Paper Details 
Original Abstract of the Article :
Hyperbilirubinaemia with or without jaundice is one of the side effects of atazanavir boosted with low-dose ritonavir (ATV/rit) related to the drug plasma levels, as a result of its metabolism by UGT1A1 - uridine diphosphate-glucuronosyl transferase. Genotyping for UGT1A1*28 before initiation of ant...See full text at original site
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引用元:
https://doi.org/10.1177/0956462414523259

データ提供:米国国立医学図書館(NLM)

Atazanavir and Hyperbilirubinemia: A Genetic Twist in the Desert

Atazanavir is a medication used to treat HIV infection. However, it can sometimes cause elevated bilirubin levels in the blood, leading to jaundice. This study investigates the genetic basis for this side effect, focusing on a specific gene called UGT1A1.

The UGT1A1 Gene: A Hidden Oasis in the Desert of Drug Metabolism

The researchers found that a specific variant of the UGT1A1 gene, called UGT1A1*28, was significantly more common in HIV-infected individuals who experienced hyperbilirubinemia while taking atazanavir. This suggests that genetic testing for this variant could be helpful in identifying individuals at higher risk of this side effect.

Personalized Medicine: A New Path Through the Desert

This study highlights the importance of personalized medicine, where treatment decisions are tailored to the individual's genetic makeup. By understanding the genetic factors that contribute to drug responses, doctors can make more informed choices about medication and minimize the risk of adverse effects.

Dr.Camel's Conclusion

This research delves into the genetic basis of atazanavir-induced hyperbilirubinemia, unveiling the role of the UGT1A1*28 variant. This study emphasizes the importance of personalized medicine in optimizing HIV treatment strategies and minimizing the risk of adverse effects. By understanding the genetic landscape of drug metabolism, we can pave a safer and more effective path through the desert of HIV treatment.

Date :
  1. Date Completed 2014-12-08
  2. Date Revised 2015-11-19
Further Info :

Pubmed ID

24516079

DOI: Digital Object Identifier

10.1177/0956462414523259

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SNS
PICO Info
in preparation
Languages

English

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