CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study.

Standard

CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study. / Rau, Thomas; Wohlleben, Gerlinde; Wuttke, Henrike; Thuerauf, Norbert; Lunkenheimer, Jens; Lanczik, Mario; Eschenhagen, Thomas.

in: CLIN PHARMACOL THER, Jahrgang 75, Nr. 5, 5, 2004, S. 386-393.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Rau, T, Wohlleben, G, Wuttke, H, Thuerauf, N, Lunkenheimer, J, Lanczik, M & Eschenhagen, T 2004, 'CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study.', CLIN PHARMACOL THER, Jg. 75, Nr. 5, 5, S. 386-393. <http://www.ncbi.nlm.nih.gov/pubmed/15116051?dopt=Citation>

APA

Rau, T., Wohlleben, G., Wuttke, H., Thuerauf, N., Lunkenheimer, J., Lanczik, M., & Eschenhagen, T. (2004). CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study. CLIN PHARMACOL THER, 75(5), 386-393. [5]. http://www.ncbi.nlm.nih.gov/pubmed/15116051?dopt=Citation

Vancouver

Rau T, Wohlleben G, Wuttke H, Thuerauf N, Lunkenheimer J, Lanczik M et al. CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study. CLIN PHARMACOL THER. 2004;75(5):386-393. 5.

Bibtex

@article{50ea3fd4e5984a998fb3bf762d2832e0,
title = "CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study.",
abstract = "OBJECTIVE: Treatment with antidepressants is frequently associated with adverse effects or insufficient clinical response. Several antidepressants are metabolized by cytochrome P450 (CYP) 2D6. The activity of this enzyme markedly varies among individuals from poor to ultrarapid metabolism on the basis of the polymorphism of the CYP2D6 gene. This association study investigated whether the CYP2D6 genotype distribution differs from that of the German white population either in patients with marked adverse effects or in nonresponders during treatment with antidepressants metabolized by CYP2D6. METHODS: By use of a retrospective, naturalistic approach, outpatient practices and hospitals in southern Germany were asked to report on patients who either had had adverse drug effects or were nonresponsive during treatment with CYP2D6-dependent antidepressants. CYP2D6 genotyping was performed by a panel of polymerase chain reaction techniques. Poor and intermediate metabolizer alleles, as well as allelic duplications of CYP2D6, were detected. RESULTS: Of 28 patients with adverse effects during treatment with a CYP2D6-dependent antidepressant, 8 (29%) had 2 inactive alleles and thus were poor metabolizers. This is a 4-fold increase as compared with the German population (P",
author = "Thomas Rau and Gerlinde Wohlleben and Henrike Wuttke and Norbert Thuerauf and Jens Lunkenheimer and Mario Lanczik and Thomas Eschenhagen",
year = "2004",
language = "Deutsch",
volume = "75",
pages = "386--393",
journal = "CLIN PHARMACOL THER",
issn = "0009-9236",
publisher = "NATURE PUBLISHING GROUP",
number = "5",

}

RIS

TY - JOUR

T1 - CYP2D6 genotype: impact on adverse effects and nonresponse during treatment with antidepressants-a pilot study.

AU - Rau, Thomas

AU - Wohlleben, Gerlinde

AU - Wuttke, Henrike

AU - Thuerauf, Norbert

AU - Lunkenheimer, Jens

AU - Lanczik, Mario

AU - Eschenhagen, Thomas

PY - 2004

Y1 - 2004

N2 - OBJECTIVE: Treatment with antidepressants is frequently associated with adverse effects or insufficient clinical response. Several antidepressants are metabolized by cytochrome P450 (CYP) 2D6. The activity of this enzyme markedly varies among individuals from poor to ultrarapid metabolism on the basis of the polymorphism of the CYP2D6 gene. This association study investigated whether the CYP2D6 genotype distribution differs from that of the German white population either in patients with marked adverse effects or in nonresponders during treatment with antidepressants metabolized by CYP2D6. METHODS: By use of a retrospective, naturalistic approach, outpatient practices and hospitals in southern Germany were asked to report on patients who either had had adverse drug effects or were nonresponsive during treatment with CYP2D6-dependent antidepressants. CYP2D6 genotyping was performed by a panel of polymerase chain reaction techniques. Poor and intermediate metabolizer alleles, as well as allelic duplications of CYP2D6, were detected. RESULTS: Of 28 patients with adverse effects during treatment with a CYP2D6-dependent antidepressant, 8 (29%) had 2 inactive alleles and thus were poor metabolizers. This is a 4-fold increase as compared with the German population (P

AB - OBJECTIVE: Treatment with antidepressants is frequently associated with adverse effects or insufficient clinical response. Several antidepressants are metabolized by cytochrome P450 (CYP) 2D6. The activity of this enzyme markedly varies among individuals from poor to ultrarapid metabolism on the basis of the polymorphism of the CYP2D6 gene. This association study investigated whether the CYP2D6 genotype distribution differs from that of the German white population either in patients with marked adverse effects or in nonresponders during treatment with antidepressants metabolized by CYP2D6. METHODS: By use of a retrospective, naturalistic approach, outpatient practices and hospitals in southern Germany were asked to report on patients who either had had adverse drug effects or were nonresponsive during treatment with CYP2D6-dependent antidepressants. CYP2D6 genotyping was performed by a panel of polymerase chain reaction techniques. Poor and intermediate metabolizer alleles, as well as allelic duplications of CYP2D6, were detected. RESULTS: Of 28 patients with adverse effects during treatment with a CYP2D6-dependent antidepressant, 8 (29%) had 2 inactive alleles and thus were poor metabolizers. This is a 4-fold increase as compared with the German population (P

M3 - SCORING: Zeitschriftenaufsatz

VL - 75

SP - 386

EP - 393

JO - CLIN PHARMACOL THER

JF - CLIN PHARMACOL THER

SN - 0009-9236

IS - 5

M1 - 5

ER -