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International Pooled Analysis of Leisure-Time Physical Activity and Premenopausal Breast Cancer in Women From 19 Cohorts
Timmins, Iain R; Jones, Michael E; O'Brien, Katie M; Adami, Hans-Olov; Aune, Dagfinn; Baglietto, Laura; Bertrand, Kimberly A; Brantley, Kristen D; Chen, Yu; Clague DeHart, Jessica; Clendenen, Tess V; Dossus, Laure; Eliassen, A Heather; Fletcher, Olivia; Fournier, Agnès; Håkansson, Niclas; Hankinson, Susan E; Houlston, Richard S; Joshu, Corinne E; Kirsh, Victoria A; Kitahara, Cari M; Koh, Woon-Puay; Linet, Martha S; Park, Hannah Lui; Lynch, Brigid M; May, Anne M; Mellemkjær, Lene; Milne, Roger L; Palmer, Julie R; Ricceri, Fulvio; Rohan, Thomas E; Ruddy, Kathryn J; Sánchez, Maria-Jose; Shu, Xiao-Ou; Smith-Byrne, Karl; Steindorf, Karen; Sund, Malin; Vachon, Celine M; Vatten, Lars J; Visvanathan, Kala; Weiderpass, Elisabete; Willett, Walter C; Wolk, Alicja; Yuan, Jian-Min; Zheng, Wei; Nichols, Hazel B; Sandler, Dale P; Swerdlow, Anthony J; Schoemaker, Minouk J
PURPOSE/OBJECTIVE:There is strong evidence that leisure-time physical activity is protective against postmenopausal breast cancer risk but the association with premenopausal breast cancer is less clear. The purpose of this study was to examine the association of physical activity with the risk of developing premenopausal breast cancer. METHODS:We pooled individual-level data on self-reported leisure-time physical activity across 19 cohort studies comprising 547,601 premenopausal women, with 10,231 incident cases of breast cancer. Multivariable Cox regression was used to estimate hazard ratios (HRs) and 95% CIs for associations of leisure-time physical activity with breast cancer incidence. HRs for high versus low levels of activity were based on a comparison of risk at the 90th versus 10th percentiles of activity. We assessed the linearity of the relationship and examined subtype-specific associations and effect modification across strata of breast cancer risk factors, including adiposity. RESULTS: CONCLUSION/CONCLUSIONS:This large, pooled analysis of cohort studies adds to evidence that engagement in higher levels of leisure-time physical activity may lead to reduced premenopausal breast cancer risk.
PMID: 38079601
ISSN: 1527-7755
CID: 5589632
World Trade Center Exposure, DNA Methylation Changes, and Cancer: A Review of Current Evidence
Tuminello, Stephanie; Nguyen, Emelie; Durmus, Nedim; Alptekin, Ramazan; Yilmaz, Muhammed; Crisanti, Maria Cecilia; Snuderl, Matija; Chen, Yu; Shao, Yongzhao; Reibman, Joan; Taioli, Emanuela; Arslan, Alan A
PMCID:10742700
PMID: 38131903
ISSN: 2075-4655
CID: 5612212
Evaluation of Socioeconomic Disparities in Follow-up Completion for Incidental Pulmonary Nodules
Thakore, Nitya L; Russo, Rienna; Hang, Tianchu; Moore, William H; Chen, Yu; Kang, Stella K
OBJECTIVE:To evaluate the association between census-tract level measures of social vulnerability and residential segregation and IPN follow up. METHODS:This retrospective cohort study included patients with IPN ≥6 mm in size or multiple subsolid/ground-glass IPNs <6 mm (with non-optional follow-up recommendations) diagnosed between January 1, 2018 and December 30, 2019 at a large urban tertiary center and followed ≥two years. Geographic sociodemographic context was characterized by 2018 U.S. Centers for Disease Control and Prevention Social Vulnerability Index (SVI) and the Index of Concentration at the Extreme (ICE), categorized in quartiles. Multivariable binomial regression models were utilized with a primary outcome of inappropriate IPN follow up (late or no follow up). Models were also stratified by nodule risk. RESULTS:The study consisted of 2,492 patients (mean age 65.6 years +/- 12.6 years; 1,361 women). Top-quartile SVI patients were more likely to have inappropriate follow up (Risk Ratio [RR]: 1.24, 95% Confidence Interval [95% CI], 1.12-1.36]), compared with the bottom quartile; risk was also elevated in top-quartile SVI subcategories of Socioeconomic Status (RR: 1.23, 95% CI, 1.13-1.34), Minority Status and Language (RR: 1.24, 95% CI, 1.03-1.48), Housing and Transportation (RR: 1.13, 95% CI, 1.02-1.26), and ICE (RR: 1.20, 95% CI, 1.11-1.30). Further, top-quartile ICE was associated with greater risk of inappropriate follow up among high-risk vs. lower-risk IPN (1.33 [1.18-1.50] vs. 1.13 [1.02-1.25]), respectively, P for interaction= 0.017). DISCUSSION/CONCLUSIONS:Local social vulnerability and residential segregation are associated with inappropriate IPN follow up and may inform policy or interventions tailored for neighborhoods.
PMID: 37473854
ISSN: 1558-349x
CID: 5536032
Utility of self-report antiretroviral adherence for predicting HIV viral load among persons who inject drugs in Hai Phong Vietnam: assessing differences by methamphetamine use
Feelemyer, Jonathan; Des Jarlais, Don C; Nagot, Nicolas; Huong, Duong Thi; Oanh, Khuat Thi Hai; Khue, Pham Minh; Thi Giang, Hoang; Tuyet Thanh, Nham Thi; Cleland, Charles M; Arasteh, Kamyar; Caniglia, Ellen; Chen, Yu; Bart, Gavin; Moles, Jean Pierre; Vinh, Vu Hai; Vallo, Roselyne; Quillet, Catherine; Rapoud, Delphine; Le, Sao M; Michel, Laurent; Laureillard, Didier; Khan, Maria R
PMID: 37909053
ISSN: 1360-0451
CID: 5614452
Long-Term Exposure to Walkable Residential Neighborhoods and Risk of Obesity-Related Cancer in the New York University Women's Health Study (NYUWHS)
India-Aldana, Sandra; Rundle, Andrew G; Quinn, James W; Clendenen, Tess V; Afanasyeva, Yelena; Koenig, Karen L; Liu, Mengling; Neckerman, Kathryn M; Thorpe, Lorna E; Zeleniuch-Jacquotte, Anne; Chen, Yu
BACKGROUND:Living in neighborhoods with higher levels of walkability has been associated with a reduced risk of obesity and higher levels of physical activity. Obesity has been linked to increased risk of 13 cancers in women. However, long-term prospective studies of neighborhood walkability and risk for obesity-related cancer are scarce. OBJECTIVES:We evaluated the association between long-term average neighborhood walkability and obesity-related cancer risk in women. METHODS:The New York University Women's Health Study (NYUWHS) is a prospective cohort with 14,274 women recruited between 1985 and 1991 in New York City and followed over nearly three decades. We geocoded residential addresses for each participant throughout follow-up and calculated an average annual measure of neighborhood walkability across years of follow-up using data on population density and accessibility to destinations associated with geocoded residential addresses. We used ICD-9 codes to characterize first primary obesity-related cancers and employed Cox proportional hazards models to assess the association between average neighborhood walkability and risk of overall and site-specific obesity-related cancers. RESULTS: DISCUSSION:Our study highlights a potential protective role of neighborhood walkability in preventing obesity-related cancers in women. https://doi.org/10.1289/EHP11538.
PMID: 37791759
ISSN: 1552-9924
CID: 5635402
Risk of post-acute sequelae of SARS-CoV-2 infection associated with pre-coronavirus disease obstructive sleep apnea diagnoses: an electronic health record-based analysis from the RECOVER initiative
Mandel, Hannah L; Colleen, Gunnar; Abedian, Sajjad; Ammar, Nariman; Bailey, L Charles; Bennett, Tellen D; Brannock, M Daniel; Brosnahan, Shari B; Chen, Yu; Chute, Christopher G; Divers, Jasmin; Evans, Michael D; Haendel, Melissa; Hall, Margaret A; Hirabayashi, Kathryn; Hornig, Mady; Katz, Stuart D; Krieger, Ana C; Loomba, Johanna; Lorman, Vitaly; Mazzotti, Diego R; McMurry, Julie; Moffitt, Richard A; Pajor, Nathan M; Pfaff, Emily; Radwell, Jeff; Razzaghi, Hanieh; Redline, Susan; Seibert, Elle; Sekar, Anisha; Sharma, Suchetha; Thaweethai, Tanayott; Weiner, Mark G; Yoo, Yun Jae; Zhou, Andrea; Thorpe, Lorna E
STUDY OBJECTIVES/OBJECTIVE:Obstructive sleep apnea (OSA) has been associated with more severe acute coronavirus disease-2019 (COVID-19) outcomes. We assessed OSA as a potential risk factor for Post-Acute Sequelae of SARS-CoV-2 (PASC). METHODS:We assessed the impact of preexisting OSA on the risk for probable PASC in adults and children using electronic health record data from multiple research networks. Three research networks within the REsearching COVID to Enhance Recovery initiative (PCORnet Adult, PCORnet Pediatric, and the National COVID Cohort Collaborative [N3C]) employed a harmonized analytic approach to examine the risk of probable PASC in COVID-19-positive patients with and without a diagnosis of OSA prior to pandemic onset. Unadjusted odds ratios (ORs) were calculated as well as ORs adjusted for age group, sex, race/ethnicity, hospitalization status, obesity, and preexisting comorbidities. RESULTS:Across networks, the unadjusted OR for probable PASC associated with a preexisting OSA diagnosis in adults and children ranged from 1.41 to 3.93. Adjusted analyses found an attenuated association that remained significant among adults only. Multiple sensitivity analyses with expanded inclusion criteria and covariates yielded results consistent with the primary analysis. CONCLUSIONS:Adults with preexisting OSA were found to have significantly elevated odds of probable PASC. This finding was consistent across data sources, approaches for identifying COVID-19-positive patients, and definitions of PASC. Patients with OSA may be at elevated risk for PASC after SARS-CoV-2 infection and should be monitored for post-acute sequelae.
PMID: 37166330
ISSN: 1550-9109
CID: 5509392
Change-plane analysis for subgroup detection with a continuous treatment
Jin, Peng; Lu, Wenbin; Chen, Yu; Liu, Mengling
Detecting and characterizing subgroups with differential effects of a binary treatment has been widely studied and led to improvements in patient outcomes and population risk management. Under the setting of a continuous treatment, however, such investigations remain scarce. We propose a semiparametric change-plane model and consequently a doubly robust test statistic for assessing the existence of two subgroups with differential treatment effects under a continuous treatment. The proposed testing procedure is valid when either the baseline function for the covariate effects or the generalized propensity score function for the continuous treatment is correctly specified. The asymptotic distributions of the test statistic under the null and local alternative hypotheses are established. When the null hypothesis of no subgroup is rejected, the change-plane parameters that define the subgroups can be estimated. This paper provides a unified framework of the change-plane method to handle various types of outcomes, including the exponential family of distributions and time-to-event outcomes. Additional extensions with nonparametric estimation approaches are also provided. We evaluate the performance of our proposed methods through extensive simulation studies under various scenarios. An application to the Health Effects of Arsenic Longitudinal Study with a continuous environmental exposure of arsenic is presented. This article is protected by copyright. All rights reserved.
PMID: 36134534
ISSN: 1541-0420
CID: 5335512
Alcohol intake and endogenous sex hormones in women: meta-analysis of cohort studies and Mendelian randomization
Tin, Sandar Tin; Smith-Byrne, Karl; Ferrari, Pietro; Rinaldi, Sabina; McCullough, Marjorie L; Teras, Lauren R; Manjer, Jonas; Giles, Graham; Marchand, Loïc Le; Haiman, Christopher A; Wilkens, Lynne R; Chen, Yu; Hankinson, Sue; Tworoger, Shelley; Eliassen, A Heather; Willett, Walter C; Ziegler, Regina G; Fuhrman, Barbara J; Sieri, Sabina; Agnoli, Claudia; Cauley, Jane; Menon, Usha; Fourkala, Evangelia Ounia; Rohan, Thomas E; Kaaks, Rudolf; Reeves, Gillian K; Key, Timothy J
BACKGROUND/UNASSIGNED:The mechanisms underlying alcohol-induced breast carcinogenesis are not fully understood but may involve hormonal changes. METHODS/UNASSIGNED:(Alcohol Dehydrogenase 1B) variant (rs1229984). RESULTS/UNASSIGNED:between alcohol intake and higher free testosterone and lower SHBG (PP4: 0.81 and 0.97 respectively). CONCLUSIONS/UNASSIGNED:Alcohol intake was associated with small increases in sex hormone concentrations, including bioavailable fractions, which may contribute to its effect on breast cancer risk.
PMID: 37645769
ISSN: 2693-5015
CID: 5738242
Chronotype and sleep duration interact to influence time to pregnancy: Results from a New York City cohort
Charifson, Mia; Ghassabian, Akhgar; Seok, Eunsil; Naidu, Mrudula; Mehta-Lee, Shilpi S; Brubaker, Sara G; Afanasyeva, Yelena; Chen, Yu; Liu, Mengling; Trasande, Leonardo; Kahn, Linda G
STUDY OBJECTIVE:To study associations between nighttime sleep characteristics and time to pregnancy. METHODS:Pregnant people age ≥18 years and<18 weeks' gestation were recruited from 3 New York University Grossman School of Medicine affiliated hospitals in Manhattan and Brooklyn (n = 1428) and enrolled into the New York University Children's Health and Environment Study. Participants in the first trimester of pregnancy were asked to recall their time to pregnancy and their sleep characteristics in the 3 months before conception. RESULTS:Participants who reported sleeping<7 hours per night tended to have shorter time to pregnancy than those who slept 7-9 hours per night (adjusted fecundability odds ratio = 1.16, 95% confidence interval: 0.94, 1.41). Participants with a sleep midpoint of 4 AM or later tended to have longer time to pregnancy compared with those with earlier sleep midpoints (before 4 AM) (adjusted fecundability odds ratio = 0.88, 95% confidence interval: 0.74, 1.04). When stratified by sleep midpoint, sleeping<7 hours was significantly associated with shorter time to pregnancy only among those whose sleep midpoint was before 4 AM (adjusted fecundability odds ratio = 1.33, 95% confidence interval: 1.07, 1.67). CONCLUSIONS:The association of sleep duration with time to pregnancy was modified by chronotype, suggesting that both biological and behavioral aspects of sleep may influence fecundability.
PMCID:10514230
PMID: 37055302
ISSN: 2352-7226
CID: 5606752
Endogenous sex steroid hormones and risk of liver cancer among US men: Results from the Liver Cancer Pooling Project
Wu, Zeni; Petrick, Jessica L; Florio, Andrea A; Guillemette, Chantal; Beane Freeman, Laura E; Buring, Julie E; Bradwin, Gary; Caron, Patrick; Chen, Yu; Eliassen, A Heather; Engel, Lawrence S; Freedman, Neal D; Gaziano, J Michael; Giovannuci, Edward L; Hofmann, Jonathan N; Huang, Wen-Yi; Kirsh, Victoria A; Kitahara, Cari M; Koshiol, Jill; Lee, I-Min; Liao, Linda M; Newton, Christina C; Palmer, Julie R; Purdue, Mark P; Rohan, Thomas E; Rosenberg, Lynn; Sesso, Howard D; Sinha, Rashmi; Stampfer, Meir J; Um, Caroline Y; Van Den Eeden, Stephen K; Visvanathan, Kala; Wactawski-Wende, Jean; Zeleniuch-Jacquotte, Anne; Zhang, Xuehong; Graubard, Barry I; Campbell, Peter T; McGlynn, Katherine A
BACKGROUND & AIMS/UNASSIGNED:Incidence rates of liver cancer in most populations are two to three times higher among men than women. The higher rates among men have led to the suggestion that androgens are related to increased risk whereas oestrogens are related to decreased risk. This hypothesis was investigated in the present study via a nested case-control analysis of pre-diagnostic sex steroid hormone levels among men in five US cohorts. METHODS/UNASSIGNED:Concentrations of sex steroid hormones and sex hormone-binding globulin were quantitated using gas chromatography-mass spectrometry and a competitive electrochemiluminescence immunoassay, respectively. Multivariable conditional logistic regression was used to calculate odds ratios (ORs) and 95% CIs for associations between hormones and liver cancer among 275 men who subsequently developed liver cancer and 768 comparison men. RESULTS/UNASSIGNED: = 1.77, 95% CI = 1.38-2.29), dihydrotestosterone (OR = 1.76, 95% CI = 1.21-2.57), oestrone (OR = 1.74, 95% CI = 1.08-2.79), total oestradiol (OR = 1.58, 95% CI=1.22-20.05), and sex hormone-binding globulin (OR = 1.63, 95% CI = 1.27-2.11) were associated with increased risk. Higher concentrations of dehydroepiandrosterone (DHEA), however, were associated with a 53% decreased risk (OR = 0.47, 95% CI = 0.33-0.68). CONCLUSIONS/UNASSIGNED:Higher concentrations of both androgens (testosterone, dihydrotestosterone) and their aromatised oestrogenic metabolites (oestrone, oestradiol) were observed among men who subsequently developed liver cancer compared with men who did not. As DHEA is an adrenal precursor of both androgens and oestrogens, these results may suggest that a lower capacity to convert DHEA to androgens, and their subsequent conversion to oestrogens, confers a lower risk of liver cancer, whereas a greater capacity to convert DHEA confers a greater risk. IMPACT AND IMPLICATIONS/UNASSIGNED:This study does not fully support the current hormone hypothesis as both androgen and oestrogen levels were associated with increased risk of liver cancer among men. The study also found that higher DHEA levels were associated with lower risk, thus suggesting the hypothesis that greater capacity to convert DHEA could be associated with increased liver cancer risk among men.
PMCID:10326694
PMID: 37425211
ISSN: 2589-5559
CID: 5537372