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Brain structure, psychosocial, and physical health in acute and chronic back pain: a UK Biobank study.
Tagliaferri, Scott D; Fitzgibbon, Bernadette M; Owen, Patrick J; Miller, Clint T; Bowe, Steven J; Belavy, Daniel L.
Afiliação
  • Tagliaferri SD; Deakin University, Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Geelong, Australia.
  • Fitzgibbon BM; Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne Victoria, Australia.
  • Owen PJ; Deakin University, Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Geelong, Australia.
  • Miller CT; Deakin University, Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Geelong, Australia.
  • Bowe SJ; Biostatistics Unit, Deakin University, Faculty of Health, Geelong, Australia.
  • Belavy DL; Deakin University, Institute for Physical Activity and Nutrition, School of Exercise and Nutrition Sciences, Geelong, Australia.
Pain ; 163(7): 1277-1290, 2022 07 01.
Article em En | MEDLINE | ID: mdl-34711762
ABSTRACT
ABSTRACT 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) mm3, P < 0.001; CWP -170 (-313, -27)mm3, P = 0.011} and higher caudate gray matter volumes (CBP 127 [38,216]mm3, P = 0.001; CWP 122 [33,210]mm3, P = 0.002) compared with pain-free controls. The CBP group also had a lower primary motor cortex volume (-215 [-382, -50]mm3, P = 0.005), whereas the CWP group had a lower amygdala gray matter volume (-27 [-52, -3]mm3, 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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Crônica Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Pain Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Crônica Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Pain Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália