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Monoamine Oxidase A Gene Methylation and Its Role in Posttraumatic Stress Disorder: First Evidence from the South Eastern Europe (SEE)-PTSD Study.


ABSTRACT: Background:Posttraumatic stress disorder is characterized by an overactive noradrenergic system conferring core posttraumatic stress disorder symptoms such as hyperarousal and reexperiencing. Monoamine oxidase A is one of the key enzymes mediating the turnover of noradrenaline. Here, DNA methylation of the monoamine oxidase A gene exonI/intronI region was investigated for the first time regarding its role in posttraumatic stress disorder risk and severity. Methods:Monoamine oxidase A methylation was analyzed via direct sequencing of sodium bisulfite-treated DNA extracted from blood cells in a total sample of N=652 (441 male) patients with current posttraumatic stress disorder, patients with remitted posttraumatic stress disorder, and healthy probands (comparison group) recruited at 5 centers in Bosnia-Herzegovina, Croatia, and the Republic of Kosovo. Posttraumatic stress disorder severity was measured by means of the Clinician-Administered Posttraumatic Stress Disorder Scale and its respective subscores representing distinct symptom clusters. Results:In the male, but not the female sample, patients with current posttraumatic stress disorder displayed hypermethylation of 3 CpGs (CpG3=43656362; CpG12=43656514; CpG13=43656553, GRCh38.p2 Assembly) as compared with remitted Posttraumatic Stress Disorder patients and healthy probands. Symptom severity (Clinician-Administered Posttraumatic Stress Disorder Scale scores) in male patients with current posttraumatic stress disorder significantly correlated with monoamine oxidase A methylation. This applied particularly to symptom clusters related to reexperiencing of trauma (cluster B) and hyperarousal (cluster D). Conclusions:The present findings suggest monoamine oxidase A gene hypermethylation, potentially resulting in enhanced noradrenergic signalling, as a disease status and severity marker of current posttraumatic stress disorder in males. If replicated, monoamine oxidase A hypermethylation might serve as a surrogate marker of a hyperadrenergic subtype of posttraumatic stress disorder guiding personalized treatment decisions on the use of antiadrenergic agents.

SUBMITTER: Ziegler C 

PROVIDER: S-EPMC5932467 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Monoamine Oxidase A Gene Methylation and Its Role in Posttraumatic Stress Disorder: First Evidence from the South Eastern Europe (SEE)-PTSD Study.

Ziegler Christiane C   Wolf Christiane C   Schiele Miriam A MA   Feric Bojic Elma E   Kucukalic Sabina S   Sabic Dzananovic Emina E   Goci Uka Aferdita A   Hoxha Blerina B   Haxhibeqiri Valdete V   Haxhibeqiri Shpend S   Kravic Nermina N   Muminovic Umihanic Mirnesa M   Cima Franc Ana A   Jaksic Nenad N   Babic Romana R   Pavlovic Marko M   Warrings Bodo B   Bravo Mehmedbasic Alma A   Rudan Dusko D   Aukst-Margetic Branka B   Kucukalic Abdulah A   Marjanovic Damir D   Babic Dragan D   Bozina Nada N   Jakovljevic Miro M   Sinanovic Osman O   Avdibegovic Esmina E   Agani Ferid F   Dzubur-Kulenovic Alma A   Deckert Jürgen J   Domschke Katharina K  

The international journal of neuropsychopharmacology 20180501 5


<h4>Background</h4>Posttraumatic stress disorder is characterized by an overactive noradrenergic system conferring core posttraumatic stress disorder symptoms such as hyperarousal and reexperiencing. Monoamine oxidase A is one of the key enzymes mediating the turnover of noradrenaline. Here, DNA methylation of the monoamine oxidase A gene exonI/intronI region was investigated for the first time regarding its role in posttraumatic stress disorder risk and severity.<h4>Methods</h4>Monoamine oxidas  ...[more]

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