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Environmental Exposures, Reproductive Windows, and Social Drivers of Young-Onset Breast Cancer

$156,000P30FY2025CANIH

Oregon Health & Science University, Portland OR

Investigators

Linked publications, trials & patents

Paper 39764100Paper 39763867Paper 39605535Paper 39435649Paper 39386578Paper 39375962Trial NCT07434128Trial NCT07278440Trial NCT07089940Trial NCT05705492Trial NCT04247425Trial NCT04172493Trial NCT04104139Trial NCT04061980Trial NCT04005690Trial NCT03961672Trial NCT03960177Trial NCT03699995Trial NCT03677531Trial NCT03649880Trial NCT03626285Trial NCT03613259Trial NCT03544125Trial NCT03479268Trial NCT03418025Trial NCT03406013Trial NCT03361436Trial NCT03347617Trial NCT03325166Trial NCT03280277Trial NCT03270059Trial NCT03261180Trial NCT03234309Trial NCT03135782Trial NCT03097588Trial NCT03028935Trial NCT03010358Trial NCT03009201Trial NCT02890979Trial NCT02869412Trial NCT02857218Trial NCT02779283Trial NCT02736617Trial NCT02522715Trial NCT02504359Trial NCT02503358Trial NCT02501759Trial NCT02498951Trial NCT02427841Trial NCT02359097Trial NCT02355262Trial NCT02312557Trial NCT02228265Trial NCT02100189Trial NCT02099864Trial NCT02092324Trial NCT02070705Trial NCT02050919Trial NCT01913015Trial NCT01748942Trial NCT01689987Trial NCT01649505Trial NCT01635413Trial NCT01620216Trial NCT01532687Trial NCT01498978Trial NCT01441882Trial NCT01422408Trial NCT01253642Trial NCT01031953Trial NCT01005914Trial NCT00983398Trial NCT00978562Trial NCT00900302Trial NCT00900068Trial NCT00900055Trial NCT00899795Trial NCT00899522Trial NCT00843167Trial NCT00822848Trial NCT00764517Trial NCT00722072Trial NCT00691652Trial NCT00662103Trial NCT00660543Trial NCT00659126Trial NCT00627276Trial NCT00516542Trial NCT00482274Trial NCT00425386Trial NCT00324324Trial NCT00303849Trial NCT00293475Trial NCT00253721Trial NCT00253643Trial NCT00238433Trial NCT00227682Trial NCT00103038Trial NCT00075387Patent 9279811

Abstract

PROJECT SUMMARY Young-onset breast cancer (YOBC), diagnosed in women <50 years old, is increasing in incidence by 1-2% annually in the U.S. and is associated with worse outcomes compared to breast cancer (BC) diagnosed later in life. Most YOBC cases occur in women without inherited genetic risk, highlighting the need to better understand environmental, reproductive, and social drivers of the disease. Emerging evidence suggests that exposures during vulnerable life stages such as puberty, pregnancy, and the postpartum period may have lasting effects on BC risk. Concurrent shifts in reproductive timing (e.g., delayed childbirth) and rising environmental exposures (e.g., air pollution, pesticides, ‘forever chemicals’ in water, lack of greenspace access) may contribute to this trend, particularly in socially disadvantaged populations. Methods: We will conduct a population-based, matched case-control study using data from the Healthy Oregon Project (HOP), a mobile health research platform with >50,000 participants statewide. YOBC cases (n=600) and age and race-matched controls (n=1,200) identified from the HOP will complete detailed surveys on reproductive history (e.g., age at menarche, parity, age at first/last birth, lactation); residential addresses and age/year at key life stages: (1) menarche, (2) each pregnancy and postpartum period, and (3) pre- diagnosis window for cases and a matched age window for controls, and current period; and social factors (e.g., education, healthcare access). Geocoded residential addresses will be linked to environmental datasets on PM2.5, pesticides, agricultural and urban greenspace, and PFAS to quantify environmental exposures during each key reproductive time window and pre-diagnosis window (cases) or current period (controls). Specific Aims: We propose to: 1) Evaluate the effects of environmental exposure mixtures during key reproductive life stages using quantile g-computation. This approach will allow us to assess the cumulative/overall impact of environmental exposure mixtures and the relative contribution of individual environmental exposure component at each time window on YOBC risk. We will compare the magnitude and direction of environmental [mixture] risk estimates between reproductive life stages and the pre- diagnosis period to identify the most critical window of vulnerability; 2) Determine how social drivers influence YOBC risk via environmental exposures and reproductive factors using structural equation modeling (SEM). We hypothesize that environmental exposures during hormonally sensitive life stages interact synergistically with reproductive timing to increase YOBC risk, with a prediction that earlier life exposures playing the most significant role, and that social disadvantage amplifies these risks. This study will identify modifiable, time-sensitive environmental exposures and provide insight into how social and reproductive factors may compound these risks, informing future YOBC prevention strategies, particularly among socioeconomically and environmentally vulnerable populations.

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