کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5630338 1580368 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Multiple sclerosis risk pathways differ in Caucasian and Chinese populations
ترجمه فارسی عنوان
مسیرهای ریسک ابتلا به مولتیپل اسکلروزیس در جمعیت قفقازی و چینی متفاوت است
کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


- We investigated potential up- and downregulation of 42 MS genes in 10 MS risk pathways.
- 31 differentially expressed genes in Chinese MS patients compared to healthy control subjects were identified.
- The expression patterns of 28 of these genes were consistent with those obtained from Caucasian MS patients.

Large-scale genome-wide association study (GWAS) datasets provide strong support for investigations of the mechanisms underlying multiple sclerosis (MS) by using pathway analysis methods. In our recent study, we conducted a three-stage pathway analysis of GWAS and expression datasets. After identifying 15 shared MS pathways in separate MS GWAS datasets, we found that dysregulated MS genes were significantly enriched in 10 of the 15 MS risk pathways. Evidence showed that 17%-30% of genes are differentially expressed among individual ethnic populations. We then verified the potential disruption of genes in the 10 MS risk pathways cited above in Chinese MS patients. Here, we investigated potential up- and down-regulation of 42 MS genes in these 10 MS risk pathways using 132 Chinese MS patients and 76 healthy control subjects. We then identified 31 differentially expressed genes in Chinese MS patients compared to healthy control subjects. Moreover, the expression patterns of 28 of these genes were consistent with those obtained from Caucasian (European and American) MS patients, although 14 genes differed from the latter group's. Our results provide clinically useful clues about the link between these risk genes and MS susceptibility in the Chinese population.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Neuroimmunology - Volume 307, 15 June 2017, Pages 63-68
نویسندگان
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