Evidence mapPaperPMID 38396997Full record

ArticleInternational journal of molecular sciences2024

High Frequencies of Genetic Variants in Patients with Atypical Femoral Fractures.

Álvaro Del Real, Raquel Cruz, Carolina Sañudo, José L Pérez-Castrillón, María I Pérez-Núñez, Jose M Olmos, José L Hernández, Carmen García-Ibarbia, Carmen Valero, Jose A Riancho

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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.

Álvaro Del RealDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.ORCID 0000-0002-1057-461X
Raquel CruzGrupo de Medicina Xenómica, Centro de Investigación en Medicina Molecular y Enfermedades Crónicas, Universidade de Santiago de Compostela (USC), 15782 Santiago de Compostela, Spain.ORCID 0000-0002-6964-8898
Carolina SañudoDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.ORCID 0000-0002-4287-1336
José L Pérez-CastrillónInternal Medicine Department, University Hospital Rio Hortega of Valladolid, 47012 Valladolid, Spain.ORCID 0000-0002-1723-217X
María I Pérez-NúñezTraumatology Department, University Hospital M. Valdecilla, 39008 Santander, Spain.ORCID 0000-0001-6423-260X
Jose M OlmosDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.
José L HernándezDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.ORCID 0000-0002-6585-8847
Carmen García-IbarbiaInternal Medicine Department, Marqués de Valdecilla University Hospital, 39008 Santander, Spain.
Carmen ValeroDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.
Jose A RianchoDepartamento de Medicina y Psiquiatría, Instituto de Investigación Sanitaria Valdecilla (IDIVAL), Facultad de Medicina, Universidad de Cantabria, 39011 Santander, Spain.ORCID 0000-0003-0691-8755
Universidad de Cantabria · ESMarqués de Valdecilla University Hospital · ESHospital Universitario Río Hortega · ESUniversidade de Santiago de Compostela · ES

Funding

Instituto de Salud Carlos III PI21/00532
6 · The paper itself

Abstract

This study explores the genetic factors associated with atypical femoral fractures (AFF), rare fractures associated with prolonged anti-resorptive therapy. AFF are fragility fractures that typically appear in the subtrochanteric or diaphyseal regions of the femur. While some cases resemble fractures in rare genetic bone disorders, the exact cause remains unclear. This study investigates 457 genes related to skeletal homeostasis in 13 AFF patients by exome sequencing, comparing the results with osteoporotic patients (

Indexed as

Bone Density Conservation AgentsBone DiseasesFemoral FracturesDiaphysesDiphosphonatesFemurHumansBone Density Conservation AgentsDiphosphonatesatypical femur fracturesgeneticsSNPs

Identifiers

PMID38396997
PMCPMC10889592
OpenAlexW4391836795

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.