Nuffield Department of Population Health, University of Oxford, Oxford, OX3 7LF, UK.
BMC Public Health. 2023 Jul 6;23(1):1300. doi: 10.1186/s12889-023-16202-9.
Whilst multi-morbidity is known to be a concern in people with cancer, very little is known about the risk of cancer in multi-morbid patients. This study aims to investigate the risk of being diagnosed with lung, colorectal, breast and prostate cancer associated with multi-morbidity.
We investigated the association between multi-morbidity and subsequent risk of cancer diagnosis in UK Biobank. Cox models were used to estimate the relative risks of each cancer of interest in multi-morbid participants, using the Cambridge Multimorbidity Score. The extent to which reverse causation, residual confounding and ascertainment bias may have impacted on the findings was robustly investigated.
Of the 436,990 participants included in the study who were cancer-free at baseline, 21.6% (99,965) were multi-morbid (≥ 2 diseases). Over a median follow-up time of 10.9 [IQR 10.0-11.7] years, 9,019 prostate, 7,994 breast, 5,241 colorectal, and 3,591 lung cancers were diagnosed. After exclusion of the first year of follow-up, there was no clear association between multi-morbidity and risk of colorectal, prostate or breast cancer diagnosis. Those with ≥ 4 diseases at recruitment had double the risk of a subsequent lung cancer diagnosis compared to those with no diseases (HR 2.00 [95% CI 1.70-2.35] p for trend < 0.001). These findings were robust to sensitivity analyses aimed at reducing the impact of reverse causation, residual confounding from known cancer risk factors and ascertainment bias.
Individuals with multi-morbidity are at an increased risk of lung cancer diagnosis. While this association did not appear to be due to common sources of bias in observational studies, further research is needed to understand what underlies this association.
尽管多疾病与癌症患者有关,但对于多疾病患者患癌症的风险知之甚少。本研究旨在调查多疾病与随后肺癌、结直肠癌、乳腺癌和前列腺癌诊断风险之间的关系。
我们在英国生物银行中调查了多疾病与随后癌症诊断之间的关联。使用剑桥多疾病评分,Cox 模型估计了多疾病患者中每个相关癌症的相对风险。稳健地调查了反向因果关系、残余混杂和检测偏差可能对研究结果的影响程度。
在基线时无癌症的 436990 名研究参与者中,21.6%(99965 人)患有多种疾病(≥2 种疾病)。在中位随访时间为 10.9[IQR 10.0-11.7]年后,诊断出 9019 例前列腺癌、7994 例乳腺癌、5241 例结直肠癌和 3591 例肺癌。排除随访的头 1 年后,多疾病与结直肠癌、前列腺癌或乳腺癌诊断风险之间没有明显关联。与无疾病者相比,招募时患有≥4 种疾病的人随后患肺癌的风险增加了一倍(HR 2.00[95%CI 1.70-2.35]p<0.001)。这些发现对旨在降低反向因果关系、已知癌症风险因素的残余混杂和检测偏差影响的敏感性分析具有稳健性。
患有多种疾病的个体患肺癌的风险增加。虽然这种关联似乎不是由于观察性研究中常见的偏倚来源,但需要进一步研究来了解这种关联的基础。