Multiplex proteomics for prediction of major cardiovascular events in type 2 diabetes

被引:45
|
作者
Nowak, Christoph [1 ]
Carlsson, Axel C. [1 ,2 ]
Ostgren, Carl Johan [3 ]
Nystrom, Fredrik H. [3 ]
Alam, Moudud [4 ]
Feldreich, Tobias [5 ]
Sundstrom, Johan [2 ]
Carrero, Juan-Jesus [6 ]
Leppert, Jerzy [7 ]
Hedberg, Par [7 ]
Henriksen, Egil [7 ]
Cordeiro, Antonio C. [8 ]
Giedraitis, Vilmantas [9 ]
Lind, Lars [2 ]
Ingelsson, Erik [10 ]
Fall, Tove [2 ]
Arnlov, Johan [1 ,5 ]
机构
[1] Karolinska Inst, Div Family Med & Primary Care, Dept Neurobiol Care Sci & Soc NVS, Alfred Nobels Alle 23, SE-14183 Huddinge, Sweden
[2] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[3] Linkoping Univ, Dept Med & Hlth Sci, Linkoping, Sweden
[4] Dalarna Univ, Sch Technol & Business Studies Stat, Falun, Sweden
[5] Dalarna Univ, Sch Hlth & Social Studies, Falun, Sweden
[6] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[7] Uppsala Univ, Ctr Clin Res, Vasteras, Sweden
[8] Dante Pazzanese Inst Cardiol, Dept Hypertens & Nephrol, Sao Paulo, Brazil
[9] Uppsala Univ, Dept Publ Hlth & Caring Sci, Geriatr, Uppsala, Sweden
[10] Stanford Univ, Sch Med, Div Cardiovasc Med, Dept Med, Stanford, CA 94305 USA
基金
欧盟地平线“2020”; 瑞典研究理事会;
关键词
Biomarkers; Major adverse cardiovascular event; Proteomics; Risk; Type; 2; diabetes; CORONARY-ARTERY-DISEASE; HEART-DISEASE; MYOCARDIAL-INFARCTION; PROTEIN BIOMARKERS; KIDNEY-DISEASE; PLASMA-LEVELS; RISK-FACTORS; ATHEROSCLEROSIS; INTERLEUKIN-27; ASSOCIATION;
D O I
10.1007/s00125-018-4641-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis Multiplex proteomics could improve understanding and risk prediction of major adverse cardiovascular events (MACE) in type 2 diabetes. This study assessed 80 cardiovascular and inflammatory proteins for biomarker discovery and prediction of MACE in type 2 diabetes. Methods We combined data from six prospective epidemiological studies of 30-77-year-old individuals with type 2 diabetes in whom 80 circulating proteins were measured by proximity extension assay. Multivariable-adjusted Cox regression was used in a discovery/replication design to identify biomarkers for incident MACE. We used gradient-boosted machine learning and lasso regularised Cox regression in a random 75% training subsample to assess whether adding proteins to risk factors included in the Swedish National Diabetes Register risk model would improve the prediction of MACE in the separate 25% test subsample. Results Of 1211 adults with type 2 diabetes (32% women), 211 experienced a MACE over a mean (+/- SD) of 6.4 +/- 2.3 years. We replicated associations (< 5% false discovery rate) between risk of MACE and eight proteins: matrix metalloproteinase (MMP)-12, IL-27 subunit alpha (IL-27a), kidney injury molecule (KIM)-1, fibroblast growth factor (FGF)-23, protein S100-A12, TNF receptor (TNFR)-1, TNFR-2 and TNF-related apoptosis-inducing ligand receptor (TRAIL-R)2. Addition of the 80-protein assay to established risk factors improved discrimination in the separate test sample from 0.686 (95% CI 0.682, 0.689) to 0.748 (95% CI 0.746, 0.751). A sparse model of 20 added proteins achieved a C statistic of 0.747 (95% CI 0.653, 0.842) in the test sample. Conclusions/interpretation We identified eight protein biomarkers, four of which are novel, for risk of MACE in community residents with type 2 diabetes, and found improved risk prediction by combining multiplex proteomics with an established risk model. Multiprotein arrays could be useful in identifying individuals with type 2 diabetes who are at highest risk of a cardiovascular event.
引用
收藏
页码:1748 / 1757
页数:10
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