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SLCO1B1*5 Allele Is Associated With Atorvastatin Discontinuation and Adverse Muscle Symptoms in the Context of Routine Care.
Author: BayeJordan, HajekCatherine, LarsonEric A, McDermaidAdam, Narayana GowdaSmitha, Nicole MyrmoeAnna, VooraDeepak, WilkeRussell A
Original Abstract of the Article :
The SLCO1B1 genotype is known to influence patient adherence to statin therapy, in part by increasing the risk for statin-associated musculoskeletal symptoms (SAMSs). The SLCO1B1*5 allele has previously been associated with simvastatin discontinuation and SAMSs. Prior analyses of the relationship be...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303592/
データ提供:米国国立医学図書館(NLM)
The Genetic Link Between Statin Adherence and Muscle Side Effects
Statins, a class of drugs widely used to lower cholesterol levels, are effective in preventing heart disease. However, some individuals experience statin-associated musculoskeletal symptoms (SAMSs), which can lead to medication discontinuation. This research explores the impact of the SLCO1B1*5 allele, a genetic variant, on statin adherence and SAMSs in patients taking atorvastatin.
The study analyzed electronic medical records from a large observational cohort, investigating the association between SLCO1B1*5 and atorvastatin discontinuation and SAMSs. The study found that individuals carrying the SLCO1B1*5 allele were significantly more likely to discontinue atorvastatin and to develop SAMSs. This finding suggests that genetic testing for SLCO1B1*5 may be helpful in predicting the risk of SAMSs and in guiding statin therapy decisions.
Personalized Medicine: Tailoring Treatment to Genetics
This research highlights the growing importance of personalized medicine, where treatment decisions are tailored to individual genetic profiles. The study's findings suggest that SLCO1B1*5 genetic testing can provide valuable information for predicting the risk of SAMSs and for optimizing statin therapy. This approach allows for more personalized and potentially more effective treatment strategies, ensuring better patient outcomes and adherence to statin therapy.
Navigating the Desert of Statin Therapy
Statins are a crucial part of cardiovascular disease prevention, but managing their potential side effects, particularly SAMSs, is essential. This study reveals the potential of genetic testing to guide statin therapy decisions, allowing for more personalized and effective treatment. It's like finding a new oasis in the desert of statin therapy, where the path to optimal health is guided by individual genetic profiles. Understanding your genetic predispositions can help you work with your healthcare provider to develop a treatment plan that maximizes benefits and minimizes risks.
Dr.Camel's Conclusion
The link between SLCO1B1*5 and statin adherence and SAMSs is a significant discovery. It highlights the power of personalized medicine to optimize treatment decisions based on individual genetic profiles. This research is a step towards a more precise and effective approach to managing cardiovascular health, like finding a hidden oasis in the desert of statin therapy, offering a personalized path to optimal well-being.
Date :
- Date Completed 2022-04-21
- Date Revised 2022-07-27
Further Info :
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