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Updated: Jul 12, 2025

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
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A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene

Published on: April 1, 2019

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在ABCB1的遗传多态性与阿托瓦斯塔丁诱导的肌肉副作用的风险增加相关:一个横截面研究

Ninoslava Lalatović1, Maša Ždralević2, Tanja Antunović3

  • 1Faculty of Medicine, University of Montenegro, Kruševac bb, 81000, Podgorica, Montenegro. nina.lalatovic32@gmail.com.

Scientific reports
|October 19, 2023
PubMed
概括

ABCB1基因的遗传变异增加了与他类药物相关的肌肉症状 (SAMS) 的风险,这是他类药物不耐受的常见原因. ABCB1基因定型可能有助于识别患有SAMS风险较高的患者.

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Hyperlipidemia, a medical condition often referred to as high cholesterol, is characterized by abnormally elevated levels of lipids in the bloodstream. When present in excess, these lipids, specifically cholesterol and triglycerides, can lead to serious health complications, often involving cardiovascular diseases. Illnesses like atherosclerosis, heart attacks, and pancreatitis have all been linked to untreated hyperlipidemia. This means controlling and regulating cholesterol and triglyceride...
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