TY - JOUR
T1 - Prefrontal cortex response to drug cues, craving, and current depressive symptoms are associated with treatment outcomes in methadone-maintained patients
AU - Huhn, Andrew S.
AU - Sweeney, Mary M.
AU - Brooner, Robert K.
AU - Kidorf, Michael S.
AU - Tompkins, D. Andrew
AU - Ayaz, Hasan
AU - Dunn, Kelly E.
N1 - Funding Information:
The work described in this article was funded by the National Institute on Drug Abuse: NIDA R21 DA035327 (Dunn). Support for ASH was provided by National Institute on Drug Abuse: NIDA T32DA07209. DAT has received medication supplies from Indivior (formerly Reckitt Benckiser Pharmaceuticals) for an investigator- initiated study, was site PI for a clinical trial sponsored by Alkermes, and provided consulting services for AstraZeneca and Theravance. HA was involved in the technology development of the brain-imaging instrument manufactured by fNIR Devices, LLC, and owns a minor share of the firm.
Publisher Copyright:
© 2018, American College of Neuropsychopharmacology.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - 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 1, 24 = 13.19, p = 0.001, ∆R 2 = 0.30), and correctly classified 86% of MMPs as either using opioids, or abstaining from opioids (χ 2 (4) = 16.28, p = 0.003). Baseline craving (p < 0.001) and HAM-D assessment (p < 0.01) were also associated with percent opioid-negative urine screens. Combining fNIRS results, baseline craving scores, and HAM-D scores created a robust predictive model (∆F 3, 22 = 16.75, p < 0.001, ∆R 2 = 0.59). These data provide preliminary evidence that the fNIRS technology may have value as an objective measure of treatment outcomes within outpatient methadone clinics. Depressive symptoms and drug craving were also correlated with opioid use in MMPs.
AB - 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 1, 24 = 13.19, p = 0.001, ∆R 2 = 0.30), and correctly classified 86% of MMPs as either using opioids, or abstaining from opioids (χ 2 (4) = 16.28, p = 0.003). Baseline craving (p < 0.001) and HAM-D assessment (p < 0.01) were also associated with percent opioid-negative urine screens. Combining fNIRS results, baseline craving scores, and HAM-D scores created a robust predictive model (∆F 3, 22 = 16.75, p < 0.001, ∆R 2 = 0.59). These data provide preliminary evidence that the fNIRS technology may have value as an objective measure of treatment outcomes within outpatient methadone clinics. Depressive symptoms and drug craving were also correlated with opioid use in MMPs.
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U2 - 10.1038/s41386-018-0252-0
DO - 10.1038/s41386-018-0252-0
M3 - Article
C2 - 30375498
AN - SCOPUS:85056751414
SN - 0893-133X
VL - 44
SP - 826
EP - 833
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 4
ER -