scholarly journals Interactive effect of genetic susceptibility with height, body mass index, and hormone replacement therapy on the risk of breast cancer

2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Sophia Harlid ◽  
Salma Butt ◽  
Malin IL Ivarsson ◽  
Jorunn Erla Eyfjörd ◽  
Per Lenner ◽  
...  
Maturitas ◽  
2005 ◽  
Vol 50 (1) ◽  
pp. 19-29 ◽  
Author(s):  
Toshiyuki Yasui ◽  
Hirokazu Uemura ◽  
Yuka Umino ◽  
Masaya Takikawa ◽  
Seiichiro Saito ◽  
...  

2012 ◽  
Vol 45 (3) ◽  
pp. 149-154 ◽  
Author(s):  
Beatriz Regina Alvares ◽  
Christian Henrique de Andrade Freitas ◽  
Rodrigo Menezes Jales ◽  
Orlando José de Almeida ◽  
Emílio Francisco Marussi

OBJECTIVE: To evaluate mammographic breast density in asymptomatic menopausal women in correlation with clinical and sonographic findings. MATERIALS AND METHODS: Mammograms and clinical and sonographic findings of 238 asymptomatic patients were retrospectively reviewed in the period from February/2022 to June/2006. The following variables were analyzed: mammographic density patterns, sonographic findings, patients' age, parity, body mass index and use of hormone replacement therapy. RESULTS: Age, parity and body mass index showed a negative correlation with breast density pattern, while use of hormone replacement therapy showed a positive correlation. Supplementary breast ultrasonography was performed in 103 (43.2%) patients. Alterations which could not be visualized at mammography were found in 34 (33%) of them, most frequently in women with breast density patterns 3 and 4. CONCLUSION: The authors concluded that breast density patterns were influenced by age, parity, body mass index and time of hormone replacement therapy. Despite not having found any malignant abnormality in the studied cases, the authors have observed a predominance of benign sonographic abnormalities in women with high breast density patterns and without mammographic abnormalities, proving the relevance of supplementary ultrasonography to identify breast lesions in such patients.


2010 ◽  
Vol 19 (12) ◽  
pp. 3119-3130 ◽  
Author(s):  
Emma J. Crosbie ◽  
Marcel Zwahlen ◽  
Henry C. Kitchener ◽  
Matthias Egger ◽  
Andrew G. Renehan

2002 ◽  
Vol 20 (3) ◽  
pp. 699-706 ◽  
Author(s):  
Giske Ursin ◽  
Chiu-Chen Tseng ◽  
Annlia Paganini-Hill ◽  
Shelley Enger ◽  
Peggy C. Wan ◽  
...  

PURPOSE: We and other investigators have previously shown that postmenopausal combined estrogen and progestin replacement therapy (EPRT) increases the risk of breast cancer and that the risk associated with EPRT is substantially higher than for estrogen replacement therapy (ERT) alone. The present study was conducted to determine whether any particular subgroup of women are at particularly high risk of breast cancer if they use EPRT and whether tumor characteristics in women who develop cancer while on ERT or EPRT are different from those in women not using ERT or EPRT. PATIENTS AND METHODS: We conducted a population-based case-control study in Los Angeles, CA, with patients diagnosed with breast cancer in the late 1980s and early 1990s. Control subjects were matched to patients on age, ethnicity, and neighborhood of residence. We present data on 1,897 postmenopausal patients and 1,637 controls aged 55 to 72 years who had not undergone a simple hysterectomy. RESULTS: Relative risk of breast cancer associated with EPRT use did not vary with body mass index (body mass index at or below v above median [24.6 kg/m2]; P = .98), alcohol intake (≥ one v < one drink per week; P = .16), parity (nulliparous v parous; P = .45), history of benign breast disease (yes v no; P = .99), or family history of breast cancer (first degree v none; P = .57). All of these results were compatible with our previously reported estimate of an increased risk of breast cancer of 5% per year of use of EPRT. Hormone users, principally EPRT users, were more likely to have hormone receptor–positive, especially progesterone-positive, tumors. CONCLUSION: We found no evidence that the risk of breast cancer associated with EPRT is limited to subgroups of women with specific cofactors. Tumors in EPRT users are more often hormone receptor–positive, indicating that they may have a better prognosis than breast cancer overall.


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