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April 19, 2013Arteriosclerosis Thrombosis and Vascular BiologyOpen Access

Genetic Risk Prediction and a 2-Stage Risk Screening Strategy for Coronary Heart Disease

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Key result

Adding a 28-variant genetic risk score to conventional risk factors improved risk discrimination for incident CHD (C-index 0.856 vs 0.851; P=0.0002).

Why the study?

Does adding a multilocus genetic risk score to conventional risk factors improve risk prediction for incident coronary heart disease in a general population?

Population

24,124 participants in 4 Finnish population-based, prospective cohorts (recruitment years 1992-2002)

Comparison

Multilocus genetic risk score added to… vs Conventional risk factors and family history alone

Design

Cohort

Follow-up

median 12 years (IQR 8.75-15.25 years)

Authors

ETEmmi TikkanenGeneral / Preventive / LipidsAHAki S. HavulinnaPreventive CardiologyAarno PalotieAarno PalotieStatens Serum Institut

Discussion

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Implication

May modestly refine CHD risk stratification in cohorts; leaves open effects on decisions and outcomes.

Study Design

Type

Cohort (n=24,124)

Multicenter

Yes

Structured PICO

Does adding a multilocus genetic risk score to conventional risk factors improve risk prediction for incident coronary heart disease in a general population?

P
Population
24,124 participants in 4 Finnish population-based, prospective cohorts (recruitment years 1992-2002)
I
Intervention
Multilocus genetic risk score (28 genetic variants) added to conventional risk factors and family history
C
Comparator
Conventional risk factors and family history alone
O
Outcome
Incident coronary heart disease (CHD) eventshard clinical

Main Result

Absolute Event Rate: 0.856% vs 0.851%

p-value: p=0.0002

Adding a 28-variant genetic risk score to conventional risk factors modestly improves CHD risk discrimination and can reclassify intermediate-risk individuals to guide statin therapy.

Cite This Study

Tikkanen et al. (2013) conducted a cohort in Coronary Heart Disease (n=24,124). Multilocus genetic risk score (28 genetic variants) vs. Conventional risk factors and family history was evaluated on Risk discrimination of CHD (C-index) (p=0.0002). Adding a 28-variant genetic risk score to conventional risk factors improved risk discrimination for incident CHD (C-index 0.856 vs 0.851; P=0.0002).

synapsesocial.com/papers/6a18d233673175fe754af392https://doi.org/10.1161/atvbaha.112.301120

Topics

Statin therapy
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