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Relationship of joint hypermobility with low Back pain and lumbar spine osteoarthritis.
Goode, Adam P; Cleveland, Rebecca J; Schwartz, Todd A; Nelson, Amanda E; Kraus, Virginia B; Hillstrom, Howard J; Hannan, Marian T; Flowers, Portia; Renner, Jordan B; Jordan, Joanne M; Golightly, Yvonne M.
  • Goode AP; Department of Orthopedic Surgery, Duke University School of Medicine, Durham, NC, USA. Adam.goode@duke.edu.
  • Cleveland RJ; Duke Clinical Research Institute, Duke University, Durham, NC, USA. Adam.goode@duke.edu.
  • Schwartz TA; Duke Department of Population Health Sciences, Durham, NC, USA. Adam.goode@duke.edu.
  • Nelson AE; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC, USA.
  • Kraus VB; Department of Medicine, University of North Carolina, Chapel Hill, NC, USA.
  • Hillstrom HJ; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC, USA.
  • Hannan MT; Department of Biostatistics, University of North Carolina, Chapel Hill, NC, USA.
  • Flowers P; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC, USA.
  • Renner JB; Department of Medicine, University of North Carolina, Chapel Hill, NC, USA.
  • Jordan JM; Duke Molecular Physiology Institute and Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
  • Golightly YM; Hospital for Special Surgery, New York, NY, USA.
BMC Musculoskelet Disord ; 20(1): 158, 2019 Apr 09.
Article en En | MEDLINE | ID: mdl-30967130
ABSTRACT

BACKGROUND:

Chronic low back pain (cLBP) affects millions of Americans and costs billions. Studies suggest a link between cLBP and joint hypermobility.

METHODS:

We conducted cross-sectional primary analyses of joint hypermobility and cLBP, lumbar spine osteoarthritis (OA), and lumbar facet joint OA (FOA) in 3 large studies-the Generalized Osteoarthritis Study, Genetics of Generalized Osteoarthritis Study, and Johnston County Osteoarthritis Project (total n = 5072). Associations of joint hypermobility and Beighton trunk flexion with cLBP and lumbar OA were estimated using separate adjusted logistic regression models. Adjusted pooled odds ratios (pORs) and 95% confidence intervals (CIs) were then summarized-using random effect univariate, multivariate crude, and adjusted models-and heterogeneity was determined (I2 statistic).

RESULTS:

In univariate models, hypermobility was associated with symptomatic FOA (pOR = 0.64 [95% CI 0.44, 0.93]) but this result was not found in the multivariate models. In multivariate adjusted models, hypermobility was not significantly associated with cLBP and lumbar OA, but trunk flexion was inversely associated with cLBP (pOR = 0.40 [95% 0.26, 0.62]), spine OA (pOR = 0.66 [95% CI 0.50, 0.87]), symptomatic spine OA (pOR = 0.39 [95% CI 0.28, 0.53]), and symptomatic FOA (pOR = 0.53 [95% CI 0.37, 0.77]). Generally, between-study heterogeneity was moderate-high.

CONCLUSIONS:

Hypermobility was not associated with cLBP or lumbar OA. The inverse association of trunk flexion with cLBP and lumbar OA may indicate a role for a flexible spine in avoiding or managing these conditions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor de la Región Lumbar / Osteoartritis de la Columna Vertebral / Inestabilidad de la Articulación / Vértebras Lumbares Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor de la Región Lumbar / Osteoartritis de la Columna Vertebral / Inestabilidad de la Articulación / Vértebras Lumbares Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article