Evidence map›Paper›PMID 40362542›Full record

ArticleInternational journal of molecular sciences2025

Bone Remodeling in Children with Acute Lymphoblastic Leukemia: A Two-Year Prospective Longitudinal Study.

Paola Muggeo, Massimo Grassi, Vito D'Ascanio, Jessica Forte, Vincenzo Brescia, Francesca Di Serio, Laura Piacente, Paola Giordano, Nicola Santoro, Maria Felicia Faienza

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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
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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.

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.

Paola MuggeoDepartment of Pediatric Oncology and Hematology, University Hospital of Policlinico, 70124 Bari, Italy.ORCID 0000-0001-8813-3200
Massimo GrassiDepartment of Pediatric Oncology and Hematology, University Hospital of Policlinico, 70124 Bari, Italy.ORCID 0000-0002-6705-6354
Vito D'AscanioInstitute of Sciences of Food Production (ISPA), Italian National Research Council (CNR), 70126 Bari, Italy.ORCID 0000-0001-7344-9712
Jessica FortePediatric Department, Ospedale Della Murgia "F. Perinei", 70022 Altamura, Italy.ORCID 0009-0008-1440-0861
Vincenzo BresciaClinical Pathology Unit, AOU Policlinico Consorziale di Bari-Ospedale Giovanni XXIII, 70124 Bari, Italy.
Francesca Di SerioClinical Pathology Unit, AOU Policlinico Consorziale di Bari-Ospedale Giovanni XXIII, 70124 Bari, Italy.ORCID 0000-0001-6089-1165
Laura PiacentePediatric Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePre-J), Medical School, University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124 Bari, Italy.
Paola GiordanoInterdisciplinary Department of Medicine, University of Bari "Aldo Moro", 70124 Bari, Italy.
Nicola SantoroDepartment of Pediatric Oncology and Hematology, University Hospital of Policlinico, 70124 Bari, Italy.ORCID 0000-0001-8853-6536
Maria Felicia FaienzaPediatric Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePre-J), Medical School, University of Bari "Aldo Moro", Piazza G. Cesare 11, 70124 Bari, Italy.ORCID 0000-0002-1899-8337

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Childhood leukemia survivors are at risk of long-term complications. Data on bone remodeling in childhood acute lymphoblastic leukemia (ALL) are limited. This 2-year prospective longitudinal study investigated bone remodeling and bone turnover markers at diagnosis, during treatment, and until stopping treatment, in ALL patients < 18 years, to clarify the influence of leukemia itself and/or chemotherapy on bone.

methodsA total of 22 ALL children (12 males, age 5.5 ± 3.6 years) underwent blood sampling at the 5 time point (T0-T4). Osteoprotegerin (OPG), receptor-activator-NF-B-ligand (RANKL), osteocalcin (OC), C-terminal-telopeptide-type-I-collagen (CTX), bone-alkaline-phosphatase (bALP), tartrate-resistant acid-phosphatase-5b (TRACP5b), procollagen-type-I-N-terminal-propeptide (P1NP), Dickkopf-1 (DKK-1), and sclerostin were assessed. Data from patients at T0 were compared to a control group of healthy children. We used the principal component analysis (PCA) for statistics.

resultsLevels of CTX, OC, P1NP, and bALP resulted lower in ALL children than controls (

conclusionsThe onset of leukemia has been revealed as a key point in determining a slowing of bone remodeling in ALL children.

Indexed as

Bone RemodelingPrecursor Cell Lymphoblastic Leukemia-LymphomaAdaptor Proteins, Signal TransducingAdolescentBiomarkersChildChild, PreschoolFemaleHumansIntercellular Signaling Peptides and ProteinsLongitudinal StudiesMaleOsteocalcinOsteoprotegerinProspective StudiesRANK LigandAdaptor Proteins, Signal TransducingBiomarkersDKK1 protein, humanIntercellular Signaling Peptides and ProteinsOsteocalcinOsteoprotegerinRANK LigandTartrate-Resistant Acid Phosphataseacute lymhpoblastic leukemia (ALL)bone remodelingbone turnoverchildrenC-terminal-telopeptide-type-I-collagen (CTX)osteocalcin (OC)procollagen-type-I-N-terminal-propeptide (P1NP)

Identifiers

PMID40362542
PMCPMC12072470

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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.