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Genetic risk-factors for anxiety in healthy individuals: polymorphisms in gene simportant for the HPA axis
University of Skövde, School of Health Sciences. University of Skövde, Digital Health Research (DHEAR). (Translationell medicin TRIM, Translational Medicine)ORCID iD: 0000-0003-2462-0178
Center for Social and Affective Neuroscience, Linköping University, Sweden.ORCID iD: 0000-0002-7992-0306
University of Skövde, School of Health Sciences. University of Skövde, Digital Health Research (DHEAR). Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, Sweden ; Department of Community Medicine, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, Norway. (Individ och samhälle VIDSOC, Individual and Society)ORCID iD: 0000-0002-4583-9315
Department of Nursing Sciences, School of Health and Welfare, Jönköping University, Sweden.
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2020 (English)In: BMC Medical Genetics, E-ISSN 1471-2350, Vol. 21, article id 184Article in journal (Refereed) Published
Abstract [en]

Background

Two 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.

Methods

DNA 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.

Results

Self-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).

Conclusion

This 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.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2020. Vol. 21, article id 184
Keywords [en]
Anxiety, Stress, HPA axis, Polymorphism, STAI
National Category
Medical and Health Sciences Psychiatry Medical Genetics Neurosciences
Research subject
Translational Medicine TRIM; Individual and Society VIDSOC
Identifiers
URN: urn:nbn:se:his:diva-19078DOI: 10.1186/s12881-020-01123-wISI: 000574511800002PubMedID: 32957930Scopus ID: 2-s2.0-85091472288OAI: oai:DiVA.org:his-19078DiVA, id: diva2:1469501
Funder
Swedish Research CouncilUniversity of Skövde
Note

CC BY 4.0 [artikel], CC0 1.0 [data]

* Correspondence: linda.handlin@his.se

The study was supported by the Swedish Research Council and the School of Health Sciences, University of Skövde, Sweden. Open access funding provided by University of Skövde.

Available from: 2020-09-22 Created: 2020-09-22 Last updated: 2024-11-18Bibliographically approved

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Lindholm, HeléneMorrison, IndiaKrettek, AlexandraHandlin, Linda

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