Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP

Objective<p>The aim of the study was to establish whether whole-blood microRNA (miRNA) profiles differ between postural tachycardia syndrome (POTS) sufferers and control subjects and to identify the miRNA that regulates plasma H<sub>2</sub>S.</p>Study Design<p>High-thro...

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Main Author: Jing Lin (50818) (author)
Other Authors: Jie Shen (31533) (author), Juan Liu (6492) (author), Wenjie Cheng (519724) (author), Lintian Li (12980726) (author), Fuyong Jiao (3170943) (author)
Published: 2022
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_version_ 1855393479702609920
author Jing Lin (50818)
author2 Jie Shen (31533)
Juan Liu (6492)
Wenjie Cheng (519724)
Lintian Li (12980726)
Fuyong Jiao (3170943)
author2_role author
author
author
author
author
author_facet Jing Lin (50818)
Jie Shen (31533)
Juan Liu (6492)
Wenjie Cheng (519724)
Lintian Li (12980726)
Fuyong Jiao (3170943)
author_role author
dc.creator.none.fl_str_mv Jing Lin (50818)
Jie Shen (31533)
Juan Liu (6492)
Wenjie Cheng (519724)
Lintian Li (12980726)
Fuyong Jiao (3170943)
dc.date.none.fl_str_mv 2022-06-30T13:35:57Z
dc.identifier.none.fl_str_mv 10.3389/fnins.2022.920477.s001
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Data_Sheet_1_Whole-Blood_MicroRNA_Sequence_Profiling_and_Identification_of_Specific_miR-21_for_Adolescents_With_Postural_Tachycardia_Syndrome_ZIP/20199410
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Neuroscience
Biological Engineering
Developmental Biology
Stem Cells
Artificial Intelligence and Image Processing
Endocrinology
Radiology and Organ Imaging
Autonomic Nervous System
Cellular Nervous System
Central Nervous System
Sensory Systems
Clinical Nursing: Tertiary (Rehabilitative)
Decision Making
Rehabilitation Engineering
Biomedical Engineering not elsewhere classified
Signal Processing
Neurogenetics
Image Processing
postural tachycardia syndrome
whole blood
high-throughput sequencing
miR-21
adolescents
dc.title.none.fl_str_mv Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description Objective<p>The aim of the study was to establish whether whole-blood microRNA (miRNA) profiles differ between postural tachycardia syndrome (POTS) sufferers and control subjects and to identify the miRNA that regulates plasma H<sub>2</sub>S.</p>Study Design<p>High-throughput sequencing was used to obtain whole-blood miRNA expression profiles for 20 POTS sufferers and 20 normal children.The thresholds for defining differentially expressed miRNAs (DEmiRNAs) were an adjusted DESeq P of <0.05 and a log2 fold variation of ≥3. The DEmiRNA target genes were identified using RNAhybrid and miRanda, and only those identified by both were considered. The combined effects of the DEmiRNAs were determined using KEGG pathway analysis. Another 40 POTS and 20 normal patients were used as validation subjects. Plasma H<sub>2</sub>S was determined with a sulfide electrode, and flow-mediated vasodilation (FMD) was performed with a color Doppler ultrasound system. miRNAs were analyzed using qRT-PCR.</p>Results<p>Totally, 13 DEmiRNAs were identified through high-throughput sequencing. In the 60-member validation group, the 13 miRNAs were verified again, and it turned out that miR-21 was significantly elevated and could diagnose POTS with a 100% specificity and 92.5% sensitivity. Overall, 198 and 481 genes, respectively, were shown to be targeted by the 13 DEmiRNAs when P values of 0.01 and 0.05 were used. The target gene of hsa-miR-21-5p was SP1 when the P-value is <0.01. DEmiRNAs were significantly enriched in 36 pathways (P < 0.05), in which PI3K/Akt signaling was closely related to vascular function. In the validation subjects, the plasma H<sub>2</sub>S and FMD were higher in the POTS sufferers (P < 0.05).</p>Conclusion<p>Elevated whole-blood miR-21 levels serve as an indicator for POTS and may explain the increased plasma H<sub>2</sub>S observed in POTS sufferers.</p>
eu_rights_str_mv openAccess
id Manara_2d0addb0f4e6dfd0e8e55d7b6c3ddbfe
identifier_str_mv 10.3389/fnins.2022.920477.s001
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/20199410
publishDate 2022
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIPJing Lin (50818)Jie Shen (31533)Juan Liu (6492)Wenjie Cheng (519724)Lintian Li (12980726)Fuyong Jiao (3170943)NeuroscienceBiological EngineeringDevelopmental BiologyStem CellsArtificial Intelligence and Image ProcessingEndocrinologyRadiology and Organ ImagingAutonomic Nervous SystemCellular Nervous SystemCentral Nervous SystemSensory SystemsClinical Nursing: Tertiary (Rehabilitative)Decision MakingRehabilitation EngineeringBiomedical Engineering not elsewhere classifiedSignal ProcessingNeurogeneticsImage Processingpostural tachycardia syndromewhole bloodhigh-throughput sequencingmiR-21adolescentsObjective<p>The aim of the study was to establish whether whole-blood microRNA (miRNA) profiles differ between postural tachycardia syndrome (POTS) sufferers and control subjects and to identify the miRNA that regulates plasma H<sub>2</sub>S.</p>Study Design<p>High-throughput sequencing was used to obtain whole-blood miRNA expression profiles for 20 POTS sufferers and 20 normal children.The thresholds for defining differentially expressed miRNAs (DEmiRNAs) were an adjusted DESeq P of <0.05 and a log2 fold variation of ≥3. The DEmiRNA target genes were identified using RNAhybrid and miRanda, and only those identified by both were considered. The combined effects of the DEmiRNAs were determined using KEGG pathway analysis. Another 40 POTS and 20 normal patients were used as validation subjects. Plasma H<sub>2</sub>S was determined with a sulfide electrode, and flow-mediated vasodilation (FMD) was performed with a color Doppler ultrasound system. miRNAs were analyzed using qRT-PCR.</p>Results<p>Totally, 13 DEmiRNAs were identified through high-throughput sequencing. In the 60-member validation group, the 13 miRNAs were verified again, and it turned out that miR-21 was significantly elevated and could diagnose POTS with a 100% specificity and 92.5% sensitivity. Overall, 198 and 481 genes, respectively, were shown to be targeted by the 13 DEmiRNAs when P values of 0.01 and 0.05 were used. The target gene of hsa-miR-21-5p was SP1 when the P-value is <0.01. DEmiRNAs were significantly enriched in 36 pathways (P < 0.05), in which PI3K/Akt signaling was closely related to vascular function. In the validation subjects, the plasma H<sub>2</sub>S and FMD were higher in the POTS sufferers (P < 0.05).</p>Conclusion<p>Elevated whole-blood miR-21 levels serve as an indicator for POTS and may explain the increased plasma H<sub>2</sub>S observed in POTS sufferers.</p>2022-06-30T13:35:57ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fnins.2022.920477.s001https://figshare.com/articles/dataset/Data_Sheet_1_Whole-Blood_MicroRNA_Sequence_Profiling_and_Identification_of_Specific_miR-21_for_Adolescents_With_Postural_Tachycardia_Syndrome_ZIP/20199410CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/201994102022-06-30T13:35:57Z
spellingShingle Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
Jing Lin (50818)
Neuroscience
Biological Engineering
Developmental Biology
Stem Cells
Artificial Intelligence and Image Processing
Endocrinology
Radiology and Organ Imaging
Autonomic Nervous System
Cellular Nervous System
Central Nervous System
Sensory Systems
Clinical Nursing: Tertiary (Rehabilitative)
Decision Making
Rehabilitation Engineering
Biomedical Engineering not elsewhere classified
Signal Processing
Neurogenetics
Image Processing
postural tachycardia syndrome
whole blood
high-throughput sequencing
miR-21
adolescents
status_str publishedVersion
title Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
title_full Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
title_fullStr Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
title_full_unstemmed Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
title_short Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
title_sort Data_Sheet_1_Whole-Blood MicroRNA Sequence Profiling and Identification of Specific miR-21 for Adolescents With Postural Tachycardia Syndrome.ZIP
topic Neuroscience
Biological Engineering
Developmental Biology
Stem Cells
Artificial Intelligence and Image Processing
Endocrinology
Radiology and Organ Imaging
Autonomic Nervous System
Cellular Nervous System
Central Nervous System
Sensory Systems
Clinical Nursing: Tertiary (Rehabilitative)
Decision Making
Rehabilitation Engineering
Biomedical Engineering not elsewhere classified
Signal Processing
Neurogenetics
Image Processing
postural tachycardia syndrome
whole blood
high-throughput sequencing
miR-21
adolescents