-
Je něco špatně v tomto záznamu ?
Safety of the Geneva Cocktail, a Cytochrome P450 and P-Glycoprotein Phenotyping Cocktail, in Healthy Volunteers from Three Different Geographic Origins
V. Rollason, M. Mouterde, Y. Daali, M. Čížková, E. Priehodová, I. Kulichová, H. Posová, J. Petanová, A. Mulugeta, E. Makonnen, A. Al-Habsi, R. Davidson, KK. Al-Balushi, K. Al-Thihli, M. Cerná, S. Al-Yahyaee, V. Černý, G. Yimer, ES. Poloni, J. Desmeules
Jazyk angličtina Země Nový Zéland
Typ dokumentu klinické zkoušky, časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 2008-06-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 2008-06-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2008-06-01 do Před 1 rokem
- MeSH
- dospělí MeSH
- fixní kombinace léků MeSH
- genotyp MeSH
- inhibitory cytochromu P450 MeSH
- léčivé přípravky metabolismus MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- P-glykoprotein genetika metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- substrátová specifita MeSH
- systém (enzymů) cytochromů P-450 genetika metabolismus MeSH
- zdraví dobrovolníci pro lékařské studie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Etiopie MeSH
- Omán MeSH
INTRODUCTION AND OBJECTIVE: Cytochrome P450 enzymes are the major drug-metabolizing enzymes in humans and the importance of drug transport proteins, in particular P-glycoprotein, in the variability of drug response has also been highlighted. Activity of cytochrome P450 enzymes and P-glycoprotein can vary widely between individuals and genotyping and/or phenotyping can help assess their activity. Several phenotyping cocktails have been developed. The Geneva cocktail is composed of a specific probe for six different cytochrome P450 enzymes and one for P-glycoprotein and was used in the context of a research aiming at exploring genotypes and phenotypes in distinct human populations (NCT02789527). The aim of the present study is to solely report the safety results of the Geneva cocktail in the healthy volunteers of these populations.MATERIALS AND METHODS: The Geneva cocktail is composed of caffeine, bupropion, flurbiprofen, omeprazole, dextromethorphan, midazolam, and fexofenadine. The volunteers fasted and avoided drinking caffeine-containing beverages or food and grapefruit juice overnight before receiving the cocktail orally. They provided blood spots for the probes' concentrations at 2, 3, and 6 h after ingestion and were asked about adverse events. RESULTS: A total of 265 healthy adult volunteers were included from Ethiopia, Oman, and the Czech Republic. The mean plasma concentrations at the 2-h sampling time of each probe drug in the total sample were: 1663 ng/mL for caffeine, 8 ng/mL for bupropion, 789 ng/mL for flurbiprofen, 6 ng/mL for dextromethorphan, 2 ng/mL for midazolam, 35 ng/mL for fexofenadine, and 103 ng/mL for omeprazole. Four adverse events were observed representing an occurrence of 1.5%. All these events were categorized as mild to moderate, non-serious, and resolved spontaneously. A causal link with the cocktail cannot be excluded because of the temporal relationship but is at most evaluated as possible according to the World Health Organization-Uppsala Monitoring Centre causal assessment system. CONCLUSIONS: In this research, healthy volunteers from three different human populations were phenotyped with the Geneva cocktail. Four adverse events were observed, confirming the safety of this cocktail that is given at lower than clinically relevant doses and therefore results in concentrations lower than those reported to cause adverse events.
Department of Family Medicine Sultan Qaboos University Hospital Muscat Sultanate of Oman
Department of Genetics College of Medicine and Health Sciences Muscat Sultanate of Oman
Department of Genetics Sultan Qaboos University Hospital Muscat Sultanate of Oman
Department of Medical Genetics 3rd Faculty of Medicine Charles University Prague Czech Republic
Department of Pharmacology and Clinical Pharmacy Sultan Qaboos University Muscat Sultanate of Oman
Institute of Genetics and Genomics of Geneva Geneva Switzerland
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21026444
- 003
- CZ-PrNML
- 005
- 20230704112750.0
- 007
- ta
- 008
- 211013s2020 nz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s40264-020-00983-8 $2 doi
- 035 __
- $a (PubMed)32851583
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a nz
- 100 1_
- $a Rollason, Victoria $u Division of Clinical Pharmacology and Toxicology, Geneva University Hospitals and University of Geneva, Rue Gabrielle-Perret-Gentil 4, 1211, Geneva, Switzerland. Victoria.Rollason@hcuge.ch
- 245 10
- $a Safety of the Geneva Cocktail, a Cytochrome P450 and P-Glycoprotein Phenotyping Cocktail, in Healthy Volunteers from Three Different Geographic Origins / $c V. Rollason, M. Mouterde, Y. Daali, M. Čížková, E. Priehodová, I. Kulichová, H. Posová, J. Petanová, A. Mulugeta, E. Makonnen, A. Al-Habsi, R. Davidson, KK. Al-Balushi, K. Al-Thihli, M. Cerná, S. Al-Yahyaee, V. Černý, G. Yimer, ES. Poloni, J. Desmeules
- 520 9_
- $a INTRODUCTION AND OBJECTIVE: Cytochrome P450 enzymes are the major drug-metabolizing enzymes in humans and the importance of drug transport proteins, in particular P-glycoprotein, in the variability of drug response has also been highlighted. Activity of cytochrome P450 enzymes and P-glycoprotein can vary widely between individuals and genotyping and/or phenotyping can help assess their activity. Several phenotyping cocktails have been developed. The Geneva cocktail is composed of a specific probe for six different cytochrome P450 enzymes and one for P-glycoprotein and was used in the context of a research aiming at exploring genotypes and phenotypes in distinct human populations (NCT02789527). The aim of the present study is to solely report the safety results of the Geneva cocktail in the healthy volunteers of these populations.MATERIALS AND METHODS: The Geneva cocktail is composed of caffeine, bupropion, flurbiprofen, omeprazole, dextromethorphan, midazolam, and fexofenadine. The volunteers fasted and avoided drinking caffeine-containing beverages or food and grapefruit juice overnight before receiving the cocktail orally. They provided blood spots for the probes' concentrations at 2, 3, and 6 h after ingestion and were asked about adverse events. RESULTS: A total of 265 healthy adult volunteers were included from Ethiopia, Oman, and the Czech Republic. The mean plasma concentrations at the 2-h sampling time of each probe drug in the total sample were: 1663 ng/mL for caffeine, 8 ng/mL for bupropion, 789 ng/mL for flurbiprofen, 6 ng/mL for dextromethorphan, 2 ng/mL for midazolam, 35 ng/mL for fexofenadine, and 103 ng/mL for omeprazole. Four adverse events were observed representing an occurrence of 1.5%. All these events were categorized as mild to moderate, non-serious, and resolved spontaneously. A causal link with the cocktail cannot be excluded because of the temporal relationship but is at most evaluated as possible according to the World Health Organization-Uppsala Monitoring Centre causal assessment system. CONCLUSIONS: In this research, healthy volunteers from three different human populations were phenotyped with the Geneva cocktail. Four adverse events were observed, confirming the safety of this cocktail that is given at lower than clinically relevant doses and therefore results in concentrations lower than those reported to cause adverse events.
- 650 _2
- $a P-glykoprotein $x genetika $x metabolismus $7 D020168
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a inhibitory cytochromu P450 $7 D065607
- 650 _2
- $a systém (enzymů) cytochromů P-450 $x genetika $x metabolismus $7 D003577
- 650 _2
- $a fixní kombinace léků $7 D004338
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a regulace genové exprese $x účinky léků $7 D005786
- 650 _2
- $a genotyp $7 D005838
- 650 _2
- $a zdraví dobrovolníci pro lékařské studie $7 D064368
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a léčivé přípravky $x metabolismus $7 D004364
- 650 _2
- $a substrátová specifita $7 D013379
- 650 _2
- $a mladý dospělý $7 D055815
- 651 _2
- $a Česká republika $7 D018153
- 651 _2
- $a Etiopie $7 D005002
- 651 _2
- $a Omán $7 D009850
- 655 _2
- $a klinické zkoušky $7 D016430
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Mouterde, Médéric $u Department of Genetics and Evolution (GENEV), Anthropology Unit, University of Geneva, 30, Quai Ernest-Ansermet, 1205 Geneva, Switzerland. Mederic.Mouterde@unige.ch
- 700 1_
- $a Daali, Youssef $u Division of Clinical Pharmacology and Toxicology, Geneva University Hospitals and University of Geneva, Rue Gabrielle-Perret-Gentil 4, 1211, Geneva, Switzerland
- 700 1_
- $a Čížková, Martina $u Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Priehodová, Edita $u Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Kulichová, Iva $u Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Posová, Helena $u Institute of Immunology and Microbiology, First Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Petanová, Jitka $u Institute of Immunology and Microbiology, First Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Mulugeta, Anwar $u Department of Pharmacology and Clinical Pharmacy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia
- 700 1_
- $a Makonnen, Eyasu $u Department of Pharmacology and Clinical Pharmacy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia $u Center for Innovative Drug Development and Therapeutic Trials for Africa, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia
- 700 1_
- $a Al-Habsi, Abir $u Oman Specialty Board, Muscat, Sultanate of Oman
- 700 1_
- $a Davidson, Robin $u Department of Family Medicine, Sultan Qaboos University Hospital, Muscat, Sultanate of Oman
- 700 1_
- $a Al-Balushi, Khalid K $u Department of Pharmacology and Clinical Pharmacy, Sultan Qaboos University, Muscat, Sultanate of Oman
- 700 1_
- $a Al-Thihli, Khalid $u Department of Genetics, Sultan Qaboos University Hospital, Muscat, Sultanate of Oman
- 700 1_
- $a Cerná, Marie $u Department of Medical Genetics, Third Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Al-Yahyaee, Said $u Department of Genetics, College of Medicine and Health Sciences, Muscat, Sultanate of Oman
- 700 1_
- $a Černý, Viktor, $u Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague, Czech Republic $d 1964- $7 xx0031073
- 700 1_
- $a Yimer, Getnet $u Global One Health Initiative, Office of International Affairs, The Ohio State University, Columbus, OH, USA
- 700 1_
- $a Poloni, Estella S $u Department of Genetics and Evolution (GENEV), Anthropology Unit, University of Geneva, 30, Quai Ernest-Ansermet, 1205 Geneva, Switzerland $u Institute of Genetics and Genomics of Geneva (iGE3), Geneva, Switzerland
- 700 1_
- $a Desmeules, Jules $u Division of Clinical Pharmacology and Toxicology, Geneva University Hospitals and University of Geneva, Rue Gabrielle-Perret-Gentil 4, 1211, Geneva, Switzerland
- 773 0_
- $w MED00001449 $t Drug safety $x 1179-1942 $g Roč. 43, č. 11 (2020), s. 1181-1189
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32851583 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20230704112747 $b ABA008
- 999 __
- $a ok $b bmc $g 1715228 $s 1146951
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 43 $c 11 $d 1181-1189 $e - $i 1179-1942 $m Drug safety $n Drug Saf $x MED00001449
- LZP __
- $a Pubmed-20211013