Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI 48109, USA.
Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI 48109, USA; Center for Precision Health Data Science, University of Michigan, Ann Arbor, MI 48109, USA; Rogel Cancer Center, University of Michigan, Ann Arbor, MI 48109, USA; Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI 48109, USA.
J Biomed Inform. 2022 Dec;136:104237. doi: 10.1016/j.jbi.2022.104237. Epub 2022 Oct 23.
Post COVID-19 condition (PCC) is known to affect a large proportion of COVID-19 survivors. Robust study design and methods are needed to understand post-COVID-19 diagnosis patterns in all survivors, not just those clinically diagnosed with PCC.
We applied a case-crossover Phenome-Wide Association Study (PheWAS) in a retrospective cohort of COVID-19 survivors, comparing the occurrences of 1,671 diagnosis-based phenotype codes (PheCodes) pre- and post-COVID-19 infection periods in the same individual using a conditional logistic regression. We studied how this pattern varied by COVID-19 severity and vaccination status, and we compared to test negative and test negative but flu positive controls.
In 44,198 SARS-CoV-2-positive patients, we foundenrichment in respiratory,circulatory, and mental health disorders post-COVID-19-infection. Top hits included anxiety disorder (p = 2.8e-109, OR = 1.7 [95 % CI: 1.6-1.8]), cardiac dysrhythmias (p = 4.9e-87, OR = 1.7 [95 % CI: 1.6-1.8]), and respiratory failure, insufficiency, arrest (p = 5.2e-75, OR = 2.9 [95 % CI: 2.6-3.3]). In severe patients, we found stronger associations with respiratory and circulatory disorders compared to mild/moderate patients. Fully vaccinated patients had mental health and chronic circulatory diseases rise to the top of the association list, similar to the mild/moderate cohort. Both control groups (test negative, test negative and flu positive) showed a different pattern of hits to SARS-CoV-2 positives.
Patients experience myriad symptoms more than 28 days after SARS-CoV-2 infection, but especially respiratory, circulatory, and mental health disorders. Our case-crossover PheWAS approach controls for within-person confounders that are time-invariant. Comparison to test negatives and test negative but flu positive patients with a similar design helped identify enrichment specific to COVID-19. This design may be applied other emerging diseases with long-lasting effects other than a SARS-CoV-2 infection. Given the potential for bias from observational data, these results should be considered exploratory. As we look into the future, we must be aware of COVID-19 survivors' healthcare needs.
据知,新冠病毒后状况(PCC)会影响很大比例的新冠幸存者。为了了解所有幸存者(不仅是临床诊断为 PCC 的幸存者)的新冠后诊断模式,需要稳健的研究设计和方法。
我们对新冠幸存者的回顾性队列应用了病例交叉表型全基因组关联研究(PheWAS),在同一个体中使用条件逻辑回归比较了新冠感染前后的 1671 个基于诊断的表型代码(PheCodes)的发生情况。我们研究了这种模式如何因新冠严重程度和疫苗接种状态而异,并与阴性测试和阴性但流感阳性对照进行了比较。
在 44198 例 SARS-CoV-2 阳性患者中,我们发现新冠感染后呼吸系统、循环系统和心理健康障碍增多。主要发现包括焦虑症(p=2.8e-109,OR=1.7[95%CI:1.6-1.8])、心律失常(p=4.9e-87,OR=1.7[95%CI:1.6-1.8])和呼吸衰竭、功能不全、骤停(p=5.2e-75,OR=2.9[95%CI:2.6-3.3])。在重症患者中,我们发现与轻症/中度患者相比,呼吸系统和循环系统疾病的关联更强。与轻症/中度队列相似,完全接种疫苗的患者的心理健康和慢性循环系统疾病上升到关联列表的首位。两个对照组(阴性测试、阴性测试和流感阳性)表现出与 SARS-CoV-2 阳性患者不同的命中模式。
患者在 SARS-CoV-2 感染后 28 天以上会出现多种症状,但尤其以呼吸系统、循环系统和心理健康障碍为主。我们的病例交叉 PheWAS 方法控制了与时间不变的个体内混杂因素有关的混杂因素。与具有相似设计的阴性测试和阴性但流感阳性患者进行比较有助于确定 COVID-19 特有的富集。这种设计可应用于其他除 SARS-CoV-2 感染外具有长期影响的新兴疾病。鉴于观察性数据可能存在偏倚,这些结果应被视为探索性的。展望未来,我们必须意识到新冠幸存者的医疗保健需求。