Evidence map›Paper›PMID 32957930›Full record

ArticleBMC medical genetics2020

Genetic risk-factors for anxiety in healthy individuals: polymorphisms in genes important for the HPA axis.

Heléne Lindholm, India Morrison, Alexandra Krettek, Dan Malm, Giovanni Novembre, Linda Handlin

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Heléne LindholmDepartment of Biomedicine, School of Health Sciences, University of Skövde, Box 408, 54128, Skövde, Sweden.
India MorrisonCenter for Social and Affective Neuroscience, Linköping University, Linköping, Sweden.
Alexandra KrettekDepartment of Public Health, School of Health Sciences, University of Skövde, Skövde, Sweden.
Dan MalmDepartment of Nursing Sciences, School of Health and Welfare, Jönköping University, Jönköping, Sweden.
Giovanni NovembreCenter for Social and Affective Neuroscience, Linköping University, Linköping, Sweden.
Linda HandlinDepartment of Biomedicine, School of Health Sciences, University of Skövde, Box 408, 54128, Skövde, Sweden. linda.handlin@his.se.ORCID http://orcid.org/0000-0003-0987-8357
University of Skövde · SELinköping University · SEJönköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTwo important aspects for the development of anxiety disorders are genetic predisposition and alterations in the hypothalamic-pituitary-adrenal (HPA) axis. In order to identify genetic risk-factors for anxiety, the aim of this exploratory study was to investigate possible relationships between genetic polymorphisms in genes important for the regulation and activity of the HPA axis and self-assessed anxiety in healthy individuals.

methodsDNA from 72 healthy participants, 37 women and 35 men, were included in the analyses. Their DNA was extracted and analysed for the following Single Nucleotide Polymorphisms (SNP)s: rs41423247 in the NR3C1 gene, rs1360780 in the FKBP5 gene, rs53576 in the OXTR gene, 5-HTTLPR in SLC6A4 gene and rs6295 in the HTR1A gene. Self-assessed anxiety was measured by the State and Trait Anxiety Inventory (STAI) questionnaire.

resultsSelf-assessed measure of both STAI-S and STAI-T were significantly higher in female than in male participants (p = 0.030 and p = 0.036, respectively). For SNP rs41423247 in the NR3C1 gene, there was a significant difference in females in the score for STAI-S, where carriers of the G allele had higher scores compared to the females that were homozygous for the C allele (p < 0.01). For the SNP rs53576 in the OXTR gene, there was a significant difference in males, where carriers of the A allele had higher scores in STAI-T compared to the males that were homozygous for the G allele (p < 0.01).

conclusionThis study shows that SNP rs41423247 in the NR3C1 gene and SNP rs53576 in the OXTR gene are associated with self-assessed anxiety in healthy individuals in a gender-specific manner. This suggests that these SNP candidates are possible genetic risk-factors for anxiety.

Indexed as

Polymorphism, Single NucleotideAdultAllelesAnxietyAnxiety DisordersFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansHypothalamo-Hypophyseal SystemMalePituitary-Adrenal SystemReceptors, GlucocorticoidReceptors, OxytocinRisk FactorsNR3C1 protein, humanOXTR protein, humanReceptors, GlucocorticoidReceptors, OxytocinAnxietyHPA axisPolymorphismSTAIStress

Identifiers

PMID32957930
PMCPMC7507731
OpenAlexW3087106776

What OpenQuestion holds

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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.