Evidence map›Paper›PMID 39292076›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2024

Can serum M30 levels be utilized as an activation marker in patients with ulcerative colitis?

Omer Burcak Binicier, Sevil Ozer Sarı, Zehra Betul Pakoz, Banu Isbilen Basok

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Article in Revista da Associacao Medica Brasileira (1992), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Omer Burcak BinicierUniversity of Health Sciences Turkey, Izmir Faculty of Medicine, Department of Gastroenterology - İzmir, Turkey.ORCID http://orcid.org/0000-0003-0040-1982
Sevil Ozer SarıUniversity of Health Sciences Turkey, Izmir Faculty of Medicine, Department of Gastroenterology - İzmir, Turkey.ORCID http://orcid.org/0000-0001-8830-0371
Zehra Betul PakozKatip Celebi University, Ataturk Training and Research Hospital, Department of Gastroenterology - İzmir, Turkey.ORCID http://orcid.org/0000-0001-5918-6178
Banu Isbilen BasokUniversity of Health Sciences Turkey, Izmir Faculty of Medicine, Department of Medical Biochemistry - İzmir, Turkey.ORCID http://orcid.org/0000-0002-1483-997X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAscertainment of disease activation is an important component of therapeutic decisions in ulcerative colitis patients and may present certain clinical challenges. The objective of this study was to determine serum levels of the M30 fragment of cytokeratin 18 and its utility as an activation marker in patients with ulcerative colitis, who are known to have increased apoptosis.

methodsA total of 60 ulcerative colitis (30 active and 30 remission) patients aged over 18 years and 29 healthy individuals as controls were included in the study. M30, C-reactive protein, and mean platelet volume were evaluated in all participants and compared between ulcerative colitis patients and controls, as well as between those with active disease or remission.

resultsAlthough ulcerative colitis patients with active disease had higher M30 levels than those in remission, the difference was not statistically significant (p=0.085). The mean M30 levels tended to increase with increasing extent of involvement, although the differences were not significant (p=0.065). The comparison of C-reactive protein and mean platelet volume according to the site of involvement, however, showed significant differences (p=0.02 and 0.004, respectively). M30 did not show significant correlations with C-reactive protein, mean platelet volume, and Mayo Score (p=0.0834, 0.768, and 0.401, respectively).

conclusionsOur results suggest that, in contrast to C-reactive protein and mean platelet volume, M30 levels do not have a significant role as an activation marker in ulcerative colitis patients. Thus, we believe that M30 may not represent an appropriate marker to be used for this purpose.

Indexed as

BiomarkersColitis, UlcerativeC-Reactive ProteinKeratin-18AdultApoptosisCase-Control StudiesFemaleHumansMaleMean Platelet VolumeMiddle AgedPeptide FragmentsSeverity of Illness IndexYoung AdultBiomarkersC-Reactive ProteinKeratin-18M30 cytokeratin-18 peptide, humanPeptide Fragments

Identifiers

PMID39292076
PMCPMC11404990

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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 Socratic graph.