نمایش پرونده ساده آیتم

dc.contributor.authorDehghan, P
dc.contributor.authorGargari, BP
dc.contributor.authorJafar-Abadi, MA
dc.contributor.authorAliasgharzadeh, A
dc.date.accessioned2018-08-26T07:56:30Z
dc.date.available2018-08-26T07:56:30Z
dc.date.issued2014
dc.identifier10.3109/09637486.2013.836738
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/48823
dc.description.abstractThere is limited evidence on the effects of prebiotics on inflammation. Therefore, the aim of this study was to evaluate the effects of inulin supplementation on inflammatory indices and metabolic endotoxemia in patients with type 2 diabetes mellitus. The participants included diabetic females (n = 49). They were divided into an intervention group (n = 24) as well as a control group (n = 25) and received 10 g/d inulin or maltodextrin for 8 weeks, respectively. Fasting blood sugar (FBS), HbA1c, insulin, high-sensitive C-reactive protein (hs-CRP), tumor necrosis factor-alpha (TNF-alpha), interleukin-10 (IL-10), and plasma lipopolysaccharide (LPS) were measured pre and post intervention. Inulin-supplemented patients exhibited a significant decrease in FBS (8.5%), HbA1c (10.4%), fasting insulin (34.3%), homeostasis model assessment of insulin resistance (HOMA-IR) (39.5%), hs-CRP (35.6%), TNF-alpha (23.1%), and LPS (27.9%) compared with the maltodextrin group (p<0.05). Increase in IL-10 was not significant in inulin compared with the maltodextrin group. It can be concluded that inulin supplementation seems to be able to modulate inflammation and metabolic endotoxemia in women with type 2 diabetes.
dc.language.isoEnglish
dc.relation.ispartofINTERNATIONAL JOURNAL OF FOOD SCIENCES AND NUTRITION
dc.subjectCytokines
dc.subjectlipopolysaccharide
dc.subjectprebiotics
dc.titleInulin controls inflammation and metabolic endotoxemia in women with type 2 diabetes mellitus: a randomized-controlled clinical trial
dc.typeArticle
dc.citation.volume65
dc.citation.issue1
dc.citation.spage117
dc.citation.epage123
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.3109/09637486.2013.836738


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم