Evidence map›Paper›PMID 34716504›Full record

ArticleMolecular biology reports2021

Investigating changes in β-adrenergic gene expression (ADRB1 and ADRB2) in Takotsubo (stress) cardiomyopathy syndrome; a pilot study.

Serap Tutgun Onrat, İbrahim Etem Dural, Zafer Yalım, Ersel Onrat

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Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Serap Tutgun OnratDepartment of Medical Genetics, Afyonkarahisar University of Health Sciences Faculty of Medicine, Zafer Sağlık Külliyesi B Blok, Kat:1, Dörtyol Mah. 2078 Sok. No:3, 03200, Afyonkarahisar, Turkey. tutgunonrat@yahoo.com.ORCID http://orcid.org/0000-0001-7863-1839
İbrahim Etem DuralDepartment of Cardiology, Afyonkarahisar University of Health Sciences Faculty of Medicine, Afyonkarahisar, Turkey.ORCID http://orcid.org/0000-0003-4005-4858
Zafer YalımDepartment of Cardiology, Afyonkarahisar University of Health Sciences Faculty of Medicine, Afyonkarahisar, Turkey.ORCID http://orcid.org/0000-0001-7736-0205
Ersel OnratDepartment of Cardiology, Afyonkarahisar University of Health Sciences Faculty of Medicine, Afyonkarahisar, Turkey.ORCID http://orcid.org/0000-0002-2215-6570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTakotsubo Cardiomyopathy (TC) is a rare disorder that is mostly caused by stress and is often misdiagnosed. We aimed to analyze Takotsubo Syndrome at the molecular level by using the Oxford Nanopore Minion Device and its protocol. METHODS AND

resultsTen patients who were previously diagnosed with Takotsubo Syndrome (increased after decrease in ejection fraction and without critical stenosis in coronary arteries) and 10 healthy individuals in the control group were included in our project. The mean age was 53 ± 12.2 for the patient group and 52.4 ± 9.9 for the control group, and the left ventricular ejection fraction was 50.3 ± 11.5 for the patient group and 64.2 ± 2.8 for the control group (p < 0.05). Peripheral blood of patients and healthy individuals was taken and their DNA was obtained. By making long reads throughout the genome, the most studied regions responsible for β-adrenergic signaling pathways; The gene expression level of cardiac β-1 ADRB1 (rs1801253-ENST00000369295.4), G > C, (Gly389Arg) and cardiac β-2 ADRB2 (rs1800888-ENSG00000169252), C > T, (Thr165Ile) adrenoceptors was investigated. As a result; no structural variation was detected leading to Takotsubo Cardiomyopathy. The results obtained from the bioinformatics analysis were also checked from the VarSome Tools and similar results were found.

conclusionsMany publications in TC susceptibility have that may lead to adrenergic pathway dysregulation, most studied adrenergic receptor genes in the similar literatures too. We searched for genetic variants in b1AR and b2AR genes in our study and however we could not find any variants in this study, we think larger numbers of cohort studies are needed.

Indexed as

AdultAgedCohort StudiesDNAGene ExpressionHumansMaleMiddle AgedPilot ProjectsPolymorphism, Single NucleotideReceptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Stress, PhysiologicalStroke VolumeTakotsubo CardiomyopathyADRB1 protein, humanADRB2 protein, humanDNAReceptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2ADRB1ADRB2CardiomyopathyExomeStressTakotsubo

Identifiers

PMID34716504
PMCPMC8555722

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.