Lin Feng, Yang Kewei, Luo Tianbo, Chen Tianqi
Department of Urology, Affiliated Hospital of Shaoxing University, Shaoxing, Zhejiang, China.
Medicine (Baltimore). 2025 Jun 6;104(23):e42814. doi: 10.1097/MD.0000000000042814.
Bladder cancer (BC) is influenced by genetic and environmental factors, with blood and urine biomarkers playing a critical role in its diagnosis and progression. However, establishing the causal association between these biomarkers and BC remains challenging due to confounding factors and reverse causation in traditional studies. Therefore, we conducted a Mendelian randomization (MR) analysis to assess the causal association between these biomarkers and BC. A bidirectional MR analysis was performed using pooled data from 35 blood and urine biomarkers, 731 immune cell types, and BC cases from the Genome-Wide Association of Transgenics and Circulating Metabolites study. Complementary analyses, including mediation analysis, 2-stage MR, and multivariate MR, were employed to investigate the potential mediating role of immune cells in this association. We further conducted sensitivity analyses to validate the stability and feasibility of our dataset. The analysis identified a causal association between BC and 2 biomarkers: calcium and sex hormone-binding globulin. Elevated calcium levels were associated with an increased risk of BC (inverse variance weighting: [OR] = 1.295, 95% [CI] = 1.062-1.578, P = .011), while higher sex hormone-binding globulin levels were linked to a decreased risk (inverse variance weighting: OR = 0.857, 95% CI = 0.741-0.991, P = .037). Notably, CD20 expression on IgD⁻ CD24⁻ B cells appeared to attenuate the positive association between calcium and BC. This study reinforces the association between specific blood and urine biomarkers and the risk of developing BC. It also highlights the mediating role of CD20 on IgD⁻ CD24⁻ B cells in the causal pathways linking these biomarkers to BC. These insights enhance our understanding of BC pathogenesis and may guide the development of targeted diagnostic and therapeutic strategies.
膀胱癌(BC)受遗传和环境因素影响,血液和尿液生物标志物在其诊断和进展中起着关键作用。然而,由于传统研究中的混杂因素和反向因果关系,确定这些生物标志物与膀胱癌之间的因果关联仍然具有挑战性。因此,我们进行了孟德尔随机化(MR)分析,以评估这些生物标志物与膀胱癌之间的因果关联。使用来自转基因和循环代谢物全基因组关联研究的35种血液和尿液生物标志物、731种免疫细胞类型以及膀胱癌病例的汇总数据进行了双向MR分析。采用了包括中介分析、两阶段MR和多变量MR在内的补充分析,以研究免疫细胞在这种关联中的潜在中介作用。我们进一步进行了敏感性分析,以验证数据集的稳定性和可行性。分析确定了膀胱癌与2种生物标志物之间的因果关联:钙和性激素结合球蛋白。钙水平升高与膀胱癌风险增加相关(逆方差加权:[OR]=1.295,95%[CI]=1.062-1.578,P=.011),而较高的性激素结合球蛋白水平与风险降低相关(逆方差加权:OR=0.857,95%CI=0.741-0.991,P=.037)。值得注意的是,IgD⁻CD24⁻B细胞上的CD20表达似乎减弱了钙与膀胱癌之间的正相关。这项研究强化了特定血液和尿液生物标志物与患膀胱癌风险之间的关联。它还突出了CD20在IgD⁻CD24⁻B细胞上在将这些生物标志物与膀胱癌联系起来的因果途径中的中介作用。这些见解增强了我们对膀胱癌发病机制的理解,并可能指导靶向诊断和治疗策略的开发。