Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Eugeniahemmet T2, 171 76, Stockholm, Sweden.
Respiratory Medicine Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Eur J Epidemiol. 2020 Nov;35(11):1087-1097. doi: 10.1007/s10654-020-00611-w. Epub 2020 Feb 11.
Findings from molecular studies suggesting that several infectious agents cause sarcoidosis are intriguing yet conflicting and likely biased due to their cross-sectional design. As done in other inflammatory diseases to overcome this issue, prospectively-collected register data could be used, but reverse causation is a threat when the onset of disease is difficult to establish. We investigated the association between infectious diseases and sarcoidosis to understand if they are etiologically related. We conducted a nested case-control study (2009-2013) using incident sarcoidosis cases from the Swedish National Patient Register (n = 4075) and matched general population controls (n = 40,688). Infectious disease was defined using inpatient/outpatient visits and/or antimicrobial dispensations starting 3 years before diagnosis/matching. Adjusted odds ratios (aOR) of sarcoidosis were estimated using conditional logistic regression and tested for robustness assuming the presence of reverse causation bias. The aOR of sarcoidosis associated with history of infectious disease was 1.19 (95% confidence interval [CI] 1.09, 1.29; 21% vs. 16% exposed cases and controls, respectively). Upper respiratory and ocular infections conferred the highest OR. Findings were similar when we altered the infection definition or varied the infection-sarcoidosis latency period (1-7 years). In bias analyses assuming one in 10 infections occurred because of preclinical sarcoidosis, the observed association was completely attenuated (aOR 1.02; 95% CI 0.90, 1.15). Our findings, likely induced by reverse causation due to preclinical sarcoidosis, do not support the hypothesis that common symptomatic infectious diseases are etiologically linked to sarcoidosis. Caution for reverse causation bias is required when the real disease onset is unknown.
研究结果表明,几种感染因子可引起结节病,这令人着迷,但也存在冲突,且由于其横断面设计,这些结果可能存在偏倚。为了克服这一问题,正如在其他炎症性疾病中所做的那样,可以使用前瞻性收集的登记数据,但当疾病发作难以确定时,就存在反向因果关系的威胁。我们调查了传染性疾病与结节病之间的关联,以了解它们是否存在病因学上的联系。我们进行了一项嵌套病例对照研究(2009-2013 年),使用瑞典国家患者登记处(n=4075)中的结节病新发病例和匹配的一般人群对照(n=40688)。使用住院/门诊就诊和/或抗生素配药记录来定义传染病,这些记录起始于诊断/匹配前 3 年。使用条件逻辑回归估计结节病的调整后比值比(aOR),并假设存在反向因果关系偏倚,对其稳健性进行检验。有传染病史与结节病相关的 aOR 为 1.19(95%置信区间 [CI] 1.09, 1.29;分别有 21%和 16%的暴露病例和对照患有结节病)。上呼吸道和眼部感染的 OR 最高。当我们改变感染定义或改变感染-结节病潜伏期(1-7 年)时,结果相似。在假设每 10 例感染中有 1 例是由于临床前结节病引起的偏倚分析中,观察到的相关性完全减弱(aOR 1.02;95%CI 0.90, 1.15)。由于临床前结节病引起的反向因果关系,我们的发现不太支持常见症状性传染病与结节病具有病因学联系的假设。当真正的疾病发作未知时,需要警惕反向因果关系偏倚。