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Evidence that anhedonia is a symptom of opioid dependence associated with recent use.

Identifieur interne : 001401 ( Main/Exploration ); précédent : 001400; suivant : 001402

Evidence that anhedonia is a symptom of opioid dependence associated with recent use.

Auteurs : Joshua B B. Garfield [Australie] ; Sue M. Cotton [Australie] ; Nicholas B. Allen [États-Unis] ; Ali Cheetham [Australie] ; Marni Kras [Australie] ; Murat Yücel [Australie] ; Dan I. Lubman [Australie]

Source :

RBID : pubmed:28551591

Descripteurs français

English descriptors

Abstract

BACKGROUND

Anhedonia is prevalent among substance-dependent populations. The hedonic allostasis model suggests this is due to the effects of addictive substances on neural substrates of reward processing. However, previous research may have been confounded by other factors likely to influence anhedonia, including tobacco use, psychopathology, and history of trauma and other stressors. Thus it remains unclear whether elevated anhedonia in substance-dependent populations is caused by substance use itself, or is due to other correlates of substance dependence.

METHODS

Multivariate analysis of covariance was conducted to test whether opioid-dependent participants' anhedonia scores were elevated, relative to a non-dependent control group, after controlling for psychosocial factors likely to influence anhedonia. Correlational analyses within opioid-dependent participants were also conducted to examine whether anhedonia was associated with recent illicit opioid use or duration of abstinence.

RESULTS

There was a modest, but significant, elevation in anhedonia in opioid-dependent participants, relative to controls (Partial η

CONCLUSION

These findings support the hypothesis that use of opioids can cause anhedonia, although other psychosocial factors may also contribute to the high prevalence of anhedonia among opioid-dependent populations.


DOI: 10.1016/j.drugalcdep.2017.03.012
PubMed: 28551591


Affiliations:


Links toward previous steps (curation, corpus...)


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<term>Adult (MeSH)</term>
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<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
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<b>BACKGROUND</b>
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<p>Anhedonia is prevalent among substance-dependent populations. The hedonic allostasis model suggests this is due to the effects of addictive substances on neural substrates of reward processing. However, previous research may have been confounded by other factors likely to influence anhedonia, including tobacco use, psychopathology, and history of trauma and other stressors. Thus it remains unclear whether elevated anhedonia in substance-dependent populations is caused by substance use itself, or is due to other correlates of substance dependence.</p>
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<p>
<b>METHODS</b>
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<p>Multivariate analysis of covariance was conducted to test whether opioid-dependent participants' anhedonia scores were elevated, relative to a non-dependent control group, after controlling for psychosocial factors likely to influence anhedonia. Correlational analyses within opioid-dependent participants were also conducted to examine whether anhedonia was associated with recent illicit opioid use or duration of abstinence.</p>
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<b>RESULTS</b>
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<b>CONCLUSION</b>
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<QualifierName UI="Q000523" MajorTopicYN="Y">psychology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013313" MajorTopicYN="N">Stress Disorders, Post-Traumatic</DescriptorName>
<QualifierName UI="Q000523" MajorTopicYN="N">psychology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D055815" MajorTopicYN="N">Young Adult</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">Anhedonia</Keyword>
<Keyword MajorTopicYN="Y">Opioid use disorder</Keyword>
<Keyword MajorTopicYN="Y">Substance dependence</Keyword>
<Keyword MajorTopicYN="Y">Trauma</Keyword>
</KeywordList>
</MedlineCitation>
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<PubMedPubDate PubStatus="received">
<Year>2016</Year>
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<Day>12</Day>
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<PubMedPubDate PubStatus="revised">
<Year>2017</Year>
<Month>02</Month>
<Day>03</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2017</Year>
<Month>03</Month>
<Day>08</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>5</Month>
<Day>30</Day>
<Hour>6</Hour>
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<PubMedPubDate PubStatus="medline">
<Year>2018</Year>
<Month>3</Month>
<Day>10</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>5</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">28551591</ArticleId>
<ArticleId IdType="pii">S0376-8716(17)30196-5</ArticleId>
<ArticleId IdType="doi">10.1016/j.drugalcdep.2017.03.012</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>États-Unis</li>
</country>
<region>
<li>Victoria (État)</li>
</region>
<settlement>
<li>Melbourne</li>
</settlement>
<orgName>
<li>Université de Melbourne</li>
</orgName>
</list>
<tree>
<country name="Australie">
<noRegion>
<name sortKey="Garfield, Joshua B B" sort="Garfield, Joshua B B" uniqKey="Garfield J" first="Joshua B B" last="Garfield">Joshua B B. Garfield</name>
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<name sortKey="Cheetham, Ali" sort="Cheetham, Ali" uniqKey="Cheetham A" first="Ali" last="Cheetham">Ali Cheetham</name>
<name sortKey="Cotton, Sue M" sort="Cotton, Sue M" uniqKey="Cotton S" first="Sue M" last="Cotton">Sue M. Cotton</name>
<name sortKey="Kras, Marni" sort="Kras, Marni" uniqKey="Kras M" first="Marni" last="Kras">Marni Kras</name>
<name sortKey="Lubman, Dan I" sort="Lubman, Dan I" uniqKey="Lubman D" first="Dan I" last="Lubman">Dan I. Lubman</name>
<name sortKey="Yucel, Murat" sort="Yucel, Murat" uniqKey="Yucel M" first="Murat" last="Yücel">Murat Yücel</name>
</country>
<country name="États-Unis">
<region name="Victoria (État)">
<name sortKey="Allen, Nicholas B" sort="Allen, Nicholas B" uniqKey="Allen N" first="Nicholas B" last="Allen">Nicholas B. Allen</name>
</region>
</country>
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