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AuthorAlser, Maha
AuthorNaja, Khaled
AuthorElrayess, Mohamed A.
Available date2024-05-27T03:10:13Z
Publication Date2024
Publication NameFrontiers in Nutrition
ResourceScopus
Identifierhttp://dx.doi.org/10.3389/fnut.2024.1368966
ISSN2296861X
URIhttp://hdl.handle.net/10576/55452
AbstractObesity is a major health problem that affects millions of individuals, and it is associated with metabolic diseases including insulin resistance (IR), type 2 diabetes (T2D), and cardiovascular diseases (CVDs). However, Body fat distribution (BFD) rather than crude obesity is now considered as a more accurate factor associated with these diseases. The factors affecting BFD vary, from genetic background, epigenetic factors, ethnicity, aging, hormonal changes, to lifestyle and medication consumptions. The main goal of controlling BFD comes from the fact that fat accumulation in different depots has a different effect on the overall health and metabolic health of individuals. It is well established that fat storage in the abdominal visceral depot is associated with metabolic disorder occurrence, while gluteal-femoral subcutaneous fat depot seems to be protective against these diseases. In this paper, we will summarize the factors affecting fat distribution. Then, we will present evidence connecting gluteal-femoral fat depot with protection against metabolic disorders including IR, T2D, and CVDs. Finally, we will list the suggested mechanisms that lead to this protective effect. The abstract is visualized in Graphical Abstract.
SponsorThe author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Qatar National Research Fund (QNRF) (grant no. NPRP13S-1230-190008).
Languageen
PublisherFrontiers Media SA
Subjectbody fat distribution
cardiovascular diseases
metabolic protection
prediabetes
thigh fat
type 2 diabetes
TitleMechanisms of body fat distribution and gluteal-femoral fat protection against metabolic disorders
TypeArticle Review
Volume Number11
dc.accessType Open Access


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