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263例共济失调毛细血管扩张症患者的死亡率和癌症发病率

Mortality and cancer incidence in 263 patients with ataxia-telangiectasia.

作者信息

Morrell D, Cromartie E, Swift M

出版信息

J Natl Cancer Inst. 1986 Jul;77(1):89-92.

PMID:3459930
Abstract

Mortality and cancer incidence were measured retrospectively in 263 ataxia-telangiectasia (A-T) homozygotes. For white and black A-T patients, respectively, all-cause mortality was 50 and 147 times higher than expected based on U.S. mortality rates. There were 52 primary cancers, representing a 61-fold cancer excess for white probands and a 184-fold excess for black probands. The cancer excess was most pronounced for lymphoma, with 252- and 750-fold excesses observed for whites and blacks, respectively. All the age-specific mortality and cancer incidence rates for blacks exceeded those for whites, and overall mortality was 3.0 times higher for black probands than for whites (P less than .001), whereas cancer incidence was 2.2 times higher (P less than .06). Among the white A-T patients, 36% of those who had died had lived at least until 20 years of age, and 33% of those still living were at least 20 years old.

摘要

对263名共济失调毛细血管扩张症(A-T)纯合子患者的死亡率和癌症发病率进行了回顾性测量。对于白种人和黑种A-T患者,全因死亡率分别比基于美国死亡率预期的高出50倍和147倍。共有52例原发性癌症,白种先证者的癌症超额发生率为61倍,黑种先证者为184倍。癌症超额发生率在淋巴瘤中最为明显,白种人和黑种人的超额发生率分别为252倍和750倍。黑种人的所有年龄特异性死亡率和癌症发病率均超过白种人,黑种先证者的总体死亡率比白种先证者高3.0倍(P<0.001),而癌症发病率高2.2倍(P<0.06)。在白种A-T患者中,36%的死亡患者至少活到了20岁,33%仍在世的患者年龄至少为20岁。

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