Occupational and Environmental Medicine, Sahlgrenska University Hospital and Sahlgrenska Academy, University of Gothenburg, P.O. Box 414, 405 30, Gothenburg, Sweden.
Department of Molecular and Clinical Medicine, Wallenberg Laboratory for Cardiovascular and Metabolic Research, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.
Environ Health. 2019 Jun 14;18(1):56. doi: 10.1186/s12940-019-0495-1.
Smoking is a strong risk factor for cardiovascular disease (CVD) and causes exposure to cadmium, which is a pro-atherosclerotic metal. Cadmium exposure has also been shown to increase the risk of CVD, even after adjustment for smoking. Our hypothesis was that part of the risk of CVD in smokers may be mediated by cadmium exposure from tobacco smoke. We examined this hypothesis in a mediation analysis, trying to assess how much of the smoking-induced CVD risk could be explained via cadmium.
We used prospective data on CVD (incidence and mortality) in a Swedish population-based cohort of 4304 middle-aged men and women (the Malmö Diet and Cancer Study). Blood cadmium was analyzed in base-line samples from 1991, and clinical events were followed up for 16-19 years based on registry data. Mediation analysis was conducted to evaluate the indirect effect (via cadmium) of smoking on CVD. Survival was analyzed by the accelerated failure time (AFT) model and the Aalen additive hazard model.
The mean blood cadmium level in the study population was 0.43 μg/L (median 0.24 μg/L) and increased with recent and current smoking. As expected, shorter survival time (AFT model) and higher incidence rate (Aalen model) were found in current smokers for all CVD outcomes and this effect seemed to be partly mediated by cadmium. For the sum of acute myocardial infarction, bypass grafts and percutaneous coronary intervention, and death in ischemic heart disease, about half of the increased risk of such events in current smokers was mediated via cadmium, with similar results for the AFT and Aalen models.
Cadmium plays an important role in smoking-induced CVDs. This provides evidence for mechanisms and is of importance for both individuals and policy makers.
吸烟是心血管疾病(CVD)的一个强烈风险因素,会导致接触到镉,镉是一种促进动脉粥样硬化的金属。镉暴露已被证明即使在调整了吸烟因素后,也会增加 CVD 的风险。我们的假设是,吸烟者患 CVD 的部分风险可能是由烟草烟雾中的镉暴露引起的。我们在中介分析中检验了这一假设,试图评估通过镉解释多少由吸烟引起的 CVD 风险。
我们使用了来自瑞典人群为基础的队列中 4304 名中年男女(马尔默饮食与癌症研究)的 CVD(发病和死亡率)的前瞻性数据。1991 年基线样本中分析了血液中的镉含量,根据登记数据,对临床事件进行了 16-19 年的随访。中介分析用于评估吸烟对 CVD 的间接影响(通过镉)。生存分析采用加速失效时间(AFT)模型和 Aalen 相加风险模型。
研究人群的平均血镉水平为 0.43μg/L(中位数 0.24μg/L),且随着近期和当前吸烟而增加。正如预期的那样,当前吸烟者的所有 CVD 结局的生存时间(AFT 模型)和发病率(Aalen 模型)都较短,这种影响似乎部分是通过镉介导的。对于急性心肌梗死、旁路移植术和经皮冠状动脉介入治疗以及缺血性心脏病导致的死亡的总和,当前吸烟者的此类事件风险增加的一半左右是通过镉介导的,AFT 和 Aalen 模型的结果相似。
镉在吸烟引起的 CVD 中起着重要作用。这为机制提供了证据,对个人和决策者都很重要。