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Achievement of LDL-C <55 mg/dL among US adults: Findings from the cvMOBIUS2 registry - 07/08/24

Doi : 10.1016/j.ahj.2024.06.012 
Ann Marie Navar, MD PhD, a, , Nishant P. Shah, MD, b, c, Peter Shrader, MA c, Laine E. Thomas, PhD d, Zahid Ahmad, MD, e, Clint Allred, MD, f, Alanna M. Chamberlain, PhD, g, Elizabeth A. Chrischilles, PhD, h, Nafeesa Dhalwani, MSc, PhD, i, Mark B. Effron, MD, j, Salim Hayek, MD, k, Laney K. Jones, MPH PharmD, l, Bethany Kalich, PharmD, i, Michael D. Shapiro, DO, m, Cezary Wójcik, MD PhD, i, Eric D. Peterson, MD MPH, a
a Department of Medicine, Division of Cardiology, UT Southwestern Medical Center, Dallas, TX, USA 
b Division of Cardiology, Duke University School of Medicine, Durham, NC, USA 
c Duke Clinical Research Institute, Durham, NC, USA 
d Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA 
e Department of Medicine, Division of Endocrinology, UT Southwestern Medical Center, Dallas, TX, USA 
f Department of Population Health, University of Utah, Salt Lake City, UT and St Luke's Health Idaho Cardiology Associates, Boise, ID 
g Department of Quantitative Health Sciences and Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA 
h Department of Epidemiology, College of Public Health, University of Iowa, Iowa City, IA, USA 
i Amgen, Thousand Oaks, CA, USA 
j Oschner Medical Center, New Orleans, LA, USA 
k Department of Cardiology, University of Michigan, Ann Arbor, MI, USA 
l Department of Genomic Health, Geisinger Clinic, Danville, PA, USA 
m Department of Cardiovascular Medicine, Wake Forest University Health Sciences, Wake Forest, NC, USA 

Reprint requests: Ann Marie Navar, MD PhD, Department of medicine, UT Southwestern Medical Center, 5323 Harry Hines Blvd. E5.722, Dallas, Tx 75390.UT Southwestern Medical Center5323 Harry Hines Blvd. E5.722DallasTx75390
In corso di stampa. Prove corrette dall'autore. Disponibile online dal Wednesday 07 August 2024
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ABSTRACT

Background

Reflecting clinical trial data showing improved outcomes with lower LDL-C levels, guidelines across the globe are increasingly recommending a goal of LDL-C <55 mg/dL in persons with atherosclerotic cardiovascular disease (ASCVD). What proportion of patients with ASCVD are already meeting those goals in the US remains understudied.

Methods

Using electronic health record data from 8 large US health systems, we evaluated lipid-lowering therapy (LLT), LDL-C levels, and factors associated with an LDL-C <55 mg/dL in persons with ASCVD treated between 1/1/2021-12/31/2021. Multivariable modeling was used to evaluate factors associated with achievement of an LDL-C <55 mg/dL.

Results

Among 167,899 eligible patients, 22.6% (38,016) had an LDL-C <55 mg/dL. While 76.1% of individuals overall were on a statin, only 38.2% were on a high-intensity statin, 5.9% were on ezetimibe, and 1.7% were on a PCSK9i monoclonal antibody (mAb). Factors associated with lower likelihood of achieving an LDL-C <55 mg/dL included: younger age (odds ratio [OR] 0.91 per 10y), female sex (OR 0.69), Black race (OR 0.76), and noncoronary artery disease forms of ASCVD including peripheral artery disease (OR 0.72) and cerebrovascular disease (OR 0.85), while high-intensity statin use was associated with increased odds of LDL-C <55 mg/dL (OR 1.55). Combination therapy (statin+ezetimibe or statin+PCSK9i mAb) was rare (4.4% and 0.5%, respectively) and was associated with higher odds of an LDL-C <55 mg/dL (OR 1.39 and 3.13, respectively).

Conclusion

Less than a quarter of US patients with ASCVD in community practice are already achieving an LDL-C <55 mg/dL. Marked increases in utilization of both high intensity statins and combination therapy with non-statin therapy will be needed to achieve LDL-C levels <55 mg/dL at the population level in secondary prevention.

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