Evidence map›Paper›PMID 26825304›Full record

ArticlePurinergic signalling2016

Functional polymorphisms in the P2X7 receptor gene are associated with stress fracture injury.

Ian Varley, Julie P Greeves, Craig Sale, Eitan Friedman, Daniel S Moran, Ran Yanovich, Peter J Wilson, Alison Gartland, David C Hughes, Trent Stellingwerff and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Purinergic signalling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
10.3field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Bone stress injuries.Nature reviews. Disease primers · 2022
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Tarsal navicular stress fractures.Current reviews in musculoskeletal medicine · 2017
    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

13 authors at 7 institutions in 3 countries.

Ian VarleyMusculoskeletal Physiology Research Group, Sport, Health and Performance Enhancement Research Centre, Nottingham Trent University, Clifton Lane, Nottingham, NG11 8NS, UK. ian.varley@ntu.ac.uk.
Julie P GreevesDepartment of Occupational Medicine, Headquarters Army Recruiting and Training Division, Trenchard Lines, Upavon, Pewsey, Wilts SN9 6BE, UK. julie.greeves143@mod.uk.
Craig SaleMusculoskeletal Physiology Research Group, Sport, Health and Performance Enhancement Research Centre, Nottingham Trent University, Clifton Lane, Nottingham, NG11 8NS, UK. craig.sale@ntu.ac.uk.
Eitan FriedmanThe Susanne Levy Gertner Oncogenetics Unit, Sheba Medical Center, Tel-Hashomer, Israel. eitan.friedman@sheba.health.gov.il.
Daniel S MoranAriel and Heller Institue, Sheba Medical Center, Ariel University, Ramat Gen, Israel. dani.moran@sheba.health.gov.il.
Ran YanovichAriel and Heller Institue, Sheba Medical Center, Ariel University, Ramat Gen, Israel. ran.yanovich@sheba.health.gov.il.
Peter J WilsonBone and Joint Research Group, Department of Musculoskeletal Biology, Institute of Ageing and Chronic Diseases, Faculty of Health and Life Sciences, University of Liverpool, Sherrington Buildings, Ashton Street, Liverpool, L69 3GE, UK. P.Wilson@liverpool.ac.uk.
Alison GartlandThe Mellanby Centre for Bone Research, Department of Human Metabolism, The University of Sheffield, Beech Hill Road, Sheffield, S10 2RX, UK. a.gartland@sheffield.ac.uk.
David C HughesMusculoskeletal Physiology Research Group, Sport, Health and Performance Enhancement Research Centre, Nottingham Trent University, Clifton Lane, Nottingham, NG11 8NS, UK. david.hughes02@ntu.ac.uk.
Trent StellingwerffCanadian Sport Institute Pacific, Pacific Institute for Sport Excellence, Victoria, BC, V9E 2C5, Canada. tstellingwerff@csipacific.ca.
Craig RansonCardiff School of Sport, Cardiff Metropolitan University, Cardiff, Wales, UK. cranson@cardiffmet.ac.uk.
William D FraserNorwich Medical School, University of East Anglia, Norwich, Norfolk, NR4 7TJ, UK. W.Fraser@uea.ac.uk.
James A GallagherBone and Joint Research Group, Department of Musculoskeletal Biology, Institute of Ageing and Chronic Diseases, Faculty of Health and Life Sciences, University of Liverpool, Sherrington Buildings, Ashton Street, Liverpool, L69 3GE, UK. J.A.Gallagher@liverpool.ac.uk.
Nottingham Trent University · GBSheba Medical Center · ILUniversity of Liverpool · GBCanadian Sport Centre Pacific · CACardiff Metropolitan University · GBUniversity of East Anglia · GBUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Military recruits and elite athletes are susceptible to stress fracture injuries. Genetic predisposition has been postulated to have a role in their development. The P2X7 receptor (P2X7R) gene, a key regulator of bone remodelling, is a genetic candidate that may contribute to stress fracture predisposition. The aim of this study is to evaluate the putative contribution of P2X7R to stress fracture injury in two separate cohorts, military personnel and elite athletes. In 210 Israeli Defense Forces (IDF) military conscripts, stress fracture injury was diagnosed (n = 43) based on symptoms and a positive bone scan. In a separate cohort of 518 elite athletes, self-reported medical imaging scan-certified stress fracture injuries were recorded (n = 125). Non-stress fracture controls were identified from these cohorts who had a normal bone scan or no history or symptoms of stress fracture injury. Study participants were genotyped for functional SNPs within the P2X7R gene using proprietary fluorescence-based competitive allele-specific PCR assay. Pearson's chi-squared (χ (2)) tests, corrected for multiple comparisons, were used to assess associations in genotype frequencies. The variant allele of P2X7R SNP rs3751143 (Glu496Ala-loss of function) was associated with stress fracture injury, whilst the variant allele of rs1718119 (Ala348Thr-gain of function) was associated with a reduced occurrence of stress fracture injury in military conscripts (P < 0.05). The association of the variant allele of rs3751143 with stress fractures was replicated in elite athletes (P < 0.05), whereas the variant allele of rs1718119 was also associated with reduced multiple stress fracture cases in elite athletes (P < 0.05). The association between independent P2X7R polymorphisms with stress fracture prevalence supports the role of a genetic predisposition in the development of stress fracture injury.

Indexed as

AdultAllelesAthletesBone RemodelingCohort StudiesDNAFemaleFractures, StressGenetic Predisposition to DiseaseGenotypeHumansIsraelMaleMilitary PersonnelPolymorphism, Single NucleotideReceptors, Purinergic P2X7DNAReceptors, Purinergic P2X7BoneP2X7 receptorStress fracture injury

Identifiers

PMID26825304
PMCPMC4749527
OpenAlexW2466136947

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.