Breast density in NF1 women: a retrospective study.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Familial Cancer Pub Date : 2024-03-01 Epub Date: 2024-01-25 DOI:10.1007/s10689-023-00355-y
R De Santis, G Cagnoli, B Rinaldi, D Consonni, Beatrice Conti, M Eoli, A Liguori, M Cosentino, G Carrafiello, O Garrone, M Giroda, C Cesaretti, M S Sfondrini, D Gambini, F Natacci
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引用次数: 0

Abstract

Neurofibromatosis type 1 (NF1) is an autosomal dominant condition caused by neurofibromin haploinsufficiency due to pathogenic variants in the NF1 gene. Tumor predisposition has long been associated with NF1, and an increased breast cancer (BC) incidence and reduced survival have been reported in recent years for women with NF1. As breast density is another known independent risk factor for BC, this study aims to evaluate the variability of breast density in patients with NF1 compared to the general population. Mammograms from 98 NF1 women affected by NF1, and enrolled onto our monocentric BC screening program, were compared with those from 300 healthy subjects to verify differences in breast density. Mammograms were independently reviewed and scored by a radiologist and using a Computer-Aided Detection (CAD) software. The comparison of breast density between NF1 patients and controls was performed through Chi-squared test and with multivariable ordinal logistic models adjusted for age, body mass index (BMI), number of pregnancies, and menopausal status.breast density was influenced by BMI and menopausal status in both NF1 patients and healthy subjects. No difference in breast density was observed between NF1 patients and the healthy female population, even after considering the potential confounding factors.Although NF1 and a highly fibroglandular breast are known risk factors of BC, in this study, NF1 patients were shown to have comparable breast density to healthy subjects. The presence of pathogenic variants in the NF1 gene does not influence the breast density value.

NF1 女性的乳房密度:一项回顾性研究。
神经纤维瘤病 1 型(NF1)是一种常染色体显性遗传病,由 NF1 基因中的致病变体导致神经纤维瘤蛋白单倍体缺乏引起。肿瘤易感性长期以来一直与 NF1 相关,近年来有报道称,NF1 女性患者的乳腺癌(BC)发病率增加,存活率降低。由于乳房密度是乳腺癌的另一个已知独立风险因素,本研究旨在评估与普通人群相比,NF1 患者乳房密度的变化情况。我们将 98 名受 NF1 影响的 NF1 妇女的乳房 X 光照片与 300 名健康受试者的乳房 X 光照片进行了比较,以验证乳房密度的差异。乳房 X 光照片由放射科医生使用计算机辅助检测 (CAD) 软件进行独立审查和评分。NF1患者和对照组之间乳腺密度的比较通过Chi-squared检验和多变量序数逻辑模型进行,并对年龄、体重指数(BMI)、怀孕次数和绝经状态进行了调整。尽管NF1和高纤维腺性乳房是已知的乳腺增生症风险因素,但在本研究中,NF1患者的乳房密度与健康受试者相当。NF1基因致病变体的存在并不影响乳腺密度值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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