Gal Inbar, Sadetzki Siegal, Gershoni-Baruch Ruth, Oberman Bernice, Carp Howard, Papa Moshe Z, Diestelman-Menachem Tal, Eisenberg-Barzilai Shlomit, Friedman Eitan
Susanne Levy Gertner Oncogenetics Unit, Chaim Sheba Medical Center, Tel-Hashomer, 52621, Israel.
Am J Hum Genet. 2004 Jun;74(6):1270-5. doi: 10.1086/421442. Epub 2004 Apr 28.
BRCA1/BRCA2 germline mutations are associated with an increased breast/ovarian cancer risk. Offspring gender ratios may be skewed against male births in BRCA1 mutation carriers. In addition, the lack of viable homozygous BRCA1/BRCA2-mutation carriers implies that recurrent miscarriages may be associated with homozygous fetuses. Jewish Israeli high-risk women who were tested for being carriers of the predominant BRCA1/BRCA2 mutations in Jewish high-risk families were analyzed for the sex of offspring and the rate of spontaneous miscarriages. Overall, 817 women participated: 393 BRCA1/BRCA2-mutation carriers (229 with breast/ovarian cancer) and 424 high-risk noncarriers (208 with breast/ovarian cancer). No differences between the male-to-female offspring ratios of all study groups were noted. Among mutation carriers, the offspring male-to-female ratio was 0.97 (444 : 460), and among mutation carriers with cancer it was 0.92 (262 : 284). Similarly, no offspring gender skewing was noted among high-risk noncarriers, regardless of health status. The rates of three or more spontaneous miscarriages among participants with at least one live birth were 4.37% (15/343) among mutation carriers and 3% (12/401) among high-risk women (P = not significant). In conclusion, the offspring gender ratio is similar in high-risk Jewish families and in the general population. The issue of the rate of recurrent miscarriages in high-risk Jewish women is unresolved.
BRCA1/BRCA2基因种系突变与乳腺癌/卵巢癌风险增加相关。BRCA1突变携带者的后代性别比可能不利于男性出生。此外,缺乏存活的纯合BRCA1/BRCA2突变携带者意味着反复流产可能与纯合胎儿有关。对在犹太高危家庭中检测是否携带主要BRCA1/BRCA2突变的以色列犹太高危女性的后代性别和自然流产率进行了分析。总体而言,817名女性参与:393名BRCA1/BRCA2突变携带者(229名患有乳腺癌/卵巢癌)和424名高危非携带者(208名患有乳腺癌/卵巢癌)。所有研究组的后代男女比例均未发现差异。在突变携带者中,后代男女比例为0.97(444:460),在患有癌症的突变携带者中为0.92(262:284)。同样,无论健康状况如何,高危非携带者中均未发现后代性别偏差。在至少有一次活产的参与者中,突变携带者的三次或更多次自然流产率为4.37%(15/343),高危女性为3%(12/401)(P=无显著性差异)。总之,高危犹太家庭的后代性别比与一般人群相似。高危犹太女性反复流产率的问题尚未解决。