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

Nowak, Christoph (author)
Karolinska Institutet,Karolinska Inst, Dept Neurobiol Care Sci & Soc NVS, Huddinge, Sweden
Carlsson, Axel C (author)
Karolinska Institutet,Uppsala universitet,Institutionen för medicinska vetenskaper,Karolinska Inst, Div Family Med & Primary Care, Dept Neurobiol Care Sci & Soc NVS, Alfred Nobels Alle 23, SE-14183 Huddinge, Sweden,Karolinska Inst, Sweden; Uppsala Univ, Sweden,Dante Pazzanese Inst Cardiol, Sao Paulo, Brazil
Östgren, Carl Johan, 1963- (author)
Linköpings universitet,Avdelningen för samhällsmedicin,Medicinska fakulteten,Region Östergötland, Vårdcentralen Ödeshög,Linkoping Univ, Linkoping, Sweden
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Nyström, Fredrik, 1963- (author)
Linköpings universitet,Avdelningen för kardiovaskulär medicin,Medicinska fakulteten,Region Östergötland, Endokrinmedicinska kliniken,Linkoping Univ, Linkoping, Sweden
Alam, Moudud, 1976- (author)
Högskolan Dalarna,Statistik,Dalarna Univ, Falun, Sweden
Rudholm Feldreich, Tobias (author)
Högskolan Dalarna,Medicinsk vetenskap,Dalarna Univ, Falun, Sweden
Sundström, Johan (author)
Uppsala universitet,Kardiovaskulär epidemiologi,Uppsala Univ, Sweden
Carrero, Juan-Jesus (author)
Karolinska Institutet,Karolinska Inst, Solna, Sweden
Leppert, Jerzy (author)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Uppsala Univ, Sweden
Hedberg, Pär (author)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Uppsala Univ, Sweden
Henriksen, Egil (author)
Uppsala universitet,Centrum för klinisk forskning, Västerås,Uppsala Univ, Sweden
Cordeiro, Antonio C. (author)
Dante Pazzanese Inst Cardiol, Dept Hypertens & Nephrol, Sao Paulo, Brazil
Giedraitis, Vilmantas (author)
Uppsala universitet,Geriatrik,Uppsala Univ, Sweden
Lind, Lars (author)
Uppsala universitet,Kardiovaskulär epidemiologi,Uppsala Univ, Sweden
Ingelsson, Erik (author)
Stanford Univ, Sch Med, Div Cardiovasc Med, Dept Med, Stanford, CA 94305 USA
Fall, Tove, 1979- (author)
Uppsala universitet,Molekylär epidemiologi,Uppsala Univ, Sweden
Ärnlöv, Johan, 1970- (author)
Högskolan Dalarna,Karolinska Institutet,Karolinska Inst, Dept Neurobiol Care Sci & Soc NVS, Huddinge, Sweden;Dalarna Univ, Falun, Sweden,Medicinsk vetenskap
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 (creator_code:org_t)
2018-05-24
2018
English.
In: Diabetologia. - : SPRINGER. - 0012-186X .- 1432-0428. ; 61:8, s. 1748-1757
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Biomarkers
Major adverse cardiovascular event
Proteomics
Risk
Type 2 diabetes
Health and Welfare

Publication and Content Type

ref (subject category)
art (subject category)

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