Literature DB >> 9322316

Quantification of lumbar intradiscal deformation during flexion and extension, by mathematical analysis of magnetic resonance imaging pixel intensity profiles.

J S Brault1, D M Driscoll, L L Laakso, R E Kappler, E F Allin, T Glonek.   

Abstract

STUDY
DESIGN: A magnetic resonance imaging study of the internal kinematic response of normal lumbar intervertebral discs to non-weight-bearing flexion and extension.
OBJECTIVES: To quantify the pattern of magnetic resonance imaging pixel intensity variation across discs, and noninvasively monitor displacement of the nucleus pulposus during sagittal-plane movements. SUMMARY OF BACKGROUND DATA: Invasive techniques used to study intradiscal movements of the nucleus pulposus have suggested that it moves posteriorly during flexion and anteriorly during extension. A noninvasive study based on magnetic resonance images gave similar results for normal young women. Quantification has been problematic, and the invasive procedures may have altered disc dynamics.
METHODS: Ten male subjects (age, 21-38 years) with healthy backs were positioned in a magnetic resonance imaging portal with their lumbar spine stabilized in flexion and extension by supporting pads. For each disc, a T2-weighted image was obtained, as was a computer-generated profile of pixel intensities along a horizontal mid-discal transect. Mathematical curve-fitting regression analysis was used to characterize the shape of the intensity profile and to compute the point of maximum pixel intensity.
RESULTS: A single equation fitted the profile for all normal discs. The intensity peak shifted posteriorly during flexion, anteriorly during extension.
CONCLUSIONS: Automated mathematical modeling of magnetic resonance imaging pixel data can be used to describe the fundamental shape of the pixel intensity profile across a normal lumbar disc, to determine the precise location of the site of maximum pixel intensity, and to measure the movement of this peak with flexion and extension. This technique may be of value in recognizing incipient degenerative changes in lumbar discs.

Entities:  

Mesh:

Year:  1997        PMID: 9322316     DOI: 10.1097/00007632-199709150-00002

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  7 in total

1.  Comparable effect of simulated side bending and side gliding positions on the direction and magnitude of lumbar disc hydration shift: in vivo MRI mechanistic study.

Authors:  Hiroshi Takasaki
Journal:  J Man Manip Ther       Date:  2015-05

2.  Nucleus pulposus deformation in response to lumbar spine lateral flexion: an in vivo MRI investigation.

Authors:  Peter J Fazey; Hiroshi Takasaki; Kevin P Singer
Journal:  Eur Spine J       Date:  2010-03-05       Impact factor: 3.134

Review 3.  Quantitative MRI as a diagnostic tool of intervertebral disc matrix composition and integrity.

Authors:  Fackson Mwale; James C Iatridis; John Antoniou
Journal:  Eur Spine J       Date:  2008-11-13       Impact factor: 3.134

4.  Effect of pathology type and severity on the distribution of MRI signal intensities within the degenerated nucleus pulposus: application to idiopathic scoliosis and spondylolisthesis.

Authors:  Delphine Périé; Daniel Curnier
Journal:  BMC Musculoskelet Disord       Date:  2010-08-26       Impact factor: 2.362

5.  In vivo morphological features of human lumbar discs.

Authors:  Weiye Zhong; Sean J Driscoll; Minfei Wu; Shaobai Wang; Zhan Liu; Thomas D Cha; Kirkham B Wood; Guoan Li
Journal:  Medicine (Baltimore)       Date:  2014-12       Impact factor: 1.889

6.  MRI signal distribution within the intervertebral disc as a biomarker of adolescent idiopathic scoliosis and spondylolisthesis.

Authors:  Julien Gervais; Delphine Périé; Stefan Parent; Hubert Labelle; Carl-Eric Aubin
Journal:  BMC Musculoskelet Disord       Date:  2012-12-03       Impact factor: 2.362

Review 7.  Tissue Engineering a Biological Repair Strategy for Lumbar Disc Herniation.

Authors:  Grace D O'Connell; J Kent Leach; Eric O Klineberg
Journal:  Biores Open Access       Date:  2015-11-01
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.