Parental chronic widespread pain and the association with chronic widespread pain in adult offspring: Family-linkage data from the Norwegian HUNT Study

J R Zadro; T I L Nilsen; D Shirley; A B Amorim; P H Ferreira; P J Mork

doi:10.1002/ejp.1237

Parental chronic widespread pain and the association with chronic widespread pain in adult offspring: Family-linkage data from the Norwegian HUNT Study

Eur J Pain. 2018 Apr 28. doi: 10.1002/ejp.1237. Online ahead of print.

Authors

J R Zadro¹, T I L Nilsen^{2

3}, D Shirley¹, A B Amorim¹, P H Ferreira¹, P J Mork²

Affiliations

¹ Discipline of Physiotherapy, Faculty of Health Sciences, The University of Sydney, NSW, Australia.
² Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway.
³ Clinic of Anaesthesia and Intensive Care, St Olavs Hospital, Trondheim University Hospital, Norway.

PMID: 29704885
DOI: 10.1002/ejp.1237

Abstract

Background: Individuals experiencing chronic widespread pain (CWP) have greater disability and poorer quality of life compared to those with other chronic painful conditions; although research identifying risk factors for CWP is lacking. We aimed to investigate whether parental CWP increases the risk of offspring CWP, and if offspring body mass index (BMI) and leisure time physical activity modify this association.

Methods: We included 6589 parent-offspring trios participating in the Norwegian HUNT Study in 1995-1997 and 2006-2008. Logistic regression was used to calculate adjusted odd ratios (ORs) (95% confidence intervals, CIs) as estimates of relative risk for offspring CWP. We analysed the joint effect of parental CWP and offspring BMI or leisure time physical activity on offspring risk of CWP and calculated the relative excess risk due to interaction (RERI).

Results: In total, 886 (13.5%) offspring developed CWP during follow-up. Having one (OR = 1.23, 95% CI, 1.05-1.44) or both parents with CWP (OR = 1.89, 95% CI, 1.50-2.38) increased the risk of offspring CWP. In analyses of joint effects, ORs were 1.84 (95% CI, 1.31-2.56) and 3.35 (95% CI, 1.94-5.77) in normal weight and obese offspring, respectively, when both parents had CWP. The estimate of RERI suggested some synergistic effect (RERI = 1.19, 95% CI, -0.68 to 3.05), although precision was low. Risk of CWP was similar in active (OR = 2.05, 95% CI, 1.56-2.70) and inactive (OR = 1.96, 95% CI, 1.31-2.91) offspring when both parents had CWP.

Conclusion: Parental CWP increases the risk of CWP in adult offspring, particularly if both parents have CWP and offspring are obese. This highlights a familial predisposition for CWP and an important target group for preventive measures.

Significance: The parent-offspring transmission of CWP is stronger in obese offspring (particularly when both parents have CWP). This study is the first to investigate the interaction between modifiable lifestyle factors, familial factors and CWP.