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首页> 外文期刊>Gynecological endocrinology: the official journal of the International Society of Gynecological Endocrinology >Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause
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Polymorphisms of estrogen receptor-α gene in Brazilian women with high breast density after menopause

机译:绝经后高乳房密度的巴西女性中雌激素受体-α基因的多态性

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The association of genetic polymorphism in the estrogen receptor alpha (ERα) gene and risk for diseases including breast cancer (BC) has been the subject of great interest. Objective: Checking on women with high breast density after menopause, the frequency of the Pvull and Xbal polymorphisms of the ERα gene and the correlation between them and the known risk factors for breast cancer. Method: Observational study with 308 women between 45 and 65 years old with high breast density, without hormonal therapy, menstruation for a year or more, breast and ovarian cancer history. It was characterized in clinical history and physical examination: menarche, menopause, parity, family history of BC, smoking, alcohol intake and body mass index. Results: The allelic and genotypic frequencies for ERα-Pvull and Xbal: p=43.99%; p=56.01%; pp=32.14%; Pp=47.73% and PP=20.13%; X=41.56%; x=58.44%; xx=33.44%; Xx=50.00% and XX=16.56%, respectively. The most frequent risk factors for BC: menarche before 12 years old (35.38%), nulliparity or first child after 28 years old (41.66%), family history of BC (19.16%) and overweight/obesity (62.01%). Conclusion: Allelic and genotypic distribution similar to literature. The risk factors for BC were more prevalent in women with high breast density but without significant associations with these polymorphisms.
机译:雌激素受体α(ERα)基因的遗传多态性与包括乳腺癌(BC)在内的疾病风险的关联一直是引起人们极大兴趣的主题。目的:检查绝经后高乳房密度的女性,ERα基因Pvull和Xbal多态性的频率及其与已知的乳腺癌危险因素的相关性。方法:对308名45岁至65岁,乳房密度高,未经荷尔蒙治疗,月经一年以上,乳腺癌和卵巢癌病史的女性进行观察性研究。它的特征在于临床病史和体格检查:初潮,更年期,产次,BC家族史,吸烟,饮酒和体重指数。结果:ERα-Pvull和Xbal的等位基因和基因型频率:p = 43.99%; p = 56.01%; pp = 32.14%; Pp = 47.73%和PP = 20.13%; X = 41.56%; x = 58.44%; xx = 33.44%; Xx = 50.00%和XX = 16.56%。 BC的最常见危险因素:12岁之前的初潮(35.38%),28岁以下的未产妇或第一个孩子(41.66%),BC的家族病史(19.16%)和超重/肥胖(6​​2.01%)。结论:等位基因和基因型分布与文献相似。乳腺密度高的女性中,BC的危险因素更为普遍,但与这些多态性没有显着相关性。

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