Hyperbilirubinemia in atazanavir treated HIV-infected patients: the impact of the UGT1A1*28 allele.

Author: HatzakisAngelos, MaltezosEfstathios, PanagopoulosPeriklis, ParaskevisDimitrios

Paper Details 
Original Abstract of the Article :
Combination antiretroviral treatment (cART) has significantly improved the life expectancy of people living with HIV. The life-long nature of cART increases the risk of side effects, which in some cases may have been caused by specific genetic characteristics. Patients treated with atazanavir (ATV) ...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488765/

データ提供:米国国立医学図書館(NLM)

Unraveling the Mystery of Hyperbilirubinemia in HIV Patients

This study investigates the impact of a specific gene variant on the occurrence of hyperbilirubinemia, a condition where bilirubin levels in the blood are elevated, in patients undergoing antiretroviral therapy for HIV. Think of it like a puzzle with pieces scattered across the vast desert of human genetics. The researchers sought to identify a specific genetic piece that contributes to the puzzle of hyperbilirubinemia.

UGT1A1*28: A Missing Piece of the Puzzle

The study reveals that the UGT1A1*28 allele, a variant in the UGT1A1 gene, is a key contributor to hyperbilirubinemia in HIV patients treated with atazanavir/ritonavir. This discovery is like finding a vital clue buried beneath the sand, providing a deeper understanding of the complex interplay between genetics and drug response.

Individualized Medicine: A Personalized Approach

This research highlights the importance of personalized medicine in treating HIV patients, taking into account individual genetic variations. By understanding the role of UGT1A1*28, doctors can tailor treatment plans to minimize the risk of hyperbilirubinemia and optimize patient outcomes.

Dr.Camel's Conclusion

The study emphasizes the significance of genetic variations in drug response, allowing for a more tailored and effective approach to HIV treatment. This research is a reminder that the human body is a complex desert of genetic information, and understanding its nuances is crucial for providing optimal care.

Date :
  1. Date Completed n.d.
  2. Date Revised 2020-10-01
Further Info :

Pubmed ID

28790862

DOI: Digital Object Identifier

PMC5488765

Related Literature

SNS
PICO Info
in preparation
Languages

English

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