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Predictors of new-onset widespread pain in older adults: results from a population-based prospective cohort study in the UK

Predictors of new-onset widespread pain in older adults: results from a population-based prospective cohort study in the UK
Predictors of new-onset widespread pain in older adults: results from a population-based prospective cohort study in the UK
Objective: in older adults, widespread pain (WP) is common, although its etiology is unclear. This study sought to identify factors associated with an increased risk of developing WP in adults age ≥50 years.

Methods: a population-based prospective study was conducted. A baseline questionnaire was administered to subjects to collect data on pain, psychological status, lifestyle and health behaviors, and sociodemographic and clinical factors. Participants free of WP (as defined by the American College of Rheumatology 1990 criteria for fibromyalgia) were followed up for 3 years, and those with new-onset WP at followup were identified. Logistic regression analyses were used to test the relationship between baseline factors and new-onset WP. Multiple imputation was used to test the results for sensitivity to missing data.

Results: in this population-based study, 4,326 subjects (1,562 reporting no pain at baseline and 2,764 reporting some pain at baseline) participated at followup. Of these participants, 800 (18.5%) reported a status of new WP at followup (of whom, 121 [7.7%] had reported no pain at baseline and 679 [24.6%] had reported some pain at baseline). The majority of the study factors were associated with new-onset WP. However, only a few factors showed a persistent association with new-onset WP in the multivariate analysis, including age (odds ratio [OR] 0.97, 95% confidence interval [95% CI] 0.96–0.99), baseline pain status (OR 1.1, 95% CI 1.08–1.2), anxiety (OR 1.5, 95% CI 1.01–2.1), physical health-related quality of life (OR 1.3, 95% CI 1.1–1.5), cognitive complaint (OR 1.3, 95% CI 1.04–1.6), and nonrestorative sleep (OR 1.9, 95% CI 1.2–2.8). These associations persisted after adjustment for the presence of diffuse osteoarthritis (OA), which led to a modest increase in model fit (C-statistic 0.738, compared with 0.731 in the model excluding diffuse OA). The results were not sensitive to missing data.

Conclusion: of the factors measured in this study, nonrestorative sleep was the strongest independent predictor of new-onset WP.
2326-5191
757-767
McBeth, John
98012716-66ba-480b-9e43-ac53b51dce61
Lacey, Rosie J.
f7ad2961-1071-47c2-9d62-42aed526bde0
Wilkie, Ross
f6c2a734-0dc7-4598-a4e5-322e5e50403a
McBeth, John
98012716-66ba-480b-9e43-ac53b51dce61
Lacey, Rosie J.
f7ad2961-1071-47c2-9d62-42aed526bde0
Wilkie, Ross
f6c2a734-0dc7-4598-a4e5-322e5e50403a

McBeth, John, Lacey, Rosie J. and Wilkie, Ross (2014) Predictors of new-onset widespread pain in older adults: results from a population-based prospective cohort study in the UK. Arthritis and Rheumatology, 66 (3), 757-767. (doi:10.1002/art.38284).

Record type: Article

Abstract

Objective: in older adults, widespread pain (WP) is common, although its etiology is unclear. This study sought to identify factors associated with an increased risk of developing WP in adults age ≥50 years.

Methods: a population-based prospective study was conducted. A baseline questionnaire was administered to subjects to collect data on pain, psychological status, lifestyle and health behaviors, and sociodemographic and clinical factors. Participants free of WP (as defined by the American College of Rheumatology 1990 criteria for fibromyalgia) were followed up for 3 years, and those with new-onset WP at followup were identified. Logistic regression analyses were used to test the relationship between baseline factors and new-onset WP. Multiple imputation was used to test the results for sensitivity to missing data.

Results: in this population-based study, 4,326 subjects (1,562 reporting no pain at baseline and 2,764 reporting some pain at baseline) participated at followup. Of these participants, 800 (18.5%) reported a status of new WP at followup (of whom, 121 [7.7%] had reported no pain at baseline and 679 [24.6%] had reported some pain at baseline). The majority of the study factors were associated with new-onset WP. However, only a few factors showed a persistent association with new-onset WP in the multivariate analysis, including age (odds ratio [OR] 0.97, 95% confidence interval [95% CI] 0.96–0.99), baseline pain status (OR 1.1, 95% CI 1.08–1.2), anxiety (OR 1.5, 95% CI 1.01–2.1), physical health-related quality of life (OR 1.3, 95% CI 1.1–1.5), cognitive complaint (OR 1.3, 95% CI 1.04–1.6), and nonrestorative sleep (OR 1.9, 95% CI 1.2–2.8). These associations persisted after adjustment for the presence of diffuse osteoarthritis (OA), which led to a modest increase in model fit (C-statistic 0.738, compared with 0.731 in the model excluding diffuse OA). The results were not sensitive to missing data.

Conclusion: of the factors measured in this study, nonrestorative sleep was the strongest independent predictor of new-onset WP.

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Accepted/In Press date: 14 November 2013
e-pub ahead of print date: 25 February 2014
Published date: 25 February 2014

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Local EPrints ID: 491372
URI: http://eprints.soton.ac.uk/id/eprint/491372
ISSN: 2326-5191
PURE UUID: f085bb3d-990a-45b1-99f7-e59f0683324e
ORCID for John McBeth: ORCID iD orcid.org/0000-0001-7047-2183

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Date deposited: 20 Jun 2024 17:09
Last modified: 21 Jun 2024 02:08

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Author: John McBeth ORCID iD
Author: Rosie J. Lacey
Author: Ross Wilkie

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