miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients

Abstract Background Childhood dilated cardiomyopathy (CDCM) is the most common cardiomyopathy in children and it is risk factor to heart failure and sudden death. Most of the different etiologic factors which have been postulated to DCM are idiopathic, and its pathogenesis remains uncertain. So it w...

Full description

Bibliographic Details
Main Authors: Alaaeldin G. Fayez, Nora N. Esmaiel, Sohair M. Salem, Engy A. Ashaat, Sonia A. El-Saiedi, Mona O. El Ruby
Format: Article
Language:English
Published: SpringerOpen 2022-09-01
Series:The Egyptian Heart Journal
Subjects:
Online Access:https://doi.org/10.1186/s43044-022-00300-x
_version_ 1811273673955344384
author Alaaeldin G. Fayez
Nora N. Esmaiel
Sohair M. Salem
Engy A. Ashaat
Sonia A. El-Saiedi
Mona O. El Ruby
author_facet Alaaeldin G. Fayez
Nora N. Esmaiel
Sohair M. Salem
Engy A. Ashaat
Sonia A. El-Saiedi
Mona O. El Ruby
author_sort Alaaeldin G. Fayez
collection DOAJ
description Abstract Background Childhood dilated cardiomyopathy (CDCM) is the most common cardiomyopathy in children and it is risk factor to heart failure and sudden death. Most of the different etiologic factors which have been postulated to DCM are idiopathic, and its pathogenesis remains uncertain. So it was worth investigating the potential DCM pathogenicity models to establish early noninvasive diagnosis parameters especially in CDCM patients. Beside that miRNAs in the circulatory blood are genetically considered the best option for noninvasive diagnosis; also, implementation of miRNAs as early diagnostic markers for children with DCM is urgent because those children have high risk to sudden heart death. We aimed to identify discriminator diagnostic circulatory miRNA expression levels in CDCM patients. Results The expression levels of miR-454-3p and miR-194-5p were found significant upregulated (p value = 0.001 and 0.018; CI 95%, respectively), while miR-875-3p was found significant downregulated (p value = 0.040; CI 95%). A receiver operating characteristic (ROC) curve analysis showed significant AUC = 1.000 and 0.798 for miR-454-3p and miR-194-5p, respectively, and the optimal discriminated diagnostic cut-points were computed by index of union (IU) method. Enrichment analysis for the potential targeted mature mRNAs by miR-454-3p and miR-194-5p pointed that Ca, Na and K ions homeostasis in cardiac sarcolemma consider potential CDCM pathogenicity model. Conclusions miR-454-3p and miR-194-5p are highly influencing noninvasive biomarkers for CDCM, and further circulatory miRNAs-implicated studies are highly recommended.
first_indexed 2024-04-12T23:03:30Z
format Article
id doaj.art-78294392449e440f9e65ee669d4e1b76
institution Directory Open Access Journal
issn 2090-911X
language English
last_indexed 2024-04-12T23:03:30Z
publishDate 2022-09-01
publisher SpringerOpen
record_format Article
series The Egyptian Heart Journal
spelling doaj.art-78294392449e440f9e65ee669d4e1b762022-12-22T03:12:58ZengSpringerOpenThe Egyptian Heart Journal2090-911X2022-09-0174111010.1186/s43044-022-00300-xmiR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patientsAlaaeldin G. Fayez0Nora N. Esmaiel1Sohair M. Salem2Engy A. Ashaat3Sonia A. El-Saiedi4Mona O. El Ruby5Human Genetics and Genome Research Institute, National Research CentreHuman Genetics and Genome Research Institute, National Research CentreHuman Genetics and Genome Research Institute, National Research CentreHuman Genetics and Genome Research Institute, National Research CentreDivision of Pediatric Cardiology, Faculty of Medicine, Cairo UniversityHuman Genetics and Genome Research Institute, National Research CentreAbstract Background Childhood dilated cardiomyopathy (CDCM) is the most common cardiomyopathy in children and it is risk factor to heart failure and sudden death. Most of the different etiologic factors which have been postulated to DCM are idiopathic, and its pathogenesis remains uncertain. So it was worth investigating the potential DCM pathogenicity models to establish early noninvasive diagnosis parameters especially in CDCM patients. Beside that miRNAs in the circulatory blood are genetically considered the best option for noninvasive diagnosis; also, implementation of miRNAs as early diagnostic markers for children with DCM is urgent because those children have high risk to sudden heart death. We aimed to identify discriminator diagnostic circulatory miRNA expression levels in CDCM patients. Results The expression levels of miR-454-3p and miR-194-5p were found significant upregulated (p value = 0.001 and 0.018; CI 95%, respectively), while miR-875-3p was found significant downregulated (p value = 0.040; CI 95%). A receiver operating characteristic (ROC) curve analysis showed significant AUC = 1.000 and 0.798 for miR-454-3p and miR-194-5p, respectively, and the optimal discriminated diagnostic cut-points were computed by index of union (IU) method. Enrichment analysis for the potential targeted mature mRNAs by miR-454-3p and miR-194-5p pointed that Ca, Na and K ions homeostasis in cardiac sarcolemma consider potential CDCM pathogenicity model. Conclusions miR-454-3p and miR-194-5p are highly influencing noninvasive biomarkers for CDCM, and further circulatory miRNAs-implicated studies are highly recommended.https://doi.org/10.1186/s43044-022-00300-xChildhood dilated cardiomyopathyNoninvasive diagnostic biomarkersmiRNAsCardiac sarcolemmaGene ontology analysis
spellingShingle Alaaeldin G. Fayez
Nora N. Esmaiel
Sohair M. Salem
Engy A. Ashaat
Sonia A. El-Saiedi
Mona O. El Ruby
miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
The Egyptian Heart Journal
Childhood dilated cardiomyopathy
Noninvasive diagnostic biomarkers
miRNAs
Cardiac sarcolemma
Gene ontology analysis
title miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
title_full miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
title_fullStr miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
title_full_unstemmed miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
title_short miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
title_sort mir 454 3p and mir 194 5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in egyptian patients
topic Childhood dilated cardiomyopathy
Noninvasive diagnostic biomarkers
miRNAs
Cardiac sarcolemma
Gene ontology analysis
url https://doi.org/10.1186/s43044-022-00300-x
work_keys_str_mv AT alaaeldingfayez mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients
AT noranesmaiel mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients
AT sohairmsalem mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients
AT engyaashaat mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients
AT soniaaelsaiedi mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients
AT monaoelruby mir4543pandmir1945ptargetingcardiacsarcolemmaionexchangetranscriptsarepotentialnoninvasivediagnosticbiomarkersforchildhooddilatedcardiomyopathyinegyptianpatients