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  • 1
    In: The FASEB Journal, Wiley, Vol. 25, No. S1 ( 2011-04)
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 1468876-1
    SSG: 12
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  • 2
    In: BMJ Open, BMJ, Vol. 12, No. 12 ( 2022-12), p. e061205-
    Abstract: To develop a breast cancer risk prediction model for Chamorro and Filipino women of the Mariana Islands and compare its performance to that of the Breast Cancer Risk Assessment Tool (BCRAT). Design Case–control study. Setting Clinics/facilities and other community-based settings on Guam and Saipan (Northern Mariana Islands). Participants 245 women (87 breast cancer cases and 158 controls) of Chamorro or Filipino ethnicity, age 25–80 years, with no prior history of cancer (other than skin cancer), residing on Guam or Saipan for at least 5 years. Primary and secondary outcome measures Breast cancer risk models were constructed using combinations of exposures previously identified to affect breast cancer risk in this population, population breast cancer incidence rates and all-cause mortality rates for Guam. Results Models using ethnic-specific relative risks performed better than those with relative risks estimated from all women. The model with the best performance among both ethnicities (the Breast Cancer Risk Model (BRISK) model; area under the receiver operating characteristic curve (AUC): 0.64 and 0.67 among Chamorros and Filipinos, respectively) included age at menarche, age at first live birth, number of relatives with breast cancer and waist circumference. The 10-year breast cancer risk predicted by the BRISK model was 1.28% for Chamorros and 0.89% for Filipinos. Performance of the BCRAT was modest among both Chamorros (AUC: 0.60) and Filipinos (AUC: 0.55), possibly due to incomplete information on BCRAT risk factors. Conclusions The ability to develop breast cancer risk models for Mariana Islands women is constrained by the small population size and limited availability of health services and data. Nonetheless, we have demonstrated that breast cancer risk prediction models with adequate discriminatory performance can be built for small populations such as in the Mariana Islands. Anthropometry, in particular waist circumference, was important for estimating breast cancer risk in this population.
    Type of Medium: Online Resource
    ISSN: 2044-6055 , 2044-6055
    Language: English
    Publisher: BMJ
    Publication Date: 2022
    detail.hit.zdb_id: 2599832-8
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2011
    In:  Breast Cancer Research and Treatment Vol. 129, No. 2 ( 2011-9), p. 565-574
    In: Breast Cancer Research and Treatment, Springer Science and Business Media LLC, Vol. 129, No. 2 ( 2011-9), p. 565-574
    Type of Medium: Online Resource
    ISSN: 0167-6806 , 1573-7217
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2011
    detail.hit.zdb_id: 2004077-5
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  • 4
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2020
    In:  Cancer Epidemiology, Biomarkers & Prevention Vol. 29, No. 10 ( 2020-10-01), p. 2019-2025
    In: Cancer Epidemiology, Biomarkers & Prevention, American Association for Cancer Research (AACR), Vol. 29, No. 10 ( 2020-10-01), p. 2019-2025
    Abstract: Incidence rates of epithelial ovarian cancer (EOC) vary across racial/ethnic groups, yet little is known about the impact of hormone-related EOC risk factors in non-Whites. Methods: Among 91,625 female Multiethnic Cohort Study participants, 155 incident EOC cases were diagnosed in Whites, 93 in African Americans, 57 in Native Hawaiians, 161 in Japanese Americans, and 141 in Latinas. We used Cox proportional hazards regression models to estimate hazard ratios (HR) and 95% confidence intervals (CI) for associations between race/ethnicity and EOC risk and between hormone-related factors and EOC risk across racial/ethnic groups. Results: Compared with Whites, African Americans and Japanese Americans had a lower multivariable-adjusted EOC risk; Native Hawaiians had a suggestive higher risk. Parity and oral contraceptive (OC) use were inversely associated with EOC risk (Pint race/ethnicity ≥ 0.43); associations were strongest among Japanese Americans (e.g., ≥4 vs. 0 children; HR = 0.45; CI, 0.26–0.79). Age at natural menopause and postmenopausal hormone (PMH) use were not associated with EOC risk in the overall population, but were positively associated with risk in Latinas (e.g., ≥5 years vs. never PMH use; HR = 2.13; CI, 1.30–3.49). Conclusions: We observed strong associations with EOC risk for parity and OC use in Japanese Americans and PMH use and age at natural menopause in Latinas. However, differences in EOC risk among racial/ethnic groups were not fully explained by established hormone-related risk factors. Impact: Our study indicates there are racial/ethnic differences in EOC risk and risk factors, and could help improve prevention strategies for non-White women.
    Type of Medium: Online Resource
    ISSN: 1055-9965 , 1538-7755
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
    detail.hit.zdb_id: 2036781-8
    detail.hit.zdb_id: 1153420-5
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  • 5
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 80, No. 16_Supplement ( 2020-08-15), p. 1169-1169
    Abstract: The impact of hormone-related factors on breast cancer risk has been well-studied; however, data on racial/ethnic minorities, especially Native Hawaiian women, remain relatively scarce. MEC participants completed a baseline questionnaire providing information on hormone-related factors. During a median follow-up of 20 years, 4,634 incident invasive breast cancer cases were identified among 81,511 postmenopausal women (20,003 White, 16,060 African American, 5,468 Native Hawaiian, 22,333 Japanese American, and 17,647 Latina). We used Cox proportional hazards regression models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for associations of: (1) race/ethnicity with estrogen receptor positive (ER+) and negative (ER-) breast cancer risk and (2) hormone-related factors with ER+ and ER- breast cancer risk across race/ethnicity. Models were adjusted for baseline age and body mass index (BMI), parity, as well as ages at menarche, menopause, and first birth. Compared to Whites, age-adjusted ER+ breast cancer risk was higher in Native Hawaiians (HR 1.42 [CI 1.26-1.60]), lower in African Americans (0.72 [0.66-0.80] ) and Latinas (0.54 [0.49-0.60]), and similar in Japanese Americans (0.97 [0.89-1.05] ). Risk for ER- disease was higher in African Americans (1.41 [1.15-1.72]) than in Whites, but no difference was observed in Native Hawaiians, Latinas or Japanese Americans. These results were unchanged after adjustment for hormone-related factors. In the full population, parity and a later age at natural menopause were associated with a decreased ER+ breast cancer risk, and postmenopausal hormone (PMH) use and a higher BMI with an increased risk. There was no significant interaction of these factors with race/ethnicity (p-value for interaction [p-int] ≥0.10). In race/ethnicity specific analyses, parity (vs nulliparity) was associated with lower ER+ breast cancer risk in Whites (0.72 [0.59-0.87]), Japanese Americans (0.57 [0.44-0.74] ), and Latinas (0.63 [0.46-0.86]). Age at menopause (≥55 vs & lt;45 years) was inversely associated with ER+ disease risk in African Americans (0.69 [0.52-0.91]) and Japanese Americans (0.69 [0.57-0.84] ). PMH use (ever vs never) increased ER+ breast cancer risk by 17-36% in all racial/ethnic groups except Native Hawaiians. BMI (≥30 vs & lt;25 kg/m2) was associated with a 22-66% increased risk of ER+ disease in all racial/ethnic groups. For ER- breast cancer, ever use of oral contraceptives was the only factor associated with risk in the full population (p-int 0.45) and we observed an increased risk of ER- disease in Whites (1.52 [1.09-2.12]) and African Americans (1.80 [1.30-2.51] ). Although we observed different associations across racial/ethnic groups for several hormone-related factors with risk of ER+ disease, these did not appear to explain the observed racial/ethnic differences in breast cancer incidence. Citation Format: Danja Sarink, Loic Le Marchand, Lenora W. Loo, Song-Yi Park, Kami K. White, V Wendy Setiawan, Anna H. Wu, Lynne R. Wilkens, Melissa A. Merritt. Racial/ethnic differences in postmenopausal breast cancer incidence and risk factors: Results from the Multiethnic Cohort (MEC) Study [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 1169.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
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    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2012
    In:  International Journal of Cancer Vol. 131, No. 5 ( 2012-09-01), p. E705-E716
    In: International Journal of Cancer, Wiley, Vol. 131, No. 5 ( 2012-09-01), p. E705-E716
    Type of Medium: Online Resource
    ISSN: 0020-7136
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 218257-9
    detail.hit.zdb_id: 1474822-8
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  • 7
    In: International Journal of Cancer, Wiley, Vol. 150, No. 2 ( 2022-01-15), p. 221-231
    Abstract: What's new? Racial/ethnic differences in hormone receptor positive and negative breast cancer risk are well‐documented; the factors contributing to these differences less so. The authors compared hormone‐related risk factors for breast cancer among a multiethnic population. They identified a number of notable differences in the impact of established risk factors ‐ particularly oral contraceptive use and BMI ‐ between racial/ethnic groups. These results reinforce the need to consider race/ethnicity in breast cancer studies and prevention recommendations.
    Type of Medium: Online Resource
    ISSN: 0020-7136 , 1097-0215
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 218257-9
    detail.hit.zdb_id: 1474822-8
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  • 8
    In: Journal of Cachexia, Sarcopenia and Muscle, Wiley, Vol. 13, No. 2 ( 2022-04), p. 987-1002
    Abstract: Age‐related loss in skeletal muscle mass, quality, and strength, known as sarcopenia, is a well‐known phenomenon of aging and is determined clinically using methods such as dual‐energy X‐ray absorptiometry (DXA). However, these clinical methods to measure sarcopenia are not practical for population‐based studies, and a five‐question screening tool known as SARC‐F has been validated to screen for sarcopenia. Methods We investigated the relationship between appendicular skeletal lean mass/height 2 (ALM/HT 2 ) (kg/m 2 ) assessed by DXA and SARC‐F in a subset of 1538 (778 men and 760 women) participants in the Multiethnic Cohort (MEC) Study after adjustment for race/ethnicity, age, and body mass index (BMI) at the time of DXA measurement. We then investigated the association between SARC‐F and mortality among 71 283 (41 757 women and 29 526 men) participants in the MEC, who responded to the five SARC‐F questions on a mailed questionnaire as part of the MEC follow‐up in 2012–2016. Results In women, SARC‐F score was significantly inversely associated with ALM/HT 2 after adjusting for race/ethnicity, and age and BMI at DXA ( r  = −0.167, P   〈  0.001); the result was similar in men although it did not reach statistical significance ( r  = −0.056, P  = 0.12). Among the 71 000+ MEC participants, SARC‐F score ≥ 4, as an indicator of sarcopenia, was higher in women (20.9%) than in men (11.2%) ( P   〈  0.0001) and increased steadily with increasing age (6.3% in 〈 70 vs. 41.3% in 90+ years old) ( P   〈  0.0001). SARC‐F score ≥ 4 was highest among Latinos (30.8% in women and 16.1% in men) and lowest in Native Hawaiian women (15.6%) and Japanese American men (8.9%). During an average of 6.8 years of follow‐up, compared with men with SARC‐F score of 0–1 (indicator of no sarcopenia), men with SARC‐F 2–3 (indicator of pre‐sarcopenia) and SARC‐F ≥ 4 had significantly increased risk of all‐cause mortality [hazard ratio (HR) = 1.00, 1.77, 3.73, P   〈  0.001], cardiovascular disease (CVD) mortality (HR = 1.00, 1.85, 3.98, P   〈  0.001), and cancer mortality (HR = 1.00, 1.46, 1.96, P   〈  0.001) after covariate adjustment. Comparable risk association patterns with SARC‐F scores were observed in women (all‐cause mortality: HR = 1.00, 1.47, 3.10, P   〈  0.001; CVD mortality: HR = 1.00, 1.59, 3.54, P   〈  0.001; cancer mortality: HR = 1.00, 1.30, 1.77, P   〈  0.001). These significant risk patterns between SARC‐F and all‐cause mortality were found across all sex–race/ethnic groups considered (12 in total). Conclusions An indicator of sarcopenia, determined using SARC‐F, showed internal validity against DXA and displayed racial/ethnic and sex differences in distribution. SARC‐F was associated with all‐cause mortality as well as cause‐specific mortality.
    Type of Medium: Online Resource
    ISSN: 2190-5991 , 2190-6009
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2586864-0
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  • 9
    In: Preventive Medicine, Elsevier BV, Vol. 69 ( 2014-12), p. 214-223
    Type of Medium: Online Resource
    ISSN: 0091-7435
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 1471564-8
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  • 10
    In: Endocrine-Related Cancer, Bioscientifica, Vol. 17, No. 1 ( 2010-03), p. 125-134
    Abstract: To add to the existing evidence that comes mostly from White populations, we conducted a nested case–control study to examine the association between sex hormones and breast cancer risk within the Multiethnic Cohort that includes Japanese American, White, Native Hawaiian, African American, and Latina women. Of the postmenopausal women for whom we had a plasma sample, 132 developed breast cancer during follow-up. Two controls per case, matched on study area (Hawaii, Los Angeles), ethnicity/race, birth year, date and time of blood draw and time fasting, were randomly selected from the women who had not developed breast cancer. Levels of estradiol (E 2 ), estrone (E 1 ), androstenedione, dehydroepiandrosterone (DHEA), and testosterone were quantified by RIA after organic extraction and Celite column partition chromatography. E 1 sulfate, DHEA sulfate (DHEAS), and sex hormone-binding globulin (SHBG) were quantified by direct immunoassays. Based on conditional logistic regression, the sex hormones were positively associated and SHBG was negatively associated with breast cancer risk. All associations, except those with DHEAS and testosterone showed a significant linear trend. The odds ratio (OR) associated with a doubling of E 2 levels was 2.26 (95% confidence interval (CI) 1.58–3.25), and the OR associated with a doubling of testosterone levels was 1.34 (95% CI 0.98–1.82). The associations in Japanese American women, who constituted 54% of our sample, were similar to or nonsignificantly stronger than in the overall group. This study provides the best evidence to date that the association between sex hormones and breast cancer risk is generalizable to an ethnically diverse population.
    Type of Medium: Online Resource
    ISSN: 1351-0088 , 1479-6821
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2010
    detail.hit.zdb_id: 2010895-3
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