Centre for Environmental Sciences, Hasselt University, Diepenbeek, Belgium.
PLoS One. 2011;6(10):e27130. doi: 10.1371/journal.pone.0027130. Epub 2011 Oct 31.
Studies on familial aggregation of cancer may suggest an overall contribution of inherited genes or a shared environment in the development of malignant disease. We performed a meta-analysis on familial clustering of prostate cancer. Out of 74 studies reporting data on familial aggregation of prostate cancer in unselected populations retrieved by a Pubmed search and browsing references, 33 independent studies meeting the inclusion criteria were used in the analysis performed with the random effects model. The pooled rate ratio (RR) for first-degree family history, i.e. affected father or brother, is 2.48 (95% confidence interval: 2.25-2.74). The incidence rate for men who have a brother who got prostate cancer increases 3.14 times (CI:2.37-4.15), and for those with affected father 2.35 times (CI:2.02-2.72). The pooled estimate of RR for two or more affected first-degree family members relative to no history in father and in brother is 4.39 (CI:2.61-7.39). First-degree family history appears to increase the incidence rate of prostate cancer more in men under 65 (RR:2.87, CI:2.21-3.74), than in men aged 65 and older (RR:1.92, CI:1.49-2.47), p for interaction = 0.002. The attributable fraction among those having an affected first-degree relative equals to 59.7% (CI:55.6-63.5%) for men at all ages, 65.2% (CI:57.7-71.4%) for men younger than 65 and 47.9% (CI:37.1-56.8%) for men aged 65 or older. For those with a family history in 2 or more first-degree family members 77.2% (CI:65.4-85.0%) of prostate cancer incidence can be attributed to the familial clustering. Our combined estimates show strong familial clustering and a significant effect-modification by age meaning that familial aggregation was associated with earlier disease onset (before age 65).
关于癌症家族聚集性的研究表明,遗传基因或恶性疾病发生过程中的共享环境可能对其整体发病有一定影响。我们对前列腺癌家族聚集性进行了荟萃分析。通过 Pubmed 检索和查阅参考文献,共检索到 74 项关于未选择人群中前列腺癌家族聚集性的研究报告数据,其中 33 项符合纳入标准的独立研究纳入了随机效应模型分析。一级亲属(即受影响的父亲或兄弟)的家族史患病风险比(RR)为 2.48(95%置信区间:2.25-2.74)。有兄弟患前列腺癌的男性发病率增加 3.14 倍(CI:2.37-4.15),有受影响父亲的男性发病率增加 2.35 倍(CI:2.02-2.72)。与父亲和兄弟均无家族史相比,两个或更多一级亲属受影响的 RR 为 4.39(CI:2.61-7.39)。一级家族史似乎使 65 岁以下男性的前列腺癌发病率增加更多(RR:2.87,CI:2.21-3.74),而对 65 岁以上男性的影响较小(RR:1.92,CI:1.49-2.47),交互检验 p 值为 0.002。所有年龄组中,有一级亲属受影响的归因分数为 59.7%(CI:55.6-63.5%),65 岁以下男性为 65.2%(CI:57.7-71.4%),65 岁及以上男性为 47.9%(CI:37.1-56.8%)。对于有 2 个或更多一级亲属家族史的男性,77.2%(CI:65.4-85.0%)的前列腺癌发病率可归因于家族聚集。我们的综合评估显示出强烈的家族聚集性,且发病年龄存在显著的修饰效应,这意味着家族聚集与疾病的早期发病(65 岁前)相关。