Chan Yi X, Knuiman Matthew W, Divitini Mark L, Brown Suzanne J, Walsh John, Yeap Bu B
School of Medicine, The University of Western Australia, Crawley, Western Australia, Australia.
Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Western Australia, Australia.
Eur J Endocrinol. 2017 Oct;177(4):297-308. doi: 10.1530/EJE-17-0197. Epub 2017 Jul 6.
Thyroid hormones modulate proliferative, metabolic and angiogenic pathways. However few studies have examined associations of thyroid hormones with cancer risk.
To explore associations of thyrotropin (TSH), free thyroxine (FT4) and anti-thyroperoxidase antibodies (TPOAb) with the incidence of all (non-skin) cancers and specific common cancers.
A prospective cohort study of a community-dwelling population aged 25-84 years in Western Australia.
Archived sera from 3649 participants in the 1994/1995 Busselton Health Survey were assayed for TSH, FT4 and TPOAb. Cancer outcomes until 30 June 2014 were ascertained using data linkage. Longitudinal analyses were performed using Cox proportional hazards regression.
During 20-year follow-up, 600 participants were diagnosed with non-skin cancer, including 126, 100, 103 and 41 prostate, breast, colorectal and lung cancers respectively. Higher TSH was associated with a lower risk of prostate cancer after adjusting for potential confounders, with a 30% lower risk for every 1 IU/L increase in TSH (adjusted hazard ratio (HR): 0.70, 95% confidence interval (CI): 0.55-0.90, = 0.005). Similarly, higher FT4 was associated with an increased risk of prostate cancer (adjusted HR: 1.11 per 1 pmol/L increase, 95% CI: 1.03-1.19, = 0.009). There were no associations of TSH, FT4 or TPOAb with all non-skin cancer events combined, or with breast, colorectal or lung cancer.
In a community-dwelling population, lower TSH and higher FT4 were associated with an increased risk of prostate cancer. Further studies are required to assess if thyroid function is a biomarker or risk factor for prostate cancer.
甲状腺激素可调节增殖、代谢和血管生成途径。然而,很少有研究探讨甲状腺激素与癌症风险之间的关联。
探讨促甲状腺激素(TSH)、游离甲状腺素(FT4)和抗甲状腺过氧化物酶抗体(TPOAb)与所有(非皮肤)癌症及特定常见癌症发病率之间的关联。
对西澳大利亚州25 - 84岁社区居住人群进行的一项前瞻性队列研究。
对1994/1995年巴瑟尔顿健康调查中3649名参与者的存档血清进行TSH、FT4和TPOAb检测。利用数据链接确定截至2014年6月30日的癌症结局。采用Cox比例风险回归进行纵向分析。
在20年的随访期间,600名参与者被诊断患有非皮肤癌,其中分别有126例、100例、103例和41例前列腺癌、乳腺癌、结直肠癌和肺癌。在调整潜在混杂因素后,较高的TSH与较低的前列腺癌风险相关,TSH每升高1 IU/L,风险降低30%(调整后风险比(HR):0.70,95%置信区间(CI):0.55 - 0.90,P = 0.005)。同样,较高的FT4与前列腺癌风险增加相关(每升高1 pmol/L,调整后HR:1.11,95% CI:1.03 - 1.19,P = 0.009)。TSH、FT4或TPOAb与所有非皮肤癌事件合并,或与乳腺癌、结直肠癌或肺癌均无关联。
在社区居住人群中,较低的TSH和较高的FT4与前列腺癌风险增加相关。需要进一步研究以评估甲状腺功能是否为前列腺癌的生物标志物或风险因素。