Sagittal spinopelvic malalignment in Parkinson disease: prevalence and associations with disease severity.
dc.contributor.author | Oh, Jae Keun | |
dc.contributor.author | Smith, Justin S | |
dc.contributor.author | Shaffrey, Christopher I | |
dc.contributor.author | Lafage, Virginie | |
dc.contributor.author | Schwab, Frank | |
dc.contributor.author | Ames, Christopher P | |
dc.contributor.author | Matsumoto, Morio | |
dc.contributor.author | Baik, Jong Sam | |
dc.contributor.author | Ha, Yoon | |
dc.date.accessioned | 2023-07-20T20:37:40Z | |
dc.date.available | 2023-07-20T20:37:40Z | |
dc.date.issued | 2014-06 | |
dc.date.updated | 2023-07-20T20:37:20Z | |
dc.description.abstract | Study designProspective study.ObjectiveOur objectives were to evaluate the prevalence of sagittal spinopelvic malalignment in a consecutive series of patients with Parkinson disease (PD) and to identify factors associated with sagittal spinopelvic deformity in this population.Summary of background dataPD is a degenerative neurological condition characterized by tremor, rigidity, bradykinesia, and loss of postural reflexes. The prevalence of spinal deformity in PD is higher than that of age-matched adults without PD.MethodsThis study was a prospective assessment of consecutive patients with PD presenting to a neurology clinic during 12 months. Inclusion criteria included age more than 21 years and diagnosis of PD. Age- and sex-matched control group was selected from patients with cervical spondylosis. Clinical and demographic factors were collected including Unified Parkinson Disease Rating Scale score and Hoehn and Yahr stage. Full-length standing spine radiographs were assessed. Patients were grouped into either low C7 sagittal vertical axis (SVA) (<5 cm) or high C7 SVA (≥5 cm) and into matched (≤10°) or mismatched (>10°) pelvic incidence (PI)-lumbar lordosis.ResultsEighty-nine patients met criteria (41 males/48 females), including 52 with low C7 SVA and 37 with high C7 SVA. Significantly higher prevalence of high C7 SVA was found in PD (41.6 vs. 16.8%; P < 0.001). The high C7 SVA group was significantly older (72.4 vs. 65.1 yr; P < 0.001) and had a higher proportion of females (68% vs. 44%; P = 0.034), greater severity of PD based on Hoehn and Yahr stage (1.89 vs. 1.37; P < 0.001) and Unified Parkinson Disease Rating Scale (30.5 vs. 17.2; P = 0.002. Unified Parkinson Disease Rating Scale significantly correlated with C7 SVA (r = 0.474). Compared with the matched (≤10°) PI-lumbar lordosis group, the mismatch PI-lumbar lordosis group had higher C7 SVA, higher PI, higher pelvic tilt, lower lumbar lordosis, and lower thoracic kyphosis (P ≤ 0.003).ConclusionPatients with PD have a high prevalence of sagittal spinopelvic malalignment than control group patients. Greater severity of PD is associated with sagittal spinopelvic malalignment.Level of evidence3. | |
dc.identifier.issn | 0362-2436 | |
dc.identifier.issn | 1528-1159 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
dc.relation.ispartof | Spine | |
dc.relation.isversionof | 10.1097/brs.0000000000000366 | |
dc.subject | Pelvis | |
dc.subject | Spine | |
dc.subject | Humans | |
dc.subject | Spinal Diseases | |
dc.subject | Parkinson Disease | |
dc.subject | Radiography | |
dc.subject | Severity of Illness Index | |
dc.subject | Prevalence | |
dc.subject | Prospective Studies | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Male | |
dc.title | Sagittal spinopelvic malalignment in Parkinson disease: prevalence and associations with disease severity. | |
dc.type | Journal article | |
duke.contributor.orcid | Shaffrey, Christopher I|0000-0001-9760-8386 | |
pubs.begin-page | E833 | |
pubs.end-page | E841 | |
pubs.issue | 14 | |
pubs.organisational-group | Duke | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Orthopaedic Surgery | |
pubs.organisational-group | Neurosurgery | |
pubs.publication-status | Published | |
pubs.volume | 39 |
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