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Updated: Jan 16, 2026

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Published on: July 2, 2013
Expression profile of long noncoding RNAs in post-stroke aphasia
Linazi Gu1, Caili Ren2, Mei Qu3
1Department of Rehabilitation Medicine, The First Affiliated Hospital of Xinjiang Medical University, Ürümqi, China.
This study investigated long noncoding RNAs (lncRNAs) in post-stroke aphasia (PSA). LncRNA RP11-227G15.3 was upregulated in PSA patients and showed a preliminary link to oral spelling, suggesting potential biomarker value.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Post-stroke aphasia (PSA) significantly impacts stroke survivors' quality of life.
- The role of long noncoding RNAs (lncRNAs) in PSA pathogenesis is not well understood.
- Identifying biomarkers for PSA is crucial for diagnosis and treatment.
Purpose of the Study:
- To explore lncRNA expression profiles in post-stroke aphasia.
- To identify potential lncRNA biomarkers associated with PSA.
- To investigate the correlation between lncRNA expression and language deficits.
Main Methods:
- High-throughput RNA sequencing (RNA-seq) was used to analyze lncRNA expression profiles.
- Quantitative polymerase chain reaction (qPCR) validated key lncRNA findings.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed.
Main Results:
- 797 differentially expressed lncRNAs were identified between PSA and stroke patients.
- LncRNA RP11-227G15.3 was found to be upregulated in PSA patients.
- A preliminary negative correlation between RP11-227G15.3 and oral spelling scores was observed.
Conclusions:
- LncRNA RP11-227G15.3 is a candidate biomarker for PSA.
- Further validation in larger cohorts is necessary to confirm its clinical utility.
- The preliminary association with oral spelling requires further investigation.
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