risk factors estimated an AUC of 0.72, which increased to 0.74 when the genetic risk score was added, revealing a better fit of the model (p < 0.0001). Conclusions: In conclusion, a multilocus genetic risk score was associated with an increased risk for coronary disease in our population. The usual model of traditional risk factors can be improved by incorporating genetic data.
引用
收藏
页码:50 / 61
页数:12
相关论文
共 50 条
  • [41] Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
    Waterworth, Dawn M.
    Ricketts, Sally L.
    Song, Kijoung
    Chen, Li
    Zhao, Jing Hua
    Ripatti, Samuli
    Aulchenko, Yurii S.
    Zhang, Weihua
    Yuan, Xin
    Lim, Noha
    Luan, Jian'an
    Ashford, Sofie
    Wheeler, Eleanor
    Young, Elizabeth H.
    Hadley, David
    Thompson, John R.
    Braund, Peter S.
    Johnson, Toby
    Struchalin, Maksim
    Surakka, Ida
    Luben, Robert
    Khaw, Kay-Tee
    Rodwell, Sheila A.
    Loos, Ruth J. F.
    Boekholdt, S. Matthijs
    Inouye, Michael
    Deloukas, Panagiotis
    Elliott, Paul
    Schlessinger, David
    Sanna, Serena
    Scuteri, Angelo
    Jackson, Anne
    Mohlke, Karen L.
    Tuomilehto, Jaako
    Roberts, Robert
    Stewart, Alexandre
    Kesaeniemi, Y. Antero
    Mahley, Robert W.
    Grundy, Scott M.
    McArdle, Wendy
    Cardon, Lon
    Waeber, Gerard
    Vollenweider, Peter
    Chambers, John C.
    Boehnke, Michael
    Abecasis, Goncalo R.
    Salomaa, Veikko
    Jaervelin, Marjo-Riitta
    Ruokonen, Aimo
    Barroso, Ines
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2010, 30 (11) : 2264 - U566
  • [42] Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort
    Yun, Sohyun
    Han, Miyeun
    Kim, Hyo Jin
    Kim, Hyunsuk
    Kang, Eunjeong
    Kim, Sangsoo
    Ahn, Curie
    Oh, Kook-Hwan
    CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2019, 23 (08) : 995 - 1003
  • [43] Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort
    Sohyun Yun
    Miyeun Han
    Hyo Jin Kim
    Hyunsuk Kim
    Eunjeong Kang
    Sangsoo Kim
    Curie Ahn
    Kook-Hwan Oh
    Clinical and Experimental Nephrology, 2019, 23 : 995 - 1003
  • [44] Genetic Risk, Lifestyle, and Coronary Artery Disease
    Kullo, Iftikhar J.
    Fan, Xiao
    Ding, Keyue
    NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (12): : 1192 - 1193
  • [45] A multilocus genetic risk score predicts coronary heart disease risk in a Chinese Han population
    Gui, Lixuan
    Wu, Fangqin
    Han, Xu
    Dai, Xiayun
    Qiu, Gaokun
    Li, Jun
    Wang, Jing
    Zhang, Xiaoming
    Wu, Tangchun
    He, Meian
    ATHEROSCLEROSIS, 2014, 237 (02) : 480 - 485
  • [46] Genetic polymorphisms and risk of coronary artery disease
    Murata, M
    Kawano, K
    Matsubara, Y
    Ishikawa, K
    Watanabe, K
    Ikeda, Y
    SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1998, 24 (03): : 245 - 250
  • [47] A Weighted Genetic Risk Score Using Known Susceptibility Variants to Predict Graves Disease Risk
    Ma, Yu-Ru
    Zhao, Shuang-Xia
    Li, Lu
    Sun, Feng
    Ye, Xiao-Ping
    Yuan, Fei-Fei
    Jiang, Dan
    Zhou, Zheng
    Zhang, Qian-Yue
    Wan, Yue-Yue
    Zhang, Guang-Ya
    Wu, Jing
    Zhang, Rui-Jia
    Fang, Ya
    Song, Huai-Dong
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2019, 104 (06): : 2121 - 2130
  • [48] Genetic Risk Score for Coronary Heart Disease: Review
    Semaev, Sergey
    Shakhtshneider, Elena
    JOURNAL OF PERSONALIZED MEDICINE, 2020, 10 (04): : 1 - 18
  • [49] Genetic Risk Score Enhances Coronary Artery Disease Risk Prediction in Individuals With Type 1 Diabetes
    Lithovius, Raija
    Antikainen, Anni A.
    Mutter, Stefan
    Valo, Erkka
    Forsblom, Carol
    Harjutsalo, Valma
    Sandholm, Niina
    Groop, Per-Henrik
    DIABETES CARE, 2022, 45 (03) : 734 - 741
  • [50] A genetic risk score predicts coronary artery disease in familial hypercholesterolaemia: enhancing the precision of risk assessment
    Ellis, Katrina L.
    Hooper, Amanda J.
    Pang, Jing
    Chan, Dick C.
    Burnett, John R.
    Bell, Damon A.
    Schultz, Carl J.
    Moses, Eric K.
    Watts, Gerald F.
    CLINICAL GENETICS, 2020, 97 (02) : 257 - 263