Key result
Lp(a) testing in ASCVD is linked to ~186% greater statin initiation versus no testing.
Why the study?
Lipoprotein (a) is an independent risk factor for atherosclerotic cardiovascular disease, but testing remains variable, and it is unclear what factors influence testing and whether it changes clinical management.
Does Lipoprotein (a) testing increase the initiation of lipid-lowering therapies in patients with established atherosclerotic cardiovascular disease?
Cohort (n=595,684)
Yes
Does Lipoprotein (a) testing increase the initiation of lipid-lowering therapies in patients with established atherosclerotic cardiovascular disease?
Lipoprotein (a) testing in real-world clinical practice is vastly underutilized (0.4%) with significant racial disparities, but obtaining a test leads to a substantially higher initiation of lipid-lowering therapies, especially non-statin therapies in those with elevated levels.
Lp(a) testing was associated with higher statin initiation in ASCVD; leaves open whether testing drives uptake or reflects confounding.
Background Lipoprotein (a) is an independent risk factor for atherosclerotic cardiovascular disease. However, lipoprotein (a) testing remains variable and it is unclear what factors influence testing and if testing changes clinical management. Methods and Results A retrospective study using electronic medical record data from 5 health systems identified an atherosclerotic cardiovascular disease cohort divided into those with and without a lipoprotein (a) test between 2019 and 2021. Baseline characteristics and lipid‐lowering therapy patterns were assessed. Multivariable regression modeling was used to determine factors associated with lipoprotein (a) testing. Among 595 684 patients with atherosclerotic cardiovascular disease, only 2587 (0.4%) were tested for lipoprotein (a). Those who were older or Black individuals were less likely to have lipoprotein (a) testing, while those with familial hypercholesterolemia, ischemic stroke/transient ischemic attack, peripheral artery disease, prior lipid‐lowering therapy, or low‐density lipoprotein cholesterol ≥130 mg/dL were more likely to be tested. Those with a lipoprotein (a) test, regardless of the lipoprotein (a) value, were more frequently initiated on any statin therapy (30.3% versus 10.6%, P < 0.001), ezetimibe (7.65% versus 0.8%, P < 0.001), or proprotein convertase substilisin/kexin type 9 inhibitor (6.7% versus 0.3%, P < 0.001) compared with those without a test. Those with an elevated lipoprotein (a) level more frequently initiated ezetimibe (11.5% versus 5.9%, P < 0.001) or proprotein convertase substilisin/kexin type 9 inhibitor (10.9% versus 4.8%, P < 0.001). Conclusions Lipoprotein (a) testing in patients with atherosclerotic cardiovascular disease is infrequent, with evidence of disparities among older or Black individuals. Testing for lipoprotein (a), regardless of level, is associated with greater initiation of any lipid‐lowering therapy, while elevated lipoprotein (a) is associated with greater initiation of nonstatin lipid‐lowering therapy. There is a critical need for multidisciplinary and inclusive approaches to raise awareness for lipoprotein (a) testing, and its implications on management.
No takes yet. Share an insight, caveat, or question.
Shah et al. (2024) conducted a cohort in Atherosclerotic Cardiovascular Disease (n=595,684). Lipoprotein (a) testing vs. No lipoprotein (a) testing was evaluated on Initiation of any statin therapy within 6 months (p=<0.001). Among patients with atherosclerotic cardiovascular disease, lipoprotein (a) testing was infrequent (0.4%) but was associated with greater initiation of statin therapy (30.3% vs 10.6%) compared to no testing.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: