Institute for Computational Biomedicine, RWTH Aachen University, Pauwelsstr. 19, 52074, Aachen, Germany.
Joint Research Center for Computational Biomedicine, RWTH Aachen University, Pauwelsstr. 19, 52074, Aachen, Germany.
BMC Infect Dis. 2021 Nov 4;21(1):1136. doi: 10.1186/s12879-021-06823-z.
The impact of biometric covariates on risk for adverse outcomes of COVID-19 disease was assessed by numerous observational studies on unstratified cohorts, which show great heterogeneity. However, multilevel evaluations to find possible complex, e.g. non-monotonic multi-variate patterns reflecting mutual interference of parameters are missing. We used a more detailed, computational analysis to investigate the influence of biometric differences on mortality and disease evolution among severely ill COVID-19 patients.
We analyzed a group of COVID-19 patients requiring Intensive care unit (ICU) treatment. For further analysis, the study group was segmented into six subgroups according to Body mass index (BMI) and age. To link the BMI/age derived subgroups with risk factors, we performed an enrichment analysis of diagnostic parameters and comorbidities. To suppress spurious patterns, multiple segmentations were analyzed and integrated into a consensus score for each analysis step.
We analyzed 81 COVID-19 patients, of whom 67 required mechanical ventilation (MV). Mean mortality was 35.8%. We found a complex, non-monotonic interaction between age, BMI and mortality. A subcohort of patients with younger age and intermediate BMI exhibited a strongly reduced mortality risk (p < 0.001), while differences in all other groups were not significant. Univariate impacts of BMI or age on mortality were missing. Comparing MV with non-MV patients, we found an enrichment of baseline CRP, PCT and D-Dimers within the MV group, but not when comparing survivors vs. non-survivors within the MV patient group.
The aim of this study was to get a more detailed insight into the influence of biometric covariates on the outcome of COVID-19 patients with high degree of severity. We found that survival in MV is affected by complex interactions of covariates differing to the reported covariates, which are hidden in generic, non-stratified studies on risk factors. Hence, our study suggests that a detailed, multivariate pattern analysis on larger patient cohorts reflecting the specific disease stages might reveal more specific patterns of risk factors supporting individually adapted treatment strategies.
许多观察性研究对未经分层的队列进行了评估,发现生物特征协变量对 COVID-19 疾病不良结局的风险有影响,但缺乏多层次的评估来寻找可能的复杂模式,例如反映参数相互干扰的多变量模式。我们使用更详细的计算分析来研究生物特征差异对重症 COVID-19 患者死亡率和疾病演变的影响。
我们分析了一组需要重症监护病房(ICU)治疗的 COVID-19 患者。为了进一步分析,将研究组根据体重指数(BMI)和年龄分为六个亚组。为了将 BMI/年龄衍生的亚组与风险因素联系起来,我们对诊断参数和合并症进行了富集分析。为了抑制虚假模式,对多个分段进行了分析,并将其整合到每个分析步骤的共识评分中。
我们分析了 81 名 COVID-19 患者,其中 67 名需要机械通气(MV)。平均死亡率为 35.8%。我们发现年龄、BMI 和死亡率之间存在复杂的、非单调的相互作用。年龄较轻和 BMI 中等的亚组患者死亡率风险显著降低(p<0.001),而其他组之间的差异则不显著。BMI 或年龄对死亡率的单变量影响不存在。将 MV 患者与非 MV 患者进行比较时,我们发现 MV 组中基线 CRP、PCT 和 D-二聚体富集,但在 MV 患者组中比较幸存者与非幸存者时则没有。
本研究旨在更详细地了解生物特征协变量对高度严重 COVID-19 患者结局的影响。我们发现,MV 的存活率受到不同的协变量的复杂相互作用的影响,这与报告的风险因素隐藏在通用的、未经分层的研究中。因此,我们的研究表明,对反映特定疾病阶段的更大患者队列进行详细的、多变量的模式分析可能会揭示更具体的风险因素模式,从而支持个体化的治疗策略。