4.1 Article Data Paper

Data of multiple regressions analysis between selected biomarkers related to glutamate excitotoxicity and oxidative stress in Saudi autistic patients

期刊

DATA IN BRIEF
卷 7, 期 -, 页码 111-116

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.dib.2016.02.025

关键词

Autism; Multiple Regression Analysis; Glutamate excitotoxicity; Oxidative stress; Detoxification; Glutathione status

资金

  1. Research Center of the Center for Female Scientific and Medical Colleges in King Saud University

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This work demonstrates data of multiple regression analysis between nine biomarkers related to glutamate excitotoxicity and impaired detoxification as two mechanisms recently recorded as autism phenotypes. The presented data was obtained by measuring a panel of markers in 20 autistic patients aged 3-15 years and 20 age and gender matching healthy controls. Levels of GSH, glutathione status (GSH/GSSG), glutathione reductase (GR), glutathione-s-transferase (GST), thioredoxin (Trx), thioredoxin reductase (TrxR) and peroxidoxins (Prxs I and III), glutamate, glutamine, glutamate/glutamine ratio glutamate dehydrogenase (GDH) in plasma and mercury (Hg) in red blood cells were determined in both groups. In Multiple regression analysis, R-2 values which describe the proportion or percentage of variance in the dependent variable attributed to the variance in the independent variables together were calculated. Moreover, beta coefficients values which show the direction either positive or negative and the contribution of the independent variable relative to the other independent variables in explaining the variation of the dependent variable were determined. A panel of inter-related markers was recorded. This paper contains data related to and supporting research articles currently published entitled Mechanism of nitrogen metabolism-related parameters and enzyme activities in the pathophysiology of autism [1], Novel metabolic biomarkers related to sulfur-dependent detoxification pathways in autistic patients of Saudi Arabia [2], and A key role for an impaired detoxification mechanism in the etiology and severity of autism spectrum disorders [3]. (C) 2016 The Author. Published by Elsevier Inc.

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