Neuroimaging MAO-B in Medication Free and Treatment Resistant Major Depressive Disorder Using Novel MAO-B Tracer [11C]SL2511.88
Neuroimaging MAO-B in Medication Free and Treatment Resistant Major Depressive Disorder Using Novel MAO-B Tracer [11C]SL2511.88
批准号:
10295180
负责人:
JEFFREY H MEYER
金额:
$21.02万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-11-10 至 2024-04-30
关键词:
AffectAgeAnteriorAntioxidantsApoptosisAstrocytesBenzylaminesBiological MarkersBrainBrain regionCessation of lifeChemicalsChronicChronic stressClinicClinicalCorpus striatum structureDataDopamineDorsalFutureGenetic MarkersGenetic TranscriptionGlucocorticoidsHealthHormonesImpaired cognitionImpairmentIntentionMajor Depressive DisorderMeasuresMetabolismMonoamine Oxidase BMoodsMotivationNerve DegenerationNeuronsNorepinephrineNuclearOxidative StressPeripheralPharmaceutical PreparationsPhenethylaminesPlayPositive ValencePositron-Emission TomographyPredispositionPrefrontal CortexProcessProteinsRecording of previous eventsResistanceRodentRoleSelective Serotonin Reuptake InhibitorSerotoninStressSystemTherapeutic EffectTracerVentral Striatumbrain cellcingulate cortexcognitive controlcognitive systemcommon treatmentcostdensityearly onsetimprovedindexinginhibitormonoamineneuroimagingnoveloxidationprotein biomarkersresponsereuptakesingle episode major depressive disordertherapeutic targettherapy resistanttranscription factor
中文摘要
项目摘要/摘要
单胺氧化酶B(MAO-B)是大脑中一种高度丰富的蛋白质,它能产生
氧化应激,去除单胺,如多巴胺和去甲肾上腺素
正常情绪,并影响对细胞凋亡的倾向。MAO-B水平和活动
是高度相关的,并且在长期应激激素暴露后增加。MAO-B活动是
在慢性不可预测的应激后,啮齿动物大脑中MAO-B的含量增加,然而,MAO-B并没有被
研究对象为最常见的早发性(45岁)严重抑郁障碍(MDD)。
使用[11C]SL25.1188正电子发射断层扫描,我们建议研究MAO-B VT是否
非药物治疗的重度抑郁症早期发病的MDD患者关键脑区升高
发作;(MDE;n=31),以及在非药物治疗中有以下病史的主要抑郁发作
耐药组(31例)和年龄匹配的健康对照组(46例)。这个
目的是提出一个令人信服的理由,即MAO-B水平在关键影响因素中经常升高
MDE过程中的调节区,尤其是耐药MDE。这样的结果可能是
应用于制定MAO-B水平升高的MDE病例与MAO-B匹配的策略
通过寻找MAO-B水平升高的低成本预测因素在临床上应用抑制剂治疗
(例如建议的临床和RDoC措施和/或额外的外周蛋白或
未来研究中的遗传生物标记物)。
英文摘要
Project Summary/Abstract
Monoamine oxidase B (MAO-B) is a highly abundant protein in the brain that generates
oxidative stress, removes monoamines such as dopamine and norepinephrine that support
normal mood, and influences the predisposition towards apoptosis. MAO-B levels and activity
are highly correlated and increase after chronic stress hormone exposure. MAO-B activity is
increased in rodent brain after chronic unpredictable stress, however, MAO-B has not been
studied in the most common early onset (age<45 years) major depressive disorder (MDD).
Using [11C]SL25.1188 positron emission tomography, we propose to study whether MAO-B VT is
elevated in key brain regions in early onset MDD during medication free major depressive
episodes; (MDE; n=31), and in medication free major depressive episodes with a history of
treatment resistance (n=31) as well as age matched healthy controls (from n=46). The
intention is to make a convincing case that MAO-B levels are frequently elevated in key affect
modulating regions during MDE, especially treatment resistant MDE. Such results could be
applied to develop strategies for matching MDE cases of elevated MAO-B level towards MAO-B
inhibitor treatments in the clinic through identifying low cost predictors of elevated MAO-B level
(such as the clinical and RDOC measures proposed and/or additional peripheral protein or
genetic biomarkers in future study).
期刊论文(1)
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会议论文
Neuroimaging MAO-B in Medication Free and Treatment Resistant Major Depressive Disorder Using Novel MAO-B Tracer [11C]SL2511.88
-
批准号:10053730
-
项目类别:
-
资助金额:$23.09万
-
财政年份:2017
-
负责人:JEFFREY H MEYER
-
依托单位:
HYPOFRACTIONATED STEREOTACTIC RADIOTHERAPY WITH VASCULAR TARGETING
-
批准号:7358304
-
项目类别:
-
资助金额:$1.03万
-
财政年份:2006
-
负责人:JEFFREY H MEYER
-
依托单位:
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