OBJECTIVES: To investigate whether symptoms of depression increase the risk of low back pain (LBP), after adjusting for genetic and environmental influences. METHODS: Baseline data of 1607 twins from the Murcia Twin Registry (Spain) were collected in 2009-2011 and follow-up data in 2013. Twins answered questions on depression-related symptomatology and LBP. Only participants not reporting chronic LBP (pain>6 mo) at baseline were included. The association between symptoms of depression and LBP was investigated using logistic regression analysis including the complete sample. Subsequent matched within pair case-control analyses were performed with all complete dizygotic twin pairs discordant for LBP, followed by monozygotic twins. RESULTS: In the total sample analysis, symptoms of depression did not significantly increase the risk of chronic LBP (OR=1.40, 95%CI: 0.96-2.03), LBP care seeking (OR=1.21, 95%CI: 0.81-1.81), or activity limiting LBP (OR=1.09, 95%CI: 0.69-1.72). State-depression (participants' symptoms at the moment of the interview) was significantly associated with future care seeking (OR=1.06, 95%CI: 1.01-1.12), and activity limiting LBP (OR=1.07, 95%CI: 1.01-1.14). A significant association was found between trait depression and activity limiting LBP (OR=1.05, 95%CI: 1.01-1.10), but not for the other LBP outcomes. No significant association was observed in any of the subsequent case-control analyses. DISCUSSION: The magnitude of the association between depression and LBP appears to be small and may be confounded by genetic and early shared environment influences, although firm conclusions could not be made due to small sample size in the case-control analysis. Additionally, the observed association is dependent on the method of assessment used for both conditions.
AD - *Arthritis & Musculoskeletal Research Group, Faculty of Health Sciences, The University of Sydney, Sydney, Australia daggerMusculoskeletal Division, The George Institute for Global Health, Sydney Medical School, The University of Sydney, Sydney, Australia double daggerInstitute of Bone and Joint Research, The Kolling Institute, Sydney Medical School, The University of Sydney, Sydney, Australia section signMurcia Twin Registry, Department of Human Anatomy and Psychobiology, University of Murcia and IMIB-Arrixaca, Murcia, Spain parallelPsychiatric Genetics Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia paragraph signCentre for Epidemiology & Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia. AN - 27977426 BT - Clin J Pain CN - [IF]: 2.527 DP - NLM ET - 2016/12/16 J2 - The Clinical journal of pain LA - eng LB - AUSOBJECTIVES: To investigate whether symptoms of depression increase the risk of low back pain (LBP), after adjusting for genetic and environmental influences. METHODS: Baseline data of 1607 twins from the Murcia Twin Registry (Spain) were collected in 2009-2011 and follow-up data in 2013. Twins answered questions on depression-related symptomatology and LBP. Only participants not reporting chronic LBP (pain>6 mo) at baseline were included. The association between symptoms of depression and LBP was investigated using logistic regression analysis including the complete sample. Subsequent matched within pair case-control analyses were performed with all complete dizygotic twin pairs discordant for LBP, followed by monozygotic twins. RESULTS: In the total sample analysis, symptoms of depression did not significantly increase the risk of chronic LBP (OR=1.40, 95%CI: 0.96-2.03), LBP care seeking (OR=1.21, 95%CI: 0.81-1.81), or activity limiting LBP (OR=1.09, 95%CI: 0.69-1.72). State-depression (participants' symptoms at the moment of the interview) was significantly associated with future care seeking (OR=1.06, 95%CI: 1.01-1.12), and activity limiting LBP (OR=1.07, 95%CI: 1.01-1.14). A significant association was found between trait depression and activity limiting LBP (OR=1.05, 95%CI: 1.01-1.10), but not for the other LBP outcomes. No significant association was observed in any of the subsequent case-control analyses. DISCUSSION: The magnitude of the association between depression and LBP appears to be small and may be confounded by genetic and early shared environment influences, although firm conclusions could not be made due to small sample size in the case-control analysis. Additionally, the observed association is dependent on the method of assessment used for both conditions.
PY - 2016 SN - 1536-5409 (Electronic)