Investigating the epigenetic profile of the inflammatory gene IL-6 in late-life depression
Identifieur interne : 000928 ( Main/Exploration ); précédent : 000927; suivant : 000929Investigating the epigenetic profile of the inflammatory gene IL-6 in late-life depression
Auteurs : Joanne Ryan [France] ; Lauren Pilkington ; Katharina Neuhaus ; Karen Ritchie [France] ; Marie-Laure Ancelin [France] ; Richard SafferySource :
- BMC Psychiatry [ 1471-244X ] ; 2017.
Abstract
It is well established that there is a link between inflammation and depression, with several studies reporting increased circulating levels of the pro-inflammatory cytokine, interleukin-6 (
The ESPRIT study of later life neuropsychiatric disorders used a random sampling framework to select non-institutionalised participants aged ≥65 years and over living in the Montpellier region of France. Major depressive disorder (MDD) was assessed using the Mini International Neuropsychiatric Interview (MINI) according to DSM-IV criteria. High levels of depressive symptoms were defined as a score of ≥16 on the Centre for Epidemiologic Studies Depression Scale (CES-D).
Individuals with depression (current MDD or high depressive symptoms) had lower
This study presents evidence that
Url:
DOI: 10.1186/s12888-017-1515-8
PubMed: 29070016
PubMed Central: 5657056
Affiliations:
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<series><title level="j">BMC Psychiatry</title>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p id="Par1">It is well established that there is a link between inflammation and depression, with several studies reporting increased circulating levels of the pro-inflammatory cytokine, interleukin-6 (<italic>IL6</italic>
), in depressed individuals. Peripheral epigenetic marks, including DNA methylation, hold promise as biomarkers for a range of complex conditions, with potential to inform diagnosis and tailor interventions. The aim of this study was to determine whether individuals with depression display differential methylation of the <italic>IL6</italic>
gene promoter compared to individuals without depression.</p>
</sec>
<sec><title>Methods</title>
<p id="Par2">The ESPRIT study of later life neuropsychiatric disorders used a random sampling framework to select non-institutionalised participants aged ≥65 years and over living in the Montpellier region of France. Major depressive disorder (MDD) was assessed using the Mini International Neuropsychiatric Interview (MINI) according to DSM-IV criteria. High levels of depressive symptoms were defined as a score of ≥16 on the Centre for Epidemiologic Studies Depression Scale (CES-D). <italic>IL6</italic>
promoter DNA methylation was measured on a sub-sample of 380 participants who provided buccal samples.</p>
</sec>
<sec><title>Results</title>
<p id="Par3">Individuals with depression (current MDD or high depressive symptoms) had lower <italic>IL6</italic>
methylation levels at one of the four sites investigated, however the effect size was small (∆ 2.4%, SE 0.009, <italic>p</italic>
= 0.006). Interestingly, antidepressant use was independently associated with higher <italic>IL-6</italic>
methylation at the same site (∆ 4.6%, SE 0.019, <italic>p</italic>
= 0.015). In multivariate linear regression analyses adjusting for covariates, including sex and smoking status, these associations remained. There was no effect modification when considering <italic>IL6</italic>
genotype.</p>
</sec>
<sec><title>Conclusion</title>
<p id="Par4">This study presents evidence that <italic>IL6</italic>
methylation may be a marker of depression status in older individuals, however further work is now needed to replicate these findings and to assess the association with inflammatory status of individuals.</p>
</sec>
</div>
</front>
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<author><name sortKey="Ormstad, H" uniqKey="Ormstad H">H Ormstad</name>
</author>
<author><name sortKey="Aass, Hc" uniqKey="Aass H">HC Aass</name>
</author>
<author><name sortKey="Malt, Uf" uniqKey="Malt U">UF Malt</name>
</author>
<author><name sortKey="Bendz, Lt" uniqKey="Bendz L">LT Bendz</name>
</author>
<author><name sortKey="Sandvik, L" uniqKey="Sandvik L">L Sandvik</name>
</author>
<author><name sortKey="Brundin, L" uniqKey="Brundin L">L Brundin</name>
</author>
<author><name sortKey="Andreassen, Oa" uniqKey="Andreassen O">OA Andreassen</name>
</author>
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</author>
<author><name sortKey="Olsson, Ah" uniqKey="Olsson A">AH Olsson</name>
</author>
<author><name sortKey="Gillberg, L" uniqKey="Gillberg L">L Gillberg</name>
</author>
<author><name sortKey="Jorgensen, Sw" uniqKey="Jorgensen S">SW Jorgensen</name>
</author>
<author><name sortKey="Brons, C" uniqKey="Brons C">C Brons</name>
</author>
<author><name sortKey="Eriksson, Kf" uniqKey="Eriksson K">KF Eriksson</name>
</author>
<author><name sortKey="Groop, L" uniqKey="Groop L">L Groop</name>
</author>
<author><name sortKey="Jansson, Pa" uniqKey="Jansson P">PA Jansson</name>
</author>
<author><name sortKey="Nilsson, E" uniqKey="Nilsson E">E Nilsson</name>
</author>
<author><name sortKey="Ronn, T" uniqKey="Ronn T">T Ronn</name>
</author>
</analytic>
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<affiliations><list><country><li>France</li>
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<tree><noCountry><name sortKey="Neuhaus, Katharina" sort="Neuhaus, Katharina" uniqKey="Neuhaus K" first="Katharina" last="Neuhaus">Katharina Neuhaus</name>
<name sortKey="Pilkington, Lauren" sort="Pilkington, Lauren" uniqKey="Pilkington L" first="Lauren" last="Pilkington">Lauren Pilkington</name>
<name sortKey="Saffery, Richard" sort="Saffery, Richard" uniqKey="Saffery R" first="Richard" last="Saffery">Richard Saffery</name>
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<country name="France"><noRegion><name sortKey="Ryan, Joanne" sort="Ryan, Joanne" uniqKey="Ryan J" first="Joanne" last="Ryan">Joanne Ryan</name>
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<name sortKey="Ancelin, Marie Laure" sort="Ancelin, Marie Laure" uniqKey="Ancelin M" first="Marie-Laure" last="Ancelin">Marie-Laure Ancelin</name>
<name sortKey="Ritchie, Karen" sort="Ritchie, Karen" uniqKey="Ritchie K" first="Karen" last="Ritchie">Karen Ritchie</name>
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