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Journal of Neural Transmission

, Volume 125, Issue 10, pp 1473–1480 | Cite as

Body height loss characterizes camptocormia in Parkinson’s disease

  • Urban M. Fietzek
  • Frauke E. Schroeteler
  • Lisa Hahn
  • Kerstin Ziegler
  • Andres O. Ceballos-Baumann
Neurology and Preclinical Neurological Studies - Original Article
  • 29 Downloads

Abstract

Axial deformities such as camptocormia or Pisa syndrome in people with Parkinson’s disease (PwP) are poorly understood. The scarcity of information may result from the shortage of reliable and responsive evaluation instruments. We evaluated the body height loss (BHL) as a new measure for PwP with axial deformities. 50 PwP with axial deformity defined by an UPDRS item 28 value of at least 2 were included in this mono-center study. We measured body height while lying supine and after 1 min of standing, providing a percentage value of BHL, and compared this measure to other clinical variables. BHL depended on the Hoehn and Yahr clinical stage and correlated with clinical scales for function and mobility, but not with timely measures of the axial disorder such as age at diagnosis or duration of disease. ANOVA showed that only lumbar flexion explained the variability of BHL (F = 21.0, p < 0.0001), but not kyphosis (F = 0.4, p = 0.74) or lateroflexion (F = 0.6, p = 0.6). Re-test reliability of BHL was good with к = 0.76 (p < 0.0001). BHL resulted from the lumbar spine and the hip joint and not from the thoracic spine or lateroflexion. This observation conforms to the concept of upper-type and lower-type camptocormia with only the latter leading to a BHL. The assessment of the BHL is shown to be a well defined, easy to perform, and reliable measure for the clinical evaluation of lower-type camptocormia.

Keywords

Parkinson’s disease Axial deformity Posture Camptocormia Body height 

Notes

Acknowledgements

We want to thank the Deutsche Stiftung Neurologie and the Deutsche Parkinson Vereinigung for generously supporting this research. We want to thank the involved patients for their collaboration.

Compliance with ethical standards

Conflict of interest

On behalf of all authors, the corresponding author states there is no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Supplementary material

702_2018_1912_MOESM1_ESM.pdf (188 kb)
Supplementary material 1 (PDF 187 KB)
702_2018_1912_MOESM2_ESM.pdf (431 kb)
Supplementary material 2 (PDF 430 KB)
702_2018_1912_MOESM3_ESM.pdf (575 kb)
Supplementary material 3 (PDF 574 KB)

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Copyright information

© Springer-Verlag GmbH Austria, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Neurology and Clinical Neurophysiology, Centre for Parkinson’s Disease and Movement DisordersSchön Klinik München SchwabingMunichGermany
  2. 2.Department of Neurology, Klinikum Rechts der IsarTechnische Universität MünchenMunichGermany

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