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Effect of Statins on Trained Immunity

Effect of Statins on Epigenetic Reprogramming of Monocytes in Patients With Elevated Levels of LDL

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02817230
Enrollment
45
Registered
2016-06-29
Start date
2015-06-30
Completion date
2017-06-01
Last updated
2023-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis

Brief summary

In this study, the investigators will determine whether patients with elevated levels of LDL are characterized by specific epigenetic changes in circulating cells of the innate immune system, compared to control subjects with healthy levels of LDL and whether regular statin treatment influences these changes.

Detailed description

Rationale: The innate immune system plays a pivotal role in the development and progression of atherosclerosis. Recently, it was reported that monocytes can develop a long-lasting immunological memory after stimulation with various microorganisms, which has been termed 'trained innate immunity'. This memory is induced by epigenetic reprogramming. Here the investigators hypothesize that monocytes of patients with elevated LDL cholesterol levels show epigenetic changes compared to normocholesterolemic subjects and that this can be reversed by treatment with statins. Objective: The main objective is to study whether patients with elevated levels of LDL show increased Histone 3 Lysine 4 trimethylation in the promoter regions of pro-inflammatory cytokines and have an augmented ex vivo Toll-Like Receptor agonist-induced cytokine production in isolated monocytes compared to controls. Subsequently the investigators will study the effect of treatment with statins on these responses. Study design: Observational study Study population: Subjects aged \>18 years who have been referred to the out-patient clinic and have LDL levels that require lipid lowering treatment and matched normocholesterolemic control subjects.

Interventions

DRUGStatin

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
CollaboratorOTHER
Erasmus Medical Center
CollaboratorOTHER
Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patients: * 18 years or older * Elevated LDL levels (\>4.9 mmol/l) * No previous cardiovascular events Controls: * Age \> 18 years * LDL cholesterol \< 3.5 mmol/l * No previous cardiovascular events

Exclusion criteria

* Current lipid lowering treatment * Known malignant disorders, auto-immune disorder, or diabetes * Inability or unwillingness to comply with the protocol requirements, or deemed by investigator to be unfit for the study * Clinical signs of acute infection * Use of anti-inflammatory medication

Design outcomes

Primary

MeasureTime frameDescription
Changes in histone methylation levels in circulating monocytesBaseline-3 months follow upHistone methylation levels on different lysines of histone 3 will be analyzed at baseline and after 3 months of statin treatment

Secondary

MeasureTime frame
Inflammatory phenotypeBaseline-3 months follow up

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026