224 research outputs found

    Urbanization, processed foods, and eating out in India

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    Urban consumption of processed and fast foods is a challenge to nutrition security. Observed differences in urban versus rural consumption are commonly attributed to higher income levels in urban areas. Yet, there is still no clear understanding of why and how urban dwellers consume differently. Using India as a case study, we analyze expenditures on processed foods and consumption of food away from home (FAFH) of urban, metropolitan, and rural populations using OLS regression models. We show that urban households spend more on processed foods and consume more FAFH than rural households. Most of this difference can be attributed to differing socio-economic and demographic factors, such as higher income, or smaller urban household size. However, even after controlling for these factors, we find differences not only between rural and urban areas but also between different urban areas: households in large metropolitan areas consume more than households in smaller non-metropolitan urban areas. These inter-urban variations suggest that the dichotomy of urban versus rural consumption does not adequately capture the full spectrum of food consumption complexities. Our findings indicate that urbanization is affecting how people consume food beyond shaping their socio-economic and demographic status. We also highlight the need to account for the role of urbanization—beyond an urban-rural dichotomy—when addressing the challenges associated with changing food consumption patterns

    Principles of early human development and germ cell program from conserved model systems

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    Human primordial germ cells (hPGCs), the precursors of sperm and eggs, originate during week 2-3 of early postimplantation development(1). Using in vitro models of hPGC induction(2-4), recent studies suggest striking mechanistic differences in specification of human and mouse PGCs(5). This may partly be due to the divergence in their pluripotency networks, and early postimplantation development(6-8). Since early human embryos are inaccessible for direct studies, we considered alternatives, including porcine embryos that, as in humans, develop as bilaminar embryonic discs. Here we show that porcine PGCs (pPGCs) originate from the posterior pre-primitive streak competent epiblast by sequential upregulation of SOX17 and BLIMP1 in response to WNT and BMP signalling. Together with human and monkey in vitro models simulating peri-gastrulation development, we show conserved principles for epiblast development for competency for PGC fate, followed by initiation of the epigenetic program(9-11), regulated by a balanced SOX17–BLIMP1 gene dosage. Our combinatorial approach using human, porcine and monkey in vivo and in vitro models, provides synthetic insights on early human development
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