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2
Copy number variation analysis on a non-Hodgkin lymphoma case-control study identifies an 11q25 duplication associated with diffuse large B-cell lymphoma.一项非霍奇金淋巴瘤病例对照研究中的拷贝数变异分析确定了一个与弥漫性大B细胞淋巴瘤相关的11q25重复。
PLoS One. 2014 Aug 18;9(8):e105382. doi: 10.1371/journal.pone.0105382. eCollection 2014.
3
Age-associated sperm DNA methylation alterations: possible implications in offspring disease susceptibility.与年龄相关的精子DNA甲基化改变:对后代疾病易感性的潜在影响。
PLoS Genet. 2014 Jul 10;10(7):e1004458. doi: 10.1371/journal.pgen.1004458. eCollection 2014 Jul.
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Tumour Biol. 2014 Sep;35(9):8913-9. doi: 10.1007/s13277-014-2082-y. Epub 2014 Jun 4.
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First births to older women continue to rise.高龄女性的头胎生育数量持续上升。
NCHS Data Brief. 2014 May(152):1-8.
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Prediagnostic telomere length and risk of B-cell lymphoma-Results from the EPIC cohort study.诊断前端粒长度与B细胞淋巴瘤风险——EPIC队列研究结果
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Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.全基因组关联研究鉴定出慢性淋巴细胞白血病的多个风险位点。
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Rate of de novo mutations and the importance of father's age to disease risk.新突变率和父亲年龄对疾病风险的重要性。
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9
Increased de novo copy number variants in the offspring of older males.老年男性后代中新的从头拷贝数变异增加。
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Perinatal and family risk factors for non-Hodgkin lymphoma in early life: a Swedish national cohort study.围生期和家庭因素与儿童期非霍奇金淋巴瘤的关系:一项瑞典全国队列研究。
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父母生育时的年龄与老年人血液系统恶性肿瘤的风险

Parental Age at Birth and Risk of Hematological Malignancies in Older Adults.

作者信息

Teras Lauren R, Gaudet Mia M, Blase Jennifer L, Gapstur Susan M

出版信息

Am J Epidemiol. 2015 Jul 1;182(1):41-8. doi: 10.1093/aje/kwu487. Epub 2015 May 11.

DOI:10.1093/aje/kwu487
PMID:25964260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4479112/
Abstract

The proportion of parents aged ≥35 years at the birth of their child continues to increase, but long-term health consequences for these children are not fully understood. A recent prospective study of 110,999 adult women showed an association between paternal-but not maternal-age at birth and sporadic hematological cancer risk. To further investigate this topic, we examined these associations in women and men in the American Cancer Society Cancer Prevention Study-II Nutrition Cohort. Among 138,003 Cancer Prevention Study-II participants, 2,532 incident hematological cancers were identified between 1992 and 2009. Multivariable-adjusted hazard ratios and 95% confidence intervals were computed by using Cox proportional hazards regression. There was no clear linear trend in the risk of hematological malignancies by either paternal or maternal age. However, there was a strong, positive association with paternal age among participants without siblings. In that group, the hazard ratio for fathers aged ≥35 years compared with <25 years at birth was 1.63 (95% confidence interval: 1.19, 2.23), and a linear dose-response association was suggested (Pspline = 0.002).There were no differences by subtype of hematological cancer. Results of this study support the need for further research to better understand the association between paternal age at birth and hematological malignancies.

摘要

孩子出生时父亲年龄≥35岁的父母比例持续上升,但这些孩子的长期健康后果尚未完全明确。最近一项针对110,999名成年女性的前瞻性研究表明,孩子出生时父亲的年龄(而非母亲的年龄)与散发性血液系统癌症风险之间存在关联。为进一步探究该主题,我们在美国癌症协会癌症预防研究II营养队列中的男性和女性中研究了这些关联。在138,003名癌症预防研究II的参与者中,1992年至2009年期间共确诊了2,532例新发血液系统癌症。采用Cox比例风险回归计算多变量调整后的风险比和95%置信区间。无论是父亲还是母亲的年龄,血液系统恶性肿瘤风险均无明显线性趋势。然而,在没有兄弟姐妹的参与者中,父亲年龄与血液系统恶性肿瘤风险呈强烈正相关。在该组中,孩子出生时父亲年龄≥35岁与<25岁相比,风险比为1.63(95%置信区间:1.19, 2.23),提示存在线性剂量反应关联(P样条 = 0.002)。血液系统癌症亚型之间无差异。本研究结果支持需要进一步开展研究,以更好地理解孩子出生时父亲年龄与血液系统恶性肿瘤之间的关联。