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Serum Insulin‐like Growth Factors Insulin‐like Growth Factor‐binding Protein‐3 and Risk of Lung Cancer Death: A Case‐control Study Nested in the Japan Collaborative Cohort (JACC) Study

机译:血清胰岛素样生长因子胰岛素样生长因子结合蛋白3和肺癌死亡风险:日本协作研究(JACC)研究中的病例对照研究

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摘要

To elucidate the roles of insulin‐like growth factors (IGFs) in the development of lung cancer, we conducted a case‐control study nested within the Japan Collaborative Cohort Study. Serum samples were collected at baseline from 39 140 men and women between 1988 and 1990. We measured serum IGF‐I, IGF‐II, and IGF‐binding protein‐3 (IGFBP‐3) in 194 case subjects who subsequently died from lung cancer during an 8‐year follow‐up and in 9351 controls. The odds ratios (ORs), adjusted for smoking and other covariates, were smaller with higher levels of IGF‐II and IGFBP‐3. The ORs across quartiles were 0.41 (95% confidence interval [CI], 0.27–0.63), 0.47 (0.31–0.71), and 0.67 (0.46–0.98) for IGF‐II (trend P=0.018), and 0.55 (95% CI, 0.37–0.81), 0.54 (0.36–0.82), and 0.67 (0.45–1.01) for IGFBP‐3 (trend P=0.037). These peptides were not independently related to lung cancer risk when mutually adjusted. The risk was increased in the highest vs. the lowest quartile of IGF‐I only after controlling for IGFBP‐3 (OR, 1.74; 95% CI, 1.08–2.81). Limiting subjects to those followed for ≥3 years strengthened the negative associations of IGF‐II and IGFBP‐3, whereas the ORs for IGF‐I generally decreased. A higher level of circulating IGFBP‐3 and/or IGF‐II may decrease lung cancer risk. Elevated serum IGF‐I may increase the risk, but this could partly be attributable to latent tumors.
机译:为了阐明胰岛素样生长因子(IGF)在肺癌发展中的作用,我们进行了一项病例对照研究,该研究嵌套在Japan Collaborative Cohort研究中。在1988年至1990年期间,从39140名男性和女性的基线收集血清样本。我们测量了194例后来死于肺癌的患者的血清IGF-I,IGF-II和IGF-结合蛋白-3(IGFBP-3)在8年的随访期间和9351个对照中。 IGF-II和IGFBP-3水平较高时,针对吸烟和其他协变量进行调整的优势比(OR)较小。 IGF-II(趋势P = 0.018)跨四分位数的OR分别为0.41(95%置信区间[CI],0.27-0.63),0.47(0.31-0.71)和0.67(0.46-0.98),以及0.55(95%) IGFBP-3的CI为0.37-0.81),0.54(0.36-0.82)和0.67(0.45-1.01)(趋势P = 0.037)。相互调整后,这些肽与肺癌的风险并不独立相关。仅在控制了IGFBP-3之后,IGF-1的最高四分之一与最低四分之一的风险才会增加(OR,1.74; 95%CI,1.08-2.81)。将受试者限制为随访≥3年的受试者会增强IGF-II和IGFBP-3的消极关联,而IGF-I的OR则总体上会降低。循环中较高的IGFBP-3和/或IGF-II水平可以降低患肺癌的风险。血清IGF-I升高可能会增加风险,但这可能部分归因于潜在的肿瘤。

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