Official Title
The Effect of miRNA and Epigenetic Modifications on Prognosis in Covid-19 Infection
Brief Title
Epigenetic Tools as Prognostic Predictors in Covid19
Protocol ID
NCT04411563
Lead Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Brief Summary
The necessity for early detection and hence improving the outcome of treatment of
pneumonia is critical especially SARS-CoV-2 induced cases. This work was designed to
evaluate the potential application of measuring circulating epigenetic markers namely,
miR-744, miR-24, miR-124, miR-155, miR-19a, miR-122, miR-21, miR-223, let-7f, miR-146,
miR-196, miR-136, P13-K, miR-9 expression, and DNA methylation profiling of the ACE2,
TMPRSS2, PARP, HOX1 genes in Coronavirus disease 2019 (COVID-19) due to SARS-CoV-2
with/without pneumonia and severe acute respiratory syndrome (SARS) patients as an
attempt to evaluate the potential benefits of these new circulating, prognostic,
epigenetic markers for Turkish patients.
Detailed Description
The objectives of this observational study are 1) To investigate why COVID-19 infection
causes different biological behavioral patterns in individuals, 2) To determine the role
of epigenetic mechanisms here to detect the difference between individuals, 3)To
determine the effectiveness of this behavior model and mechanisms on clinical treatment
and to ensure that the results obtained are a step for further treatment studies, 4) To
evaluate whether the data obtained in MicroRNA analysis is a predictive marker on
prognosis. Material and methods Study design This is an observational prospective cohort
study. In the power analysis performed with the G * power 3.1 programs related to our
study, the effect size for the lymphocyte percentage and C-reactive protein was found to
be 0.57 (Effective Treatment of Severe COVID-19 Patients with Tocilizumab) (alpha
probability of error = 0.05); in the sample width analysis, taking the power value 0.80,
the total number of patients to be collected was 105 (105/3 = 35 for each group).
Patient's criteria This study was approved by the Clinical Research Ethics Committee
(2011- CREC-40) at Bakırköy Dr.Sadi Konuk Training and Research Hospital and informed
consent will be obtained from all patients according to the rules of the Declaration of
Helsinki. Approval of the local ethical committee number is 2020/143 (2011-CREC-40).
Patients enrolled in this study will be admitted to the Infectious Diseases and Clinical
Microbiology Department and the Intensive Care Department from May 2020 to September
2020. Diagnosis of COVID 19 will be depending upon the presence of specific lesions in
lungs confirmed by computed tomography (CT), and/or laboratory findings according to the
Republic of Turkey Ministry of Health diagnostic criteria.
Inclusion criteria All patients between the ages of 18 and 65 included will suffer from
COVID 19, and specific treatment should not yet be initiated. COVID 19 diagnosis of
patients will be based on full medical history, thorough clinical examination,
radiological imaging, laboratory assessment, and SARS-CoV-2 analysis by RT-PCR.
Exclusion criteria
1. People with chronic lung disease or previous AC surgery
2. People with immune deficiency or cancer patients
3. Patients receiving immunosuppressive therapy for autoimmune disease
4. People with neurological diseases affecting the respiratory muscles, such as
hypotonia.
On the basis of the inclusion and exclusion criteria 105 patients subjects will be
included in this study, divided into three groups; group I (n = 35) patients are mild,
group II (n = 35) patients are moderate, and group III (n = 35) patients are severe and
critical. Mild and moderate cases are usually defined as those without severe pneumonia
or severe acute respiratory syndrome. Mild symptoms are low-grade fever (not more than 38
degrees celsius), dry cough, fatigue, sore throat, headache, the new loss of taste, and
smell. Patients with normal or mild pneumonia findings of radiological imaging and blood
lymphocyte count ≥800 / µl and serum CRP≤40 mg /l, ferritin ≤500ng/ml, D-Dimer ≤1000
ng/ml will be included in group I. Moderate symptoms are fever of about 38,5-39 degrees
celsius, chills, deep cough, fatigue and body aches, muscle pain, the general feeling of
being unwell. Patients with bilateral diffuse pneumonia findings of radiological imaging
or blood lymphocyte count <800 / µl or serum CRP> 40 mg / l or ferritin> 500ng / ml or
D-Dimer> 1000 ng / ml will be included in group II. Severe symptoms are all the common
symptoms mentioned above along with shortness of breath, chest discomfort,
confusion/unresponsiveness, bluish face/lips, possible gastrointestinal issues, like
diarrhea or nausea. Patients with ICU (intensive care unit) admission criteria, such as
confusion or tachycardia (> 125 / min) or respiratory distress or tachypnea (> 22 / min)
or hypotension <90/60 mmHg or SPO2 <93%will be included in group III. Also, patients with
the central nervous system and heart involvement will be directly included in the severe
case group.
Specimen collection and handling About 10 ml of peripheral venous blood will be collected
under strict aseptic conditions by clean venipuncture using vacuum blood collection tubes
and will be distributed as 3 ml in EDTA tubes for complete blood count and DNA
extraction, 3 ml in another sterile special RNA protective tube (stored at -80 °C) for
miRNA extraction. In addition, 4 ml in a plane tube will be allowed to clot at the room
temperature and then will be centrifuged at 3000 rpm for 10 minutes and the collected
serum will be stored at -80°C to be used for analyzing cytokine, and other specific
tests.On the 7th day of treatment, second samples will be taken under the same conditions
and finally, on the 21st day, third samples will be taken.
Laboratory investigations RNA Extraction was done according to the miRNeasy Serum/Plasma
Advanced Kit (cat. no. 217204) https:// www.qiagen.com/
The expressions of selected miRNAs and genes were analyzed using Real-Time PCR. The list
of required kits, chemicals and consumables is as follows:
miRCURY LNA RT Kit (Cat No: 339340) miRCURY LNA miRNA PCR Assay (200) (Cat No: 339306)
miRCURY LNA SYBR Green PCR Kit (600) (Cat No: 339346) miRCURY LNA SYBR Green PCR Kit
(200) (Cat No: 339345) PAXgene Blood miRNA Kit (50) (Cat No: 763134) miRNeasy
Serum/Plasma Kit (50) (Cat No: 217184) PCR Tubes 0.2 ml (1000) (Cat No: 981005) TF/10UL
FILTER TIPS FOR P-10,RAC (Cat No: TF-10-R-S) TF/100UL FILTER TIPS FOR (Cat No:
TF-100-R-S) TF /1000UL UNIVERSAL FILTER TIPS (Cat No: TF-1000-R-S)
Kit and consumables required for DNA methylation analysis:
ZymoResearch EZ DNA Methylation-Gold™ Kit 200 Preps (Cat no: D5006) ZymoResearch Human
Methylated & Non-methylated DNA Set (DNA w/ primers) 1 set (Cat no: D5014) ZymoResearch
ZymoTaq qPCR Premix 200 Reactions (Cat no: E2055) Primary synthesis consumable for 1 gene
region AXYGEN 0.5ml Thin Wall PCR Tubes,Flat Cap. Clear1000 (Cat no: PCR-05-C) Capp 2.0ml
Boil-Proof Microtubes. Clear 1000 (Cat no: MCT-200-C) Capp 10 ul Dnase, Rnase Free Bulk
Pipet tips 10 rack (Cat no: 5.030.010) Capp 200 ul Dnase, Rnase Free Bulk Pipet ucu
(Yellow Tips) 10 rack (Cat no: 4.130.075) Capp 1000 ul Dnase, Rnase Free Bulk Pipet ucu
(Blue Tips) 10 rack (Cat no: 4.130.135) Bio Molecular Systems Mic Tubes and Caps 1 Box:
20 racks of 48 tubes/rack, 960 Tubes in Strips of 4 with matching caps (Cat no:
MIC-TUBES960).
The motivation element behind the choice of miRNAs in the current work is a product of
the following integrated online databases for miRNA target prediction and functional
analysis.http://microrna.osumc.edu, https://www.genecards.org.
http://www.mirdb.org/miRDB/ Gene association networks with ACE2, TMPRSS2, PARP, HOX1
genes in COVID 19 cases were analyzed using GeneMANIA (Multiple Association Network
Integration Algorithm) for prediction of possible functional interactions among them
(http://www. genemania.org).
Study Period
Enrollment Count
105 participants
Eligibility Criteria
Inclusion Criteria:
- All patients between the ages of 18 and 65 included will suffer from COVID 19, and
specific treatment should not yet be initiated.
- COVID 19 diagnosis of patients will be based on full medical history, thorough
clinical examination, radiological imaging, laboratory assessment, and SARS-CoV-2
analysis by RT-PCR.
Exclusion Criteria:
- People with chronic lung disease or previous AC surgery
- People with immune deficiency or cancer patients
- Patients receiving immunosuppressive therapy for autoimmune disease
- People with neurological diseases affecting the respiratory muscles, such as
hypotonia.
Filters
Prognosis
UNKNOWN
ADULT
OLDER_ADULT