Is obesity genetic disease?

dc.contributor.authorDuran, Tugce
dc.contributor.authorZainalbden, Hasanain Akram
dc.contributor.authorKocak, Nadir
dc.date.accessioned2020-03-26T19:32:31Z
dc.date.available2020-03-26T19:32:31Z
dc.date.issued2017
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractObesity is a complex disease that has unfavorable impacts for all ethnic populations in worldwide. Genetics, environment and lifestyle are among aetiological factors of this disease. Genetic contribution associated with this disease is generally classified into 2 types: monogenic syndromes that display severe obesity, and the polygenic model of common obesity. Single-gene mutations can cause severe obesity resulting from alteration in central and peripheral appetite control mechanisms. Candidate gene and genome-wide association studies have led to the identification of nine loci associated with Mendelian forms of obesity and 58 loci contributing to polygenic obesity. These loci explain a small fraction of the heritability for obesity and many genes remain to be identified. The interaction of several polymorphisms and epigenetic modifications open a new research field for common obesity. As a result, still remains to be a mystery.en_US
dc.identifier.doi10.5455/jtomc.2017.03.032en_US
dc.identifier.endpage534en_US
dc.identifier.issn1300-1744en_US
dc.identifier.issue4en_US
dc.identifier.startpage531en_US
dc.identifier.urihttps://dx.doi.org/10.5455/jtomc.2017.03.032
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TWpnME9EUXhNUT09
dc.identifier.urihttps://hdl.handle.net/20.500.12395/34480
dc.identifier.volume24en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofİnönü Üniversitesi Turgut Özal Tıp Merkezi Dergisien_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectGenel ve Dahili Tıpen_US
dc.titleIs obesity genetic disease?en_US
dc.typeOtheren_US

Dosyalar