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1.
Nat Metab ; 3(9): 1217-1227, 2021 09.
Artículo en Inglés | MEDLINE | ID: mdl-34552269

RESUMEN

How lifespan and body weight vary as a function of diet and genetic differences is not well understood. Here we quantify the impact of differences in diet on lifespan in a genetically diverse family of female mice, split into matched isogenic cohorts fed a low-fat chow diet (CD, n = 663) or a high-fat diet (HFD, n = 685). We further generate key metabolic data in a parallel cohort euthanized at four time points. HFD feeding shortens lifespan by 12%: equivalent to a decade in humans. Initial body weight and early weight gains account for longevity differences of roughly 4-6 days per gram. At 500 days, animals on a HFD typically gain four times as much weight as control, but variation in weight gain does not correlate with lifespan. Classic serum metabolites, often regarded as health biomarkers, are not necessarily strong predictors of longevity. Our data indicate that responses to a HFD are substantially modulated by gene-by-environment interactions, highlighting the importance of genetic variation in making accurate individualized dietary recommendations.


Asunto(s)
Interacción Gen-Ambiente , Longevidad , Aumento de Peso , Animales , Peso Corporal , Estudios de Cohortes , Dieta Alta en Grasa , Ratones , Ratones Endogámicos C57BL
2.
Cell Syst ; 12(3): 235-247.e9, 2021 03 17.
Artículo en Inglés | MEDLINE | ID: mdl-33472028

RESUMEN

The challenge of precision medicine is to model complex interactions among DNA variants, phenotypes, development, environments, and treatments. We address this challenge by expanding the BXD family of mice to 140 fully isogenic strains, creating a uniquely powerful model for precision medicine. This family segregates for 6 million common DNA variants-a level that exceeds many human populations. Because each member can be replicated, heritable traits can be mapped with high power and precision. Current BXD phenomes are unsurpassed in coverage and include much omics data and thousands of quantitative traits. BXDs can be extended by a single-generation cross to as many as 19,460 isogenic F1 progeny, and this extended BXD family is an effective platform for testing causal modeling and for predictive validation. BXDs are a unique core resource for the field of experimental precision medicine.


Asunto(s)
Medicina de Precisión , Animales , Modelos Animales de Enfermedad , Ratones
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