Evidence map›Paper›PMID 35725492›Full record

ArticleItalian journal of pediatrics2022

Assessment of biochemical bone markers of osteoporosis in children with thalassemia major.

Tanju Çelik, Özlem Sangün, Şule Ünal, Ali Balcı, Sedat Motor

Open access · goldAbstract read
In one paragraph

Article in Italian journal of pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 12 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

5 authors at 4 institutions in 1 country.

Tanju ÇelikSchool of Medicine, Pediatrics, Mustafa Kemal University, Hatay, Turkey. dr.tanju35@hotmail.com.ORCID https://orcid.org/0000-0003-3522-9406
Özlem SangünDepartment of Pediatric Endocrinology, Antakya State Hospital, Hatay, Turkey.ORCID https://orcid.org/0000-0002-9079-4574
Şule ÜnalDepartment of Pediatric Hematology and Oncology, Antakya State Hospital, Hatay, Turkey.ORCID https://orcid.org/0000-0002-3842-8788
Ali BalcıSchool of Medicine, Department of Radiology, 9 Eylul University, Hatay, Turkey.ORCID https://orcid.org/0000-0002-5781-2910
Sedat MotorSchool of Medicine, Department of Biochemistry, Mustafa Kemal University, Hatay, Turkey.ORCID https://orcid.org/0000-0003-1004-8086
Dokuz Eylül University · TRDr. Behçet Uz Çocuk Hastalıkları Hastanesi · TRHacettepe University · TRMustafa Kemal University · TR

Funding

Mustafa Kemal Üniversitesi 1106 M 0107
6 · The paper itself

Abstract

backgroundBeta thalassemia major (β-TM) is a common cause of skeletal morbidity and is associated with increased bone fracture risk, particularly in inadequately transfused children. The aim of this study was to investigate some potential biochemical markers as possible early predictors of BMD variations in children with β-TM.

methodsThe study included 38 children with β-TM and 40 sex-age matched controls. All patients were subjected to BMD assessment by dual-energy X-ray absorptiometry (DEXA). Serum beta-crosslaps (beta-CTx), osteoprotegerin (OPG), receptor activator of nuclear factor-kappa B ligand (RANKL), urinary deoxypyridinoline (DPD) and ferritin levels were compared between the groups.

resultsSerum OPG levels were significantly lower in thalassemic children than in controls. The mean ratio of RANKL/OPG was significantly higher in the thalassemic patients than in the control group. Osteoporosis was detected in 10 (3 female and 7 male) of 38 patients (26.3%) according to the femur Z score and in 6 of them (4 male and 2 female) (15.8%) according to the spine Z score.

conclusionsSerum OPG concentrations can be used as a biochemical marker in screening patients with beta-thalassemia major for the development of osteoporosis.

Indexed as

beta-ThalassemiaOsteoporosisBiomarkersBone DensityCase-Control StudiesChildFemaleHumansMaleBiomarkersBone markersBone mineralization disordersOsteoporosis

Identifiers

PMID35725492
PMCPMC9210807
OpenAlexW4283160267

What OpenQuestion holds

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Registered trials

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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.