Pereira Andreia, Mendonça Maria Isabel, Borges Sofia, Freitas Sónia, Henriques Eva, Rodrigues Mariana, Freitas Ana Isabel, Sousa Ana Célia, Brehm António, Reis Roberto Palma Dos
Unidade de Investigação, Hospital Dr. Nélio Mendonça, Funchal - Portugal.
Laboratório de Genética Humana, Universidade da Madeira, Funchal - Portugal.
Arq Bras Cardiol. 2018 Jul;111(1):50-61. doi: 10.5935/abc.20180107. Epub 2018 Jul 2.
Genetic risk score can quantify individual's predisposition to coronary artery disease; however, its usefulness as an independent risk predictor remains inconclusive.
To evaluate the incremental predictive value of a genetic risk score to traditional risk factors associated with coronary disease.
Thirty-three genetic variants previously associated with coronary disease were analyzed in a case-control population with 2,888 individuals. A multiplicative genetic risk score was calculated and then divided into quartiles, with the 1st quartile as the reference class. Coronary risk was determined by logistic regression analysis. Then, a second logistic regression was performed with traditional risk factors and the last quartile of the genetic risk score. Based on this model, two ROC curves were constructed with and without the genetic score and compared by the Delong test. Statistical significance was considered when p values were less than 0.05.
The last quartile of the multiplicative genetic risk score revealed a significant increase in coronary artery disease risk (OR = 2.588; 95% CI: 2.090-3.204; p < 0.0001). The ROC curve based on traditional risk factors estimated an AUC of 0.72, which increased to 0.74 when the genetic risk score was added, revealing a better fit of the model (p < 0.0001).
In conclusion, a multilocus genetic risk score was associated with an increased risk for coronary disease in our population. The usual model of traditional risk factors can be improved by incorporating genetic data.
遗传风险评分可量化个体患冠状动脉疾病的易感性;然而,其作为独立风险预测指标的效用仍无定论。
评估遗传风险评分对与冠心病相关的传统风险因素的增量预测价值。
在一个包含2888名个体的病例对照人群中,分析了33个先前与冠心病相关的基因变异。计算了一个乘法遗传风险评分,然后将其分为四分位数,以第一四分位数作为参照组。通过逻辑回归分析确定冠心病风险。然后,对传统风险因素和遗传风险评分的最后四分位数进行第二次逻辑回归。基于该模型,构建了有和没有遗传评分的两条ROC曲线,并通过德龙检验进行比较。当p值小于0.05时,认为具有统计学意义。
乘法遗传风险评分的最后四分位数显示冠心病风险显著增加(OR = 2.588;95% CI:2.090 - 3.204;p < 0.0001)。基于传统风险因素的ROC曲线估计AUC为0.72,加入遗传风险评分后增至0.74,表明模型拟合度更好(p < 0.0001)。
总之,在我们的人群中,多基因座遗传风险评分与冠心病风险增加相关。纳入遗传数据可改善传统风险因素的常用模型。