Paper Details 
Original Abstract of the Article :
<b>Background:</b> Statin intolerance impacts approximately 10% of statin users, with side effects ranging from mild myalgia to extreme intolerance resulting in myopathy and rhabdomyolysis. Statin intolerance results in poor adherence to therapy and can impact statin efficacy. Many genetic variants...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517257/

データ提供:米国国立医学図書館(NLM)

Statin Intolerance: Genetic Clues for Personalized Treatment

Statins, a class of drugs used to lower cholesterol, can be a lifeline for those at risk of heart disease, but some people experience unpleasant side effects. This is like crossing a desert, where some travelers may be better equipped than others for the journey. This study explores the connection between genetic variations and statin response, looking for clues to personalize treatment and avoid these side effects.

Two Variants Linked to Statin Efficacy

The research identified two specific genetic variants, one in the ABCB1 gene and another in the LILRB5 gene, that were associated with statin efficacy. It's like discovering two hidden springs in the desert, offering a better path for some travelers. Individuals with certain combinations of these variants showed a greater reduction in non-HDL cholesterol levels when taking statins.

The Promise of Precision Medicine

These findings highlight the potential of genetic testing to personalize statin therapy. This is like having a customized map for navigating the desert, tailoring the journey to the individual's needs. By understanding a person's genetic makeup, doctors can make more informed decisions about statin treatment, potentially improving outcomes and reducing side effects.

Dr.Camel's Conclusion

This research takes us a step closer to precision medicine, where treatments are tailored to individual genetic profiles. It's like developing a more sophisticated set of tools for navigating the desert, ensuring a safer and more effective journey for everyone. As we continue to explore the complexities of genetics, we're opening up exciting new possibilities for personalized healthcare.

Date :
  1. Date Completed n.d.
  2. Date Revised 2021-10-22
Further Info :

Pubmed ID

34659336

DOI: Digital Object Identifier

PMC8517257

Related Literature

SNS
PICO Info
in preparation
Languages

English

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