Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
JNCI Cancer Spectr. 2022 Mar 2;6(2). doi: 10.1093/jncics/pkac019.
Higher circulating vitamin D has been associated with improved overall cancer survival, but data for organ-specific cancers are mixed.
We examined the association between prediagnostic serum 25-hydroxyvitamin D [25(OH)D], the recognized biomarker of vitamin D status, and cancer survival in 4038 men and women diagnosed with 1 of 11 malignancies during 22 years of follow-up (median = 15.6 years) within the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. Multivariable-adjusted proportional hazards regression estimated hazard ratios (HR) and 95% confidence intervals (CI) for associations between baseline 25(OH)D concentration and subsequent cancer survival; we also stratified on the common vitamin D binding protein isoforms (Gc1f, Gc1s, and Gc2) defined by two single-nucleotide polymorphisms (rs7041 and rs4588) in the vitamin D binding protein gene GC. All P values were 2-sided.
Higher 25(OH)D concentrations were associated with greater overall cancer survival (HR for cancer mortality = 0.83, 95% CI = 0.70 to 0.98 for highest vs lowest quintile; Ptrend = .05) and lung cancer survival (HR = 0.63, 95% CI = 0.44 to 0.90; Ptrend = .03). These associations were limited to cases expressing the Gc2 isoform (HR = 0.38 for Gc2-2, 95% CI = 0.14 to 1.05 for highest vs lowest quintile; Ptrend = .02; and HR = 0.30 for Gc1-2/Gc2-2 combined, 95% CI = 0.16 to 0.56; Ptrend < .001 for overall and lung cancer, respectively).
Higher circulating 25(OH)D was associated with improved overall and lung cancer survival. As this was especially evident among cases with the genetically determined Gc2 isoform of vitamin D binding protein, such individuals may gain a cancer survival advantage by maintaining higher 25(OH)D blood concentrations.
较高的循环维生素 D 与改善整体癌症存活率有关,但针对特定器官癌症的数据则存在差异。
我们在前列腺癌、肺癌、结直肠癌和卵巢癌筛查试验中,对 4038 名男性和女性进行了为期 22 年的随访(中位数=15.6 年),这些人在随访期间被诊断出患有 11 种恶性肿瘤中的 1 种,研究了诊断前血清 25-羟维生素 D [25(OH)D](维生素 D 状态的公认生物标志物)与癌症存活率之间的关联。使用多变量调整的比例风险回归估计了基线 25(OH)D 浓度与随后癌症存活率之间的风险比(HR)和 95%置信区间(CI);我们还根据维生素 D 结合蛋白基因 GC 中的两个单核苷酸多态性(rs7041 和 rs4588)定义的常见维生素 D 结合蛋白同工型(Gc1f、Gc1s 和 Gc2)进行了分层。所有 P 值均为双侧。
较高的 25(OH)D 浓度与整体癌症存活率的提高有关(癌症死亡率的 HR=0.83,95%CI=0.70 至 0.98,最高与最低五分位数相比;Ptrend=0.05)和肺癌存活率(HR=0.63,95%CI=0.44 至 0.90;Ptrend=0.03)。这些关联仅限于表达 Gc2 同工型的病例(HR=0.38,95%CI=0.14 至 1.05,最高与最低五分位数相比;Ptrend=0.02;HR=0.30,Gc1-2/Gc2-2 联合,95%CI=0.16 至 0.56;Ptrend<0.001 用于整体和肺癌)。
较高的循环 25(OH)D 与整体和肺癌的存活率提高有关。由于这种情况在具有遗传决定的维生素 D 结合蛋白 Gc2 同工型的病例中尤为明显,因此通过维持较高的 25(OH)D 血液浓度,此类个体可能获得癌症存活率优势。