Pironti Alejandro, Pfeifer Nico, Walter Hauke, Jensen Björn-Erik O, Zazzi Maurizio, Gomes Perpétua, Kaiser Rolf, Lengauer Thomas
Department of Computational Biology and Applied Algorithmics, Max-Planck-Institut für Informatik, Saarbrücken, Germany.
Medizinisches Infektiologiezentrum Berlin, Berlin, Germany.
PLoS One. 2017 Apr 10;12(4):e0174992. doi: 10.1371/journal.pone.0174992. eCollection 2017.
Antiretroviral treatment history and past HIV-1 genotypes have been shown to be useful predictors for the success of antiretroviral therapy. However, this information may be unavailable or inaccurate, particularly for patients with multiple treatment lines often attending different clinics. We trained statistical models for predicting drug exposure from current HIV-1 genotype. These models were trained on 63,742 HIV-1 nucleotide sequences derived from patients with known therapeutic history, and on 6,836 genotype-phenotype pairs (GPPs). The mean performance regarding prediction of drug exposure on two test sets was 0.78 and 0.76 (ROC-AUC), respectively. The mean correlation to phenotypic resistance in GPPs was 0.51 (PhenoSense) and 0.46 (Antivirogram). Performance on prediction of therapy-success on two test sets based on genetic susceptibility scores was 0.71 and 0.63 (ROC-AUC), respectively. Compared to geno2pheno[resistance], our novel models display a similar or superior performance. Our models are freely available on the internet via www.geno2pheno.org. They can be used for inferring which drug compounds have previously been used by an HIV-1-infected patient, for predicting drug resistance, and for selecting an optimal antiretroviral therapy. Our data-driven models can be periodically retrained without expert intervention as clinical HIV-1 databases are updated and therefore reduce our dependency on hard-to-obtain GPPs.
抗逆转录病毒治疗史和既往HIV-1基因型已被证明是抗逆转录病毒治疗成功的有用预测指标。然而,这些信息可能无法获取或不准确,特别是对于经常在不同诊所接受多种治疗方案的患者。我们训练了用于从当前HIV-1基因型预测药物暴露的统计模型。这些模型是基于63742条来自有已知治疗史患者的HIV-1核苷酸序列以及6836个基因型-表型对(GPPs)进行训练的。在两个测试集上预测药物暴露的平均性能分别为0.78和0.76(ROC-AUC)。在GPPs中与表型耐药性的平均相关性在PhenoSense中为0.51,在Antivirogram中为0.46。基于遗传易感性评分在两个测试集上预测治疗成功的性能分别为0.71和0.63(ROC-AUC)。与geno2pheno[耐药性]相比,我们的新模型表现出相似或更优的性能。我们的模型可通过www.geno2pheno.org在互联网上免费获取。它们可用于推断HIV-1感染患者先前使用过哪些药物化合物、预测耐药性以及选择最佳抗逆转录病毒治疗方案。随着临床HIV-1数据库的更新,我们的数据驱动模型可以在无需专家干预的情况下定期重新训练,从而减少我们对难以获得的GPPs的依赖。