At the Zorab Symposium in Oxford, 2006, we showed that semicircular canal (SCC) anomalies occurring with posterior basicranium asymmetry affect the oculovestibular system in human beings. As a consequence, we proposed the hypothesis of a descending direct vestibulospinal and cognitive top-down effect on some scoliosis. We will show that some SCC anomalies detected with MRI modelling are malformations frequently found in scoliosis. 445 patients (323 women, mean age 21 years; 122 men, mean age 24 years) with instability, imbalance, and spatial disorientation were submitted to T2 MRI modelling. 95 of 445 patients had scoliosis: 57 thoracolumbar scoliosis, 24 thoracic scoliosis, and 14 lumbar deformation. We processed the data acquired with G.E.MRI (1.5T), T2- 3D Fiesta with a set of Brainvisa modules (http://brainvisa.info/).Introduction
Methods
The Proprio-oculo-vestibular system is involved in scoliosis. In Congress ZORAB, Oxford 2006, we showed correlations between morphological semicircular canals (SCC) anomalies and vestibular dysfunctions associated with oculomotor anomalies. We will describe a set of specific anomalies in adolescent idiopathic scoliosis (AIS) in favour of an altered perception of space. The study included 95 patients with AIS: 57 had thoracolumbar scoliosis, 24 thoracic scoliosis, and 14 lumbar deformation. Patients were submitted to a set of tests: (1) three-dimensional vestibular evaluation with semicircular canal-specific horizontal and vertical stimulations; (2) measurement of the static ocular torsion; (3) ocular smooth pursuits analyses with a new automatised programme; and (4) posturographic recording (static and dynamic tests). The tests were done before and after treatment (vestibular training and oculomotor training).Introduction
Methods
The assessment of vestibular function throws new light on scoliosis. Vestibular morphological anomalies are frequent in scoliosis. This communication has two aims:
to correlate the dysfunctions of the semi-circular canal system with morphological anomalies. to include the vestibular assessment in the management of the scoliotic subject. These anomalies are demonstrated by graphic modelling from MRI images (see abstract of Dr. Rousié). The examination of the proprio-oculo-labyrinthine system is done by Videonystagmography (VNG) and Videooculography (VOG). We able to test both horizontal and vertical canal function to give a 3D vestibular assessment. We use these tests to measure primitive vestibular dissymmetry (PVD). We compare the 3D endolymphatic morphology with the 3D vestibular function.
In the In the The difference between the results obtained with the caloric test and the kinetic tests is in connection with the phenomena of central compensation. On the vestibular level there is a close connection between the scoliosis, the vestibular morphological anomalies and the vestibular examination.
The vestibular assessment and vestibular rehabilitation are necessary because of the close connections between the anomalies of the proprio-oculo-labyrinthin and the scoliosis.
Control group (CG):32 subjects, 26W. &
6M., fr. 8 to 51. AIS group (AISG):93 subjects, 77W. &
16M., fr. 6 to 63. AIS were classified according to – Amplitude of spine deformation (d°) G1: 8 to10°, G2: 10 to 15°, G3:15 to 40° – Location of deformation (Ponsetti class.): TL=thoracolumbar, T=thoracic, L=lumbar.
Step1: 3D Basicranium measurements in both groups with Brainvisa processing: ( Step2: 3D anatomical study of semicircular canals in both groups with original modelling software.
AIS showed a pathognomic increase of these Human traits. Inside AIS subgroups, TL &
G3 revealed highest levels of asymmetry and rotation. We will discuss, thanks to AIS homozygosis twins in mirror, genetic origins for these specific P.B. &
Cerebellum asymmetries. Modelling of semi-circular canals revealed significative malformations in AIS compared to normal group. Again, T.L. and G3 revealed highest scores of canals anomalies. We highlighted a specific malformation in AIS: abnormal connexion between lateral &
posterior canal. We will demonstrate, thanks to same AIS twins, genetic origins of this malformation and propose a genetic hypothesis to link the different results.