Pharmacogenetics and Pharmacotherapy of Military Personnel Suffering from Post-traumatic Stress Disorder
- Publication type:
- Journal article
- Metadata:
-
- Autoren
- Janine Nass
- Thomas Efferth
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000407196400004&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.2174/1570159X15666161111113514
- eISSN
- 1875-6190
- Externe Identifier
- Clarivate Analytics Document Solution ID: FC9YG
- PubMed Identifier: 27834145
- ISSN
- 1570-159X
- Ausgabe der Veröffentlichung
- 6
- Zeitschrift
- CURRENT NEUROPHARMACOLOGY
- Schlüsselwörter
- DNA
- genetics
- mental diseases
- pharmacology
- single nucleotide polymorphisms
- gene-environment interactions
- Paginierung
- 831 - 860
- Datum der Veröffentlichung
- 2017
- Status
- Published
- Titel
- Pharmacogenetics and Pharmacotherapy of Military Personnel Suffering from Post-traumatic Stress Disorder
- Sub types
- Review
- Ausgabe der Zeitschrift
- 15
Data source: Web of Science (Lite)
- Other metadata sources:
-
- Autoren
- Janine Naß
- Thomas Efferth
- DOI
- 10.2174/1570159x15666161111113514
- ISSN
- 1570-159X
- Ausgabe der Veröffentlichung
- 6
- Zeitschrift
- Current Neuropharmacology
- Sprache
- en
- Datum der Veröffentlichung
- 2017
- Status
- Published
- Herausgeber
- Bentham Science Publishers Ltd.
- Herausgeber URL
- http://dx.doi.org/10.2174/1570159x15666161111113514
- Datum der Datenerfassung
- 2017
- Titel
- Pharmacogenetics and Pharmacotherapy of Military Personnel Suffering from Post-traumatic Stress Disorder
- Ausgabe der Zeitschrift
- 15
Data source: Crossref
- Abstract
- <h4>Background</h4>Posttraumatic stress disorder (PTSD) is a severe problem among soldiers with combating experience difficult to treat. The pathogenesis is still not fully understood at the psychological level. Therefore, genetic research became a focus of interest. The identification of single nucleotide polymorphisms (SNPs) may help to predict, which persons are at high risk to develop PTSD as a starting point to develop novel targeted drugs for treatment.<h4>Methods</h4>We conducted a systematic review on SNPs in genes related to PTSD pathology and development of targeted pharmacological treatment options based on PubMed database searches. We focused on clinical trials with military personnel.<h4>Results</h4>SNPs in 22 human genes have been linked to PTSD. These genes encode proteins acting as neurotransmitters and receptors, downstream signal transducers and metabolizing enzymes. Pharmacological inhibitors may serve as drug candidates for PTSD treatment, e.g. β2 adrenoreceptor antagonists, dopamine antagonists, partial dopamine D2 receptor agonists, dopamine β hydroxylase inhibitors, fatty acid amid hydrolase antagonists, glucocorticoid receptor agonists, tropomyosin receptor kinase B agonists, selective serotonin reuptake inhibitors, catechol-O-methyltransferase inhibitors, gamma-amino butyric acid receptor agonists, glutamate receptor inhibitors, monoaminoxidase B inhibitors, N-methyl-d-aspartate receptor antagonists.<h4>Conclusion</h4>The combination of genetic and pharmacological research may lead to novel targetbased drug developments with improved specificity and efficacy to treat PTSD. Specific SNPs may be identified as reliable biomarkers to assess individual disease risk. Focusing on soldiers suffering from PTSD will not only help to improve treatment options for this specific group, but for all PTSD patients and the general population.
- Addresses
- Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, Johannes Gutenberg University, Staudinger Weg 5, 55128 Mainz. Germany.
- Autoren
- Janine Naß
- Thomas Efferth
- Thomas Efferth
- DOI
- 10.2174/1570159x15666161111113514
- eISSN
- 1875-6190
- Externe Identifier
- PubMed Identifier: 27834145
- PubMed Central ID: PMC5652029
- Open access
- true
- ISSN
- 1570-159X
- Ausgabe der Veröffentlichung
- 6
- Zeitschrift
- Current neuropharmacology
- Schlüsselwörter
- Animals
- Humans
- Genetic Predisposition to Disease
- Stress Disorders, Post-Traumatic
- Military Personnel
- Clinical Trials as Topic
- Gene-Environment Interaction
- Sprache
- eng
- Medium
- Open access status
- Open Access
- Paginierung
- 831 - 860
- Datum der Veröffentlichung
- 2017
- Status
- Published
- Publisher licence
- CC BY-NC
- Datum der Datenerfassung
- 2016
- Titel
- Pharmacogenetics and Pharmacotherapy of Military Personnel Suffering from Post-traumatic Stress Disorder.
- Sub types
- Systematic Review
- review-article
- Review
- Journal Article
- Ausgabe der Zeitschrift
- 15
Files
https://europepmc.org/articles/PMC5652029?pdf=render
Data source: Europe PubMed Central
- Abstract
- BACKGROUND: Posttraumatic stress disorder (PTSD) is a severe problem among soldiers with combating experience difficult to treat. The pathogenesis is still not fully understood at the psychological level. Therefore, genetic research became a focus of interest. The identification of single nucleotide polymorphisms (SNPs) may help to predict, which persons are at high risk to develop PTSD as a starting point to develop novel targeted drugs for treatment. METHODS: We conducted a systematic review on SNPs in genes related to PTSD pathology and development of targeted pharmacological treatment options based on PubMed database searches. We focused on clinical trials with military personnel. RESULTS: SNPs in 22 human genes have been linked to PTSD. These genes encode proteins acting as neurotransmitters and receptors, downstream signal transducers and metabolizing enzymes. Pharmacological inhibitors may serve as drug candidates for PTSD treatment, e.g. β2 adrenoreceptor antagonists, dopamine antagonists, partial dopamine D2 receptor agonists, dopamine β hydroxylase inhibitors, fatty acid amid hydrolase antagonists, glucocorticoid receptor agonists, tropomyosin receptor kinase B agonists, selective serotonin reuptake inhibitors, catechol-O-methyltransferase inhibitors, gamma-amino butyric acid receptor agonists, glutamate receptor inhibitors, monoaminoxidase B inhibitors, N-methyl-d-aspartate receptor antagonists. CONCLUSION: The combination of genetic and pharmacological research may lead to novel targetbased drug developments with improved specificity and efficacy to treat PTSD. Specific SNPs may be identified as reliable biomarkers to assess individual disease risk. Focusing on soldiers suffering from PTSD will not only help to improve treatment options for this specific group, but for all PTSD patients and the general population.
- Date of acceptance
- 2016
- Autoren
- Janine Naß
- Thomas Efferth
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/27834145
- DOI
- 10.2174/1570159X15666161111113514
- eISSN
- 1875-6190
- Externe Identifier
- PubMed Central ID: PMC5652029
- Ausgabe der Veröffentlichung
- 6
- Zeitschrift
- Curr Neuropharmacol
- Schlüsselwörter
- DNA
- gene-environment interactions
- genetics
- mental diseases
- pharmacology
- single nucleotide polymorphisms
- Animals
- Clinical Trials as Topic
- Gene-Environment Interaction
- Genetic Predisposition to Disease
- Humans
- Military Personnel
- Stress Disorders, Post-Traumatic
- Sprache
- eng
- Country
- United Arab Emirates
- Paginierung
- 831 - 860
- PII
- CN-EPUB-79662
- Datum der Veröffentlichung
- 2017
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2018
- Titel
- Pharmacogenetics and Pharmacotherapy of Military Personnel Suffering from Post-traumatic Stress Disorder.
- Sub types
- Journal Article
- Review
- Systematic Review
- Ausgabe der Zeitschrift
- 15
Data source: PubMed
- Beziehungen:
- Property of