FV 16 Brain arousal regulation as response predictor for antidepressant therapy in major depression

2017 ◽  
Vol 128 (10) ◽  
pp. e313-e314
Author(s):  
F. Schmidt ◽  
C. Sander ◽  
U. Hegerl
2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Frank M. Schmidt ◽  
Christian Sander ◽  
Marie-Elisa Dietz ◽  
Claudia Nowak ◽  
Thomas Schröder ◽  
...  

1988 ◽  
Vol 33 (7) ◽  
pp. 606-610 ◽  
Author(s):  
Vikram K. Yeragani ◽  
Robert Pohl ◽  
Asaf Aleem ◽  
Richard Balon ◽  
Paul Sherwood ◽  
...  

The symptom of carbohydrate craving and increased appetite (CHH) was studied in 180 outpatients receiving antidepressant treatment. One hundred and fifty-eight of these patients had a DSM-III diagnosis of panic disorder and 17, major depression. The incidence of CHH was similar in both diagnostic groups. Thus, antidepressant treatment is associated with CHH in patients with diagnoses, other than depression. Desipramine was least likely to induce CHH compared to imipramine, amitriptyline and doxepin. Most patients who developed CHH on imipramine no longer experienced this side effect when switched to desipramine. CHH was not more frequent among women and not associated with antidepressant dosage or treatment response. Histamine H-1 receptor blockade may be an important factor in the etiology of CHH.


2021 ◽  
Vol 74 (3-4) ◽  
pp. 117-122
Author(s):  
Sladjana Vojvodic ◽  
Gabor Katona ◽  
Miroslav Sarac

Introduction. The combinatorial pharmacogenomic test has shown the potential to predict antidepressant response, tolerability, selection, and dosage in the treatment of a major depressive disorder. A case of successful management of antidepressant therapy adjustment is reported by using the combinatorial pharmacogenomic test. Case Report. A 53-year old man, severely disabled due to a rare genetic disease, Usher syndrome type 3, was treated with numerous antidepressants. However, episodes of major depression recurred, along with frequent suicidal thoughts. A combinatorial pharmacogenomic test was considered to design a potentially effective antidepressant therapy. Conclusion. According to the results of the combinatorial pharmacogenomic test, the patient constantly received inadequate antidepressant therapy, which did not lead to an improvement of depression due to moderate gene-drug interaction. The patient was prescribed nortriptyline, which proved to be one of the few most adequate according to the test. He showed improvement with subjectively more tolerable depression without suicidal thoughts and episodes of major depression. This case showed that the combinatorial pharmacogenomic testing may contribute to better selection of antidepressant therapy.


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