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| DOI | 10.1080/15592294.2017.1414127 | ||||
| Año | 2018 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Epigenetic age is an indicator of biological aging, capturing the impact of environmental and behavioral influences across time on cellular function. Deviance between epigenetic age and chronological age (AgeAccel) is a predictor of health. Pubertal timing has similarly been associated with cancer risk and mortality rate among females. We examined the association between AgeAccel and pubertal timing and adolescent breast composition in the longitudinal Growth and Obesity Cohort Study. AgeAccel was estimated in whole blood using the Horvath method at breast Tanner 2 (B2) and 4 (B4). Total breast volume, absolute fibro-glandular volume (FGV), and %FGV were evaluated at B4 using dual X-ray absorptiometry. The impact of AgeAccel (mean: 0; SD: 3.78) across puberty on the time to breast development (thelarche), menarche, and pubertal tempo (thelarche to menarche) was estimated using accelerated failure time models; generalized estimating equations were used to evaluate associations with breast density. A five-year increase in average adolescent AgeAccel was associated with a significant decrease in time to menarche [hazard ratio (HR): 1.37; 95% confidence interval (CI): 1.04, 1.80] adjusting for birth weight, maternal pre-pregnancy body mass index, maternal height, maternal education, B2 height, fat percentage, and cell composition. AgeAccel displayed a stronger inverse association with pubertal tempo (HR: 1.48; 95% CI: 1.10, 1.99). A five-year increase in AgeAccel was associated with 5% greater %FGV, adjusting for B4 percent body fat, and maternal traits (95% CI: 1.01, 1.10). Our study provides unique insight into the influence of AgeAccel on pubertal development in girls, which may have implications for adult health.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Binder, Alexandra M. | Mujer |
UNIV CALIF LOS ANGELES - Estados Unidos
UCLA Fielding School of Public Health - Estados Unidos |
| 2 | Corvalan, Camila | Mujer |
Universidad de Chile - Chile
|
| 3 | MERICQ-GUILA, MARIA VERONICA | Mujer |
Universidad de Chile - Chile
|
| 4 | PEREIRA-SCALABRINO, ANA INES | Mujer |
Universidad de Chile - Chile
|
| 5 | SANTOS-GOMEZ, JOSE LUIS | Mujer |
Pontificia Universidad Católica de Chile - Chile
|
| 6 | Horvath, Steve | Hombre |
UNIV CALIF LOS ANGELES - Estados Unidos
David Geffen School of Medicine at UCLA - Estados Unidos |
| 7 | Shepherd, John A. | Hombre |
UNIV CALIF LOS ANGELES - Estados Unidos
University of California, San Francisco - Estados Unidos |
| 8 | Michels, Karin B. | Mujer |
UNIV CALIF LOS ANGELES - Estados Unidos
UCLA Fielding School of Public Health - Estados Unidos |
| Fuente |
|---|
| National Institutes of Health |
| National Institute of Environmental Health Sciences |
| National Cancer Institute |
| U.S. Department of Health and Human Services |
| NCI NIH HHS |
| U.S. Public Health Service |
| US Department of Health and Human Services |
| NIEHS NIH HHS |
| Department of Health and Human Services |
| Public Health Service |
| BCERP |
| Breast Cancer |
| Agradecimiento |
|---|
| This work was supported by Public Health Service grant R01CA158313 from the National Cancer Institute, National Institutes of Health, US Department of Health and Human Services (to KBM), and by the Breast Cancer and the Environment Research Program (BCERP) award grant U01ES026130 from the National Institute of Environmental Health Sciences and the National Cancer Institute, National Institutes of Health, Department of Health and Human Services (to KBM). |