Evidence map›Paper›PMID 36892078›Full record

ArticleJournal of the American Heart Association2023

Attenuation of Hypocretin/Orexin Signaling Is Associated With Increased Mortality After Myocardial Infarction.

Peter Wohlfahrt, Dominik Jenča, Vojtěch Melenovský, Petr Jarolím, Dana Dlouhá, Marek Šramko, Martin Kotrč, Michael Želízko, Jolana Mrázková, Jan Piťha and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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

12 authors at 3 institutions in 2 countries.

Peter WohlfahrtDepartment of Preventive Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0003-2390-526X
Dominik JenčaDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0003-0432-8460
Vojtěch MelenovskýDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0001-8921-7078
Petr JarolímDepartment of Pathology Brigham and Women's Hospital Boston MA.ORCID 0000-0002-9612-8652
Dana DlouháExperimental Medicine Centre Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0001-7167-1336
Marek ŠramkoFirst Medical School Charles University Prague Czech Republic.
Martin KotrčDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0002-2068-0379
Michael ŽelízkoDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.
Jolana MrázkováDepartment of Pathology Brigham and Women's Hospital Boston MA.ORCID 0000-0002-7694-3107
Jan PiťhaDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0001-9310-0067
Věra AdámkováDepartment of Preventive Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.ORCID 0000-0001-8679-3184
Josef KautznerDepartment of Cardiology Institute for Clinical and Experimental Medicine (IKEM) Prague Czech Republic.
Institute of Clinical and Experimental Medicine · CZCharles University · CZBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background The hypocretin/orexin system has been shown to play a role in heart failure. Whether it also influences myocardial infarction (MI) outcomes is unknown. We evaluated the effect of the rs7767652 minor allele T associated with decreased transcription of the hypocretin/orexin receptor-2 and circulating orexin A concentrations on mortality risk after MI. Methods and Results Data from a single-center, prospectively designed registry of consecutive patients hospitalized for MI at a large tertiary cardiology center were analyzed. Patients without previous history of MI or heart failure were included. A random population sample was used to compare allele frequencies in the general population. Out of 1009 patients (aged 64±12 years, 74.6% men) after MI, 6.1% were homozygotes (TT) and 39.4% heterozygotes (CT) for minor allele. Allele frequencies in the MI group did not differ from 1953 subjects from general population (χ

Indexed as

Heart FailureMyocardial InfarctionFemaleHumansMaleOrexin ReceptorsOrexinsStroke VolumeVentricular Function, LeftOrexin ReceptorsOrexinshypocretin/orexin receptor‐2hypocretin/orexin systeminflammationmortalitymyocardial infarctionoutcomesrecovery

Identifiers

PMID36892078
PMCPMC10111544
OpenAlexW4323653588

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.