Brain structure, psychosocial, and physical health in acute and chronic back pain: a UK Biobank study

被引:18
作者
Tagliaferri, Scott D. [1 ]
Fitzgibbon, Bernadette M. [2 ]
Owen, Patrick J. [1 ]
Miller, Clint T. [1 ]
Bowe, Steven J. [3 ]
Belavy, Daniel L. [1 ,4 ]
机构
[1] Deakin Univ, Inst Phys Act & Nutr, Sch Exercise & Nutr Sci, Geelong, Vic, Australia
[2] Monash Univ, Sch Publ Hlth & Prevent Med, Dept Epidemiol & Prevent Med, Fac Med, Melbourne, Vic, Australia
[3] Deakin Univ, Fac Hlth, Biostat Unit, Geelong, Vic, Australia
[4] Univ Appl Sci, Div Physiotherapy, Dept Appl Hlth Sci, Hsch Gesundheit, Bochum, Germany
关键词
UK Biobank; Spine; Biopsychosocial; Spinal; RISK-FACTORS; MUSCULOSKELETAL PAIN; PROGNOSTIC-FACTORS; SOCIAL-ISOLATION; DEPRESSION; ANXIETY; COHORT; EPIDEMIOLOGY; LEVEL;
D O I
10.1097/j.pain.0000000000002524
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Brain structure, psychosocial, and physical factors underpin back pain conditions; however, less is known about how these factors differ based on pain duration and location. We examined, cross-sectionally, 11,106 individuals from the UK Biobank who (1) were pain-free (n = 5616), (2) had acute back pain (n = 1746), (3) had chronic localised back pain (CBP; n = 1872), or (4) had chronic back pain and additional chronic pain sites (CWP; n = 1872). We found differences in structural brain measures in the chronic pain groups alone. Both CBP and CWP groups had lower primary somatosensory cortex {CBP mean difference (MD) (95% confidence interval [CI]): -250 (-393, -107) mm(3), P < 0.001; CWP: -170 (-313, -27)mm(3), P = 0.011} and higher caudate gray matter volumes (CBP: 127 [38,216]mm(3), P = 0.001; CWP: 122 [33,210]mm(3), P = 0.002) compared with pain-free controls. The CBP group also had a lower primary motor cortex volume (-215 [-382, -50]mm(3), P = 0.005), whereas the CWP group had a lower amygdala gray matter volume (-27 [-52, -3]mm(3), P = 0.021) compared with pain-free controls. Differences in gray matter volumes in some regions may be moderated by sex and body mass index. Psychosocial factors and body mass index differed between all groups and affected those with widespread pain the most (all, P < 0.001), whereas grip strength was only compromised in individuals with widespread pain (-1.0 [-1.4, -0.5] kg, P < 0.001) compared with pain-free controls. Longitudinal research is necessary to confirm these interactions to determine the process of pain development in relation to assessed variables and covariates. However, our results suggest that categorised pain duration and the number of pain sites warrant consideration when assessing markers of brain structure, psychosocial, and physical health.
引用
收藏
页码:1277 / 1290
页数:14
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