Prefrontal cortex response to drug cues, craving, and current depressive symptoms are associated with treatment outcomes in methadone-maintained patients

Methadone maintenance is an effective treatment for opioid use disorder, yet many methadone-maintained patients (MMPs) continue to struggle with chronic relapse. The current study evaluated whether functional near-infrared spectroscopy (fNIRS) could identify prefrontal cortex (PFC) markers of ongoin...

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Veröffentlicht in:Neuropsychopharmacology (New York, N.Y.) N.Y.), 2019-03, Vol.44 (4), p.826-833
Hauptverfasser: Huhn, Andrew S, Sweeney, Mary M, Brooner, Robert K, Kidorf, Michael S, Tompkins, D Andrew, Ayaz, Hasan, Dunn, Kelly E
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Sprache:eng
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Zusammenfassung:Methadone maintenance is an effective treatment for opioid use disorder, yet many methadone-maintained patients (MMPs) continue to struggle with chronic relapse. The current study evaluated whether functional near-infrared spectroscopy (fNIRS) could identify prefrontal cortex (PFC) markers of ongoing opioid use in MMPs, and whether clinical measures of depression and self-report measures of craving would also be associated with opioid use. MMPs (n = 29) underwent a drug cue reactivity paradigm during fNIRS measurements of PFC reactivity. Self-reported opioid craving (measured by a visual analog scale; 0-100) was collected before and after drug cue reactivity, and depressive symptoms were assessed via the 17-item Hamilton Depression Rating Scale (HAM-D). Hierarchical regression and partial correlations were used to evaluate associations between weekly urine drug screens over a 90-day follow-up period and fNIRS, craving, and HAM-D assessments. Neural response to drug cues in the left lateral PFC, controlling for age, sex, and days in treatment was significantly associated with percent opioid-negative urine screens during follow-up (∆F  = 13.19, p = 0.001, ∆R  = 0.30), and correctly classified 86% of MMPs as either using opioids, or abstaining from opioids (χ (4) = 16.28, p = 0.003). Baseline craving (p 
ISSN:0893-133X
1740-634X
DOI:10.1038/s41386-018-0252-0