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DNA Methylation and Inflammatory Signatures Associated with Suicide Risk and Treatment in US Veterans

DNA Methylation and Inflammatory Signatures Associated with Suicide Risk and Treatment in US Veterans
DNA 甲基化和炎症特征与美国退伍军人的自杀风险和治疗相关
批准号:
10268157
负责人:
FATEMEH G HAGHIGHI
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-10-01 至 2022-09-30
关键词:
AffectAmbulatory Care FacilitiesAmericanAnimal ModelAnxietyAutopsyBehavioralBiological MarkersBloodBlood specimenBrainCaringCause of DeathClinicalClinical ResearchComplexDNA MethylationDataDeath CertificatesDepressed moodDisease susceptibilityEnvironmentEnvironmental Risk FactorEpigenetic ProcessEtiologyEventExposure toFeeling suicidalFollow-Up StudiesFutureGene ExpressionGene Expression RegulationGeneral PopulationGenesGeneticGenetic TranscriptionHistonesHospitalizationImmune System DiseasesImmunologicsIncidenceInflammationInflammatoryInflammatory ResponseLifeLinkLiteratureLongitudinal StudiesMajor Depressive DisorderMeasuresMediatingMental DepressionMental disordersMethylationModificationPeripheral Nervous SystemPersonsPlasmaPositioning AttributePsychiatric therapeutic procedurePsychological StressPsychopathologyPublic HealthRecording of previous eventsRecoveryResearchResearch PersonnelResourcesRisk FactorsRisk MarkerRoleSamplingStressSuicideSuicide attemptSuicide preventionTailTimeTreatment EfficacyVeteransVeterans Health AdministrationVisitWorkbehavioral responsechildhood adversityclinical careclinical practicecombatcombat veterancytokinedepressive symptomsepigenetic markerexpectationexperimental studyfollow up assessmentfollow-upgene environment interactiongene repressiongenome-wideimprovedinflammatory markermethylation patternmilitary servicemilitary veteranneuron lossperipheral bloodprogramspublic health relevanceresponsestressorsuicidalsuicidal actsuicidal behaviorsuicidal risksuicide attemptersuicide brainsuicide ratesuicide victimtraittreatment responsetreatment strategy

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 DESCRIPTION (provided by applicant): Suicide is a leading cause of death among U.S. Veterans. Therefore, understanding the etiological basis for the risk of suicide is of dire importance to our Veteran population. Stress i a crucial factor in risk of suicide. Specifically for Veterans, exposure to traumatic environmental events during combat, military service, or post- deployment stressful situations related to readjustment to civilian life are key contributors to the increase risk of suicide. These stressors can affect the diathesis for suicidal acts and can serve as triggers or precipitants of suicidal acts. Biological markers or stable behavioral traits for suicide risk factors likely interact in a complex manner that might benefit from approaches that can examine gene by environment interactions. Epigenetics is the bridge, connecting environment with genetics, by mediating the influence of environmental factors such as stress in altered regulation of gene expression related to suicide. We will investigate DNA methylation patterns associated with suicide risk in Veterans undergoing psychiatric treatment at the JJP VAMC using a genome- scale approach. Additionally, through subsequent follow-up studies, we will assess how DNA methylation patterns are altered following treatment. Such a longitudinal study is unprecedented and provides an opportunity to identify biological markers of suicide risk and treatment response. Moreover, the role of the inflammatory response in the stress diathesis in suicide risk will also be investigated in these studies. Together the epigenetic and inflammatory markers of suicide risk and treatment will identify objective measures that we can use in clinical settings to identif Veterans at risk of suicide and to determine the efficacy of treatment course and response.
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