Quantifying serotonin transporters by PET with [11C]‐DASB before and after interferon‐α treatment. Issue 11 (4th August 2014)
- Record Type:
- Journal Article
- Title:
- Quantifying serotonin transporters by PET with [11C]‐DASB before and after interferon‐α treatment. Issue 11 (4th August 2014)
- Main Title:
- Quantifying serotonin transporters by PET with [11C]‐DASB before and after interferon‐α treatment
- Authors:
- Shapiro, Peter A.
Sloan, Richard P.
Deochand, Chetram
Franceschi, Ana M.
Delorenzo, Christine
Mann, J. John
Parsey, Ramin V. - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <sec id="syn21766-sec-0001" sec-type="section"> <title>Background</title> <p>Interferon‐α (IFN‐α) therapy is frequently associated with disabling depression, fatigue, and related neuropsychiatric effects. Although depression in major depressive disorder is associated with low serotonin transporter binding, animal models suggest that IFN‐associated mood effects are linked to increased presynaptic serotonin transporter binding. This study tested the hypotheses that IFN administration to human subjects increases presynaptic serotonin binding activity, and that this effect correlates with incident depression symptoms.</p> </sec> <sec id="syn21766-sec-0002" sec-type="section"> <title>Methods</title> <p>Positron emission tomography (PET) scans using [<sup>11</sup>C]‐DASB were obtained for nine hepatitis C patients before and after IFN‐α treatment for 8 weeks. Serotonin transporter binding was estimated using the likelihood estimation in graphical analysis (LEGA) model and measured as the volume of distribution (<italic>V</italic><sub>T</sub>) divided by the free fraction of ligand (<italic>f</italic><sub>P</sub>). Depression was measured with the Structured Clinical Interview for DSM‐IV Diagnosis (SCID) and the Hamilton Rating Scale for Depression (HAM‐D).</p> </sec> <sec id="syn21766-sec-0003" sec-type="section"> <title>Results</title> <p>Compared to pre‐IFN treatment values, changes in serotonin transporter binding and<abstract abstract-type="main"> <title>ABSTRACT</title> <sec id="syn21766-sec-0001" sec-type="section"> <title>Background</title> <p>Interferon‐α (IFN‐α) therapy is frequently associated with disabling depression, fatigue, and related neuropsychiatric effects. Although depression in major depressive disorder is associated with low serotonin transporter binding, animal models suggest that IFN‐associated mood effects are linked to increased presynaptic serotonin transporter binding. This study tested the hypotheses that IFN administration to human subjects increases presynaptic serotonin binding activity, and that this effect correlates with incident depression symptoms.</p> </sec> <sec id="syn21766-sec-0002" sec-type="section"> <title>Methods</title> <p>Positron emission tomography (PET) scans using [<sup>11</sup>C]‐DASB were obtained for nine hepatitis C patients before and after IFN‐α treatment for 8 weeks. Serotonin transporter binding was estimated using the likelihood estimation in graphical analysis (LEGA) model and measured as the volume of distribution (<italic>V</italic><sub>T</sub>) divided by the free fraction of ligand (<italic>f</italic><sub>P</sub>). Depression was measured with the Structured Clinical Interview for DSM‐IV Diagnosis (SCID) and the Hamilton Rating Scale for Depression (HAM‐D).</p> </sec> <sec id="syn21766-sec-0003" sec-type="section"> <title>Results</title> <p>Compared to pre‐IFN treatment values, changes in serotonin transporter binding and depression symptoms were not significant. There was no correlation between changes in serotonin transporter binding and depression symptoms.</p> </sec> <sec id="syn21766-sec-0004" sec-type="section"> <title>Limitations</title> <p>The study is limited by small sample size, minimal effect on observed mood symptoms within the sample, and brief duration of follow‐up.</p> </sec> <sec id="syn21766-sec-0005" sec-type="section"> <title>Conclusion</title> <p>These findings do not support the hypothesis of an IFN‐induced change in serotonin transporter function as the cause of incident depressive symptoms in patients treated with IFN‐α. Additional study of these possible relationships should be of longer duration and include more subjects with more pronounced changes in mood. <bold>Synapse 68:548–555, 2014</bold>. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Synapse. Volume 68:Issue 11(2014)
- Journal:
- Synapse
- Issue:
- Volume 68:Issue 11(2014)
- Issue Display:
- Volume 68, Issue 11 (2014)
- Year:
- 2014
- Volume:
- 68
- Issue:
- 11
- Issue Sort Value:
- 2014-0068-0011-0000
- Page Start:
- 548
- Page End:
- 555
- Publication Date:
- 2014-08-04
- Subjects:
- Synapses -- Periodicals
612 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2396 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/syn.21766 ↗
- Languages:
- English
- ISSNs:
- 0887-4476
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8585.880200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3464.xml