4.1 Article

Central sensitization in alcohol use disorder: correlates of pain, addiction and health-related quality of life

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JOURNAL OF ADDICTIVE DISEASES
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ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
DOI: 10.1080/10550887.2023.2237396

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Central nervous system sensitization; alcoholism; Fibromyalgia; chronic pain; >

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This study is the first to use a validated surrogate measure to describe central sensitization in a clinical sample with alcohol use disorder (AUD). It found that greater central sensitization was associated with worse health-related quality of life. Participants with higher central sensitization expressed greater endorsement of pain as a reason for AUD onset, maintenance, escalation, treatment delay, and relapse.
BackgroundCentral sensitization is an important mechanism underlying many chronic pain conditions. Chronic pain and alcohol use disorder (AUD) are highly comorbid. Despite great scientific interest in brain mechanisms linking chronic pain and AUD, progress has been impeded by difficulty assessing central sensitization in AUD.ObjectiveThe present study is the first to employ a validated surrogate measure to describe central sensitization in a clinical sample with AUD.MethodsParticipants with AUD (n = 99) were recruited from an academic addiction treatment center. A well-established surrogate measure of central sensitization, The American College of Rheumatology Fibromyalgia Survey Criteria (ACRFMS) was administered. Participants also responded to questions about quality of life (RAND-36), and AUD. Descriptive analyses and Spearman's rho correlations were performed.ResultsChronic pain and evidence of central sensitization were prevalent. Greater central sensitization was associated with worse health-related quality of life. Participants higher in central sensitization expressed greater endorsement of pain as a reason for AUD onset, maintenance, escalation, treatment delay, and relapse.ConclusionThe present study bolsters prior assertions that AUD and chronic pain might compound one another via progressive sensitization of shared brain circuitry. These results may inform future mechanistic research and precision AUD treatment.

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