Evidence map›Paper›PMID 40425732›Full record

ArticleScientific reports2025

Assessment of bone status and bone turnover in pediatric patients with familiar hypomagnesemia with hypercalciuria and nephrocalcinosis.

Beata Bieniaś, Anna Wieczorkiewicz-Płaza, Marcin Zaniew, Barbara Pulcer, Maria Szczepańska, Anna Moczulska, Anna Rogowska-Kalisz, Marcin Tkaczyk, Danuta Ostalska-Nowicka, Katarzyna Zachwieja and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Beata BieniaśDepartment of Pediatric Nephrology, Medical University of Lublin, Lublin, Poland. beata.bienias@umlub.pl.
Anna Wieczorkiewicz-PłazaDepartment of Pediatric Nephrology, Medical University of Lublin, Lublin, Poland.
Marcin ZaniewDepartment of Pediatrics, University of Zielona Góra, Zielona Góra, Poland.
Barbara PulcerDepartment of Pediatric Nephrology and Neurology, Municipal Hospital, Chorzów, Poland.
Maria SzczepańskaDepartment of Pediatrics, Faculty of Medical Sciences in Zabrze, SUM in Katowice, Katowice, Poland.
Anna MoczulskaDepartment of Pediatric Nephrology and Hypertension, Jagiellonian University Medical College, Kraków, Poland.
Anna Rogowska-KaliszDepartment of Pediatrics, Immunology and Nephrology, Polish Mother's Memorial Hospital Research Institute, Łódź, Poland.
Marcin TkaczykDepartment of Pediatrics, Immunology and Nephrology, Polish Mother's Memorial Hospital Research Institute, Łódź, Poland.
Danuta Ostalska-NowickaDepartment of Pediatric Nephrology and Hypertension, Poznań University of Medical Sciences, Poznań, Poland.
Katarzyna ZachwiejaDepartment of Pediatric Nephrology and Hypertension, Jagiellonian University Medical College, Kraków, Poland.
Jan ZawadzkiDepartment of Nephrology, Kidney Transplantation and Hypertension, Children's Memorial Health Institute, Warszawa, Poland.
Martin KonradDepartment of General Pediatrics, University Children's Hospital, Münster, Germany.
Przemysław SikoraDepartment of Pediatric Nephrology, Medical University of Lublin, Lublin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familiar hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare monogenic tubulopathy. Although some of its features are potentially harmful for skeletal homeostasis, this problem has not been systematically evaluated so far. To evaluate bone mineral density (BMD) in correlation with selected mineral parameters and bone turnover markers (BTMs) to determine the risk of bone mass loss in pediatric patients with FHHNC. The study comprised 28 FHHNC patients aged 4-18 years and 33 healthy, sex - and age matched controls. 6 FHHNC patients showed normal kidney function whereas the remaining 22 presented with CKD grade II- III (median eGFR 73 ml/min/1.73m

Indexed as

Bone RemodelingHypercalciuriaNephrocalcinosisRenal Tubular Transport, Inborn ErrorsAdolescentBiomarkersBone DensityCalciumCase-Control StudiesChildChild, PreschoolFemaleFibroblast Growth Factor-23HumansMagnesiumMaleBiomarkersCalciumFGF23 protein, humanFibroblast Growth Factor-23MagnesiumBone mineral densityBone turnover markersFHHNC

Identifiers

PMID40425732
PMCPMC12116731

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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.