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Insulin resistance and the development of breast cancer in premenopausal women: the Kangbuk Samsung Health Study

Authors
Lee, JeesunChang, YoosooKim, YejinPark, BoyoungRyu, Seungho
Issue Date
Jan-2022
Publisher
SPRINGER
Keywords
Breast neoplasms; Insulin resistance; Premenopause; Cohort studies
Citation
BREAST CANCER RESEARCH AND TREATMENT, v.192, no.2, pp.401 - 409
Indexed
SCIE
SCOPUS
Journal Title
BREAST CANCER RESEARCH AND TREATMENT
Volume
192
Number
2
Start Page
401
End Page
409
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/139823
DOI
10.1007/s10549-022-06513-7
ISSN
0167-6806
Abstract
Purpose Research on the role of insulin resistance (IR) in breast cancer risk in premenopausal women is scarce. We aimed to investigate the relationship between IR and the development of breast cancer in premenopausal women. Methods We analyzed the prospective association of IR and incident breast cancer in premenopausal women without breast cancer at baseline using a subsample of the Kangbuk Samsung Health Study. Results Among 134,488 Korean premenopausal women, 696 women developed incident breast cancers during a median follow-up of 4.34 years. After adjustment for dense breast and other potential confounders, HR (95% CI) for incident breast cancer comparing HOMA-IR quintiles 2, 3, 4, and 5 to the first quintile was 0.91 (0.71–1.17), 0.89 (0.69–1.15), 0.75 (0.57–0.98), and 0.87 (0.65–1.16), respectively (P for trend = 0.117), while HR (95% CI) comparing insulin quintiles 2, 3, 4, and 5 to the first quintile was 1.02 (0.80–1.30), 0.90 (0.69–1.16), 0.72 (0.54–0.96), and 0.96 (0.72–1.28), respectively (P for trend = 0.151). This pattern did not significantly differ by obesity. These results were attenuated and no longer significant in time-dependent analyses where updated status of insulin and other covariates over time were treated as time-varying covariates. Conclusion Our findings do not support the positive relationship of IR with the development of breast cancer in premenopausal women, unlike in postmenopausal women. Thus, the role of IR as a risk factor for breast cancer may differ by menopausal status.
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