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231225s2020 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2020.108612
|2 doi
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|a pubmed24n1054.xml
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|a (DE-627)NLM316392863
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|a (NLM)33069854
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|a (PII)S1521-6616(20)30772-5
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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| 100 |
1 |
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|a Zhang, Bo
|e verfasserin
|4 aut
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| 245 |
1 |
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|a A simple and highly efficient method of IFI44L methylation detection for the diagnosis of systemic lupus erythematosus
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|c 2020
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 14.05.2021
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|a Date Revised 14.05.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2020 Elsevier Inc. All rights reserved.
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|a Systemic lupus erythematosus (SLE) is a complex heterogenous autoimmune disease that can be challenging to diagnose. We previously identified the IFN-induced protein 44-like (IFI44L) methylation marker for SLE diagnosis, which can be detected by pyrosequencing. Although the previous technique has high sensitivity and specificity, it requires special equipment and high cost for detection. Here, we established a high-resolution melting-quantitative polymerase chain reaction (HRM-qPCR) assay to detect the methylation of IFI44L promoter for the diagnosis of SLE. The result was determined according to the standard melting curve of the methylation level of the IFI44L promoter region. The sensitivity was 88.571% and the specificity was 97.087%. The HRM-qPCR and pyrosequencing results presented good consistency when both methods were used to detect the methylation of the IFI44L promoter for SLE diagnosis. Furthermore, the HRM-qPCR method can be used to distinguish SLE from other autoimmune diseases, infectious diseases and virus-related cancers
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4 |
|a Journal Article
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|a Research Support, Non-U.S. Gov't
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4 |
|a Biomarker
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| 650 |
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4 |
|a DNA methylation
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| 650 |
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4 |
|a HRM-qPCR
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| 650 |
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4 |
|a IFI44L
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| 650 |
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4 |
|a SLE
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| 650 |
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7 |
|a IFI44L protein, human
|2 NLM
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| 650 |
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|a Tumor Suppressor Proteins
|2 NLM
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| 700 |
1 |
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|a Liu, Limin
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Zhou, Tian
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Shi, Xiaoli
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Wu, Haijing
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Xiang, Zhongyuan
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Zhao, Ming
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Lu, Qianjin
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 221(2020) vom: 01. Dez., Seite 108612
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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| 773 |
1 |
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|g volume:221
|g year:2020
|g day:01
|g month:12
|g pages:108612
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| 856 |
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|u http://dx.doi.org/10.1016/j.clim.2020.108612
|3 Volltext
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