Department of Genetics, Franklin College of Arts and Sciences, University of Georgia, Athens, GA, USA; School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai, PR China.
Department of Genetics, Franklin College of Arts and Sciences, University of Georgia, Athens, GA, USA; College of Life Sciences, Wuhan University, Wuhan, PR China.
Brain Behav Immun. 2021 Jan;91:383-392. doi: 10.1016/j.bbi.2020.10.019. Epub 2020 Oct 24.
Our understanding of risk factors for COVID‑19, including pre-existing medical conditions and genetic variations, is limited. To what extent the pre-existing clinical condition and genetic background have implications for COVID-19 still needs to be explored.
Our study included 389,620 participants of European descent from the UK Biobank, of whom 3,884 received the COVID-19 test and 1,091 were tested positive for COVID-19. We examined the association of COVID-19 status with an extensive list of 974 medical conditions and 30 blood biomarkers. Additionally, we tested the association of genetic variants in two key genes related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, angiotensin-converting enzyme 2 (ACE2) and transmembrane protease serine 2 (TMPRSS2), with COVID-19 or any other phenotypes.
The most significant risk factors for COVID-19 include Alzheimer's disease (OR = 2.29, 95% CI: 1.25-4.16), dementia (OR = 2.16, 95% CI: 1.36-3.42), and the overall category of delirium, dementia, amnestic and other cognitive disorders (OR = 1.90, 95% CI: 1.24-2.90). Evidence suggesting associations of genetic variants in SARS-CoV-2 infection-related genes with COVID-19 (rs7282236, OR = 1.33, 95% CI: 1.14-1.54, p = 2.31 × 10) and other phenotypes, such as an immune deficiency (p = 5.65 × 10) and prostate cancer (p = 1.1 × 10), was obtained.
Our unbiased and extensive search identified pre-existing Alzheimer's disease and dementia as top risk factors for hospital admission due to COVID-19, highlighting the importance of providing special protective care for patients with cognitive disorders during this pandemic. We also obtained evidence suggesting a direct association of genetic variants with COVID-19.
我们对 COVID-19 风险因素的了解有限,包括先前存在的医疗状况和遗传变异。先前的临床状况和遗传背景在多大程度上与 COVID-19 有关仍需进一步探讨。
我们的研究包括来自英国生物库的 389620 名欧洲血统的参与者,其中 3884 人接受了 COVID-19 检测,1091 人 COVID-19 检测呈阳性。我们检查了 COVID-19 状况与广泛的 974 种医疗状况和 30 种血液生物标志物之间的关联。此外,我们还测试了与严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染相关的两个关键基因(血管紧张素转换酶 2(ACE2)和跨膜蛋白酶丝氨酸 2(TMPRSS2)中的遗传变异与 COVID-19 或任何其他表型之间的关联。
COVID-19 的最显著危险因素包括阿尔茨海默病(OR=2.29,95%CI:1.25-4.16)、痴呆症(OR=2.16,95%CI:1.36-3.42)和谵妄、痴呆症、遗忘症和其他认知障碍的总体类别(OR=1.90,95%CI:1.24-2.90)。有证据表明,SARS-CoV-2 感染相关基因中的遗传变异与 COVID-19(rs7282236,OR=1.33,95%CI:1.14-1.54,p=2.31×10)和其他表型(如免疫缺陷症(p=5.65×10)和前列腺癌(p=1.1×10))有关。
我们的无偏见和广泛搜索确定了先前存在的阿尔茨海默病和痴呆症是因 COVID-19 住院的最高危险因素,这突显了在大流行期间为认知障碍患者提供特殊保护护理的重要性。我们还获得了遗传变异与 COVID-19 直接相关的证据。