Literature DB >> 35154403

Glenoid version: the role of genetic and environmental factors on its variability. An MRI study on asymptomatic elderly twins.

S Gumina1,2, C Villani1, S Carbone3, T Venditto1, V Candela1,2.   

Abstract

BACKGROUND: Glenoid version is the most variable parameter of the shoulder joint. No authors investigated if intrinsic genetic factors or influences from extrinsic sources are responsible for its variability. AIM: We compared glenoid version between elderly monozygotic and dizygotic twins intending to separate the contributions of genetics from shared and unique environments.
METHODS: Glenoid version of the dominant shoulder was assessed by MRI using Friedman's method in 30 pairs of elderly twins (16 monozygotic-14 dizygotic; mean age ± SD: 63.72 ± 3.37, 53-72). Heritability was estimated as twice the difference between the intraclass correlation coefficients for monozygotic and dizygotic pairs. The influence of shared environment was calculated as the difference between monozygotic correlation coefficient and the heritability index. According to job category, one way analysis of variance was used to estimate the differences between groups in the total sample and within zygosity groups.
RESULTS: Glenoid version angle in monozygotic and dizygotic twins was -2° (SD: 2°) and -3° (SD: 3°), respectively (p = 0.334). Heritability index was 0.98, while the contributions of shared and unique environment were 0 and 0.02, respectively. According to working classes, no significant differences were found between the groups (p = 0.732, F = 0.31).
CONCLUSIONS: Glenoid version is mainly genetically determined and only marginally influenced by environments.Level of evidence: III.
© 2020 The British Elbow & Shoulder Society.

Entities:  

Keywords:  Glenoid version; genetic predisposition for glenoid version; glenoid retroversion; glenoid surgery; twin methodology; twin study

Year:  2020        PMID: 35154403      PMCID: PMC8832706          DOI: 10.1177/1758573220947027

Source DB:  PubMed          Journal:  Shoulder Elbow        ISSN: 1758-5732


  25 in total

1.  Agenesis of the scapula in Emx2 homozygous mutants.

Authors:  M Pellegrini; S Pantano; M P Fumi; F Lucchini; A Forabosco
Journal:  Dev Biol       Date:  2001-04-01       Impact factor: 3.582

2.  The use of computerized tomography in the measurement of glenoid version.

Authors:  R J Friedman; K B Hawthorne; B M Genez
Journal:  J Bone Joint Surg Am       Date:  1992-08       Impact factor: 5.284

3.  Glenoid version and size: does gender, ethnicity, or body size play a role?

Authors:  Hristo Ivanov Piponov; David Savin; Neal Shah; Domenic Esposito; Brian Schwartz; Vincent Moretti; Benjamin Goldberg
Journal:  Int Orthop       Date:  2016-04-22       Impact factor: 3.075

4.  Magnetic resonance imaging is comparable to computed tomography for determination of glenoid version but does not accurately distinguish between Walch B2 and C classifications.

Authors:  Jeremiah T Lowe; Edward J Testa; Xinning Li; Suzanne Miller; Joseph P DeAngelis; Andrew Jawa
Journal:  J Shoulder Elbow Surg       Date:  2016-10-17       Impact factor: 3.019

5.  Comparative analysis of 2 glenoid version measurement methods in variable axial slices on 3-dimensionally reconstructed computed tomography scans.

Authors:  Gregory Cunningham; John Freebody; Margaret M Smith; Mohy E Taha; Allan A Young; Benjamin Cass; Bruno Giuffre
Journal:  J Shoulder Elbow Surg       Date:  2018-05-31       Impact factor: 3.019

6.  High incidence of posterior glenoid dysplasia of the shoulder in young baseball players.

Authors:  Kengo Kirimura; Masashi Nagao; Masahiro Sugiyama
Journal:  J Shoulder Elbow Surg       Date:  2018-09-17       Impact factor: 3.019

7.  Double acromion and coracoid processes.

Authors:  J G McClure; R B Raney
Journal:  J Bone Joint Surg Am       Date:  1974-06       Impact factor: 5.284

8.  Glenoid deformity secondary to brachial plexus birth palsy.

Authors:  M L Pearl; B W Edgerton
Journal:  J Bone Joint Surg Am       Date:  1998-05       Impact factor: 5.284

9.  Targeted disruption of Pax1 defines its null phenotype and proves haploinsufficiency.

Authors:  B Wilm; E Dahl; H Peters; R Balling; K Imai
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

10.  Expression of a homeobox gene in the chick wing bud following application of retinoic acid and grafts of polarizing region tissue.

Authors:  G Oliver; E M De Robertis; L Wolpert; C Tickle
Journal:  EMBO J       Date:  1990-10       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.