ApoB test outperforms LDL for guiding cholesterol treatment

A new study indicates that measuring apolipoprotein B could help prevent more heart attacks and strokes than the standard LDL cholesterol test used by millions of Americans.

Researchers at Northwestern University modeled outcomes for 250,000 adults eligible for statin therapy. They compared three strategies for intensifying treatment when targets were missed: LDL below 100 mg/dL, non-HDL below 118 mg/dL, and ApoB below 78.7 mg/dL.

The ApoB approach prevented more cardiovascular events and proved cost-effective for U.S. healthcare payers, according to the analysis published in JAMA. Lead author Ciaran Kohli-Lynch noted that the test counts harmful particles more directly than conventional measures.

The findings arrive as updated guidelines encourage earlier cholesterol-lowering therapy. Coauthors included John Wilkins and Samuel Luebbe. The study received support from the American Heart Association.

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Scientific illustration of HELZ2 protein in the liver regulating cholesterol release.
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UT Southwestern researchers identify HELZ2 protein that controls the liver’s release of cholesterol-carrying particles

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Scientists at UT Southwestern Medical Center report they have identified a protein, HELZ2, that acts as a key regulator of how many cholesterol-carrying particles the liver releases into the bloodstream by affecting the gene APOB. The study was published in the American Heart Association journal Circulation and could inform future research into heart disease and fatty liver disease.

An experimental therapy called VERVE-102 lowered LDL cholesterol by up to 62 percent after a single dose in an early safety study. The results come from a Phase I trial involving 35 patients with high cholesterol or early cardiovascular disease. Data were published this week in the New England Journal of Medicine.

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Researchers from the University of Barcelona and the University of Oregon report that short DNA molecules known as polypurine reverse Hoogsteen hairpins (PPRHs) suppressed the PCSK9 gene and reduced blood cholesterol in a mouse model. In transgenic mice carrying the human PCSK9 gene, a single injection of one candidate (HpE12) cut plasma PCSK9 by 50% and total cholesterol by 47% three days later, according to findings published in Biochemical Pharmacology.

Research presented at ASM Microbe 2026 reported that removing a bile acid receptor called FXR reduced artery plaque in mice exposed to sleep apnea-like conditions, pointing to a potential gut-driven pathway behind cardiovascular risk.

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A major Cochrane review of 17 clinical trials involving over 20,000 participants has concluded that drugs targeting amyloid beta in the brain provide no meaningful benefits for patients with mild cognitive impairment or early Alzheimer’s. These treatments also raise the risk of brain swelling and bleeding. Researchers urge a shift to alternative pathways for future treatments.

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