The effect of renin-angiotensin system blockers on spinal cord dysfunction and imaging features of spinal cord compression in patients with symptomatic cervical spondylosis.


Journal

The spine journal : official journal of the North American Spine Society
ISSN: 1878-1632
Titre abrégé: Spine J
Pays: United States
ID NLM: 101130732

Informations de publication

Date de publication:
04 2020
Historique:
received: 11 04 2019
revised: 31 10 2019
accepted: 02 12 2019
pubmed: 11 12 2019
medline: 29 6 2021
entrez: 11 12 2019
Statut: ppublish

Résumé

Cervical spondylosis may lead to spinal cord compression, poor vascular perfusion, and ultimately, cervical myelopathy. Studies suggest a neuroprotective effect of renin-angiotensin system (RAS) inhibitors in the brain, but limited data exist regarding their impact on the spinal cord. To investigate whether RAS blockers and other antihypertensive drugs are correlated with preoperative functional status and imaging markers of cord compression in patients with symptomatic cervical spondylosis. Retrospective observational study. Individuals with symptomatic degenerative cervical stenosis who underwent surgery. Imaging features of spinal cord compression and functional status (modified Japanese Orthopedic Association [mJOA] and Nurick grading scales). Two hundred sixty-six operative patients with symptomatic degenerative cervical stenosis were included. Demographic data, comorbidities, antihypertensive medications, and functional status (including mJOA and Nurick grading scales) were collected. We evaluated canal compromise, cord compromise, surface area of T2 signal cord change, and pixel intensity of signal cord change compared with normal cord on T2-weighted magnetic resonance imaging sequences. Of 266 patients, 41.7% were women, 58.3% were men; median age was 57.2 years; 20.6% smoked tobacco; 24.7% had diabetes mellitus. One hundred forty-nine patients (55.8%) had hypertension, 142 (95.3%) of these were taking antihypertensive medications (37 angiotensin-II receptor blockers [ARBs], 44 angiotensin-converting enzyme inhibitors, and 61 other medications). Patients treated with ARBs displayed a higher signal intensity ratio (ie, less signal intensity change in the compressed cord area) compared with untreated patients without hypertension (p=.004). Patients with hypertension had worse preoperative mJOA and Nurick scores than those without (p<.001). In the multivariate analysis, ARBs remained an independent beneficial factor for lower signal intensity change (p=.04), whereas hypertension remained a risk factor for worse preoperative neurological status (p<.01). In our study, patients with hypertension who were treated with RAS inhibitors had decreased T2-weighted signal intensity change than untreated patients without hypertension. Patients with hypertension also had worse preoperative functional status. Prospective case-control studies may deepen understanding of RAS modulators in the imaging and functional status of chronic spinal cord compression.

Sections du résumé

BACKGROUND CONTEXT
Cervical spondylosis may lead to spinal cord compression, poor vascular perfusion, and ultimately, cervical myelopathy. Studies suggest a neuroprotective effect of renin-angiotensin system (RAS) inhibitors in the brain, but limited data exist regarding their impact on the spinal cord.
PURPOSE
To investigate whether RAS blockers and other antihypertensive drugs are correlated with preoperative functional status and imaging markers of cord compression in patients with symptomatic cervical spondylosis.
STUDY DESIGN
Retrospective observational study.
PATIENT SAMPLE
Individuals with symptomatic degenerative cervical stenosis who underwent surgery.
OUTCOME MEASURES
Imaging features of spinal cord compression and functional status (modified Japanese Orthopedic Association [mJOA] and Nurick grading scales).
METHODS
Two hundred sixty-six operative patients with symptomatic degenerative cervical stenosis were included. Demographic data, comorbidities, antihypertensive medications, and functional status (including mJOA and Nurick grading scales) were collected. We evaluated canal compromise, cord compromise, surface area of T2 signal cord change, and pixel intensity of signal cord change compared with normal cord on T2-weighted magnetic resonance imaging sequences.
RESULTS
Of 266 patients, 41.7% were women, 58.3% were men; median age was 57.2 years; 20.6% smoked tobacco; 24.7% had diabetes mellitus. One hundred forty-nine patients (55.8%) had hypertension, 142 (95.3%) of these were taking antihypertensive medications (37 angiotensin-II receptor blockers [ARBs], 44 angiotensin-converting enzyme inhibitors, and 61 other medications). Patients treated with ARBs displayed a higher signal intensity ratio (ie, less signal intensity change in the compressed cord area) compared with untreated patients without hypertension (p=.004). Patients with hypertension had worse preoperative mJOA and Nurick scores than those without (p<.001). In the multivariate analysis, ARBs remained an independent beneficial factor for lower signal intensity change (p=.04), whereas hypertension remained a risk factor for worse preoperative neurological status (p<.01).
CONCLUSIONS
In our study, patients with hypertension who were treated with RAS inhibitors had decreased T2-weighted signal intensity change than untreated patients without hypertension. Patients with hypertension also had worse preoperative functional status. Prospective case-control studies may deepen understanding of RAS modulators in the imaging and functional status of chronic spinal cord compression.

Identifiants

pubmed: 31821888
pii: S1529-9430(19)31114-3
doi: 10.1016/j.spinee.2019.12.002
pii:
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

519-529

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Alexander Perdomo-Pantoja (A)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Alejandro Chara (A)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Samuel Kalb (S)

Division of Neurological Surgery, St. Joseph's Hospital and Medical Center, Barrow Neurological Institute, Phoenix, AZ, USA.

Joshua Casaos (J)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

A Karim Ahmed (AK)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Zachary Pennington (Z)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Ethan Cottrill (E)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Sohan Shah (S)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Bowen Jiang (B)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Amir Manbachi (A)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Corinna Zygourakis (C)

Department of Neurosurgery, Stanford University School Of Medicine, Stanford, CA, USA.

Timothy F Witham (TF)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA.

Nicholas Theodore (N)

Department of Neurosurgery, Johns Hopkins University School Of Medicine, Baltimore, MD, USA. Electronic address: Theodore@jhmi.edu.

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Classifications MeSH