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Advisor(s)
Abstract(s)
The inclusion of a genetic risk score (GRS) can modify the risk prediction of coronary artery disease (CAD), providing
an advantage over the use of traditional models. The predictive value of the genetic information on the recurrence
of major adverse cardiovascular events (MACE) remains controversial. A total of 33 genetic variants previously
associated with CAD were genotyped in 1587 CAD patients from the GENEMACOR study. Of these, 18 variants
presented an hazard ratio >1, so they were selected to construct a weighted GRS (wGRS). MACE discrimination and
reclassification were evaluated by C-Statistic, Net Reclassification Index and Integrated Discrimination Improvement
methodologies. After the addition of wGRS to traditional predictors, the C-index increased from 0.566 to 0.572
(p=0.0003). Subsequently, adding wGRS to traditional plus clinical risk factors, this model slightly improved from 0.620
to 0.622 but with statistical significance (p=0.004). NRI showed that 17.9% of the cohort was better reclassified when
the primary model was associated with wGRS. The Kaplan-Meier estimator showed that, at 15-year follow-up, the
group with a higher number of risk alleles had a significantly higher MACE occurrence (p=0.011). In CAD patients,
wGRS improved MACE risk prediction, discrimination and reclassification over the conventional factors, providing
better cost-effective therapeutic strategies.
Description
Keywords
Traditional risk factors genetic risk score events risk discrimination and reclassification Net Reclassification Index secondary prevention of coronary artery disease
Citation
Mendonça MI, Henriques E, Borges S, et al. Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population. Genet Mol Biol. 2021;44(2):e20200448. Published 2021 Jun 11. doi:10.1590/1678-4685-GMB-2020-0448