2015
DOI: 10.1007/s11606-015-3212-y
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Chronic Pain and DepressionAmong Primary Care Patients Treated with Buprenorphine

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Cited by 38 publications
(33 citation statements)
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References 65 publications
(85 reference statements)
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“…The compound best studied in this context is buprenorphine, which is a partial μ receptor agonist with a weak κ receptor antagonistic profile. Buprenorphine was found to produce antidepressant and anxiolytic effects in mice, which were mediated through the κ receptor (Falcon et al , ), although clinical observations in chronic pain patients treated with buprenorphine failed to detect lasting mood effects (Stein et al , ). Overall, compounds simultaneously targeting μ and κ receptors, either as agonist/agonist or agonist/antagonist, have shown some clinical efficacy, although the main limitations of chronic μ receptor activation, such as abuse liability, constipation and respiratory depression, are still apparent.…”
Section: Rationale For the Development Of Multi‐targeting Opioid Ligandsmentioning
confidence: 99%
“…The compound best studied in this context is buprenorphine, which is a partial μ receptor agonist with a weak κ receptor antagonistic profile. Buprenorphine was found to produce antidepressant and anxiolytic effects in mice, which were mediated through the κ receptor (Falcon et al , ), although clinical observations in chronic pain patients treated with buprenorphine failed to detect lasting mood effects (Stein et al , ). Overall, compounds simultaneously targeting μ and κ receptors, either as agonist/agonist or agonist/antagonist, have shown some clinical efficacy, although the main limitations of chronic μ receptor activation, such as abuse liability, constipation and respiratory depression, are still apparent.…”
Section: Rationale For the Development Of Multi‐targeting Opioid Ligandsmentioning
confidence: 99%
“…Up to 62% of OMT patients endorse chronic pain (Jamison et al, 2000; Rosenblum et al, 2003; Ilgen et al, 2006; Barry et al, 2008, 2009b; Dunn et al, 2014; Stein et al, 2015; Voon et al, 2015), compared to 30.7% in the general population (Johannes et al, 2010) and there is also growing evidence that OMT patients may have a different experience of pain relative to the general population. Many OMT patients show signs of opioid-induced hyperalgesia, a super-sensitivity to pain that is hypothesized to occur following extended exposure to opioid agonists (Brush, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…It has been demonstrated that similar to the MMT patient population, a large proportion of OUD patients with other medication-assisted treatments (e.g., buprenorphine and naloxone) also report chronic pain Mark, Dilonardo, Vandivort, & Miller, 2013;Stein et al, 2015). However, the extent to which findings from our study are generalizable to patients with OUD who receive other forms of medication-assisted treatment is currently unclear.…”
mentioning
confidence: 72%