We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure [email protected]
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
By
James W. Murrough, Department of Psychiatry Mount Sinai School of Medicine New York, NY, USA,
Sanjay J. Mathew, Department of Psychiatry and Behavioral Sciences Baylor College of Medicine Houston, TX, USA
This chapter reviews the neurochemical imaging literature in the anxiety disorders, focusing on key findings in post-traumatic stress disorder (PTSD), panic disorder (PD), social anxiety disorder (SAD) and generalized anxiety disorder (GAD). It provides a partial review of preclinical and human investigations of several neurochemical systems relevant to neurochemical imaging of anxiety disorders: namely the 5-HT, gamma-aminobutyric acid-benzodiazepine (GABA-BZD) and dopamine (DA) systems. Genetic analyses of polymorphisms of the major DA metabolizing enzyme catechol-O-methyltransferase (COMT) have suggested an association between specific polymorphisms and anxiety disorders, although these findings await replication. Several studies have utilized 1H-magnetic resonance spectroscopy (MRS) to investigate potential abnormalities in N-acetyl-aspartate (NAA), choline (CHO), creatine (CR) or lactate in GAD. As anxiety disorders are frequently comorbid with mood disorders, investigations of patients with anxious depression may be informative in determining specificity of neurochemical abnormalities.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.