Evidence map›Paper›PMID 39126371›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2024

Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fractures.

Wei Zhou, Joel Ås, Catherine Shore-Lorenti, Hanh H Nguyen, Denise M van de Laarschot, Shoshana Sztal-Mazer, Vivian Grill, Christian M Girgis, Bruno H Ch Stricker, Bram C J van der Eerden and 9 more

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2024. 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. Review
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

19 authors.

Wei ZhouDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0002-6748-6303
Joel ÅsDepartment of Medical Sciences, Uppsala University Hospital, Uppsala 75185, Sweden.
Catherine Shore-LorentiDepartment of Medicine, School of Clinical Sciences, Monash University, Clayton VIC 3168, Australia.
Hanh H NguyenDepartment of Medicine, School of Clinical Sciences, Monash University, Clayton VIC 3168, Australia.ORCID 0000-0002-8846-6168
Denise M van de LaarschotDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Shoshana Sztal-MazerDepartment of Endocrinology and Diabetes, The Alfred Hospital, Melbourne VIC 3004, Australia.
Vivian GrillDepartment of Endocrinology and Diabetes, Western Health, Melbourne VIC 3011, Australia.
Christian M GirgisDepartment of Diabetes and Endocrinology, Westmead Hospital, Westmead, NSW 2145, Australia.
Bruno H Ch StrickerDepartment of Epidemiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam 3015 GD, The Netherlands.
Bram C J van der EerdenDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Rajesh V ThakkerAcademic Endocrine Unit, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 9DU, United Kingdom.
Natasha M Appelman-DijkstraDepartment of Internal Medicine, division endocrinology, Leiden University Medical Center, Leiden 2333 ZA, The Netherlands.ORCID 0000-0001-5035-127X
Mia WadeliusDepartment of Medical Sciences, Uppsala University Hospital, Uppsala 75185, Sweden.
Roderick J Clifton-BlighFaculty of Medicine and Health, The Sydney University, Camperdown NSW 2050, Australia.
Pär HallbergDepartment of Medical Sciences, Uppsala University Hospital, Uppsala 75185, Sweden.
Annemieke J M H VerkerkDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Jeroen G J van RooijDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Peter R EbelingDepartment of Medicine, School of Clinical Sciences, Monash University, Clayton VIC 3168, Australia.
M Carola ZillikensDepartment of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.ORCID 0000-0001-9186-3423

Funding

Jaap Schouten FoundationNational Health and Medical Research Council of Australia GNT1197958National Institute for Health ResearchNetherlands Consortium for Healthy Aging 050-060-810NIHR Senior Investigator Award NF- SI-0514-10091Wellcome TrustWellcome Trust Investigator Award 106995/Z/15/Z
6 · The paper itself

Abstract

Several small genetic association studies have been conducted for atypical femur fracture (AFF) without replication of results. We assessed previously implicated and novel genes associated with AFFs in a larger set of unrelated AFF cases using whole exome sequencing (WES). We performed gene-based association analysis on 139 European AFF cases and 196 controls matched for bisphosphonate use. We tested all rare, protein-altering variants using both candidate gene and hypothesis-free approaches. In the latter, genes suggestively associated with AFFs (uncorrected p-values <.01) were investigated in a Swedish whole-genome sequencing replication study and assessed in 46 non-European cases. In the candidate gene analysis, PLOD2 showed a suggestive signal. The hypothesis-free approach revealed 10 tentative associations, with XRN2, SORD, and PLOD2 being the most likely candidates for AFF. XRN2 and PLOD2 showed consistent direction of effect estimates in the replication analysis, albeit not statistically significant. Three SNPs associated with SORD expression according to the GTEx portal were in linkage disequilibrium (R2 ≥ 0.2) with an SNP previously reported in a genome-wide association study of AFF. The prevalence of carriers of variants for both PLOD2 and SORD was higher in Asian versus European cases. While we did not identify genes enriched for damaging variants, we found suggestive evidence of a role for XRN2, PLOD2, and SORD, which requires further investigation. Our findings indicate that genetic factors responsible for AFFs are not widely shared among AFF cases. The study provides a stepping-stone for future larger genetic studies of AFF.

Indexed as

Femoral FracturesGenetic Predisposition to DiseasePolymorphism, Single NucleotideAgedCohort StudiesFemaleHumansMaleMiddle AgedProcollagen-Lysine, 2-Oxoglutarate 5-DioxygenasePLOD2 protein, humanProcollagen-Lysine, 2-Oxoglutarate 5-Dioxygenaseatypical femur fracturesbisphosphonatesgeneosteoporosiswhole exome sequencing

Identifiers

PMID39126371
PMCPMC11371903

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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.