ReviewMethodist DeBakey cardiovascular journal2026
Is the Commitment to LDL-C Eternal?
Review in Methodist DeBakey cardiovascular journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Low-density lipoprotein cholesterol (LDL-C) has been the cornerstone of cardiovascular risk assessment and therapy since 1988. Every guideline group and consensus report has repeated and reinforced this commitment. Yet in 2019, the European Society of Cardiology/European Atherosclerosis Society Lipid Guidelines declared that (1) apolipoprotein B (apoB) was a more accurate marker of cardiovascular risk than LDL-C or non-high-density lipoprotein cholesterol (HDL-C); (2) that apoB was a more accurate marker of the adequacy of therapy to lower cardiovascular risk than LDL-C or non-HDL-C; (3) that apoB was essential to diagnose disorders such as type III hyperlipoproteinemia and familial combined hyperlipidemia; and (4) that apoB could be measured more accurately, particularly at low concentrations, than LDL-C or non-HDL-C. Yet LDL-C remained the dominant metric for clinical care in their recommendations, and in the 7 years since, there has been minimal organized teaching about apoB in either Europe or the United States. In 2026, the American College of Cardiology/American Heart Association/Multisociety dyslipidemia guideline followed virtually the same course. Based on the evidence, apoB was ranked above both LDL-C and HDL-C for assessment of risk and the effectiveness of therapy. However, the actual recommendations ranked apoB below both and, as written, make it unlikely that apoB will be commonly used in clinical care for either purpose. How can this be, and what can we learn? LDL-C transformed cardiovascular care, and the effort to teach patients and doctors about LDL-C is unprecedented. How much of the resistance to apoB is the concern that it is too late to change? How many who write the guidelines have routinely used apoB in their clinical care? I believe that an unreasonable commitment to continuity of message and too closed a process of deliberation and review have produced this unprecedented contradiction between the guideline recommendations and the evidence. This article outlines the critical need to re-evaluate the framework and procedural standards governing our current guidelines.
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Registered trials
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