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dc.creatorSzarc vel Szic, Katarzyna
dc.creatorDeclerck, Ken
dc.creatorVidaković, Melita
dc.creatorVanden Berghe, Wim
dc.date.accessioned2023-11-13T13:59:18Z
dc.date.available2023-11-13T13:59:18Z
dc.date.issued2015
dc.identifier.issn1868-7075
dc.identifier.urihttp://radar.ibiss.bg.ac.rs/handle/123456789/6316
dc.description.abstractThe progressively older population in developed countries is reflected in an increase in the number of people suffering from age-related chronic inflammatory diseases such as metabolic syndrome, diabetes, heart and lung diseases, cancer, osteoporosis, arthritis, and dementia. The heterogeneity in biological aging, chronological age, and aging-associated disorders in humans have been ascribed to different genetic and environmental factors (i.e., diet, pollution, stress) that are closely linked to socioeconomic factors. The common denominator of these factors is the inflammatory response. Chronic low-grade systemic inflammation during physiological aging and immunosenescence are intertwined in the pathogenesis of premature aging also defined as 'inflammaging.' The latter has been associated with frailty, morbidity, and mortality in elderly subjects. However, it is unknown to what extent inflammaging or longevity is controlled by epigenetic events in early life. Today, human diet is believed to have a major influence on both the development and prevention of age-related diseases. Most plant-derived dietary phytochemicals and macro- and micronutrients modulate oxidative stress and inflammatory signaling and regulate metabolic pathways and bioenergetics that can be translated into stable epigenetic patterns of gene expression. Therefore, diet interventions designed for healthy aging have become a hot topic in nutritional epigenomic research. Increasing evidence has revealed that complex interactions between food components and histone modifications, DNA methylation, non-coding RNA expression, and chromatin remodeling factors influence the inflammaging phenotype and as such may protect or predispose an individual to many age-related diseases. Remarkably, humans present a broad range of responses to similar dietary challenges due to both genetic and epigenetic modulations of the expression of target proteins and key genes involved in the metabolism and distribution of the dietary constituents. Here, we will summarize the epigenetic actions of dietary components, including phytochemicals, and macro- and micronutrients as well as metabolites, that can attenuate inflammaging. We will discuss the challenges facing personalized nutrition to translate highly variable interindividual epigenetic diet responses to potential individual health benefits/risks related to aging disease.sr
dc.language.isoensr
dc.publisherLondon: BMCsr
dc.relationCOST Epigenetics from bench to bedside, TD0905sr
dc.relationCOST Epigenetic Chemical Biology CM1406sr
dc.relationCOST Interindividual variation in response to consumption of plant food bioactives, FA1403sr
dc.relationbilateral project ‘Pavle Savić’ (451-03-3455/2013-09/12/02)sr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173020/RS//sr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceClinical Epigeneticssr
dc.subjectAgingsr
dc.subjectEpigeneticssr
dc.subjectInflammationsr
dc.subjectMetabolismsr
dc.subjectOxidative stresssr
dc.subjectPersonalized nutritionsr
dc.subjectPhytochemicalssr
dc.titleFrom inflammaging to healthy aging by dietary lifestyle choices: is epigenetics the key to personalized nutrition?sr
dc.typearticlesr
dc.rights.licenseBYsr
dc.rights.holder© 2015, vel Szic et al.; licensee BioMed Centralsr
dc.citation.volume7
dc.identifier.doi10.1186/s13148-015-0068-2
dc.identifier.pmid25861393
dc.identifier.scopus2-s2.0-84983059084
dc.identifier.wos000352257400001
dc.citation.spage33
dc.type.versionpublishedVersionsr
dc.identifier.fulltexthttps://radar.ibiss.bg.ac.rs/bitstream/id/15536/bitstream_15536.pdf
dc.citation.rankM21


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