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霍奇金病患者的生育力、生殖结局及子代健康:一项包括染色体检查的调查

Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations.

作者信息

Swerdlow A J, Jacobs P A, Marks A, Maher E J, Young T, Barber J C, Vaughan Hudson G

机构信息

Epidemiological Monitoring Unit, London School of Hygiene and Tropical Medicine, UK.

出版信息

Br J Cancer. 1996 Jul;74(2):291-6. doi: 10.1038/bjc.1996.355.

Abstract

Reproductive outcomes and health of offspring were investigated in 340 patients with Hodgkin's disease first treated at Mount Vernon Hospital, Middlesex, England, at ages under 40 (females) or 45 (males) during 1970-91. Information on offspring was obtained from case-notes and postal questionnaires to the patients. Eleven men and 16 women who had conceived any children after treatment were then interviewed. There was no excess of stillbirths, low birthweight or cogenital malformations, and no cancers have occurred in the 49 offspring after treatment. There was a significant excess of twins, compared with national expectations, in offspring of female patients (RR = 8.52, P = 0.025). Aggregation of series from the literature also showed an excess of twins. Chromosomes from cultures of peripheral lymphocytes from 45 children born to 25 patients (11 men and 14 women) after treatment were examined for numerical abnormalities and for structural abnormalities at the 550 or greater band level of resolution. All were normal except in one child with Down's syndrome (47, XY, +21), for whom we found the origin of the trisomy was from the parent without Hodgkin's disease. The chromosome constitution was also abnormal in one miscarriage (69, XXY; originating from the parent without Hodgkin's disease) and one termination (45, X; for with the parental origin could not be determined) after treatment. The study adds to previous questionnaire data and for the first time provides data also from chromosome analysis, that offspring of patients treated in adulthood for Hodgkin's disease are not at greatly raised risk of genotoxic or other adverse outcomes as a consequence of their parent's treatment. The numbers of offspring assessed in the literature remains small, however, and surveillance of larger numbers of subjects is needed to enable reliable treatment-specific analyses.

摘要

对1970年至1991年间在英国米德尔塞克斯郡弗农山医院首次接受治疗、年龄在40岁以下(女性)或45岁以下(男性)的340例霍奇金病患者的生殖结局和子代健康状况进行了调查。通过病历记录和向患者发放邮政调查问卷获取子代的相关信息。随后对11名治疗后生育子女的男性和16名治疗后生育子女的女性进行了访谈。未发现死产、低出生体重或先天性畸形增多的情况,治疗后的49名子代中也未发生癌症。与全国预期相比,女性患者子代中的双胞胎数量显著增多(相对危险度=8.52,P=0.025)。对文献系列的汇总分析也显示双胞胎数量增多。对25例患者(11名男性和14名女性)治疗后所生45名儿童的外周淋巴细胞培养染色体进行了检查,以检测其数目异常以及在分辨率为550条带或更高条带水平的结构异常。除1例唐氏综合征患儿(47, XY, +21)外,所有染色体均正常,我们发现该三体的起源来自未患霍奇金病的父母一方。治疗后1例流产(69, XXY;起源于未患霍奇金病的父母一方)和1例终止妊娠(45, X;无法确定亲代来源)的染色体组成也异常。该研究补充了之前的问卷调查数据,并且首次提供了染色体分析数据,表明成年期接受霍奇金病治疗的患者的子代,不会因其父母的治疗而面临显著增加的遗传毒性或其他不良结局风险。然而,文献中评估的子代数量仍然较少,需要对更多受试者进行监测,以便能够进行可靠的针对特定治疗的分析。

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