Evidence map›Paper›PMID 35409072›Full record

ArticleInternational journal of molecular sciences2022

Biomarkers of Glucose Metabolism Alterations and the Onset of Metabolic Syndrome in Survivors of Childhood Acute Lymphoblastic Leukemia.

Katarzyna Konończuk, Katarzyna Muszyńska-Rosłan, Karolina Konstantynowicz-Nowicka, Maryna Krawczuk-Rybak, Adrian Chabowski, Eryk Latoch

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.3field-weighted citation impact, top 5% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  3. GLUT5-overexpression-related tumorigenic implications.Molecular medicine (Cambridge, Mass.) · 2024
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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

6 authors at 1 institution in 1 country.

Katarzyna KonończukDepartment of Pediatric Oncology and Hematology, Medical University of Bialystok, 15-274 Białystok, Poland.ORCID 0000-0003-0540-8040
Katarzyna Muszyńska-RosłanDepartment of Pediatric Oncology and Hematology, Medical University of Bialystok, 15-274 Białystok, Poland.
Karolina Konstantynowicz-NowickaDepartment of Physiology, Medical University of Bialystok, 15-222 Białystok, Poland.
Maryna Krawczuk-RybakDepartment of Pediatric Oncology and Hematology, Medical University of Bialystok, 15-274 Białystok, Poland.
Adrian ChabowskiDepartment of Physiology, Medical University of Bialystok, 15-222 Białystok, Poland.ORCID 0000-0002-7407-8156
Eryk LatochDepartment of Pediatric Oncology and Hematology, Medical University of Bialystok, 15-274 Białystok, Poland.ORCID 0000-0002-7667-7953
Medical University of Białystok · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Owing to advances in treatment modalities and supportive care, overall survival rates have reached up to 90% among children with acute lymphoblastic leukemia (ALL). However, due to the underlying illness and therapy, they are at a greater risk of developing lifestyle diseases. Hence, special attention is paid to early detection of the components of metabolic syndrome (MetS). This study aimed at investigating the association of plasma levels of nine diabetes markers with being overweight and components of MetS in ALL survivors. The study included 56 subjects with mean age of 12.36 ± 5.15 years. The commercially available Bio-Plex Pro Human Diabetes 10-Plex Panel kit was used to evaluate levels of diabetes biomarkers. ALL survivors presented statistically higher concentrations of GIP (p = 0.026), glucagon (p = 0.001), leptin (p = 0.022), and PAI-1 (p = 0.047), whereas the concentration of ghrelin was lower (p < 0.001) compared to the control group. Moreover, subjects within normal BMI range showed higher GIP (p = 0.005) and lower ghrelin concentration (p < 0.001) compared to healthy peers. At least one risk factor of MetS was present in 58.9% of participants, who showed significantly higher levels of C-peptide (p = 0.028), leptin (p = 0.003), and PAI-1 (p = 0.034) than survivors who did not meet any MetS criteria. In conclusion, ALL survivors are at greater risk of disturbances in carbohydrate metabolism. Understanding the pathogenesis and applicability of diabetes markers is crucial for developing strategies to prevent metabolic syndrome in ALL survivors.

Indexed as

Metabolic SyndromePrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentBiomarkersChildGhrelinGlucoseHumansLeptinPlasminogen Activator Inhibitor 1SurvivorsBiomarkersGhrelinGlucoseLeptinPlasminogen Activator Inhibitor 1ALLCCSchildhood cancer survivorschildrenC-peptidediabetes biomarkersgastric inhibitory peptide (GIP)ghrelinglucagoninsulinleptinobesityoverweightplasminogen activator inhibitor-1 (PAI-1)resistinvisfatin

Identifiers

PMID35409072
PMCPMC8998892
OpenAlexW4220694781

What OpenQuestion holds

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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.