Evidence map›Paper›PMID 38650024›Full record

ArticleBiomarker research2024

MicroRNAs predict early complications of autologous hematopoietic stem cell transplantation.

Damian Mikulski, Mateusz Nowicki, Izabela Dróżdż, Ewelina Perdas, Piotr Strzałka, Kacper Kościelny, Małgorzata Misiewicz, Konrad Stawiski, Agnieszka Wierzbowska, Wojciech Fendler

Open access · goldAbstract readLetter
In one paragraph

Article in Biomarker research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 2 countries.

Damian MikulskiDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
Mateusz NowickiDepartment of Hematology, Medical University of Lodz, Lodz, Poland.
Izabela DróżdżDepartment of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
Ewelina PerdasDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
Piotr StrzałkaDepartment of Hematology, Medical University of Lodz, Lodz, Poland.
Kacper KościelnyDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
Małgorzata MisiewiczDepartment of Hematology, Medical University of Lodz, Lodz, Poland.
Konrad StawiskiDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland.
Agnieszka WierzbowskaDepartment of Hematology, Medical University of Lodz, Lodz, Poland.
Wojciech FendlerDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Lodz, Poland. wojciech.fendler@umed.lodz.pl.
Medical University of Lodz · PLLublin Oncology Center · PLDana-Farber Cancer Institute · US

Funding

Narodowe Centrum Nauki 2019/33/B/NZ5/00536Narodowe Centrum Nauki 2022/45/N/NZ6/02904
6 · The paper itself

Abstract

Autologous hematopoietic stem cell transplantation (AHSCT) remains the most prevalent type of stem cell transplantation. In our study, we investigated the changes in circulating miRNAs in AHSCT recipients and their potential to predict early procedure-related complications. We collected serum samples from 77 patients, including 54 with multiple myeloma, at four key time points: before AHSCT, on the day of transplantation (day 0), and at days + 7 and + 14 post-transplantation. Through serum miRNA-seq analysis, we identified altered expression patterns and miRNAs associated with the AHSCT procedure. Validation using qPCR confirmed deviations in the levels of miRNAs at the beginning of the procedure in patients who subsequently developed bacteremia: hsa-miR-223-3p and hsa-miR-15b-5p exhibited decreased expression, while hsa-miR-126-5p had increased level. Then, a neural network model was constructed to use miRNA levels for the prediction of bacteremia. The model achieved an accuracy of 93.33% (95%CI: 68.05-99.83%), with a sensitivity of 100% (95%CI: 67.81-100.00%) and specificity of 90.91% (95%CI: 58.72-99.77%) in predicting bacteremia with mean of 6.5 ± 3.2 days before occurrence. In addition, we showed unique patterns of miRNA expression in patients experiencing platelet engraftment delay which involved the downregulation of hsa-let-7f-5p and upregulation of hsa-miR-96-5p; and neutrophil engraftment delay which was associated with decreased levels of hsa-miR-125a-5p and hsa-miR-15b-5p. Our findings highlight the significant alterations in serum miRNA levels during AHSCT and suggest the clinical utility of miRNA expression patterns as potential biomarkers that could be harnessed to improve patient outcomes, particularly by predicting the risk of bacteremia during AHSCT.

Indexed as

Autologous hematopoietic stem cell transplantBacteremiaBiomarkersHsa-miR-126-5pHsa-miR-15b-5pHsa-miR-223-3pmiRNA

Identifiers

PMID38650024
PMCPMC11036737
OpenAlexW4395013490

What OpenQuestion holds

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LicenceCC BY
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.