Evaluating the effects of bempedoic acid on lipid profiles and cardiovascular risk: An umbrella review of meta-analyses
Our findings show that bempedoic acid significantly reduces the risk of MACE, nonfatal MI, coronary and noncoronary revascularization, and hospitalizations for unstable angina. While results on cardiovascular mortality are mixed, suggesting a need for further study, bempedoic acid proves to be an effective treatment for improving lipid profiles and reducing cardiovascular events, especially in patients who cannot tolerate statins. It presents a valuable option for cardiovascular risk management, potentially enhancing patient outcomes and quality of life. Further research is needed to assess its long-term benefits and broader applicability.
Authors
- Anim Asif
- Umair Baig (ORCID: https://orcid.org/0000-0002-9881-1981)
- Aatkah Naseer
- Owais Ali
- Sheena Shamoon (ORCID: https://orcid.org/0000-0002-4663-4979)
- Rubaid Azhar Dhillon (ORCID: https://orcid.org/0000-0002-6859-1789)
- Palak Patel (ORCID: https://orcid.org/0000-0001-5805-3023)
- Sameer Bhimani
- Vikash Kumar Karmani (ORCID: https://orcid.org/0000-0001-8622-0300)
- Adina Amir
- Shahzeb Saeed
- Ashik Ali
Institutions
- Charleston Area Medical Center (US)
- Rawalpindi Medical University (PK)
- New York Medical College (US)
- Riphah International University (PK)
- Sindh Institute of Urology and Transplantation (PK)
- Karachi Institute of Heart Diseases (PK)
- Jinnah Sindh Medical University (PK)
- Harlem Hospital Center (US)
- Dow University of Health Sciences (PK)
- SRM Dental College (IN)
- The Wright Center for Graduate Medical Education (US)
- SRM University (IN)
- National Institute of Cardiovascular Diseases (PK)
- Saint Michael's Medical Center (US)
- Pakistan Institute of Medical Sciences (PK)
Publication Details
- Journal
- Qatar medical journal
- Published
- 2025-06-30
- DOI
- https://doi.org/10.5339/qmj.2025.51
- Citations
- 1
- Primary Topic
- Lipoproteins and Cardiovascular Health
- Type
- article
- Field-Weighted Citation Impact
- 2.01