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Pregled bibliografske jedinice broj: 681740

CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study


Miroševic Skvrce, Nikica; Božina, Nada; Zibar, Lada; Barišic, Ivan; Pejnovic, Lana; Macolic Šarinic, Viola
CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study // Pharmacogenomics, 14 (2013), 12; 1419-1431 doi:10.2217/pgs.13.135 (podatak o recenziji nije dostupan, prethodno priopćenje, znanstveni)


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Naslov
CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study

Autori
Miroševic Skvrce, Nikica ; Božina, Nada ; Zibar, Lada ; Barišic, Ivan ; Pejnovic, Lana ; Macolic Šarinic, Viola

Izvornik
Pharmacogenomics (1462-2416) 14 (2013), 12; 1419-1431

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, prethodno priopćenje, znanstveni

Ključne riječi
adverse drug reactions; CYP2C9; ABCG2; drug interactions; fluvastatin; hydroxymethylglutaryl-CoA reductase inhibitors; pharmacogenetics

Sažetak
Aim was to investigate whether an association exists between fluvastatin-induced adverse drug reactions (ADRs) and polymorphisms in genes encoding the metabolizing enzyme CYP2C9 and the drug transporter ABCG2 in renal transplant recipients (RTRs). Fifty-two RTRs that experienced fluvastatin ADRs and 52 controls matched for age, gender, dose of fluvastatin and immunosuppressive use were enrolled in the study. Genotyping for CYP2C9*2, *3 and ABCG2 421C>A variants was performed by real- time PCR. RESULTS: CYP2C9 homozygous and heterozygous mutant allele (*2 or *3) carriers had 2.5-times greater odds of developing adverse effects (χ² = 4.370 ; degrees of freedom = 1 ; p = 0.037 ; φ = 0.21, odds ratio [OR]: 2.44 ; 95% CI: 1.05-5.71). Patients who were the carriers of at least one mutant CYP2C9 allele (*2 or *3) and who were receiving CYP2C9 inhibitors, had more than six-times greater odds of having adverse effects than those without the inhibitor included in their therapy (p = 0.027 ; OR: 6.59 ; 95% CI: 1.24-35.08). Patients with ABCG2 421CA or AA (taken together) had almost four-times greater odds of developing adverse effects than those with ABCG2 421CC genotype (χ² = 6.190 ; degrees of freedom = 1 ; p = 0.013 ; φ = 0.24, OR: 3.81 ; 95% CI: 1.27-11.45). Patients with A allele had 2.75- times (95% CI: 1.02-7.40) greater odds of developing adverse effects than those with C allele. Our preliminary data demonstrate an association between fluvastatin-induced ADRs in RTRs and genetic variants in the CYP2C9 and ABCG2 genes.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb

Poveznice na cjeloviti tekst rada:

doi www.futuremedicine.com

Citiraj ovu publikaciju:

Miroševic Skvrce, Nikica; Božina, Nada; Zibar, Lada; Barišic, Ivan; Pejnovic, Lana; Macolic Šarinic, Viola
CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study // Pharmacogenomics, 14 (2013), 12; 1419-1431 doi:10.2217/pgs.13.135 (podatak o recenziji nije dostupan, prethodno priopćenje, znanstveni)
Miroševic Skvrce, N., Božina, N., Zibar, L., Barišic, I., Pejnovic, L. & Macolic Šarinic, V. (2013) CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study. Pharmacogenomics, 14 (12), 1419-1431 doi:10.2217/pgs.13.135.
@article{article, author = {Miro\v{s}evic Skvrce, Nikica and Bo\v{z}ina, Nada and Zibar, Lada and Bari\v{s}ic, Ivan and Pejnovic, Lana and Macolic \v{S}arinic, Viola}, year = {2013}, pages = {1419-1431}, DOI = {10.2217/pgs.13.135}, keywords = {adverse drug reactions, CYP2C9, ABCG2, drug interactions, fluvastatin, hydroxymethylglutaryl-CoA reductase inhibitors, pharmacogenetics}, journal = {Pharmacogenomics}, doi = {10.2217/pgs.13.135}, volume = {14}, number = {12}, issn = {1462-2416}, title = {CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study}, keyword = {adverse drug reactions, CYP2C9, ABCG2, drug interactions, fluvastatin, hydroxymethylglutaryl-CoA reductase inhibitors, pharmacogenetics} }
@article{article, author = {Miro\v{s}evic Skvrce, Nikica and Bo\v{z}ina, Nada and Zibar, Lada and Bari\v{s}ic, Ivan and Pejnovic, Lana and Macolic \v{S}arinic, Viola}, year = {2013}, pages = {1419-1431}, DOI = {10.2217/pgs.13.135}, keywords = {adverse drug reactions, CYP2C9, ABCG2, drug interactions, fluvastatin, hydroxymethylglutaryl-CoA reductase inhibitors, pharmacogenetics}, journal = {Pharmacogenomics}, doi = {10.2217/pgs.13.135}, volume = {14}, number = {12}, issn = {1462-2416}, title = {CYP2C9 and ABCG2 polymorphisms as risk factors for developing adverse drug reactions in renal transplant patients taking fluvastatin: a case- control study}, keyword = {adverse drug reactions, CYP2C9, ABCG2, drug interactions, fluvastatin, hydroxymethylglutaryl-CoA reductase inhibitors, pharmacogenetics} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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