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Association of Repeatedly Measured High-Sensitivity-Assayed Troponin I with Cardiovascular Disease Events in a General Population from the MORGAM/BiomarCaRE Study.
Hughes, Maria F; Ojeda, Francisco; Saarela, Olli; Jørgensen, Torben; Zeller, Tanja; Palosaari, Tarja; O'Doherty, Mark G; Borglykke, Anders; Kuulasmaa, Kari; Blankenberg, Stefan; Kee, Frank.
Affiliation
  • Hughes MF; UKCRC Centre of Excellence for Public Health Northern Ireland, Queens University Belfast, Northern Ireland; maria.hughes@qub.ac.uk.
  • Ojeda F; Department of General and Interventional Cardiology, Hamburg University Heart Center, Hamburg, Germany.
  • Saarela O; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Lübeck/Kiel.
  • Jørgensen T; MRC Epidemiology Unit, University of Cambridge, United Kingdom.
  • Zeller T; Department of General and Interventional Cardiology, Hamburg University Heart Center, Hamburg, Germany.
  • Palosaari T; Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
  • O'Doherty MG; National Institute for Health and Welfare THL, Helsinki, Finland.
  • Borglykke A; Research Centre for Prevention and Health, Centre of Health, Capital Region, Glostrup, Denmark.
  • Kuulasmaa K; Institute of Public Health, University of Copenhagen, Copenhagen, Denmark.
  • Blankenberg S; Faculty of Medicine, University of Aalborg, Aalborg, Denmark.
  • Kee F; Department of General and Interventional Cardiology, Hamburg University Heart Center, Hamburg, Germany.
Clin Chem ; 63(1): 334-342, 2017 Jan.
Article in En | MEDLINE | ID: mdl-28062627
ABSTRACT

BACKGROUND:

High-sensitivity troponin I (hs-cTnI) concentrations reflect myocardial stress. The role of hs-cTnI in predicting long-term changes in the risk of cardiovascular disease (CVD) in general populations is not clearly defined.

METHODS:

We investigated whether the change in 3 repeated measures of hs-cTnI collected 5 years apart in a prospective Danish study (3875 participants, initially aged 30-60 years, 51% female, disease free at baseline) improves 10-year prediction of incident CVD compared to using a single most recent hs-cTnI measurement. The change process was modelled using a joint (longitudinal and survival) model and compared to a Cox model using a single hs-cTnI measure adjusted for classic CVD risk factors, and evaluated using discrimination statistics.

RESULTS:

Median hs-cTnI concentrations changed from 2.6 ng/L to 3.4 ng/L over 10 years. The change in hs-cTnI predicts 10-year risk of CVD (581 events); the joint model gave a hazard ratio of 1.31 per interquartile difference in hs-cTnI (95% CI 1.15-1.48) after adjustment for CVD risk factors. However, the joint model performed only marginally better (c-index improvement 0.0041, P = 0.03) than using a single hs-cTnI measure (c-index improvement 0.0052, P = 0.04) for prediction of CVD, compared to a model incorporating CVD risk factors without hs-cTnI (c-index 0.744).

CONCLUSIONS:

The change in hs-cTnI in 5-year intervals better predicts risk of CVD in the general population, but the most recent measure of hs-cTnI, (at 10 years) is as effective in predicting CVD risk. This simplifies the use of hs-cTnI as a prognostic marker for primary prevention of CVD in the general population.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Troponin I Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Clin Chem Journal subject: QUIMICA CLINICA Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Troponin I Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Clin Chem Journal subject: QUIMICA CLINICA Year: 2017 Document type: Article