Evidence map›Paper›PMID 30744588›Full record

ArticleBMC psychiatry2019

Variation in the CACNB2 gene is associated with functional connectivity of the Hippocampus in bipolar disorder.

Fang Liu, Xiaohong Gong, Xudong Yao, Lingling Cui, Zhiyang Yin, Chao Li, Yanqing Tang, Fei Wang

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Deficiency of Intellectual Disability-Related GeneFrontiers in cell and developmental biology · 2021
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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

8 authors at 2 institutions in 1 country.

Fang LiuDepartment of Psychiatry, First Affiliated Hospital, China Medical University, 155 Nanjing North Street, Shenyang, 110001, Liaoning, China.
Xiaohong GongA605, Building School of Life SCiences, Songhu Road 2005, Dinstric Yangpu, Shanghai, China.
Xudong YaoDepartment of Psychiatry, First Affiliated Hospital, China Medical University, 155 Nanjing North Street, Shenyang, 110001, Liaoning, China.
Lingling CuiDepartment of Radiology, First Affiliated Hospital, China Medical University, Shenyang, Liaoning, People's Republic of China.
Zhiyang YinDepartment of Psychiatry, First Affiliated Hospital, China Medical University, 155 Nanjing North Street, Shenyang, 110001, Liaoning, China.
Chao LiDepartment of Radiology, First Affiliated Hospital, China Medical University, Shenyang, Liaoning, People's Republic of China.
Yanqing TangDepartment of Psychiatry, First Affiliated Hospital, China Medical University, 155 Nanjing North Street, Shenyang, 110001, Liaoning, China. yanqingtang@163.com.
Fei WangDepartment of Psychiatry, First Affiliated Hospital, China Medical University, 155 Nanjing North Street, Shenyang, 110001, Liaoning, China. fei.wang@cmu.edu.cn.
China Medical University · CNUniversity of Electronic Science and Technology of China · CN

Funding

Frontotemporal Neural Systems in Biopolar Disorder and SchizophreniaK01MH086621 · NIMH · YALE UNIVERSITY · PI WANG, FEI · 2009 to 2013
$893k
NIMH NIH HHS K01 MH086621
6 · The paper itself

Abstract

backgroundCalcium voltage-gated channel auxiliary subunit β2 is a protein that, in humans, is encoded by the CACNB2 gene. The β2 subunit is an auxiliary protein of voltage-gated calcium channels, which is predominantly expressed in hippocampal pyramidal neurons. A single-nucleotide polymorphism at the CACNB2 gene (rs11013860) has been reported in genome-wide association studies to be associated with bipolar disorder (BD). However, the neural effects of rs11013860 expression are unknown. Thus, the current study investigated the mechanisms of how the CACNB2 gene influences hippocampal-cortical limbic circuits in patients with bipolar disorder (BD).

methodsA total of 202 subjects were studied [69 BD patients and 133 healthy controls (HC)]. Participants agreed to undergo resting-state functional magnetic resonance imaging (rs-fMRI) and have blood drawn for genetic testing. Participants were found to belong to either a CC group homozygous for the C-allele (17 BD, 41 HC), or an A-carrier group carrying the high risk A-allele (AA/CA genotypes; 52 BD, 92 HC). Brain activity was assessed using resting-state functional connectivity (rs-FC) analyses.

resultsA main effect of genotype showed that the rs-FC of the AA/CA group was elevated more than that of the CC-group between the hippocampus and the regions of right-inferior temporal, fusiform, and left-inferior occipital gyri. Additionally, a significant diagnosis × genotype interaction was noted between the hippocampus and right pars triangularis. Furthermore, in BD patients, the AA/CA group showed lower rs-FC when compared to that of the CC group. Additionally, individuals from HC within the AA/CA group showed higher rs-FC than that of the CC group. Finally, within C-allele-carrying groups, individuals with BD showed significantly increased rs-FC compared to that of HC.

conclusionsOur study demonstrates that BD patients with the CACNB2 rs11013860 AA/CA genotype may exhibit altered hippocampal-cortical connectivity.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultBipolar DisorderCalcium Channels, L-TypeFemaleGenome-Wide Association StudyGenotypeHippocampusHumansMagnetic Resonance ImagingMaleNerve NetYoung AdultCACNB2 protein, humanCalcium Channels, L-Type11,013,860Bipolar disorderCACNB2Resting-state functional connectivity (rs-FC)

Identifiers

PMID30744588
PMCPMC6371424
OpenAlexW2917892572

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.