S100B Serum Levels Predict Treatment Response in Patients with Melancholic Depression

Autor: Ambree, O, Bergink, Veerle, Grosse, L, Alferink, J, Drexhage, Hemmo, Rothermundt, M, Arolt, V, Birkenhager, T.K.
Přispěvatelé: Psychiatry, Immunology
Rok vydání: 2015
Předmět:
Adult
Male
medicine.medical_specialty
Imipramine
Time Factors
Venlafaxine Hydrochloride
Venlafaxine
S100 Calcium Binding Protein beta Subunit
Melancholic depression
Severity of Illness Index
treatment resistance
03 medical and health sciences
0302 clinical medicine
Internal medicine
Severity of illness
medicine
Humans
Major depression
Pharmacology (medical)
antidepressant response
Psychiatry
predictive biomarker
neurotrophic factor
False Negative Reactions
Depression (differential diagnoses)
Aged
Pharmacology
Psychiatric Status Rating Scales
Depressive Disorder
Middle Aged
medicine.disease
Prognosis
Antidepressive Agents
030227 psychiatry
3. Good health
Psychiatry and Mental health
Treatment Outcome
Linear Models
Biomarker (medicine)
Antidepressant
Female
Psychology
030217 neurology & neurosurgery
Biomarkers
Blood Chemical Analysis
medicine.drug
Research Article
Zdroj: International Journal of Neuropsychopharmacology
International Journal of Neuropsychopharmacology, 19(3). Oxford University Press
ISSN: 1469-5111
1461-1457
Popis: Background: There is an ongoing search for biomarkers in psychiatry, for example, as diagnostic tools or predictors of treatment response. The neurotrophic factor S100 calcium binding protein B (S100B) has been discussed as a possible predictor of antidepressant response in patients with major depression, but also as a possible biomarker of an acute depressive state. The aim of the present study was to study the association of serum S100B levels with antidepressant treatment response and depression severity in melancholically depressed inpatients. Methods: After a wash-out period of 1 week, 40 inpatients with melancholic depression were treated with either venlafaxine or imipramine. S100B levels and Hamilton Depression Rating Scale (HAM-D) scores were assessed at baseline, after 7 weeks of treatment, and after 6 months. Results: Patients with high S100B levels at baseline showed a markedly better treatment response defined as relative reduction in HAM-D scores than those with low baseline S100B levels after 7 weeks (P=.002) and 6 months (P=.003). In linear regression models, S100B was a significant predictor for treatment response at both time points. It is of interest to note that nonresponders were detected with a predictive value of 85% and a false negative rate of 7.5%. S100B levels were not associated with depression severity and did not change with clinical improvement. Conclusions: Low S100B levels predict nonresponse to venlafaxine and imipramine with high precision. Future studies have to show which treatments are effective in patients with low levels of S100B so that this biomarker will help to reduce patients' burden of nonresponding to frequently used antidepressants.
Databáze: OpenAIRE