TY - JOUR
T1 - Low-fat dietary pattern and breast cancer mortality by metabolic syndrome components
T2 - a secondary analysis of the Women’s Health Initiative (WHI) randomised trial
AU - Pan, Kathy
AU - Aragaki, Aaron K.
AU - Neuhouser, Marian L.
AU - Simon, Michael S.
AU - Luo, Juhua
AU - Caan, Bette
AU - Snetselaar, Linda
AU - Mortimer, Joanne E.
AU - Manson, Jo Ann E.
AU - Kroenke, Candyce
AU - Lane, Dorothy
AU - Reding, Kerryn
AU - Rohan, Thomas E.
AU - Chlebowski, Rowan T.
N1 - Funding Information:
Funding information The WHI program is supported by the National Heart, Lung and Blood Institute, National Institutes of Health, Department of Health and Human Services through contracts N01WH22110, 24152, 32100-2, 32105-6, 32108-9, 32111-13, 32115, 32118-32119, 32122, 42107-26, 42129-32 and 44221. HHSN268201600003C, HHSN268201600004C and R25CA203650 also partially supported the development of this paper.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Cancer Research UK.
PY - 2021/8/3
Y1 - 2021/8/3
N2 - Background: In the Women’s Health Initiative (WHI) dietary modification (DM) randomised trial, the low-fat dietary intervention reduced deaths from breast cancer (P = 0.02). Extending these findings, secondary analysis examined dietary intervention influence on breast cancer mortality by metabolic syndrome (MS) components. Methods: In total, 48,835 postmenopausal women with no prior breast cancer were randomised to a low-fat dietary intervention or comparison groups. Four MS components were determined at entry in 45,833 participants: (1) high waist circumference, (2) high blood pressure, (3) high cholesterol and (4) diabetes history. Forest plots of hazard ratios (HRs) were generated with P-values for interaction between randomisation groups and MS component score. Primary outcome was death from breast cancer by metabolic syndrome score. Results: HRs and 95% confidence intervals (CI) for dietary intervention influence on death from breast cancer were with no MS components (n = 10,639), HR 1.09, 95% CI 0.63–1.87; with 1–2 MS components (n = 30,948), HR 0.80, 95% CI 0.62–1.02; with 3–4 MS components (n = 4,246), HR 0.31, 95% CI 0.14–0.69 (interaction P = 0.01). Conclusions: While postmenopausal women with 3–4 MS components were at higher risk of death from breast cancer, those randomised to a low-fat dietary intervention more likely had reduction in this risk. Registry: ClinicalTrials.gov (NCT00000611).
AB - Background: In the Women’s Health Initiative (WHI) dietary modification (DM) randomised trial, the low-fat dietary intervention reduced deaths from breast cancer (P = 0.02). Extending these findings, secondary analysis examined dietary intervention influence on breast cancer mortality by metabolic syndrome (MS) components. Methods: In total, 48,835 postmenopausal women with no prior breast cancer were randomised to a low-fat dietary intervention or comparison groups. Four MS components were determined at entry in 45,833 participants: (1) high waist circumference, (2) high blood pressure, (3) high cholesterol and (4) diabetes history. Forest plots of hazard ratios (HRs) were generated with P-values for interaction between randomisation groups and MS component score. Primary outcome was death from breast cancer by metabolic syndrome score. Results: HRs and 95% confidence intervals (CI) for dietary intervention influence on death from breast cancer were with no MS components (n = 10,639), HR 1.09, 95% CI 0.63–1.87; with 1–2 MS components (n = 30,948), HR 0.80, 95% CI 0.62–1.02; with 3–4 MS components (n = 4,246), HR 0.31, 95% CI 0.14–0.69 (interaction P = 0.01). Conclusions: While postmenopausal women with 3–4 MS components were at higher risk of death from breast cancer, those randomised to a low-fat dietary intervention more likely had reduction in this risk. Registry: ClinicalTrials.gov (NCT00000611).
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U2 - 10.1038/s41416-021-01379-w
DO - 10.1038/s41416-021-01379-w
M3 - Article
C2 - 34006923
AN - SCOPUS:85106273583
SN - 0007-0920
VL - 125
SP - 372
EP - 379
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 3
ER -