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Muscular and Renal Safety of Ticagrelor with High-Intensity Statins: Retrospective Cohort Findings
Abdullah S Alshammari1, Amer A Shalwala2, Mohammed A Alnuhait1
1Pharmaceutical Practices Department, College of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.
Insights
Combining ticagrelor with high-intensity statins increases the risk of muscle complications in acute coronary syndrome patients. This real-world study found significantly more muscle issues in patients on both drugs, highlighting safety concerns.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Ticagrelor is a key antiplatelet for acute coronary syndromes (ACS).
- Combination therapy with high-intensity statins is standard for ACS.
- Potential drug-drug interactions between ticagrelor and statins may cause adverse events, including muscular and renal issues.
Purpose of the Study:
- To evaluate the real-world risk of muscular and renal complications from co-administering ticagrelor with high-intensity statins in Saudi Arabia.
Main Methods:
- Retrospective observational cohort study of 577 adult patients at Makkah Cardiology Center.
- Patients received high-intensity statins, with or without ticagrelor.
- Primary outcomes: statin-associated muscular complications (myalgia, myopathy, myositis, rhabdomyolysis) and acute kidney injury (AKI).
Main Results:
- Muscle-related complications were significantly higher in the ticagrelor-statin combination group (20.2%) versus statin monotherapy (10.5%) (P=0.001).
- Hypertension was the only significant comorbidity linked to increased muscle complications.
- A non-significant trend towards increased AKI was noted in the combination group.
Conclusions:
- Co-administration of ticagrelor and high-intensity statins is associated with an increased risk of muscle-related adverse events.
- The study suggests cautious use of this combination therapy.
- Further prospective studies are needed to confirm AKI findings and optimize safety.
Introduction:
Ticagrelor is a widely used antiplatelet agent approved in over 70 countries, including the European Union and the United States, for reducing thrombotic events in patients with acute coronary syndromes (ACS). In clinical practice, combining ticagrelor with high-intensity statins is considered standard therapy for ACS. However, recent pharmacodynamic studies and case reports suggest potential drug-drug interactions that may increase the risk of adverse events, particularly muscular and renal complications. This study aimed to evaluate these risks in a real-world clinical setting in Saudi Arabia.
Methods:
This retrospective observational cohort study was conducted at the Makkah Cardiology Center, Saudi Arabia. The study included adult patients (n = 577) who were prescribed high-intensity statins, with or without concurrent ticagrelor. The primary outcomes were the incidence of statin-associated muscular complications-defined as myalgia, myopathy, myositis, or rhabdomyolysis-and acute kidney injury (AKI). Clinical data were extracted from the hospital information system, and statistical comparisons were conducted between patients receiving statin monotherapy and those receiving combination therapy.
Results:
The cohort consisted predominantly of male patients (74.5%). Muscle-related complications were significantly more common in the group receiving both ticagrelor and statins (20.2%) compared to the statin-only group (10.5%) (P = 0.001). Among comorbid conditions, hypertension was the only factor significantly associated with a higher incidence of muscle-related complications. Although a trend toward increased AKI incidence was observed in the combination therapy group, this difference did not reach statistical significance.
Conclusion:
This study highlights potential safety concerns related to the co-administration of ticagrelor and high-intensity statins, particularly the increased risk of muscle-related complications. While the findings on AKI were inconclusive, the results support the need for cautious use of this combination and call for larger prospective studies to further evaluate its safety profile and optimize treatment strategies.
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