Evidence map›Paper›PMID 26909604›Full record

ArticleOncotarget2016

CEACAM1 and MICA as novel serum biomarkers in patients with acute and recurrent pericarditis.

Gal Markel, Massimo Imazio, Nira Koren-Morag, Gilli Galore-Haskel, Jacob Schachter, Michal Besser, Davide Cumetti, Silvia Maestroni, Arie Altman, Yehuda Shoenfeld and 2 more

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Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Gal MarkelElla Lemelbaum Institute of Melanoma, Sheba Medical Center, Tel Hashomer, Israel.
Massimo ImazioCardiology Department, Maria Vittoria Hospital, Torino, Italy.
Nira Koren-MoragDepartment of Epidemiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gilli Galore-HaskelElla Lemelbaum Institute of Melanoma, Sheba Medical Center, Tel Hashomer, Israel.
Jacob SchachterElla Lemelbaum Institute of Melanoma, Sheba Medical Center, Tel Hashomer, Israel.
Michal BesserElla Lemelbaum Institute of Melanoma, Sheba Medical Center, Tel Hashomer, Israel.
Davide CumettiInternal Medicine, Ospedali Riuniti, Bergamo, Italy.
Silvia MaestroniInternal Medicine, Ospedali Riuniti, Bergamo, Italy.
Arie AltmanInternal Medicine B, Sheba Medical Center, Tel Hashomer, Israel.
Yehuda ShoenfeldZabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel.
Antonio BrucatoInternal Medicine, Ospedali Riuniti, Bergamo, Italy.
Yehuda AdlerTalpiot Medical Leadership Program, Sheba Medical Center, Tel Hashomer, Israel.
Sheba Medical Center · ILAzienda Ospedaliero Universitaria Ospedali Riuniti · ITTel Aviv University · ILOspedale Maria Vittoria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe immune response plays a significant role in pericarditis, but the mechanisms of disease are poorly defined. Further, efficient monitoring and predictive clinical tools are unavailable. Carcinoembryonic antigen cell adhesion molecule 1 (CEACAM1) is an immune-inhibitory protein, while MHC class I chain related protein A (MICA) and B (MICB) have an immune-stimulating function. METHODS AND

resultsSerum CEACAM1, MICA and MICB concentrations were measured by ELISA in ~50 subjects of each group: acute pericarditis (AP), recurrent pericarditis (RP) and lupus (SLE) patients, metastatic melanoma patients as well as healthy donors. Serum CEACAM1 was dramatically elevated in AP and RP patients, but not in SLE patients, and displayed a highly accurate profile in ROC curve analyses. MICA and MICB were elevated in some pericarditis patients. All markers were enhanced in metastatic melanoma patients irrespective of neoplastic pericardial involvement. Etiology-guided analysis of RP patients showed that very low MICA levels were associated with idiopathic RP, while high MICA was associated with autoimmune and post-operative RP. Importantly, MICA was significantly associated with recurrences, independently of other potentially confounding parameters such as age, time of follow up or treatment modality.

conclusionsHere we report for the first time on CEACAM1 as a potentially novel biomarker for pericarditis, as well as on MICA as an innovative prognostic marker in these patients. Determination of the roles of these immune factors, as well as their diagnostic and prognostic values should be determined in future prospective studies.

Indexed as

Biomarkers, TumorCell Adhesion Molecule-1Cell Adhesion MoleculesEnzyme-Linked Immunosorbent AssayFemaleHistocompatibility Antigens Class IHumansImmunoglobulinsMaleMiddle AgedPericarditisPrognosisBiomarkers, TumorCADM1 protein, humanCell Adhesion Molecule-1Cell Adhesion MoleculesHistocompatibility Antigens Class IImmunoglobulinsMHC class I-related chain AMICB antigenbiomarkersMICAMICBpericarditisserum

Identifiers

PMID26909604
PMCPMC4951257
OpenAlexW2293248285

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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.