Vanderbilt University Medical Center, Nashville, Tennessee.
Lehigh Valley Health Network, Allentown, Pennsylvania.
Arthritis Care Res (Hoboken). 2018 Nov;70(11):1630-1636. doi: 10.1002/acr.23553.
Phenome-wide association studies (PheWAS) scan across billing codes in the electronic health record (EHR) and re-purpose clinical EHR data for research. In this study, we examined whether PheWAS could function as an EHR-based discovery tool for systemic lupus erythematosus (SLE) and identified novel clinical associations in male versus female patients with SLE.
We used a de-identified version of the Vanderbilt University Medical Center EHR, which includes more than 2.8 million subjects. We performed EHR-based PheWAS to compare SLE patients with age-, sex-, and race-matched control subjects and to compare male SLE patients with female SLE patients, controlling for multiple testing using a false discovery rate (FDR) P value of 0.05.
We identified 1,097 patients with SLE and 5,735 matched control subjects. In a comparison of patients with SLE and matched controls, SLE patients were shown to be more likely to have International Classification of Diseases, Ninth Revision codes related to the SLE disease criteria. In the PheWAS of male versus female SLE patients, with adjustment for age and race, male patients were shown to be more likely to have atrial fibrillation (odds ratio 4.50, false discovery rate P = 3.23 × 10 ). Chart review confirmed atrial fibrillation, with the majority of patients developing atrial fibrillation after the SLE diagnosis and having multiple risk factors for atrial fibrillation. After adjustment for age, sex, race, and coronary artery disease, SLE disease status was shown to be significantly associated with atrial fibrillation (P = 0.002).
Using PheWAS to compare male and female patients with SLE, we identified a novel association of an increased incidence of atrial fibrillation in male patients. SLE disease status was shown to be independently associated with atrial fibrillation, even after adjustment for age, sex, race, and coronary artery disease. These results demonstrate the utility of PheWAS as an EHR-based discovery tool for SLE.
全基因组关联研究(PheWAS)扫描电子健康记录(EHR)中的计费代码,并重新利用临床 EHR 数据进行研究。在这项研究中,我们检查了 PheWAS 是否可以作为红斑狼疮(SLE)的基于 EHR 的发现工具,并确定了 SLE 男性和女性患者之间的新的临床关联。
我们使用了范德比尔特大学医学中心 EHR 的一个去识别版本,其中包含超过 280 万患者。我们进行了基于 EHR 的 PheWAS,以比较 SLE 患者与年龄、性别和种族匹配的对照组,并比较男性 SLE 患者与女性 SLE 患者,使用 FDR P 值为 0.05 进行了多重测试控制。
我们确定了 1097 名 SLE 患者和 5735 名匹配的对照组。在 SLE 患者与匹配对照组的比较中,SLE 患者更有可能出现与 SLE 疾病标准相关的国际疾病分类,第九版代码。在男性与女性 SLE 患者的 PheWAS 中,在调整年龄和种族后,男性患者更有可能出现心房颤动(优势比 4.50,FDR P = 3.23×10)。图表审查证实了心房颤动,大多数患者在 SLE 诊断后出现心房颤动,并存在多种心房颤动的危险因素。在调整年龄、性别、种族和冠状动脉疾病后,SLE 疾病状态与心房颤动显著相关(P = 0.002)。
使用 PheWAS 比较 SLE 男性和女性患者,我们发现男性患者心房颤动发生率增加的新关联。即使在调整年龄、性别、种族和冠状动脉疾病后,SLE 疾病状态与心房颤动仍独立相关。这些结果表明 PheWAS 作为 SLE 的基于 EHR 的发现工具具有实用性。