4.2 Article

Altered serum pro-inflammatory cytokines in children with Down's syndrome

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EUROPEAN CYTOKINE NETWORK
卷 23, 期 2, 页码 64-67

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JOHN LIBBEY EUROTEXT LTD
DOI: 10.1684/ecn.2012.0307

关键词

Down's syndrome; pro-inflammatory cytokines; TNF-alpha; IFN-gamma

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  1. Tehran University of Medical Sciences, Tehran, Iran

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There are reports showing that pro-inflammatory cytokines are dysregulated in patients with Down's syndrome (DS). However, most of these reports concern adults. We analyzed cytokine levels in serum samples from children with DS, and compared them with samples from intellectually disabled (ID), and healthy, control children. Blood samples were collected from 24 DS, 24 age-/sex-matched ID, and 24 age-/sex-matched healthy, control children. Serum levels of the cytokines IL-5, IL-10, IL-13, IFN-gamma, and TNF-alpha were measured using a sandwich ELISA method,. The age range of the children was 1-15 years, with a mean +/- SD of 5.75 +/- 4.36 years. TNF-alpha levels were significantly higher in the DS and ID groups compared with those found in healthy, control children (P<0.05). The DS and ID groups had significantly higher IFN-gamma levels compared with healthy, control children (P = 0.0002 and P<0.01, respectively), with significant higher levels in the DS than the ID group (P<0.05). Serum from the ID group showed significantly higher IL-10 levels compared with those from the DS group (P<0.05), but not the healthy, control group. Significant correlations were found between the differences in TNF-alpha and IFN-gamma levels, in both ID (rs = 0.558; P = 0.005) and DS children (rs = 0.405; P<0.05). There were no significant differences found in serum levels of IL-13 between the groups, and IL-5 was not detectable in any of the serum samples. Levels of TNF-alpha and IFN-gamma were increased, and IL-10 decreased in serum from children with DS. It may be that these differences contribute to the clinical symptoms seen in DS: consequently, these pro-inflammatory cytokines might be useful as early biomarkers of the disorders associated with DS.

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