Next Article in Journal
Ex Vivo Activation of Red Blood Cell Senescence by Plasma from Sickle-Cell Disease Patients: Correlation between Markers and Adhesion Consequences during Acute Disease Events
Next Article in Special Issue
Osteopontin in Cardiovascular Diseases
Previous Article in Journal
Long-Term Tri-Modal In Vivo Tracking of Engrafted Cartilage-Derived Stem/Progenitor Cells Based on Upconversion Nanoparticles
Previous Article in Special Issue
Circulating Biomarkers Reflecting Destabilization Mechanisms of Coronary Artery Plaques: Are We Looking for the Impossible?
 
 
Article
Peer-Review Record

Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes

Biomolecules 2021, 11(7), 962; https://doi.org/10.3390/biom11070962
by Andrey V. Zhelankin 1,*, Daria A. Stonogina 2, Sergey V. Vasiliev 2, Konstantin A. Babalyan 1, Elena I. Sharova 1, Yurii V. Doludin 3, Dmitry Y. Shchekochikhin 2, Eduard V. Generozov 1 and Anna S. Akselrod 2
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Biomolecules 2021, 11(7), 962; https://doi.org/10.3390/biom11070962
Submission received: 16 April 2021 / Revised: 11 June 2021 / Accepted: 24 June 2021 / Published: 29 June 2021
(This article belongs to the Special Issue Molecular Biomarkers In Cardiology 2021)

Round 1

Reviewer 1 Report

This article shows some methodological and design flaws. 

miRNAs selection is not well justified and is based on several publications mostly older than 10 years old, although great advances in the miRNAs area have been done. More importantly, the patient's design is not based on the current classification of the ESC (references non included). STEMI and non STEMI (includes UA) and most of the patients of these group are hypertensive patients. 

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

Authors selected very carefully the miRNAs to evaluate by qPCR and potentially justify their usage as biomarkers. However, the explanation of the results is a bit complicated, and would recommend to try to reduce and simplify the sections. Also I would recommends authors explain better and divide in columns the different comparisons made in table 3.

The authors very nicely take into account the hemolysis in the samples, plus the selection of the reference miRNA seems very well founded. 

I would also suggest to do a final working model of miRNAs secreted by the platelets / heart / endothelial cells that authors propose as biomarkers to better depict which miRNAs work for every type of CVD.

 

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

This manuscript is a resubmission of an earlier submission. The following is a list of the peer review reports and author responses from that submission.


Back to TopTop