Abstract 4366576: Treatment Implications of LDL-Cholesterol and Apolipoprotein B Discordance: Insights from the Very Large Database of Lipids (VLDbL) and the National Health and Examination Survey (NHANES)

Background: ApoB-containing lipoproteins, including LDL, are well-established causes of atherosclerotic cardiovascular disease (ASCVD). While typically highly correlated, apoB and LDL-C levels can diverge due to differences in lipid composition and response to lipid-lowering therapies (LLT). Furthermore, the definition of cutpoints can influence clinically-relevant discordance between LDL-C and apoB, which may inform guideline-directed treatment. Recent proposals suggest aligning LDL-C and apoB goals using equivalent cutpoints (<55, <70, and <100 mg/dL). Clarifying the prevalence and impact of discordance has important implications for clinical care. Objectives: To quantify the prevalence of LDL-C and apoB discordance among US adults when applying equivalent LDL-C and apoB goals. Methods: We included 298,578 adults (age ≥18) with available apoB and LDL-C measurements from the Very Large Database of Lipids (VLDbL), a population-representative convenience sample with clinical lipid measurements obtained in 2015-2019. We also included 2,707 statin-treated adults from the National Health and Nutrition Examination Survey (NHANES) from 2005-2016 to assess the effects of statin use on discordance. The Martin-Hopkins equation was used to calculate LDL-C. Equivalent goals of <55, <70, and <100 mg/dL for LDL-C and apoB were applied. Results: In VLDbL (mean age 56 years, 57% female), 43.2% had apoB and LDL-C discordance ( Table 1 ). In NHANES statin-treated individuals (mean age 66 years, 47% female), 33.9% had apoB and LDL-C discordance. Among those reaching LDL-C goals of <55, <70, and <100 mg/dL, apoB was discordantly elevated in up to 33%, 12%, and 2%, respectively, for equivalent goals ( Figure 1 ). In contrast, among those reaching apoB goals of <55, <70, and <100 mg/dL, LDL-C was discordantly elevated in up to 61%, 56%, and 49%, respectively, for equivalent goals ( Figure 2 ). Conclusions: LDL-C and apoB discordance was prevalent among US adults, most often due to discordant LDL-C elevation in those reaching equivalent apoB goals, with less discordance in statin-treated adults. These results suggest that using LDL-C and apoB individually as treatment goals could lead to substantially different patient populations eligible for LLT to reduce ASCVD risk, while utilizing both as complementary goals could maximize eligibility for LLT. Taken together, these findings suggest an opportunity for an individualized approach to ASCVD risk optimization.

Authors

Institutions

Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4366576
Primary Topic
Lipoproteins and Cardiovascular Health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 4366576: Treatment Implications of LDL-Cholesterol and Apolipoprotein B Discordance: Insights from the Very Large Database of Lipids (VLDbL) and the National Health and Examination Survey (NHANES)

Daniel Soffer, Seth S. Martin, Pamela B. Morris, Eugenia Gianos et al.
Circulation
Lipoproteins and Cardiovascular Health
article

Abstract 4366576: Treatment Implications of LDL-Cholesterol and Apolipoprotein B Discordance: Insights from the Very Large Database of Lipids (VLDbL) and the National Health and Examination Survey (NHANES)

Daniel Soffer, Seth S. Martin, Pamela B. Morris, Eugenia Gianos, Fátima Rodríguez, Françoise A. Marvel, Ann Marie Návar, Allison W. Peng, Sohail Zahid, Michael Shapiro, Roger S. Blumenthal
article en

Abstract

Background: ApoB-containing lipoproteins, including LDL, are well-established causes of atherosclerotic cardiovascular disease (ASCVD). While typically highly correlated, apoB and LDL-C levels can diverge due to differences in lipid composition and response to lipid-lowering therapies (LLT). Furthermore, the definition of cutpoints can influence clinically-relevant discordance between LDL-C and apoB, which may inform guideline-directed treatment. Recent proposals suggest aligning LDL-C and apoB goals using equivalent cutpoints (<55, <70, and <100 mg/dL). Clarifying the prevalence and impact of discordance has important implications for clinical care. Objectives: To quantify the prevalence of LDL-C and apoB discordance among US adults when applying equivalent LDL-C and apoB goals. Methods: We included 298,578 adults (age ≥18) with available apoB and LDL-C measurements from the Very Large Database of Lipids (VLDbL), a population-representative convenience sample with clinical lipid measurements obtained in 2015-2019. We also included 2,707 statin-treated adults from the National Health and Nutrition Examination Survey (NHANES) from 2005-2016 to assess the effects of statin use on discordance. The Martin-Hopkins equation was used to calculate LDL-C. Equivalent goals of <55, <70, and <100 mg/dL for LDL-C and apoB were applied. Results: In VLDbL (mean age 56 years, 57% female), 43.2% had apoB and LDL-C discordance ( Table 1 ). In NHANES statin-treated individuals (mean age 66 years, 47% female), 33.9% had apoB and LDL-C discordance. Among those reaching LDL-C goals of <55, <70, and <100 mg/dL, apoB was discordantly elevated in up to 33%, 12%, and 2%, respectively, for equivalent goals ( Figure 1 ). In contrast, among those reaching apoB goals of <55, <70, and <100 mg/dL, LDL-C was discordantly elevated in up to 61%, 56%, and 49%, respectively, for equivalent goals ( Figure 2 ). Conclusions: LDL-C and apoB discordance was prevalent among US adults, most often due to discordant LDL-C elevation in those reaching equivalent apoB goals, with less discordance in statin-treated adults. These results suggest that using LDL-C and apoB individually as treatment goals could lead to substantially different patient populations eligible for LLT to reduce ASCVD risk, while utilizing both as complementary goals could maximize eligibility for LLT. Taken together, these findings suggest an opportunity for an individualized approach to ASCVD risk optimization.

CirculationVol. 152(Suppl_3)
Northwell Health (US), Johns Hopkins University (US), Palo Alto University (US), Lenox Hill Hospital (US), Star Technology and Research (United States) (US), Southwestern Medical Center (US), Johns Hopkins Hospital (US), Southwestern Medical Center (US), Wake Forest University (US), University of Pennsylvania (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 50%
Lipoproteins and Cardiovascular Health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.