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Genetic risk-factors for anxiety in healthy individuals: polymorphisms in genes important for the HPA axis
Department of Biomedicine, School of Health Sciences, University of Skövde.
Center for Social and Affective Neuroscience, Linköping University, Linköping.
Department of Public Health, School of Health Sciences, University of Skövde.
Jönköping University, School of Health and Welfare, HHJ, Dep. of Nursing Science. Jönköping University, School of Health and Welfare, HHJ. IMPROVE (Improvement, innovation, and leadership in health and welfare).
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2020 (English)In: BMC Medical Genetics, E-ISSN 1471-2350, Vol. 21, no 1, 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
Springer Nature, 2020. Vol. 21, no 1, article id 184
Keywords [en]
Anxiety, HPA axis, Polymorphism, STAI, Stress
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Nursing
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URN: urn:nbn:se:hj:diva-50789DOI: 10.1186/s12881-020-01123-wISI: 000574511800002PubMedID: 32957930Scopus ID: 2-s2.0-85091472288Local ID: GOA HHJ 2020OAI: oai:DiVA.org:hj-50789DiVA, id: diva2:1474083
Available from: 2020-10-07 Created: 2020-10-07 Last updated: 2024-01-17Bibliographically approved

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Malm, Dan

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