Lumbar spine abnormalities in patients with obstructive sleep apnoea.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 08 2021
Historique:
received: 19 01 2021
accepted: 28 07 2021
entrez: 11 8 2021
pubmed: 12 8 2021
medline: 9 11 2021
Statut: epublish

Résumé

Previous studies suggested cervical spondylosis as a risk factor for development of obstructive sleep apnoea (OSA). We aimed to assess lumbar disc degeneration in patients with OSA and correlate the findings with symptoms and disease severity. Twenty-seven patients with OSA and 29 non-OSA controls underwent sleep studies and lumbar magnetic resonance imaging (MRI), and completed the Epworth Sleepiness Scale and the 24-item Roland-Morris Disability Questionnaire (RMDQ) questionnaires. Plasma klotho was determined with enzyme-linked immunosorbent assay. Patients with OSA had higher number of disc bulges (4.6 ± 3.7 vs. 1.7 ± 2.5, p < 0.01) and anterior spondylophytes (2.7 ± 4.2 vs. 0.8 ± 2.1, p < 0.01), increased disc degeneration (total Pfirrmann score 16.7 ± 4.7 vs. 13.2 ± 4.1, p < 0.01) and vertebral fatty degeneration (7.8 ± 4.7 vs. 3.8 ± 3.7, p < 0.01). There was no difference in the RMDQ score (0/0-3.5/ vs. 0/0-1/, p > 0.05). Markers of OSA severity, including the oxygen desaturation index and percentage of total sleep time spent with saturation < 90% as well as plasma levels of klotho were correlated with the number of disc bulges and anterior spondylophytes (all p < 0.05). OSA is associated with lumbar spondylosis. Our study highlights the importance of lumbar imaging in patients with OSA reporting lower back pain.

Identifiants

pubmed: 34376739
doi: 10.1038/s41598-021-95667-3
pii: 10.1038/s41598-021-95667-3
pmc: PMC8355280
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16233

Informations de copyright

© 2021. The Author(s).

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Auteurs

Adam Domonkos Tarnoki (AD)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary. tarnoki2@gmail.com.

David Laszlo Tarnoki (DL)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary.

Csaba Oláh (C)

Department of Neurosurgery, Borsod-Abaúj-Zemplén County and University Teaching Hospital, Miskolc, Hungary.

Marcell Szily (M)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary.

Daniel T Kovacs (DT)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary.

András Dienes (A)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary.

Marton Piroska (M)

Medical Imaging Centre, Semmelweis University, 78/A Üllői street, 1082, Budapest, Hungary.

Bianka Forgo (B)

Department of Radiology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Marina Pinheiro (M)

Faculty of Health Sciences, Discipline of Physiotherapy, The University of Sydney, Musculoskeletal Health, Sydney, Australia.

Paulo Ferreira (P)

Faculty of Health Sciences, Discipline of Physiotherapy, The University of Sydney, Musculoskeletal Health, Sydney, Australia.

László Kostyál (L)

Department of Neurosurgery, Borsod-Abaúj-Zemplén County and University Teaching Hospital, Miskolc, Hungary.

Martina Meszaros (M)

Department of Pulmonology, Semmelweis University, Budapest, Hungary.
Department of Pulmonology, University Hospital Zurich, Zurich, Switzerland.

Judit Pako (J)

National Koranyi Institute for Pulmonology, Budakeszi, Hungary.

Laszlo Kunos (L)

Department of Pulmonology, Semmelweis University, Budapest, Hungary.

Andras Bikov (A)

Department of Pulmonology, Semmelweis University, Budapest, Hungary.
Wythenshawe Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, UK.

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