5-HTTLPR-environment interplay and its effects on neural reactivity in adolescents
5-HTTLPR-environment interplay and its effects on neural reactivity in adolescents
It is not known how 5-HTTLPR genotype x childhood adversity (CA) interactions that are associated with an increased risk for affective disorders in population studies operate at the neural systems level. We hypothesized that healthy adolescents at increased genetic and environmental risk for developing mood disorders (depression and anxiety) would demonstrate increased amygdala reactivity to emotional stimuli compared to those with only one such risk factor or those with none. Participants (n=67) were classified into one of 4 groups dependent on being homozygous for the long or short alleles within the serotonin-transporter-linked polymorphic region (5-HTTLPR) of the SLC6A4 gene and exposure to CA in the first 11 years of life (present or absent). A functional magnetic resonance imaging investigation was undertaken which involved viewing emotionally-salient face stimuli. In addition, we assessed the role of other variables hypothesized to influence amygdala reactivity, namely recent negative life-events (RNLE) assessed at ages 14 and 17, current anxiety symptoms and psychiatric history. We replicated prior findings demonstrating moderation by gene variants in 5-HTTLPR, but found no support for an effect of CA on amygdala reactivity. We also found a significant effect of RNLE aged 17 with amygdala reactivity demonstrating additive, but not interactive effects with 5-HTTLPR. A whole-brain analysis found a 5-HTTLPR×CA interaction in the lingual gyrus whereby CA appears to differentially modify neural reactivity depending on genotype. These results demonstrate that two different forms of environmental adversities interplay with 5-HTTLPR and thereby differentially impact amygdala and cortical reactivity.
1670-1680
Walsh, Nicholas
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Dalgleish, Tim
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Dunn, Valerie
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Abbott, Rosemary
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St Clair, Michelle
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Owens, Matthew
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Fairchild, Graeme
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Kerslake, William
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Hiscox, Lucy
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Passamonti, Luca
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Ewbank, Michael
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Ban, Maria
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Calder, Andrew
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Goodyer, Ian
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15 November 2012
Walsh, Nicholas
964e94a4-4645-4851-8f0e-a07d6e422992
Dalgleish, Tim
556cd082-2a3a-4079-accd-504f02f2fee8
Dunn, Valerie
bd22521b-fb76-47c6-a408-02a3e296db23
Abbott, Rosemary
f9ee0b6a-6a4b-47b6-a5b1-5f8d564c3675
St Clair, Michelle
c8d70dba-f7c8-4214-b11d-6e9391a2460b
Owens, Matthew
bdb0dd82-db76-4106-806e-2ab06629d132
Fairchild, Graeme
f99bc911-978e-48c2-9754-c6460666a95f
Kerslake, William
bdb12941-6cb2-48e6-8b9f-2975ed1c6dd1
Hiscox, Lucy
fdb04253-51f6-4c4c-bf1a-cbb8cc13b1aa
Passamonti, Luca
71e1cf10-463b-45f0-acc2-0d74459d9f20
Ewbank, Michael
87325a1f-7185-4f8d-b657-14c653ca2b87
Ban, Maria
3a722c5a-6d96-4420-9518-249ad32b6ea0
Calder, Andrew
4981a9bf-43f0-484a-8dfd-e8d8981de0d8
Goodyer, Ian
d8750313-5d41-4f80-8f47-c90007cbf469
Walsh, Nicholas, Dalgleish, Tim, Dunn, Valerie, Abbott, Rosemary, St Clair, Michelle, Owens, Matthew, Fairchild, Graeme, Kerslake, William, Hiscox, Lucy, Passamonti, Luca, Ewbank, Michael, Ban, Maria, Calder, Andrew and Goodyer, Ian
(2012)
5-HTTLPR-environment interplay and its effects on neural reactivity in adolescents.
NeuroImage, 63 (3), .
(doi:10.1016/j.neuroimage.2012.07.067).
(PMID:23034517)
Abstract
It is not known how 5-HTTLPR genotype x childhood adversity (CA) interactions that are associated with an increased risk for affective disorders in population studies operate at the neural systems level. We hypothesized that healthy adolescents at increased genetic and environmental risk for developing mood disorders (depression and anxiety) would demonstrate increased amygdala reactivity to emotional stimuli compared to those with only one such risk factor or those with none. Participants (n=67) were classified into one of 4 groups dependent on being homozygous for the long or short alleles within the serotonin-transporter-linked polymorphic region (5-HTTLPR) of the SLC6A4 gene and exposure to CA in the first 11 years of life (present or absent). A functional magnetic resonance imaging investigation was undertaken which involved viewing emotionally-salient face stimuli. In addition, we assessed the role of other variables hypothesized to influence amygdala reactivity, namely recent negative life-events (RNLE) assessed at ages 14 and 17, current anxiety symptoms and psychiatric history. We replicated prior findings demonstrating moderation by gene variants in 5-HTTLPR, but found no support for an effect of CA on amygdala reactivity. We also found a significant effect of RNLE aged 17 with amygdala reactivity demonstrating additive, but not interactive effects with 5-HTTLPR. A whole-brain analysis found a 5-HTTLPR×CA interaction in the lingual gyrus whereby CA appears to differentially modify neural reactivity depending on genotype. These results demonstrate that two different forms of environmental adversities interplay with 5-HTTLPR and thereby differentially impact amygdala and cortical reactivity.
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Published date: 15 November 2012
Organisations:
Psychology
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Local EPrints ID: 346483
URI: http://eprints.soton.ac.uk/id/eprint/346483
PURE UUID: 76164afc-daf0-4738-bebf-373ee7ab2f43
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Date deposited: 03 Jan 2013 14:46
Last modified: 14 Mar 2024 12:37
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Author:
Nicholas Walsh
Author:
Tim Dalgleish
Author:
Valerie Dunn
Author:
Rosemary Abbott
Author:
Michelle St Clair
Author:
Matthew Owens
Author:
Graeme Fairchild
Author:
William Kerslake
Author:
Lucy Hiscox
Author:
Luca Passamonti
Author:
Michael Ewbank
Author:
Maria Ban
Author:
Andrew Calder
Author:
Ian Goodyer
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