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Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding

BACKGROUND: The 5-HT(4) receptor provides a novel potential target for antidepressant treatment. No studies exist to elucidate the 5-HT(4) receptor’s in vivo distribution in the depressed state or in populations that may display trait markers for major depression disorder (MDD). The aim of this stud...

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Autores principales: Madsen, Karine, Torstensen, Eva, Holst, Klaus K., Haahr, Mette E., Knorr, Ulla, Frokjaer, Vibe G., Brandt-Larsen, Malene, Iversen, Pernille, Fisher, Patrick M., Knudsen, Gitte M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368872/
https://www.ncbi.nlm.nih.gov/pubmed/25522384
http://dx.doi.org/10.1093/ijnp/pyu034
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author Madsen, Karine
Torstensen, Eva
Holst, Klaus K.
Haahr, Mette E.
Knorr, Ulla
Frokjaer, Vibe G.
Brandt-Larsen, Malene
Iversen, Pernille
Fisher, Patrick M.
Knudsen, Gitte M.
author_facet Madsen, Karine
Torstensen, Eva
Holst, Klaus K.
Haahr, Mette E.
Knorr, Ulla
Frokjaer, Vibe G.
Brandt-Larsen, Malene
Iversen, Pernille
Fisher, Patrick M.
Knudsen, Gitte M.
author_sort Madsen, Karine
collection PubMed
description BACKGROUND: The 5-HT(4) receptor provides a novel potential target for antidepressant treatment. No studies exist to elucidate the 5-HT(4) receptor’s in vivo distribution in the depressed state or in populations that may display trait markers for major depression disorder (MDD). The aim of this study was to determine whether familial risk for MDD is associated with cerebral 5-HT(4) receptor binding as measured with [(11)C]SB207145 brain PET imaging. Familial risk is the most potent risk factor of MDD. METHODS: We studied 57 healthy individuals (mean age 36 yrs, range 20–86; 21 women), 26 of which had first-degree relatives treated for MDD. RESULTS: We found that having a family history of MDD was associated with lower striatal 5-HT(4) receptor binding (p = 0.038; in individuals below 40 years, p = 0.013). Further, we found evidence for a “risk-dose effect” on 5-HT(4) receptor binding, since the number of first-degree relatives with a history of MDD binding correlated negatively with 5-HT(4) receptor binding in both the striatum (p = 0.001) and limbic regions (p = 0.012). CONCLUSIONS: Our data suggest that the 5-HT(4) receptor is involved in the neurobiological mechanism underlying familial risk for depression, and that lower striatal 5-HT(4) receptor binding is associated with increased risk for developing MDD. The finding is intriguing considering that the 5-HT(4) receptor has been suggested to be an effective target for antidepressant treatment.
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spelling pubmed-43688722015-09-01 Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding Madsen, Karine Torstensen, Eva Holst, Klaus K. Haahr, Mette E. Knorr, Ulla Frokjaer, Vibe G. Brandt-Larsen, Malene Iversen, Pernille Fisher, Patrick M. Knudsen, Gitte M. Int J Neuropsychopharmacol Research Article BACKGROUND: The 5-HT(4) receptor provides a novel potential target for antidepressant treatment. No studies exist to elucidate the 5-HT(4) receptor’s in vivo distribution in the depressed state or in populations that may display trait markers for major depression disorder (MDD). The aim of this study was to determine whether familial risk for MDD is associated with cerebral 5-HT(4) receptor binding as measured with [(11)C]SB207145 brain PET imaging. Familial risk is the most potent risk factor of MDD. METHODS: We studied 57 healthy individuals (mean age 36 yrs, range 20–86; 21 women), 26 of which had first-degree relatives treated for MDD. RESULTS: We found that having a family history of MDD was associated with lower striatal 5-HT(4) receptor binding (p = 0.038; in individuals below 40 years, p = 0.013). Further, we found evidence for a “risk-dose effect” on 5-HT(4) receptor binding, since the number of first-degree relatives with a history of MDD binding correlated negatively with 5-HT(4) receptor binding in both the striatum (p = 0.001) and limbic regions (p = 0.012). CONCLUSIONS: Our data suggest that the 5-HT(4) receptor is involved in the neurobiological mechanism underlying familial risk for depression, and that lower striatal 5-HT(4) receptor binding is associated with increased risk for developing MDD. The finding is intriguing considering that the 5-HT(4) receptor has been suggested to be an effective target for antidepressant treatment. Oxford University Press 2014-12-19 /pmc/articles/PMC4368872/ /pubmed/25522384 http://dx.doi.org/10.1093/ijnp/pyu034 Text en © The Author 2014. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Madsen, Karine
Torstensen, Eva
Holst, Klaus K.
Haahr, Mette E.
Knorr, Ulla
Frokjaer, Vibe G.
Brandt-Larsen, Malene
Iversen, Pernille
Fisher, Patrick M.
Knudsen, Gitte M.
Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title_full Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title_fullStr Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title_full_unstemmed Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title_short Familial Risk for Major Depression is Associated with Lower Striatal 5-HT(4) Receptor Binding
title_sort familial risk for major depression is associated with lower striatal 5-ht(4) receptor binding
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368872/
https://www.ncbi.nlm.nih.gov/pubmed/25522384
http://dx.doi.org/10.1093/ijnp/pyu034
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