Environmental Epidemiology of Cancer Group, Centre for Research in Epidemiology and Population Health, Institut National de la Santé et de la Recherche Médicale U1018, Villejuif, France;
Blood. 2013 Nov 14;122(20):3492-9. doi: 10.1182/blood-2013-04-497586. Epub 2013 Sep 9.
Ultraviolet radiation (UVR) exposure has been inversely associated with Hodgkin lymphoma (HL) risk, but only inconsistently, only in a few studies, and without attention to HL heterogeneity. We conducted a pooled analysis of HL risk focusing on type and timing of UVR exposure and on disease subtypes by age, histology, and tumor-cell Epstein-Barr virus (EBV) status. Four case-control studies contributed 1320 HL cases and 6381 controls. We estimated lifetime, adulthood, and childhood UVR exposure and history of sunburn and sunlamp use. We used 2-stage estimation with mixed-effects models and weighted pooled effect estimates by inverse marginal variances. We observed statistically significant inverse associations with HL risk for UVR exposures during childhood and adulthood, sunburn history, and sunlamp use, but we found no significant dose-response relationships. Risks were significant only for EBV-positive HL (pooled odds ratio, 0.56; 95% confidence interval, 0.35 to 0.91 for the highest overall UVR exposure category), with a significant linear trend for overall exposure (P = .03). Pooled relative risk estimates were not heterogeneous across studies. Increased UVR exposure may protect against HL, particularly EBV-positive HL. Plausible mechanisms involving UVR induction of regulatory T cells or the cellular DNA damage response suggest opportunities for new prevention targets.
紫外线辐射(UVR)暴露与霍奇金淋巴瘤(HL)风险呈负相关,但这种关联仅在少数研究中得到一致观察,且没有关注 HL 的异质性。我们针对 UVR 暴露的类型和时间以及按年龄、组织学和肿瘤细胞 EBV 状态划分的疾病亚型,进行了一项 HL 风险的汇总分析。四项病例对照研究共纳入了 1320 例 HL 病例和 6381 例对照。我们估计了终生、成年期和儿童期 UVR 暴露以及晒伤和太阳灯使用史。我们使用两阶段估计和混合效应模型,通过逆边际方差对加权汇总效应进行估计。我们观察到 UVR 暴露、晒伤史和太阳灯使用与 HL 风险呈显著负相关,但未发现剂量-反应关系。仅对于 EBV 阳性 HL,风险具有统计学意义(最高 UVR 暴露类别汇总比值比为 0.56;95%置信区间为 0.35 至 0.91),整体暴露呈线性趋势(P =.03)。各研究间的汇总相对风险估计无显著异质性。增加 UVR 暴露可能有助于预防 HL,特别是 EBV 阳性 HL。涉及 UVR 诱导调节性 T 细胞或细胞 DNA 损伤反应的合理机制提示了新的预防靶点的机会。