Evidence map›Paper›PMID 37076969›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2023

Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients.

Wei Zhou, Jeroen Gj van Rooij, Denise M van de Laarschot, Zografia Zervou, Hennie Bruggenwirth, Natasha M Appelman-Dijkstra, Peter R Ebeling, Serwet Demirdas, Annemieke Jmh Verkerk, M Carola Zillikens

Open access · hybridAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.1field-weighted citation impact, top 50% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Identification of hypophosphatasia in adults with persistent hypophosphatasemia: clinical-genetic characterization and a validated diagnostic tool.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Identifying rare variants in genes related to bone phenotypes in a cohort of postmenopausal women.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
    Article
  8. Article
  9. Family-based whole-exome sequencing implicates a variant in lysyl oxidase like 4 in atypical femur fractures.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  10. Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fractures.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  11. 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 3 institutions in 2 countries.

Wei ZhouDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0002-6748-6303
Jeroen Gj van RooijDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.
Denise M van de LaarschotDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0002-7701-6663
Zografia ZervouDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.
Hennie BruggenwirthDepartment of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.
Natasha M Appelman-DijkstraDepartment of Internal Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-5035-127X
Peter R EbelingDepartment of Medicine, School of Clinical Sciences, Monash University, Clayton, Australia.ORCID 0000-0002-2921-3742
Serwet DemirdasDepartment of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.
Annemieke Jmh VerkerkDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0002-7523-3656
M Carola ZillikensDepartment of Internal Medicine, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0001-9186-3423
Erasmus MC · NLLeiden University Medical Center · NLMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atypical femur fractures (AFFs), considered rare associations of bisphosphonates, have also been reported in patients with monogenic bone disorders without bisphosphonate use. The exact association between AFFs and monogenic bone disorders remains unknown. Our aim was to determine the prevalence of monogenic bone disorders in a Dutch AFF cohort. AFF patients were recruited from two specialist bone centers in the Netherlands. Medical records of the AFF patients were reviewed for clinical features of monogenic bone disorders. Genetic variants identified by whole-exome sequencing in 37 candidate genes involved in monogenic bone disorders were classified based on the American College of Medical Genetics and Genomics (ACMG) classification guidelines. Copy number variations overlapping the candidate genes were also evaluated using DNA array genotyping data. The cohort comprises 60 AFF patients (including a pair of siblings), with 95% having received bisphosphonates. Fifteen AFF patients (25%) had clinical features of monogenic bone disorders. Eight of them (54%), including the pair of siblings, had a (likely) pathogenic variant in either PLS3, COL1A2, LRP5, or ALPL. One patient carried a likely pathogenic variant in TCIRG1 among patients not suspected of monogenic bone disorders (2%). In total, nine patients in this AFF cohort (15%) had a (likely) pathogenic variant. In one patient, we identified a 12.7 Mb deletion in chromosome 6, encompassing TENT5A. The findings indicate a strong relationship between AFFs and monogenic bone disorders, particularly osteogenesis imperfecta and hypophosphatasia, but mainly in individuals with symptoms of these disorders. The high yield of (likely) pathogenic variants in AFF patients with a clinical suspicion of these disorders stresses the importance of careful clinical evaluation of AFF patients. Although the relevance of bisphosphonate use in this relationship is currently unclear, clinicians should consider these findings in medical management of these patients. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Indexed as

Bone Density Conservation AgentsFemoral FracturesVacuolar Proton-Translocating ATPasesCollagen Type IDiphosphonatesDNA Copy Number VariationsFemurHumansPrevalenceBone Density Conservation AgentsCollagen Type ICollagen Type I, alpha2 SubunitDiphosphonatesTCIRG1 protein, humanVacuolar Proton-Translocating ATPasesATYPICAL FEMUR FRACTURESBISPHOSPHONATESCOPY NUMBER VARIATIONSGENETICSMONOGENIC BONE DISORDEROSTEOPOROSISWHOLE-EXOME SEQUENCING

Identifiers

PMID37076969
PMCPMC10946469
OpenAlexW4366464254

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.