Evidence map›Paper›PMID 33454842›Full record

ArticlePflugers Archiv : European journal of physiology2021

Atrial fibrillation rhythm is associated with marked changes in metabolic and myofibrillar protein expression in left atrial appendage.

Julie H Rennison, Ling Li, Cheryl R Lin, Beth S Lovano, Laurie Castel, Sojin Youn Wass, Catherine C Cantlay, Meghan McHale, A Marc Gillinov, Reena Mehra and 5 more

Open access · greenAbstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  20. Alpha and beta myosin isoforms and human atrial and ventricular contraction.Cellular and molecular life sciences : CMLS · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Julie H RennisonDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0002-6250-1930
Ling LiProteomics Research Core Services, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
Cheryl R LinDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.
Beth S LovanoDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.
Laurie CastelDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.
Sojin Youn WassDepartment of Cardiovascular Medicine, Heart & Vascular Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0001-9354-0011
Catherine C CantlayDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.
Meghan McHaleDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.
A Marc GillinovDepartment of Cardiothoracic Surgery, Cleveland Clinic, Cleveland, OH, 44195, USA.
Reena MehraDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0002-6222-2675
Belinda B WillardProteomics Research Core Services, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0001-6884-6369
Jonathan D SmithDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0002-0415-386X
Mina K ChungDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0002-7835-6045
John BarnardCleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland Clinic, Cleveland, OH, 44195, USA.ORCID https://orcid.org/0000-0003-2403-8268
David R Van WagonerDepartment of Cardiovascular and Metabolic Sciences, Cleveland Clinic, 9500 Euclid Avenue, M/S ND50, Cleveland, OH, 44195, USA. vanwagd@ccf.org.ORCID http://orcid.org/0000-0001-8250-9828
Cleveland Clinic · US

Funding

Functional Genomics of Atrial Fibrillation in Human AtriaR01HL111314 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BARNARD, JOHN, CHUNG, MINA KAY · 2012 to 2019
$6.1M
High-End Instrumentation (HEI) Grant Program (S10)S10OD023436 · OD · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2017 to 2017
$873k
American Heart Association-American Stroke Association 18SFRN34110067American Heart Association-American Stroke Association 18SFRN34170442NHLBI NIH HHS R01 HL111314NIH HHS S10 OD023436
6 · The paper itself

Abstract

Atrial fibrillation (AF) is strongly associated with risk of stroke and heart failure. AF promotes atrial remodeling that increases risk of stroke due to left atrial thrombogenesis, and increases energy demand to support high rate electrical activity and muscle contraction. While many transcriptomic studies have assessed AF-related changes in mRNA abundance, fewer studies have assessed proteomic changes. We performed a proteomic analysis on left atrial appendage (LAA) tissues from 12 patients with a history of AF undergoing elective surgery; atrial rhythm was documented at time of surgery. Proteomic analysis was performed using liquid chromatography with mass spectrometry (LC/MS-MS). Data-dependent analysis identified 3090 unique proteins, with 408 differentially expressed between sinus rhythm and AF. Ingenuity Pathway Analysis of differentially expressed proteins identified mitochondrial dysfunction, oxidative phosphorylation, and sirtuin signaling among the most affected pathways. Increased abundance of electron transport chain (ETC) proteins in AF was accompanied by decreased expression of ETC complex assembly factors, tricarboxylic acid cycle proteins, and other key metabolic modulators. Discordant changes were also evident in the contractile unit with both up and downregulation of key components. Similar pathways were affected in a comparison of patients with a history of persistent vs. paroxysmal AF, presenting for surgery in sinus rhythm. Together, these data suggest that while the LAA attempts to meet the energetic demands of AF, an uncoordinated response may reduce ATP availability, contribute to tissue contractile and electrophysiologic heterogeneity, and promote a progression of AF from paroxysmal episodes to development of a substrate amenable to persistent arrhythmia.

Indexed as

AgedAtrial AppendageAtrial FibrillationFemaleHumansMaleMiddle AgedProteomicsAtrial fibrillationCalcium signalingLeft atriumMetabolismMitochondriaProteomics

Identifiers

PMID33454842
PMCPMC7940600
OpenAlexW3125421304

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.