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Radiological and clinical predictors of scoliosis in patients with Chiari malformation type I and spinal cord syrinx from the Park-Reeves Syringomyelia Research Consortium.
J Neurosurg Pediatr. 2019 Aug 16 [Online ahead of print]JN

Abstract

OBJECTIVE

Scoliosis is frequently a presenting sign of Chiari malformation type I (CM-I) with syrinx. The authors' goal was to define scoliosis in this population and describe how radiological characteristics of CM-I and syrinx relate to the presence and severity of scoliosis.

METHODS

A large multicenter retrospective and prospective registry of pediatric patients with CM-I (tonsils ≥ 5 mm below the foramen magnum) and syrinx (≥ 3 mm in axial width) was reviewed for clinical and radiological characteristics of CM-I, syrinx, and scoliosis (coronal curve ≥ 10°).

RESULTS

Based on available imaging of patients with CM-I and syrinx, 260 of 825 patients (31%) had a clear diagnosis of scoliosis based on radiographs or coronal MRI. Forty-nine patients (5.9%) did not have scoliosis, and in 516 (63%) patients, a clear determination of the presence or absence of scoliosis could not be made. Comparison of patients with and those without a definite scoliosis diagnosis indicated that scoliosis was associated with wider syrinxes (8.7 vs 6.3 mm, OR 1.25, p < 0.001), longer syrinxes (10.3 vs 6.2 levels, OR 1.18, p < 0.001), syrinxes with their rostral extent located in the cervical spine (94% vs 80%, OR 3.91, p = 0.001), and holocord syrinxes (50% vs 16%, OR 5.61, p < 0.001). Multivariable regression analysis revealed syrinx length and the presence of holocord syrinx to be independent predictors of scoliosis in this patient cohort. Scoliosis was not associated with sex, age at CM-I diagnosis, tonsil position, pB-C2 distance (measured perpendicular distance from the ventral dura to a line drawn from the basion to the posterior-inferior aspect of C2), clivoaxial angle, or frontal-occipital horn ratio. Average curve magnitude was 29.9°, and 37.7% of patients had a left thoracic curve. Older age at CM-I or syrinx diagnosis (p < 0.0001) was associated with greater curve magnitude whereas there was no association between syrinx dimensions and curve magnitude.

CONCLUSIONS

Syrinx characteristics, but not tonsil position, were related to the presence of scoliosis in patients with CM-I, and there was an independent association of syrinx length and holocord syrinx with scoliosis. Further study is needed to evaluate the nature of the relationship between syrinx and scoliosis in patients with CM-I.

Authors+Show Affiliations

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.2Department of Epidemiology, University of Iowa, Iowa City, Iowa.3Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.3Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.4Department of Neurosurgery, Neuroscience Institute, All Children's Hospital, St. Petersburg, Florida.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.5Department of Radiology, Washington University School of Medicine, St. Louis, Missouri.6Department of Pediatric Neurosurgery, University of Utah School of Medicine, Salt Lake City, Utah.3Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.7Department of Neurological Surgery, The Ohio State University College of Medicine, Columbus, Ohio.8Division of Pediatric Neurosurgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.9Division of Neurosurgery, University of Alabama School of Medicine, Birmingham, Alabama.10Department of Pediatric Surgery and Neurosurgery, The University of Texas McGovern Medical School, Houston, Texas.11Department of Neurological Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.12Department of Neurosurgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.13Department of Neurosurgery, The Mayo Clinic, Rochester, Minnesota.14Department of Neurosurgery, Johns Hopkins School of Medicine, Baltimore, Maryland.15Department of Neurosurgery, Stanford Child Health Research Institute, Stanford, California.16Department of Neurosurgery, Wake Forest Baptist Medical Center, Winston-Salem, North Carolina.17Department of Neurosurgery, Barrow Neurological Institute, Phoenix, Arizona.18Department of Pediatric Neurosurgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.19Department of Pediatric Neurosurgery, University of Florida College of Medicine, Jacksonville, Florida.20Department of Neurological Surgery, Columbia University College of Physicians and Surgeons, New York, New York.21Department of Neurological Surgery, Oregon Health & Science University, Portland, Oregon.21Department of Neurological Surgery, Oregon Health & Science University, Portland, Oregon.8Division of Pediatric Neurosurgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.22Department of Neurosurgery, Children's Healthcare of Atlanta, Georgia.23Department of Neurosurgery, Baylor College of Medicine, Houston, Texas.24Department of Neurosurgery, University of Washington Medicine, Seattle, Washington.25Department of Neurosurgery, Duke University School of Medicine, Durham, North Carolina.26Department of Neurosurgery, University of Minnesota Medical School, Minneapolis, Minnesota.27Department of Neurosurgery, Children's Hospital Colorado, Aurora, Colorado.28Department of Neurosurgery, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.9Division of Neurosurgery, University of Alabama School of Medicine, Birmingham, Alabama.29Department of Neurosurgery, Children's National Medical Center, Washington, DC.30Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee.30Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee.31Division of Neurosurgery, Children's Hospital Los Angeles, California.32Department of Neurosurgery, University of Iowa Hospitals, Iowa City, Iowa.33Department of Pediatric Neurosurgery, Miami Children's Hospital and University of Miami Miller School of Medicine, Miami, Florida.34Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana.35Department of Neurosurgery, University of Michigan, Ann Arbor, Michigan.12Department of Neurosurgery, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania.36Department of Orthopedic Surgery, Washington University School of Medicine, St. Louis, Missouri.27Department of Neurosurgery, Children's Hospital Colorado, Aurora, Colorado.31Division of Neurosurgery, Children's Hospital Los Angeles, California.37Department of Neurosurgery, The University of British Columbia, Vancouver, British Columbia, Canada.38Department of Neurosurgery, University of Vermont College of Medicine, Burlington, Vermont.39Arnold Palmer Hospital for Children, Orlando, Florida.40Department of Neurosurgery, Boston Children's Hospital, Boston, Massachusetts.41Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin.42Division of Neurosurgery, Children's Hospital of Philadelphia, Pennsylvania.43Department of Neurosurgery, Dartmouth Geisel School of Medicine, Hanover, New Hampshire.44Department of Neurosurgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas.45Department of Neurological Surgery, Weill Cornell Medical Center, New York, New York.46Department of Neurological Surgery, Levine Children's Hospital, Charlotte, North Carolina.46Department of Neurological Surgery, Levine Children's Hospital, Charlotte, North Carolina.47Department of Neurosurgery, Medical University of South Carolina, Charleston, South Carolina; and.48Department of Neurosurgery, Oklahoma University Medical Center, Oklahoma City, Oklahoma.5Department of Radiology, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

31419800

Citation

Strahle, Jennifer M., et al. "Radiological and Clinical Predictors of Scoliosis in Patients With Chiari Malformation Type I and Spinal Cord Syrinx From the Park-Reeves Syringomyelia Research Consortium." Journal of Neurosurgery. Pediatrics, 2019, pp. 1-8.
Strahle JM, Taiwo R, Averill C, et al. Radiological and clinical predictors of scoliosis in patients with Chiari malformation type I and spinal cord syrinx from the Park-Reeves Syringomyelia Research Consortium. J Neurosurg Pediatr. 2019.
Strahle, J. M., Taiwo, R., Averill, C., Torner, J., Shannon, C. N., Bonfield, C. M., Tuite, G. F., Bethel-Anderson, T., Rutlin, J., Brockmeyer, D. L., Wellons, J. C., Leonard, J. R., Mangano, F. T., Johnston, J. M., Shah, M. N., Iskandar, B. J., Tyler-Kabara, E. C., Daniels, D. J., Jackson, E. M., ... Limbrick, D. D. (2019). Radiological and clinical predictors of scoliosis in patients with Chiari malformation type I and spinal cord syrinx from the Park-Reeves Syringomyelia Research Consortium. Journal of Neurosurgery. Pediatrics, 1-8. https://doi.org/10.3171/2019.5.PEDS18527
Strahle JM, et al. Radiological and Clinical Predictors of Scoliosis in Patients With Chiari Malformation Type I and Spinal Cord Syrinx From the Park-Reeves Syringomyelia Research Consortium. J Neurosurg Pediatr. 2019 Aug 16;1-8. PubMed PMID: 31419800.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Radiological and clinical predictors of scoliosis in patients with Chiari malformation type I and spinal cord syrinx from the Park-Reeves Syringomyelia Research Consortium. AU - Strahle,Jennifer M, AU - Taiwo,Rukayat, AU - Averill,Christine, AU - Torner,James, AU - Shannon,Chevis N, AU - Bonfield,Christopher M, AU - Tuite,Gerald F, AU - Bethel-Anderson,Tammy, AU - Rutlin,Jerrel, AU - Brockmeyer,Douglas L, AU - Wellons,John C, AU - Leonard,Jeffrey R, AU - Mangano,Francesco T, AU - Johnston,James M, AU - Shah,Manish N, AU - Iskandar,Bermans J, AU - Tyler-Kabara,Elizabeth C, AU - Daniels,David J, AU - Jackson,Eric M, AU - Grant,Gerald A, AU - Couture,Daniel E, AU - Adelson,P David, AU - Alden,Tord D, AU - Aldana,Philipp R, AU - Anderson,Richard C E, AU - Selden,Nathan R, AU - Baird,Lissa C, AU - Bierbrauer,Karin, AU - Chern,Joshua J, AU - Whitehead,William E, AU - Ellenbogen,Richard G, AU - Fuchs,Herbert E, AU - Guillaume,Daniel J, AU - Hankinson,Todd C, AU - Iantosca,Mark R, AU - Oakes,W Jerry, AU - Keating,Robert F, AU - Khan,Nickalus R, AU - Muhlbauer,Michael S, AU - McComb,J Gordon, AU - Menezes,Arnold H, AU - Ragheb,John, AU - Smith,Jodi L, AU - Maher,Cormac O, AU - Greene,Stephanie, AU - Kelly,Michael, AU - O'Neill,Brent R, AU - Krieger,Mark D, AU - Tamber,Mandeep, AU - Durham,Susan R, AU - Olavarria,Greg, AU - Stone,Scellig S D, AU - Kaufman,Bruce A, AU - Heuer,Gregory G, AU - Bauer,David F, AU - Albert,Gregory, AU - Greenfield,Jeffrey P, AU - Wait,Scott D, AU - Van Poppel,Mark D, AU - Eskandari,Ramin, AU - Mapstone,Timothy, AU - Shimony,Joshua S, AU - Dacey,Ralph G, AU - Smyth,Matthew D, AU - Park,Tae Sung, AU - Limbrick,David D, Y1 - 2019/08/16/ PY - 2018/11/02/received PY - 2019/05/09/accepted PY - 2019/8/17/entrez PY - 2019/8/17/pubmed PY - 2019/8/17/medline KW - AIS = adolescent idiopathic scoliosis KW - CM-1 = Chiari malformation type I KW - CXA = clivoaxial angle KW - Chiari KW - PRSRC = Park-Reeves Syringomyelia Research Consortium KW - deformity KW - pB–C2 = measured perpendicular distance from the ventral dura to a line drawn from the basion to the posterior-inferior aspect of C2 KW - scoliosis KW - spine KW - syringomyelia KW - tonsil SP - 1 EP - 8 JF - Journal of neurosurgery. Pediatrics JO - J Neurosurg Pediatr N2 - OBJECTIVE: Scoliosis is frequently a presenting sign of Chiari malformation type I (CM-I) with syrinx. The authors' goal was to define scoliosis in this population and describe how radiological characteristics of CM-I and syrinx relate to the presence and severity of scoliosis. METHODS: A large multicenter retrospective and prospective registry of pediatric patients with CM-I (tonsils ≥ 5 mm below the foramen magnum) and syrinx (≥ 3 mm in axial width) was reviewed for clinical and radiological characteristics of CM-I, syrinx, and scoliosis (coronal curve ≥ 10°). RESULTS: Based on available imaging of patients with CM-I and syrinx, 260 of 825 patients (31%) had a clear diagnosis of scoliosis based on radiographs or coronal MRI. Forty-nine patients (5.9%) did not have scoliosis, and in 516 (63%) patients, a clear determination of the presence or absence of scoliosis could not be made. Comparison of patients with and those without a definite scoliosis diagnosis indicated that scoliosis was associated with wider syrinxes (8.7 vs 6.3 mm, OR 1.25, p < 0.001), longer syrinxes (10.3 vs 6.2 levels, OR 1.18, p < 0.001), syrinxes with their rostral extent located in the cervical spine (94% vs 80%, OR 3.91, p = 0.001), and holocord syrinxes (50% vs 16%, OR 5.61, p < 0.001). Multivariable regression analysis revealed syrinx length and the presence of holocord syrinx to be independent predictors of scoliosis in this patient cohort. Scoliosis was not associated with sex, age at CM-I diagnosis, tonsil position, pB-C2 distance (measured perpendicular distance from the ventral dura to a line drawn from the basion to the posterior-inferior aspect of C2), clivoaxial angle, or frontal-occipital horn ratio. Average curve magnitude was 29.9°, and 37.7% of patients had a left thoracic curve. Older age at CM-I or syrinx diagnosis (p < 0.0001) was associated with greater curve magnitude whereas there was no association between syrinx dimensions and curve magnitude. CONCLUSIONS: Syrinx characteristics, but not tonsil position, were related to the presence of scoliosis in patients with CM-I, and there was an independent association of syrinx length and holocord syrinx with scoliosis. Further study is needed to evaluate the nature of the relationship between syrinx and scoliosis in patients with CM-I. SN - 1933-0715 UR - https://www.unboundmedicine.com/medline/citation/31419800/Radiological_and_clinical_predictors_of_scoliosis_in_patients_with_Chiari_malformation_type_I_and_spinal_cord_syrinx_from_the_Park_Reeves_Syringomyelia_Research_Consortium_ DB - PRIME DP - Unbound Medicine ER -