Evidence map›Paper›PMID 28857330›Full record

ArticleThe American journal on addictions2017

Increased habenular connectivity in opioid users is associated with an α5 subunit nicotinic receptor genetic variant.

Kaylah Curtis, Humsini Viswanath, Kenia M Velasquez, David L Molfese, Mark J Harding, Eduardo Aramayo, Philip R Baldwin, Elisa Ambrosi, Alok Madan, Michelle Patriquin and 5 more

Open access · greenAbstract read
In one paragraph

Article in The American journal on addictions, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Habenula Connectivity and Intravenous Ketamine in Treatment-Resistant Depression.The international journal of neuropsychopharmacology · 2021
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  12. Mu opioid receptors in the medial habenula contribute to naloxone aversion.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Kaylah CurtisMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Humsini ViswanathMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Kenia M VelasquezMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
David L MolfeseMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Mark J HardingMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Eduardo AramayoMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Philip R BaldwinMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Elisa AmbrosiMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Alok MadanMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Michelle Patriquin
B Christopher FruehUniversity of Hawaii, Department of Psychology, Hilo, Hawaii.
J Christopher FowlerMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Thomas R KostenMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
David A NielsenMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.
Ramiro SalasMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, Texas.ORCID http://orcid.org/0000-0002-1105-566X
Michael E. DeBakey VA Medical Center · USBaylor College of Medicine · USUniversity of Hawaii at Hilo · US

Funding

Role of Habenula in Tobacco AddictionK01DA026539 · NIDA · BAYLOR COLLEGE OF MEDICINE · PI SALAS, RAMIRO · 2010 to 2013
$516k
Functional Imaging of the Habenula in Tobacco SmokersR03DA029167 · NIDA · BAYLOR COLLEGE OF MEDICINE · PI SALAS, RAMIRO · 2011 to 2011
$230k
Multimodal Imaging of Reward Brain Centers in Tobacco Smoking VeteransI01CX000994 · VA · MICHAEL E DEBAKEY VA MEDICAL CENTER · PI SALAS, RAMIRO · 2014 to 2016
–
CSRD VA I01 CX000994NIDA NIH HHS K01 DA026539NIDA NIH HHS R03 DA029167
6 · The paper itself

Abstract

BACKGROUND AND

objectivesOpioid use disorder (OUD) is a chronic disorder with relapse based on both desire for reinforcement (craving) and avoidance of withdrawal. The aversive aspect of dependence and relapse has been associated with a small brain structure called the habenula, which expresses large numbers of both opioid and nicotinic receptors. Additionally, opioid withdrawal symptoms can be induced in opioid-treated rodents by blocking not only opioid, but also nicotinic receptors. This receptor co-localization and cross-induction of withdrawal therefore might lead to genetic variation in the nicotinic receptor influencing development of human opioid dependence through its impact on the aversive components of opioid dependence.

methodsWe studied habenular resting state functional connectivity with related brain structures, specifically the striatum. We compared abstinent psychiatric patients who use opioids (N = 51) to psychiatric patients who do not (N = 254) to identify an endophenotype of opioid use that focused on withdrawal avoidance and aversion rather than the more commonly examined craving aspects of relapse.

resultsWe found that habenula-striatal connectivity was stronger in opioid-using patients. Increased habenula-striatum connectivity was observed in opioid-using patients with the low risk rs16969968 GG genotype, but not in patients carrying the high risk AG or AA genotypes.

conclusionsWe propose that increased habenula-striatum functional connectivity may be modulated by the nicotinic receptor variant rs16969968 and may lead to increased opioid use. SCIENTIFIC SIGNIFICANCE: Our data uncovered a promising brain target for development of novel anti-addiction therapies and may help the development of personalized therapies against opioid abuse. (Am J Addict 2017;26:751-759).

Indexed as

HabenulaOpioid-Related DisordersSubstance Withdrawal SyndromeAdultAvoidance LearningConnectomeCorpus StriatumFemaleGenetic Predisposition to DiseaseHumansMagnetic Resonance ImagingMaleNerve Tissue ProteinsReceptors, NicotinicCHRNA5 protein, humanNerve Tissue Proteinsnicotinic receptor alpha5 subunit, humanReceptors, Nicotinic

Identifiers

PMID28857330
PMCPMC5745069
OpenAlexW2750640935

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.