Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK
Cancer Research UK Oxford Centre, Department of Oncology, University of Oxford, Oxford, UK.
Thorax. 2022 Jan;77(1):65-73. doi: 10.1136/thoraxjnl-2021-217080. Epub 2021 Sep 27.
Conflicting evidence has emerged regarding the relevance of smoking on risk of COVID-19 and its severity.
We undertook large-scale observational and Mendelian randomisation (MR) analyses using UK Biobank. Most recent smoking status was determined from primary care records (70.8%) and UK Biobank questionnaire data (29.2%). COVID-19 outcomes were derived from Public Health England SARS-CoV-2 testing data, hospital admissions data, and death certificates (until 18 August 2020). Logistic regression was used to estimate associations between smoking status and confirmed SARS-CoV-2 infection, COVID-19-related hospitalisation, and COVID-19-related death. Inverse variance-weighted MR analyses using established genetic instruments for smoking initiation and smoking heaviness were undertaken (reported per SD increase).
There were 421 469 eligible participants, 1649 confirmed infections, 968 COVID-19-related hospitalisations and 444 COVID-19-related deaths. Compared with never-smokers, current smokers had higher risks of hospitalisation (OR 1.80, 95% CI 1.26 to 2.29) and mortality (smoking 1-9/day: OR 2.14, 95% CI 0.87 to 5.24; 10-19/day: OR 5.91, 95% CI 3.66 to 9.54; 20+/day: OR 6.11, 95% CI 3.59 to 10.42). In MR analyses of 281 105 White British participants, genetically predicted propensity to initiate smoking was associated with higher risks of infection (OR 1.45, 95% CI 1.10 to 1.91) and hospitalisation (OR 1.60, 95% CI 1.13 to 2.27). Genetically predicted higher number of cigarettes smoked per day was associated with higher risks of all outcomes (infection OR 2.51, 95% CI 1.20 to 5.24; hospitalisation OR 5.08, 95% CI 2.04 to 12.66; and death OR 10.02, 95% CI 2.53 to 39.72).
Congruent results from two analytical approaches support a causal effect of smoking on risk of severe COVID-19.
关于吸烟与 COVID-19 风险及其严重程度的相关性,出现了相互矛盾的证据。
我们使用英国生物库进行了大规模的观察性和孟德尔随机化(MR)分析。最近的吸烟状况是根据初级保健记录(70.8%)和英国生物库问卷调查数据(29.2%)确定的。COVID-19 结局是从英格兰公共卫生署 SARS-CoV-2 检测数据、住院数据和死亡证明中得出的(截至 2020 年 8 月 18 日)。逻辑回归用于估计吸烟状况与确诊的 SARS-CoV-2 感染、COVID-19 相关住院和 COVID-19 相关死亡之间的关联。使用已建立的用于吸烟起始和吸烟量的遗传工具进行了逆方差加权 MR 分析(每增加一个标准差报告)。
纳入了 421469 名合格参与者,其中 1649 人确诊感染,968 人因 COVID-19 住院,444 人因 COVID-19 死亡。与从不吸烟者相比,当前吸烟者的住院风险更高(比值比 1.80,95%置信区间 1.26 至 2.29)和死亡风险(吸烟 1-9 支/天:比值比 2.14,95%置信区间 0.87 至 5.24;10-19 支/天:比值比 5.91,95%置信区间 3.66 至 9.54;20+/天:比值比 6.11,95%置信区间 3.59 至 10.42)。在对 281465 名白种英国人的 MR 分析中,遗传预测的吸烟起始倾向与更高的感染风险(比值比 1.45,95%置信区间 1.10 至 1.91)和住院风险(比值比 1.60,95%置信区间 1.13 至 2.27)相关。遗传预测每天吸烟量更高与所有结局的风险增加相关(感染比值比 2.51,95%置信区间 1.20 至 5.24;住院比值比 5.08,95%置信区间 2.04 至 12.66;死亡比值比 10.02,95%置信区间 2.53 至 39.72)。
两种分析方法的一致结果支持吸烟对严重 COVID-19 风险的因果效应。