Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects.

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Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects. / Wuttke, Henrike; Rau, Thomas; Roland, Heide; Bergmann, Klaus; Böhm, Michael; Weil, Joachim; Werner, Dierk; Eschenhagen, Thomas.

in: CLIN PHARMACOL THER, Jahrgang 72, Nr. 4, 4, 2002, S. 429-437.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Wuttke, H, Rau, T, Roland, H, Bergmann, K, Böhm, M, Weil, J, Werner, D & Eschenhagen, T 2002, 'Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects.', CLIN PHARMACOL THER, Jg. 72, Nr. 4, 4, S. 429-437. <http://www.ncbi.nlm.nih.gov/pubmed/12386645?dopt=Citation>

APA

Wuttke, H., Rau, T., Roland, H., Bergmann, K., Böhm, M., Weil, J., Werner, D., & Eschenhagen, T. (2002). Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects. CLIN PHARMACOL THER, 72(4), 429-437. [4]. http://www.ncbi.nlm.nih.gov/pubmed/12386645?dopt=Citation

Vancouver

Bibtex

@article{e296fdcc7af94fc1970bd21aeddee9bf,
title = "Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects.",
abstract = "OBJECTIVE: The CYP2D6 genotype is a major determinant of interindividual differences in metoprolol plasma clearance. Cytochrome P450 2D6 (CYP2D6) poor metabolizers exhibit 3- to 10-fold higher plasma concentrations after administration of metoprolol than extensive metabolizers. However, the impact of the CYP2D6 genotype on the occurrence of adverse effects of metoprolol remains controversial. This study addressed whether the incidence of poor metabolizers was higher in patients with metoprolol-associated adverse effects than in the German population at large. METHODS: Approximately 1200 German physicians were asked to report on patients who had experienced pronounced adverse effects in association with administration of metoprolol. CYP2D6 genotypes were determined with a combination of allele-specific polymerase chain reaction and polymerase chain reaction-restriction fragment length polymorphism. The adverse effects, consisting of symptoms related to beta-adrenergic receptor blockade and nonspecific symptoms, were recorded by use of a standardized questionnaire. RESULTS: Twenty-four patients were included in the study. Nine patients had 2 null alleles (poor metabolizer genotype; 38%); the remaining 15 had either 1 null allele (n = 7) or no null alleles (n = 8). Therefore the occurrences of poor metabolizer genotypes in the study population were 4.9- and 5.2-fold more frequent, respectively, than that found in unselected members of the German population in two large studies (P",
author = "Henrike Wuttke and Thomas Rau and Heide Roland and Klaus Bergmann and Michael B{\"o}hm and Joachim Weil and Dierk Werner and Thomas Eschenhagen",
year = "2002",
language = "Deutsch",
volume = "72",
pages = "429--437",
journal = "CLIN PHARMACOL THER",
issn = "0009-9236",
publisher = "NATURE PUBLISHING GROUP",
number = "4",

}

RIS

TY - JOUR

T1 - Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects.

AU - Wuttke, Henrike

AU - Rau, Thomas

AU - Roland, Heide

AU - Bergmann, Klaus

AU - Böhm, Michael

AU - Weil, Joachim

AU - Werner, Dierk

AU - Eschenhagen, Thomas

PY - 2002

Y1 - 2002

N2 - OBJECTIVE: The CYP2D6 genotype is a major determinant of interindividual differences in metoprolol plasma clearance. Cytochrome P450 2D6 (CYP2D6) poor metabolizers exhibit 3- to 10-fold higher plasma concentrations after administration of metoprolol than extensive metabolizers. However, the impact of the CYP2D6 genotype on the occurrence of adverse effects of metoprolol remains controversial. This study addressed whether the incidence of poor metabolizers was higher in patients with metoprolol-associated adverse effects than in the German population at large. METHODS: Approximately 1200 German physicians were asked to report on patients who had experienced pronounced adverse effects in association with administration of metoprolol. CYP2D6 genotypes were determined with a combination of allele-specific polymerase chain reaction and polymerase chain reaction-restriction fragment length polymorphism. The adverse effects, consisting of symptoms related to beta-adrenergic receptor blockade and nonspecific symptoms, were recorded by use of a standardized questionnaire. RESULTS: Twenty-four patients were included in the study. Nine patients had 2 null alleles (poor metabolizer genotype; 38%); the remaining 15 had either 1 null allele (n = 7) or no null alleles (n = 8). Therefore the occurrences of poor metabolizer genotypes in the study population were 4.9- and 5.2-fold more frequent, respectively, than that found in unselected members of the German population in two large studies (P

AB - OBJECTIVE: The CYP2D6 genotype is a major determinant of interindividual differences in metoprolol plasma clearance. Cytochrome P450 2D6 (CYP2D6) poor metabolizers exhibit 3- to 10-fold higher plasma concentrations after administration of metoprolol than extensive metabolizers. However, the impact of the CYP2D6 genotype on the occurrence of adverse effects of metoprolol remains controversial. This study addressed whether the incidence of poor metabolizers was higher in patients with metoprolol-associated adverse effects than in the German population at large. METHODS: Approximately 1200 German physicians were asked to report on patients who had experienced pronounced adverse effects in association with administration of metoprolol. CYP2D6 genotypes were determined with a combination of allele-specific polymerase chain reaction and polymerase chain reaction-restriction fragment length polymorphism. The adverse effects, consisting of symptoms related to beta-adrenergic receptor blockade and nonspecific symptoms, were recorded by use of a standardized questionnaire. RESULTS: Twenty-four patients were included in the study. Nine patients had 2 null alleles (poor metabolizer genotype; 38%); the remaining 15 had either 1 null allele (n = 7) or no null alleles (n = 8). Therefore the occurrences of poor metabolizer genotypes in the study population were 4.9- and 5.2-fold more frequent, respectively, than that found in unselected members of the German population in two large studies (P

M3 - SCORING: Zeitschriftenaufsatz

VL - 72

SP - 429

EP - 437

JO - CLIN PHARMACOL THER

JF - CLIN PHARMACOL THER

SN - 0009-9236

IS - 4

M1 - 4

ER -