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The brain-derived neurotrophic factor pathway, life stress, and chronic multi-site musculoskeletal pain.
Generaal, Ellen; Milaneschi, Yuri; Jansen, Rick; Elzinga, Bernet M; Dekker, Joost; Penninx, Brenda W J H.
  • Generaal E; Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands e.generaal@ggzingeest.nl.
  • Milaneschi Y; Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.
  • Jansen R; Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.
  • Elzinga BM; Institute of Psychology, Leiden University, Leiden, The Netherlands Leiden Institute for Brain and Cognition, Leiden, The Netherlands.
  • Dekker J; Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands Department of Rehabilitation Medicine, VU University Medical Center, Amsterdam, The Netherlands.
  • Penninx BW; Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.
Mol Pain ; 122016.
Article en En | MEDLINE | ID: mdl-27145806
ABSTRACT

INTRODUCTION:

Brain-derived neurotrophic factor (BDNF) disturbances and life stress, both independently and in interaction, have been hypothesized to induce chronic pain. We examined whether (a) the BDNF pathway (val(66)met genotype, gene expression, and serum levels), (b) early and recent life stress, and (c) their interaction are associated with the presence and severity of chronic multi-site musculoskeletal pain.

METHODS:

Cross-sectional data are from 1646 subjects of the Netherlands Study of Depression and Anxiety. The presence and severity of chronic multi-site musculoskeletal pain were determined using the Chronic Pain Grade (CPG) questionnaire. The BDNF val(66)met polymorphism, BDNF gene expression, and BDNF serum levels were measured. Early life stress before the age of 16 was assessed by calculating a childhood trauma index using the Childhood Trauma Interview. Recent life stress was assessed as the number of recent adverse life events using the List of Threatening Events Questionnaire.

RESULTS:

Compared to val(66)val, BDNF met carriers more often had chronic pain, whereas no differences were found for BDNF gene expression and serum levels. Higher levels of early and recent stress were both associated with the presence and severity of chronic pain (p < 0.001). No interaction effect was found for the BDNF pathway with life stress in the associations with chronic pain presence and severity.

CONCLUSIONS:

This study suggests that the BDNF gene marks vulnerability for chronic pain. Although life stress did not alter the impact of BDNF on chronic pain, it seems an independent factor in the onset and persistence of chronic pain.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estrés Psicológico / Transducción de Señal / Factor Neurotrófico Derivado del Encéfalo / Dolor Musculoesquelético / Dolor Crónico Tipo de estudio: Qualitative_research Límite: Adult / Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estrés Psicológico / Transducción de Señal / Factor Neurotrófico Derivado del Encéfalo / Dolor Musculoesquelético / Dolor Crónico Tipo de estudio: Qualitative_research Límite: Adult / Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article