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RESEARCH PRODUCT

Glutamatergic hypofunction in medication-free major depression: Secondary effects of affective diagnosis and relationship to peripheral glutaminase.

David J. LythgoeToby WiseMatthew TaylorFrancesco CappelloAntonella Marino GammazzaAnthony J. CleareDanilo ArnoneSteve C.r. WilliamsAllan H. YoungAndres Herane-vives

subject

OncologyAdultMalemedicine.medical_specialtyMagnetic Resonance SpectroscopyBipolar disorderGlutamineMood disorderGlutamic AcidNeuroimagingGyrus Cinguli03 medical and health sciencesGlutamatergicYoung Adult0302 clinical medicineGlutaminaseInternal medicinemental disordersmedicineHumansBipolar disorderMajor depressive episodeDepression (differential diagnoses)Anterior cingulate cortexDepressive Disorder MajorDepressionbusiness.industryGlutaminaseGlutamate receptorBipolar disorder; depression; neuroimaging; magnetic resonance; mood disordersMiddle Agedmedicine.disease030227 psychiatryPsychiatry and Mental healthClinical Psychologymedicine.anatomical_structureMood disordersMagnetic resonanceCase-Control StudiesFemalemedicine.symptombusiness030217 neurology & neurosurgery

description

BackgroundThere is uncertainty as to whether alterations in glutamatergic function in affective disorders differ between unipolar and bipolar disorders and between depressive and euthymic states. Additionally, there are currently no available blood-based markers of central glutamatergic function to support clinical diagnosis and aid brain based investigations. MethodsIn this study, we measured levels of glutamate in the dorsal anterior cingulate cortex in-vivo using 1H-Magnetic Resonance Spectroscopy in medication free unipolar and bipolar patients (n=29, 20 unipolar and 9 bipolar) experiencing a major depressive episode, in comparison with a group of matched healthy controls (n=20). We also analysed peripheral glutaminase measured in serum to examine the relationship between central and peripheral measures. ResultsAnterior cingulate glutamate levels were reduced in both unipolar and bipolar depression groups relative to healthy controls, although this only reached significance in the unipolar group. Peripheral glutaminase levels did not differentiate bipolar from unipolar depression and a positive correlation with central glutamate levels did not reach statistical significance. LimitationsThe sample of bipolar disorder patients was relatively small due to the difficulties involved in finding medication-free patients experiencing a depressive episode.ConclusionsThese results suggest that glutamatergic hypofunction might represent a state marker for a depressive episode irrespective of diagnosis. Peripheral glutaminase did not index central glutamate levels in this study, which could potentially reflect a small magnitude of the effect requiring larger samples for detection.

10.1016/j.jad.2018.02.059https://pubmed.ncbi.nlm.nih.gov/29544167