4.5 Review

The ABCG2 transporter and its relations with the pharmacokinetics, drug interaction and lipid-lowering effects of statins

Journal

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/17425255.2011.538383

Keywords

ABCG2; LDL-C; pharmacogenetics; pharmacokinetics; polymorphisms; statins

Funding

  1. Research Grants Council of the Hong Kong Special Administrative Region, China [CUHK 4472/06 M]
  2. AstraZeneca
  3. Bayer
  4. Boehringer Ingelheim
  5. Daiichi Sankyo
  6. Kowa
  7. Merck
  8. Merck Sharp and Dohme
  9. Novartis
  10. Otsuka
  11. Pfizer
  12. Roche
  13. Sanofi-Aventis
  14. Servier
  15. School of Pharmacy
  16. Faculty of Medicine (CUHK)

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Areas covered in this review: We review and evaluate the associations of the ABCG2 polymorphism on the pharmacokinetics and clinical efficacy of statins. What the reader will gain: This article gives a detailed overview of the ABCG2 transporter and extensively reviews its relations with the pharmacokinetics and lipid-lowering effects of statins. This review also discusses the potential role of the ABCG2 polymorphism in the clinical outcomes in statin-treated patients and statin-drug interactions. Take home message: The impact of the ABCG2 421C > A polymorphism on the disposition of the statins varies between different drugs and the effect on systemic exposure was greater in the case of rosuvastatin than other statins. This genetic variant was associated with greater low-density lipoprotein cholesterol response to rosuvastatin in Chinese and caucasian patients. The effect of the ABCG2 421C > A polymorphism on the lipid response to other substrate statins and clinical outcomes need to be evaluated in future studies.

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