Enhanced Cortisol Increase Upon Awakening Is Associated With Greater Pain Ratings but Not Salivary Cortisol or Soluble Tumor Necrosis Factor-α Receptor II Responses to Acute Pain

OBJECTIVES:The cortisol awakening response (CAR) is related to psychosocial factors and health in potentially significant ways, suggesting that it may be a distinctive marker of hypothalamic-pituitary-adrenal axis function and dysfunction. This study sought to expand upon previous work that examined...

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Veröffentlicht in:The Clinical journal of pain 2012-05, Vol.28 (4), p.291-299
Hauptverfasser: Goodin, Burel R, Quinn, Noel B, King, Christopher D, Page, Gayle G, Haythornthwaite, Jennifer A, Edwards, Robert R, Stapleton, Laura M, McGuire, Lynanne
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container_end_page 299
container_issue 4
container_start_page 291
container_title The Clinical journal of pain
container_volume 28
creator Goodin, Burel R
Quinn, Noel B
King, Christopher D
Page, Gayle G
Haythornthwaite, Jennifer A
Edwards, Robert R
Stapleton, Laura M
McGuire, Lynanne
description OBJECTIVES:The cortisol awakening response (CAR) is related to psychosocial factors and health in potentially significant ways, suggesting that it may be a distinctive marker of hypothalamic-pituitary-adrenal axis function and dysfunction. This study sought to expand upon previous work that examined the association between CAR and ratings of laboratory-evoked acute pain stimulation. In addition to evoked pain ratings, this study also tested whether CAR was prospectively related with salivary cortisol and soluble tumor necrosis factor-α receptor II responses to acute pain stimulation. METHODS:This study included 36 healthy, pain-free volunteers of both sexes recruited through posted study flyers. Prior to completion of laboratory pain testing, salivary cortisol samples were obtained at home over the course of a single morning according to the following time frameupon awakening, and 15, 30, and 60 minute after awakening. After collection of saliva, study participants brought their home saliva samples to the laboratory for assay and subsequently completed acute experimental pain testing procedures. RESULTS:Cluster analysis of CAR revealed two distinct groups with similar patterns of cortisol response to awakening; increased and flattened. Relative to flattened CAR, increased CAR was associated with greater ratings of pain intensity and unpleasantness. Salivary cortisol was significantly increased and soluble tumor necrosis factor-α receptor II significantly decreased after pain testing, but neither of these responses differed as a function of increased versus flattened CAR. DISCUSSION:CAR may be a marker for stress sensitivity and/or the anticipation of impending stress, which could explain why the increased CAR cohort reported greater acute pain ratings.
doi_str_mv 10.1097/AJP.0b013e31822cf542
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This study sought to expand upon previous work that examined the association between CAR and ratings of laboratory-evoked acute pain stimulation. In addition to evoked pain ratings, this study also tested whether CAR was prospectively related with salivary cortisol and soluble tumor necrosis factor-α receptor II responses to acute pain stimulation. METHODS:This study included 36 healthy, pain-free volunteers of both sexes recruited through posted study flyers. Prior to completion of laboratory pain testing, salivary cortisol samples were obtained at home over the course of a single morning according to the following time frameupon awakening, and 15, 30, and 60 minute after awakening. After collection of saliva, study participants brought their home saliva samples to the laboratory for assay and subsequently completed acute experimental pain testing procedures. RESULTS:Cluster analysis of CAR revealed two distinct groups with similar patterns of cortisol response to awakening; increased and flattened. Relative to flattened CAR, increased CAR was associated with greater ratings of pain intensity and unpleasantness. Salivary cortisol was significantly increased and soluble tumor necrosis factor-α receptor II significantly decreased after pain testing, but neither of these responses differed as a function of increased versus flattened CAR. DISCUSSION:CAR may be a marker for stress sensitivity and/or the anticipation of impending stress, which could explain why the increased CAR cohort reported greater acute pain ratings.</description><identifier>ISSN: 0749-8047</identifier><identifier>EISSN: 1536-5409</identifier><identifier>DOI: 10.1097/AJP.0b013e31822cf542</identifier><identifier>PMID: 21904196</identifier><identifier>CODEN: CJPAEU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Adult ; Analgesics ; Biological and medical sciences ; Blood Pressure - physiology ; Cold Temperature - adverse effects ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Hydrocortisone - metabolism ; Male ; Medical sciences ; Neurology ; Neuropharmacology ; Pain - etiology ; Pain - metabolism ; Pain - psychology ; Pain Measurement ; Pharmacology. Drug treatments ; Pituitary-Adrenal Function Tests - methods ; Pressure - adverse effects ; Saliva - metabolism ; Self Report ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. 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Psychology</subject><subject>Humans</subject><subject>Hydrocortisone - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Pain - etiology</subject><subject>Pain - metabolism</subject><subject>Pain - psychology</subject><subject>Pain Measurement</subject><subject>Pharmacology. Drug treatments</subject><subject>Pituitary-Adrenal Function Tests - methods</subject><subject>Pressure - adverse effects</subject><subject>Saliva - metabolism</subject><subject>Self Report</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. 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Psychology</topic><topic>Humans</topic><topic>Hydrocortisone - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Pain - etiology</topic><topic>Pain - metabolism</topic><topic>Pain - psychology</topic><topic>Pain Measurement</topic><topic>Pharmacology. Drug treatments</topic><topic>Pituitary-Adrenal Function Tests - methods</topic><topic>Pressure - adverse effects</topic><topic>Saliva - metabolism</topic><topic>Self Report</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. 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source MEDLINE; Journals@Ovid Complete
subjects Adult
Analgesics
Biological and medical sciences
Blood Pressure - physiology
Cold Temperature - adverse effects
Female
Fundamental and applied biological sciences. Psychology
Humans
Hydrocortisone - metabolism
Male
Medical sciences
Neurology
Neuropharmacology
Pain - etiology
Pain - metabolism
Pain - psychology
Pain Measurement
Pharmacology. Drug treatments
Pituitary-Adrenal Function Tests - methods
Pressure - adverse effects
Saliva - metabolism
Self Report
Somesthesis and somesthetic pathways (proprioception, exteroception, nociception)
interoception
electrolocation. Sensory receptors
TNF Receptor-Associated Factor 2 - metabolism
Vertebrates: nervous system and sense organs
Wakefulness - physiology
Young Adult
title Enhanced Cortisol Increase Upon Awakening Is Associated With Greater Pain Ratings but Not Salivary Cortisol or Soluble Tumor Necrosis Factor-α Receptor II Responses to Acute Pain
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