Evidence map›Paper›PMID 27413371›Full record

ArticleInternational journal of endocrinology2016

Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome.

Stefano Stagi, Mariarosaria Di Tommaso, Cristina Manoni, Perla Scalini, Francesco Chiarelli, Alberto Verrotti, Elisabetta Lapi, Sabrina Giglio, Laura Dosa, Maurizio de Martino

Open access · goldAbstract read
In one paragraph

Article in International journal of endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Clinical practice guidelines for the management of differences of sex development in Japan.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Review
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  17. Review
  18. Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular FindingsJournal of clinical research in pediatric endocrinology · 2018
    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

10 authors at 4 institutions in 1 country.

Stefano StagiDepartment of Health Sciences, University of Florence, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Mariarosaria Di TommasoDepartment of Health Sciences, University of Florence, Careggi Hospital, 50134 Florence, Italy.
Cristina ManoniDepartment of Health Sciences, University of Florence, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Perla ScaliniDepartment of Health Sciences, University of Florence, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Francesco ChiarelliDepartment of Paediatrics, University of Chieti, 66100 Chieti, Italy.
Alberto VerrottiDepartment of Paediatrics, University of L'Aquila, 67100 L'Aquila, Italy.
Elisabetta LapiGenetics and Molecular Medicine Unit, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Sabrina GiglioGenetics and Molecular Medicine Unit, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Laura DosaGenetics and Molecular Medicine Unit, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Maurizio de MartinoDepartment of Health Sciences, University of Florence, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Meyer Children's Hospital · ITUniversity of Florence · ITUniversity of Chieti-Pescara · ITUniversity of L'Aquila · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective. Klinefelter syndrome (KS) has long-term consequences on bone health. However, studies regarding bone status and metabolism during childhood and adolescence are very rare. Patients. This cross-sectional study involved 40 (mean age: 13.7 ± 3.8 years) KS children and adolescents and 80 age-matched healthy subjects. For both patient and control groups, we evaluated serum levels of ionised and total calcium, phosphate, total testosterone, luteinising hormone, follicle stimulating hormone, parathyroid hormone (PTH), 25-hydroxyvitamin D (25(OH)D), 1,25-dihydroxyvitamin D, osteocalcin, bone alkaline phosphatase, and urinary deoxypyridinoline concentrations. We also calculated the z-scores of the phalangeal amplitude-dependent speed of sound (AD-SoS) and the bone transmission time (BTT). Results. KS children and adolescents showed significantly reduced AD-SoS (p < 0.005) and BTT (p < 0.0005) z-scores compared to the controls. However, KS patients presented significantly higher PTH (p < 0.0001) and significantly lower 25(OH)D (p < 0.0001), osteocalcin (p < 0.05), and bone alkaline phosphatase levels (p < 0.005). Interestingly, these metabolic bone disorders were already present in the prepubertal subjects. Conclusions. KS children and adolescents exhibited impaired bone mineral status and metabolism with higher PTH levels and a significant reduction of 25-OH-D and bone formation markers. Interestingly, this impairment was already evident in prepubertal KS patients. Follow-ups should be scheduled with KS patients to investigate and ameliorate bone mineral status and metabolism until the prepubertal ages.

Identifiers

PMID27413371
PMCPMC4927985
OpenAlexW2443640479

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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.