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Thyroid dysfunction and breast cancer risk among women in the UK Biobank cohort

机译:英国Biobank Cohort中甲状腺功能障碍和乳腺癌风险

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摘要

This study aimed to evaluate the association between thyroid dysfunction and breast cancer risk. We included 239,436 females of the UK Biobank cohort. Information on thyroid dysfunction, personal and family medical history, medications, reproductive factors, lifestyle, and socioeconomic characteristics was retrieved from baseline self‐reported data and hospital inpatient databases. Breast cancer diagnoses were identified through population‐based registries. We computed Cox models to estimate hazard ratios (HRs) of breast cancer incidence for thyroid dysfunction diagnosis and treatments, and examined potential confounding and effect modification by comorbidities and breast cancer risk factors. In our study, 3,227 (1.3%) and 20,762 (8.7%) women had hyper‐ and hypothyroidism prior to the baseline. During a median follow‐up of 7.1 years, 5,326 (2.2%) women developed breast cancer. Compared to no thyroid dysfunction, there was no association between hypothyroidism and breast cancer risk overall (HR = 0.93, 95% confidence interval (CI): 0.84–1.02, 442 cases), but we found a decreased risk more than 10 years after hypothyroidism diagnosis (HR=0.85, 95%CI 0.74–0.97, 226 cases). There was no association with hyperthyroidism overall (HR=1.08, 95%CI 0.86–1.35, 79 cases) but breast cancer risk was elevated among women with treated hyperthyroidism (HR=1.38, 95%CI: 1.03–1.86, 44 cases) or aged 60 years or more at hyperthyroidism diagnosis (HR=1.74, 95%CI: 1.01–3.00, 113 cases), and 5–10 years after hyperthyroidism diagnosis (HR=1.58, 95%CI: 1.06–2.33, 25 cases). In conclusion, breast cancer risk was reduced long after hypothyroidism diagnosis, but increased among women with treated hyperthyroidism. Future studies are needed to determine whether the higher breast cancer risk observed among treated hyperthyroidism could be explained by hyperthyroidism severity, type of treatment or aetiology.
机译:本研究旨在评估甲状腺功能障碍与乳腺癌风险之间的关联。我们包括英国Biobank Cohort的239,436名女性。从基线自我报告的数据和医院住院数据库中检索有关甲状腺功能障碍,个人和家庭病史,药物,生殖因素,生活方式和社会经济特征的信息。通过基于人口的注册管理机构确定乳腺癌诊断。我们计算了COX模型以估计乳腺癌的危险比(HRS)乳腺癌发病率为甲状腺功能障碍诊断和治疗,并通过合并症和乳腺癌危险因素进行了潜在的混杂性和作用改性。在我们的研究中,3,227名(1.3%)和20,762名(8.7%)女性在基线之前具有超和甲状腺功能亢进症。在7.1岁的中位随访期间,5,326名(2.2%)妇女发育乳腺癌。与无甲状腺功能障碍相比,甲状腺功能减退症和乳腺癌风险之间没有关联(HR = 0.93,95%置信区间(CI):0.84-1.02,442例),但我们发现甲状腺功能减退症后10年以上的风险降低诊断(HR = 0.85,95%CI 0.74-0.97,226例)。总体上没有甲状腺功能亢进症(HR = 1.08,95%CI 0.86-1.35,79例)但乳腺癌风险升高(HR = 1.38,95%CI:1.03-1.86,44例)或在甲状腺功能亢进诊断(HR = 1.74,95%CI:1.01-3.00,113例)和甲状腺功能亢进诊断(HR = 1.58,95%:1.06-2.33,25例)和5-10岁以上的60岁或更多总之,甲状腺功能减退症诊断后乳腺癌风险较长,但患有治疗甲状腺功能亢进的妇女增加。需要未来的研究来确定在治疗的甲状腺功能亢进中观察到的乳腺癌风险是否可以通过甲状腺功能亢进严重程度,治疗类型或治疗方法来解释。

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