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具有额外X染色体女性的死亡率和癌症发病率:英国的一项队列研究。

Mortality and cancer incidence in women with extra X chromosomes: a cohort study in Britain.

作者信息

Swerdlow Anthony J, Schoemaker Minouk J, Higgins Craig D, Wright Alan F, Jacobs Patricia A

机构信息

Section of Epidemiology, Institute of Cancer Research, Sutton, SM2 5NG, UK.

出版信息

Hum Genet. 2005 Nov;118(2):255-60. doi: 10.1007/s00439-005-0043-7. Epub 2005 Nov 15.

Abstract

About one woman in 1,000 has an extra X chromosome, but such women have no recognised characteristic somatic features and little is known about their long-term health and cancer risks. We conducted a cohort study of mortality and cancer incidence in 542 women diagnosed with X polysomy at 25 cytogenetic centres in Britain since 1959. Fifty-nine deaths occurred during follow-up to mid-2004. Mortality was significantly raised (standardised mortality ratio (SMR) = 2.5 (95% confidence interval (CI) 1.9-3.2)), with excess deaths due particularly to cardiovascular disease (SMR = 2.5 (95% CI 1.5-3.8)) and respiratory disease (SMR = 4.0 (95% CI 1.7-7.9)). Risks of cancer incidence and cancer mortality overall were not raised, but there was significantly raised mortality from non-Hodgkin's lymphoma (NHL) (SMR = 10.4 (95% CI 1.3-37.6); based on 2 cases). The data indicate that mortality in women diagnosed with X polysomy is considerably raised. The raised risk of NHL is seen also in males with more than one X chromosome, and hence although unexpected and based on small numbers, it might indicate the action of a gene on the X chromosome, possibly in the pseudoautosomal region, that escapes X-inactivation.

摘要

每1000名女性中约有1人有一条额外的X染色体,但这类女性没有公认的特征性躯体特征,人们对她们的长期健康和癌症风险知之甚少。我们对自1959年以来在英国25个细胞遗传学中心被诊断为X多体性的542名女性进行了一项关于死亡率和癌症发病率的队列研究。在随访至2004年年中期间有59人死亡。死亡率显著升高(标准化死亡率比(SMR)=2.5(95%置信区间(CI)1.9 - 3.2)),尤其因心血管疾病(SMR = 2.5(95%CI 1.5 - 3.8))和呼吸系统疾病(SMR = 4.0(95%CI 1.7 - 7.9))导致的死亡人数过多。总体癌症发病率和癌症死亡率风险并未升高,但非霍奇金淋巴瘤(NHL)的死亡率显著升高(SMR = 10.4(95%CI 1.3 - 37.6);基于2例)。数据表明,被诊断为X多体性的女性死亡率大幅升高。在有一条以上X染色体的男性中也观察到NHL风险升高,因此,尽管出乎意料且基于少量病例,但这可能表明X染色体上一个基因的作用,可能在拟常染色体区域,该基因逃避了X染色体失活。

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