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Factors Associated with Lipoprotein(a) Testing Among Multiethnic Individuals
Sumeet Brar1, Qiwen Huang2, Xiaowei Yan2
1Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Journal of General Internal Medicine
|October 25, 2024
Summary
Lipoprotein(a) [Lp(a)] testing is recommended but remains low in real-world use. Significant disparities in Lp(a) testing exist among racial and ethnic groups, highlighting a need for improved access.
Area of Science:
- Cardiovascular Medicine
- Clinical Epidemiology
- Health Services Research
Background:
- Lipoprotein(a) [Lp(a)] is a recognized causal risk factor for atherosclerotic cardiovascular disease (ASCVD).
- Clinical guidelines advocate for the integration of Lp(a) testing into routine patient care.
- Understanding current Lp(a) testing patterns is crucial for addressing ASCVD risk.
Purpose of the Study:
- To investigate real-world, contemporary clinical testing patterns for Lp(a).
- To examine Lp(a) testing prevalence across diverse, multiethnic populations.
- To identify factors associated with Lp(a) testing utilization.
Main Methods:
- A nested case-control study was conducted within a large Northern Californian health system (2010-2021).
- Incident density matching was employed to select controls for cases (up to 1:5 ratio).
- Conditional logistic regression analyzed associations between Lp(a) testing and patient characteristics.
Main Results:
- Only 1.0% of 1,484,410 individuals underwent Lp(a) testing; median level was 35 mg/dL.
- South Asian individuals showed higher testing likelihood (OR=3.19), while Black and Hispanic individuals had lower rates.
- History of ASCVD (OR=2.14) and frequent primary care visits (OR=1.99) were associated with increased testing.
Conclusions:
- Real-world Lp(a) testing rates are low, with notable disparities based on race, ethnicity, and healthcare utilization.
- Expanding access to Lp(a) testing is essential for equitable ASCVD risk assessment and treatment.
- Addressing testing disparities will be vital as novel Lp(a)-targeted therapies emerge.
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