Evidence map›Paper›PMID 34154308›Full record

ArticleTurkish journal of medical sciences2021

Can omentin-1 be a prognostic marker in surgical intensive care patients?

Yücel Gültekin, İsmail Biri, Afig Gojayev, Selen Yılmaz Işıkhan, Oytun Portakal Akçin, Yusuf Alper Kılıç

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Article in Turkish journal of medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

6 authors.

Yücel GültekinDepartment of General Surgery, Faculty of Medicine, Uşak University, Uşak, Turkey.
İsmail BiriDeparment of General Surgery, Koru Ankara Hospital, Ankara, Turkey.
Afig GojayevDepartment of Surgical Oncology, Faculty of Medicine, Ankara University, Ankara, Turkey.
Selen Yılmaz IşıkhanDeparment of Biostatistics, Vocational Higher School of Social Sciences and Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Oytun Portakal AkçinDeparment of Medical Biochemistry, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Yusuf Alper KılıçDeparment of General Surgery, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: A member of the adipokine family, omentin-1 is selectively secreted from visceral fat tissue and the omentum. It has been shown that omentin-1 is involved in the pathogenesis of certain diseases and can be used as a prognostic marker. This study first investigated the prognostic significance of omentin-1 in surgical intensive care patients. In addition, the relationship between omentin-1 and laboratory and clinical parameters commonly used in intensive care units (ICUs) was evaluated. Materials and methods: One hundred and fifty-four patients hospitalized in the surgical ICU were included in the study. Blood samples for omentin-1 were collected from the patients displaying clinical condition changes. Changes in omentin-1 levels were observed during the hospital stay of the patients. A total of 423 blood samples were evaluated. Omentin-1 levels were compared to the laboratory parameters routinely monitored in the ICU and the prognostic significance of omentin-1 for surgical intensive care patients was investigated. Results: The median APACHE II score of all patients was (median-IQR, 8.0–6.0 ng/mL). Omentin-1 levels of the alive patients in the ICU (median-IQR, 339.04–407.68 ng/mL) were significantly higher compared to dead patients (median-IQR, 166.40–363.60 ng/mL). Omentin-1 levels were higher in nonsepsis patients compared to the levels of the patients in sepsis and septic shock (p < 0.001). Omentin-1 values were negatively correlated with the C-reactive protein and procalcitonin levels, body temperature, and the SOFA (sequential organ failure assessment score) scores and they were positively correlated with albumin, prealbumin, and glucose levels. Conclusion: Omentin-1 may play a role in the complex constructs of inflammation and metabolic events in intensive care patients. Reduced omentin-1 levels in surgical intensive care patients were associated with poor prognosis and increased mortality.

Indexed as

SepsisShock, SepticAdolescentAdultCritical CareCytokinesFemaleGPI-Linked ProteinsHumansIntensive Care UnitsLectinsMaleMiddle AgedPostoperative ComplicationsPrognosisSurgical Procedures, OperativeCytokinesGPI-Linked ProteinsITLN1 protein, humanLectinsIntensive careomentinprognostic marker

Identifiers

PMID34154308
PMCPMC8742475

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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.