Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
182 subjects diagnosed with depression and treated with these drugs were clinically and therapeutically characterized and submitted to the quantification of drug/metabolite plasma concentrations and genotyping of ABCB1, CYP2C9, CYP2C19, and CYP2D6 genes.
|
31120287 |
2020 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
Influence of CYP2C19 Metabolizer Status on Escitalopram/Citalopram Tolerability and Response in Youth With Anxiety and Depressive Disorders.
|
30837874 |
2019 |
Depressive disorder
|
0.380 |
GeneticVariation
|
disease |
BEFREE |
Thus, we studied the effects of polymorphisms of the CYP2C19 gene on raw plasma drug concentrations in Japanese patients with depression.
|
29570504 |
2018 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
In humans, we found that the absence of CYP2C19 was associated with a bilateral hippocampal volume increase in two independent healthy cohorts (N=386 and 1032) and a lower prevalence of major depressive disorder and depression severity in African-Americans (N=3848).
|
27895323 |
2017 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
Herein, we present the case of a 29-year-old male with diagnoses of depression and obsessive compulsive disorder who had trialed and failed a dozen psychiatric medications, many of which are subject to metabolism by CYP2D6 and/or CYP2C19, and had most recently been taking clomipramine for approximately 2.5 years.
|
28470111 |
2017 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
PSYGENET |
We report the effect of CYP2C19 and CYP2D6 genotypes on steady state morning concentrations of escitalopram and N-desmethylescitalopram and the ratio of this metabolite to the parent drug in 196 adult patients with depression in GENDEP, a clinical pharmacogenomic trial.
|
21926427 |
2012 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
We report the effect of CYP2C19 and CYP2D6 genotypes on steady state morning concentrations of escitalopram and N-desmethylescitalopram and the ratio of this metabolite to the parent drug in 196 adult patients with depression in GENDEP, a clinical pharmacogenomic trial.
|
21926427 |
2012 |
Depressive disorder
|
0.380 |
GeneticVariation
|
disease |
BEFREE |
The Sequenced Treatment Alternatives to Relieve Depression sample was used to examine the relationship between variations in the CYP2C19 and CYP2D6 genes and remission of depressive symptoms and tolerance to treatment with citalopram.
|
21192344 |
2011 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
PSYGENET |
The Sequenced Treatment Alternatives to Relieve Depression sample was used to examine the relationship between variations in the CYP2C19 and CYP2D6 genes and remission of depressive symptoms and tolerance to treatment with citalopram.
|
21192344 |
2011 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
PSYGENET |
We evaluated whether cytochrome P450 (CYP) poor metabolizer polymorphisms of CYP2D6 and CYP2C19 are relevant for the outcome (measured by length of hospitalization) during treatment with psychotropic medications in patients with depression or schizophrenia.
|
16812949 |
2006 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
BEFREE |
Genetic tests suitable for the routine laboratory are now available for some important metabolizing enzymes (e.g., CYP2D6, CYP2C19) identifying those individuals who are slow or fast metabolizers of certain drugs, many of which are widely used in the treatment of depression (e.g., tricyclic antidepressants).
|
11412815 |
2001 |
Depressive disorder
|
0.380 |
Biomarker
|
disease |
PSYGENET |
Genetic tests suitable for the routine laboratory are now available for some important metabolizing enzymes (e.g., CYP2D6, CYP2C19) identifying those individuals who are slow or fast metabolizers of certain drugs, many of which are widely used in the treatment of depression (e.g., tricyclic antidepressants).
|
11412815 |
2001 |