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Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction
BACKGROUND: Nearly 6 million deaths and over a half trillion dollars in healthcare costs worldwide are attributed to tobacco smoking each year. Extensive research efforts have been pursued to elucidate the molecular underpinnings of smoking addiction and facilitate cessation. In this study, we genot...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605997/ https://www.ncbi.nlm.nih.gov/pubmed/28927378 http://dx.doi.org/10.1186/s12864-017-4124-5 |
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author | Qian, David C. Molfese, David L. Jin, Jennifer L. Titus, Alexander J. He, Yixuan Li, Yafang Vaissié, Maxime Viswanath, Humsini Baldwin, Philip R. Krahe, Ralf Salas, Ramiro Amos, Christopher I. |
author_facet | Qian, David C. Molfese, David L. Jin, Jennifer L. Titus, Alexander J. He, Yixuan Li, Yafang Vaissié, Maxime Viswanath, Humsini Baldwin, Philip R. Krahe, Ralf Salas, Ramiro Amos, Christopher I. |
author_sort | Qian, David C. |
collection | PubMed |
description | BACKGROUND: Nearly 6 million deaths and over a half trillion dollars in healthcare costs worldwide are attributed to tobacco smoking each year. Extensive research efforts have been pursued to elucidate the molecular underpinnings of smoking addiction and facilitate cessation. In this study, we genotyped and obtained both resting state and task-based functional magnetic resonance imaging from 64 non-smokers and 42 smokers. Smokers were imaged after having smoked normally (“sated”) and after having not smoked for at least 12 h (“abstinent”). RESULTS: While abstinent smokers did not differ from non-smokers with respect to pairwise resting state functional connectivities (RSFCs) between 12 brain regions of interest, RSFCs involving the caudate and putamen of sated smokers significantly differed from those of non-smokers (P < 0.01). Further analyses of caudate and putamen activity during elicited experiences of reward and disappointment show that caudate activity during reward (CR) correlated with smoking status (P = 0.015). Moreover, abstinent smokers with lower CR experienced greater withdrawal symptoms (P = 0.024), which suggests CR may be related to smoking urges. Associations between genetic variants and CR, adjusted for smoking status, were identified by genome-wide association study (GWAS). Genes containing or exhibiting caudate-specific expression regulation by these variants were enriched within Gene Ontology terms that describe cytoskeleton functions, synaptic organization, and injury response (P < 0.001, FDR < 0.05). CONCLUSIONS: By integrating genomic and imaging data, novel insights into potential mechanisms of caudate activation and homeostasis are revealed that may guide new directions of research toward improving our understanding of addiction pathology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4124-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5605997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56059972017-09-20 Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction Qian, David C. Molfese, David L. Jin, Jennifer L. Titus, Alexander J. He, Yixuan Li, Yafang Vaissié, Maxime Viswanath, Humsini Baldwin, Philip R. Krahe, Ralf Salas, Ramiro Amos, Christopher I. BMC Genomics Research Article BACKGROUND: Nearly 6 million deaths and over a half trillion dollars in healthcare costs worldwide are attributed to tobacco smoking each year. Extensive research efforts have been pursued to elucidate the molecular underpinnings of smoking addiction and facilitate cessation. In this study, we genotyped and obtained both resting state and task-based functional magnetic resonance imaging from 64 non-smokers and 42 smokers. Smokers were imaged after having smoked normally (“sated”) and after having not smoked for at least 12 h (“abstinent”). RESULTS: While abstinent smokers did not differ from non-smokers with respect to pairwise resting state functional connectivities (RSFCs) between 12 brain regions of interest, RSFCs involving the caudate and putamen of sated smokers significantly differed from those of non-smokers (P < 0.01). Further analyses of caudate and putamen activity during elicited experiences of reward and disappointment show that caudate activity during reward (CR) correlated with smoking status (P = 0.015). Moreover, abstinent smokers with lower CR experienced greater withdrawal symptoms (P = 0.024), which suggests CR may be related to smoking urges. Associations between genetic variants and CR, adjusted for smoking status, were identified by genome-wide association study (GWAS). Genes containing or exhibiting caudate-specific expression regulation by these variants were enriched within Gene Ontology terms that describe cytoskeleton functions, synaptic organization, and injury response (P < 0.001, FDR < 0.05). CONCLUSIONS: By integrating genomic and imaging data, novel insights into potential mechanisms of caudate activation and homeostasis are revealed that may guide new directions of research toward improving our understanding of addiction pathology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4124-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-19 /pmc/articles/PMC5605997/ /pubmed/28927378 http://dx.doi.org/10.1186/s12864-017-4124-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Qian, David C. Molfese, David L. Jin, Jennifer L. Titus, Alexander J. He, Yixuan Li, Yafang Vaissié, Maxime Viswanath, Humsini Baldwin, Philip R. Krahe, Ralf Salas, Ramiro Amos, Christopher I. Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title | Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title_full | Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title_fullStr | Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title_full_unstemmed | Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title_short | Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
title_sort | genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605997/ https://www.ncbi.nlm.nih.gov/pubmed/28927378 http://dx.doi.org/10.1186/s12864-017-4124-5 |
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