First-born twin has a higher risk of acute leukemia in a population-based assessment of cancer in twins in California, and lower than anticipated rate of twin concordance.

Eric M Nickels, Naying Zhou, Joseph L Wiemels
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Abstract

We assessed cancer concordance, cancer incidence in the healthy twin of cancer probands, and cancer risk in relation to birth order in pediatric and adolescent/young adult twins via a population-based study in California from 1982-2022. Twin subjects born in California between 1982-2017 who were diagnosed with leukemia from 0-39 years of age were identified through linked birth and California Cancer Registry (1988-2022) data. Two concordant-twin leukemias cases were identified across 255 total twin pairs with leukemia for an overall rate of leukemia concordance of 0.9%. One concordant twin pair was identified among 199 pairs with lymphoid leukemia (0.5%) and one within 34 pairs with acute myeloid leukemia (2.9%). A significant association was identified between twin plurality birth order and development of leukemia (OR 1.18, 95% CI 1-1.39, P=0.049), an effect which was strongest in lymphoid leukemias (2.21, 1.44-3.39, P=1.65e-4). Assessment of DNA methylation markers associated with birth order showed significantly reduced methylation in first-born twin cases compared to second-born (P=8.53e-12) in a subset of 41 twins discordant for lymphoid leukemia. Overall cancer concordance in twins was comparable to the lower range of previous estimates from different world regions. Concordance in lymphoid leukemias was quite lower than expected, indicating concordant leukemia is rarer than previously appreciated. We identified a strong association between twin plurality birth order and development of pediatric cancer. While the underlying cause of this finding is uncertain, we identified significant differences in DNA methylation at previously described sites associated with birth order, suggesting a similar biological mechanism.
在对加利福尼亚州双胞胎患癌症情况进行的人群评估中,头生双胞胎患急性白血病的风险较高,双胞胎一致率低于预期。
我们通过 1982-2022 年间在加利福尼亚州开展的一项基于人群的研究,评估了儿童和青少年/年轻成人双胞胎的癌症一致性、癌症原告健康双胞胎的癌症发病率以及癌症风险与出生顺序的关系。1982-2017年间出生在加利福尼亚州的双胞胎受试者在0-39岁期间被诊断出患有白血病,这些受试者是通过关联的出生和加利福尼亚癌症登记(1988-2022年)数据确定的。在总共 255 对患有白血病的双胞胎中,发现了两例一致的双胞胎白血病病例,总体白血病一致率为 0.9%。在 199 对淋巴性白血病患者中发现了一对同卵双胞胎(0.5%),在 34 对急性髓性白血病患者中发现了一对同卵双胞胎(2.9%)。研究发现,孪生多胞胎的出生顺序与白血病发病之间存在明显的关联(OR 1.18,95% CI 1-1.39,P=0.049),这种效应在淋巴性白血病中最强(2.21,1.44-3.39,P=1.65e-4)。对与出生顺序相关的DNA甲基化标记的评估显示,在41对淋巴细胞白血病不一致的双胞胎子集中,头胎双胞胎的甲基化程度明显低于二胎(P=8.53e-12)。双胞胎患癌症的总体一致性与世界不同地区之前估计的较低范围相当。淋巴白血病的一致性比预期的要低得多,这表明白血病的一致性比以前所认识到的要罕见。我们发现,双胞胎多胞胎的出生顺序与小儿癌症的发生有密切关系。虽然这一发现的根本原因尚不确定,但我们发现在以前描述过的与出生顺序相关的位点上,DNA 甲基化存在显著差异,这表明存在类似的生物学机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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