4.2 Article

Fat mass and fat distribution are associated with low back pain intensity and disability: results from a cohort study

Journal

ARTHRITIS RESEARCH & THERAPY
Volume 19, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s13075-017-1242-z

Keywords

Obesity; Body composition; Fat mass; Fat-free mass; Low back pain

Categories

Funding

  1. National Health and Medical Research Council (NHMRC) [233200]
  2. Australian Government Department of Health and Ageing
  3. Abbott Australasia Pty Ltd
  4. Alphapharm Pty Ltd
  5. AstraZeneca
  6. Bristol-Myers Squibb
  7. City Health Centre-Diabetes Service-Canberra
  8. Department of Health and Community Services - Northern Territory
  9. Department of Health and Human Services - Tasmania
  10. Department of Health - New South Wales
  11. Department of Health - Western Australia
  12. Department of Health - South Australia
  13. Department of Human Services - Victoria
  14. Diabetes Australia
  15. Diabetes Australia Northern Territory
  16. Eli Lilly Australia
  17. Estate of the Late Edward Wilson
  18. GlaxoSmithKline
  19. Jack Brockhoff Foundation
  20. Janssen-Cilag
  21. Kidney Health Australia
  22. Marian and FH Flack Trust
  23. Menzies Research Institute
  24. Merck Sharp Dohme
  25. Novartis Pharmaceuticals
  26. Novo Nordisk Pharmaceuticals
  27. Pfizer Pty Ltd
  28. Pratt Foundation
  29. Queensland Health
  30. Roche Diagnostics Australia
  31. Royal Prince Alfred Hospital, Sydney
  32. Sanofi Aventis
  33. sanofi-synthelabo
  34. Victorian Government's Operational Infrastructure Support (OIS) Program
  35. AFA-ARA Heald Fellowship - Australian Rheumatology Association
  36. NHMRC Career Development Fellowship [1011975, 1065464, 1063574]
  37. NHMRC Research Fellowship
  38. NHMRC Senior Research Fellowship

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Background: Determining the association between body composition and low back pain (LBP) will improve our understanding of the mechanisms by which obesity affects LBP, and inform novel approaches to managing LBP. The aim of this study was to examine the relationship between body composition and LBP intensity and disability. Methods: A total of 5058 participants (44% men) of the Australian Diabetes, Obesity and Lifestyle Study were assessed for LBP intensity and disability using the Chronic Pain Grade Questionnaire (2013-2014). Body mass index (BMI) and waist circumference were directly obtained. Fat mass and percentage fat were estimated from bioelectrical impedance analysis at study inception (1999-2000). Results: Eighty-two percent of participants reported LBP, of whom 27% also reported LBP disability. BMI, waist circumference, percent fat, and fat mass were each positively associated with LBP intensity and disability at 12 years after adjustment for potential confounders. LBP intensity and disability showed significant dose-responses to sex-specific quartiles of BMI, waist circumference, percent fat and fat mass. For example, the adjusted OR for LBP intensity in women increased with increasing fat mass quartiles [Q1: 1, Q2: 1.05 (95% CI 0.84-1.32); Q3: 1. 25 (1.00-1.57); and Q4: 1.78 (1.42-2.24); p < 0.001]. Conclusions: Fat mass and distribution are associated with LBP intensity and disability, suggesting systemic metabolic factors associated with adiposity play a major role in the pathogenesis of LBP. Clarifying the mechanisms will facilitate developing novel preventive and therapeutic approaches for LBP.

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