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A multidisciplinary assessment of pain in juvenile idiopathic arthritis.
Upadhyay, Jaymin; Lemme, Jordan; Cay, Mariesa; Van Der Heijden, Hanne; Sibai, Diana; Goodlett, Benjamin; Lo, Jeffery; Hoyt, Kacie; Taylor, Maria; Hazen, Melissa M; Halyabar, Olha; Meidan, Esra; Schreiber, Rudy; Chang, Margaret H; Nigrovic, Peter A; Jaimes, Camilo; Henderson, Lauren A; Ecklund, Kirsten; Sundel, Robert P.
Afiliación
  • Upadhyay J; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, MA, USA. Electronic address: jaymin.upadhyay@childrens.harvard.edu.
  • Lemme J; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Cay M; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, MA, USA.
  • Van Der Heijden H; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Faculty of Psychology and Neuroscience, Section Neuropsychology & Psychopharmacology Maastricht University, Maastricht, the Netherlands; Faculty of Science, Biomedi
  • Sibai D; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Goodlett B; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Lo J; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Hoyt K; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Taylor M; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Hazen MM; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Halyabar O; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Meidan E; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Schreiber R; Faculty of Psychology and Neuroscience, Section Neuropsychology & Psychopharmacology Maastricht University, Maastricht, the Netherlands.
  • Chang MH; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Nigrovic PA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jaimes C; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Henderson LA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Ecklund K; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Sundel RP; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Semin Arthritis Rheum ; 51(4): 700-711, 2021 08.
Article en En | MEDLINE | ID: mdl-34139523
INTRODUCTION: Pain is prevalent in juvenile idiopathic arthritis (JIA). Unknowns regarding the biological drivers of pain complicate therapeutic targeting. We employed neuroimaging to define pain-related neurobiological features altered in JIA. METHODS: 16 male and female JIA patients (12.7 ± 2.8 years of age) on active treatment were enrolled, together with age- and sex-matched controls. Patients were assessed using physical examination, clinical questionnaires, musculoskeletal MRI, and structural neuroimaging. In addition, functional magnetic resonance imaging (fMRI) data were collected during the resting-state, hand-motor task performance, and cold stimulation of the hand and knee. RESULTS: Patients with and without pain and with and without inflammation (joint and systemic) were evaluated.  Pain severity was associated with more physical stress and poorer cognitive function. Corrected for multiple comparisons, morphological analysis revealed decreased cortical thickness within the insula cortex and a negative correlation between caudate nucleus volume and pain severity. Functional neuroimaging findings suggested alteration within neurocircuitry structures regulating emotional pain processing (anterior insula) in addition to the default-mode and sensorimotor networks. CONCLUSIONS: Patients with JIA may exhibit changes in neurobiological circuits related to pain. These preliminary findings suggest mechanisms by which pain could potentially become dissociated from detectable joint pathology and persist independently of inflammation or treatment status.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Juvenil Tipo de estudio: Etiology_studies Límite: Female / Humans / Male Idioma: En Revista: Semin Arthritis Rheum Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Juvenil Tipo de estudio: Etiology_studies Límite: Female / Humans / Male Idioma: En Revista: Semin Arthritis Rheum Año: 2021 Tipo del documento: Article