Evidence map›Paper›PMID 40813253›Full record

ReviewClinical medicine & research2025

Low HDL-The Challenge.

Shereif H Rezkalla, Robert A Kloner

Abstract readReview
In one paragraph

Review in Clinical medicine & research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Longevity.Clinical medicine & research · 2026
    Review
  2. Journal of clinical medicine · 2026
    Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Shereif H RezkallaEmeritus Physician, Marshfield Clinic Health System, 1000 North Oak Avenue, Marshfield, WI 54449, and Adjunct Professor of Medicine, University of Wisconsin, School of Medicine; E-mail: rezkalla.shereif@marshfieldclinic.org rezkalla.shereif@marshfieldclinic.org.
Robert A KlonerChief Science Officer, Scientific Director of Cardiovascular Research Institute, Huntington Medical Research Institutes, Pasadena, CA; and Professor of Medicine (Clinical Scholar), Cardiovascular Division, Dept. of Medicine, Keck School of Medicine of University of Southern California, Los Angeles, CA; Email: robert.kloner@hmri.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main function of high-density lipoprotein (HDL) is to remove low-density lipoprotein (LDL) from blood vessels through reverse cholesterol transport. In addition, HDL has anti-inflammatory and antioxidant properties. Low HDL level is an independent risk factor for development of coronary artery disease. To manage patients with low HDL levels, general measures such as lifestyle modification, controlling acute metabolic syndrome, and participating in regular endurance exercise are essential. Smoking cessation is a must, and it will often improve HDL levels by 5% to 10%. While statin therapy is the backbone therapy for controlling LDL levels, it also results in elevation of HDL levels by at least 5%. Specific pharmacologic interventions to improve HDL level and function have been disappointing. Cholesteryl ester transfer protein (CETP) is the key metabolic pathway to transfer HDL to LDL; thus, CETP inhibitors result in elevation of HDL levels. Several products were tested in large controlled studies, such as dalcetrapib and evacetrapib; neither resulted in any clinical benefit. Anacetrapib only resulted in very limited benefit and is no longer under active development. The most recent study utilized apolipoprotein A1 infusion in high-risk patients shortly after acute myocardial infarction. There was no benefit in the primary end point of myocardial infarction, stroke, or death. In patients with low HDL, a strategy of having LDL as low as can be possibly achieved may be the most appropriate approach.

Indexed as

Cholesterol, HDLLipoproteins, HDLAnticholesteremic AgentsCholesterol Ester Transfer ProteinsCoronary Artery DiseaseHumansHydroxymethylglutaryl-CoA Reductase InhibitorsRisk FactorsAnticholesteremic AgentsCholesterol Ester Transfer ProteinsCholesterol, HDLHydroxymethylglutaryl-CoA Reductase InhibitorsLipoproteins, HDLAtherosclerotic vascular diseaseDyslipidemiaElevated LDLLow HDLManagement

Identifiers

PMID40813253
PMCPMC12352915

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.