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Updated: Jun 6, 2026

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
No evidence of impaired endothelial function or altered inflammatory state in patients with familial
Anders Hovland1, Inger Aagnes, Ole-Lars Brekke
1Coronary Care Unit, Department of Internal Medicine, Nordland Hospital, Prinsens gate, N-8092 Bodø, Norway. anders.w.hovland@gmail.com
Insights
Familial hypercholesterolemia (FH) patients on statins showed no differences in endothelial function or inflammatory markers compared to healthy individuals. This suggests statin therapy may normalize these cardiovascular risk factors in FH.
Area of Science:
- Cardiovascular Medicine
- Clinical Research
- Biomarker Analysis
Background:
- Familial hypercholesterolemia (FH) significantly elevates the risk of premature atherosclerosis.
- Inflammation and endothelial dysfunction are key contributors to FH-related cardiovascular events.
Purpose of the Study:
- To compare inflammatory cytokines and endothelial function in statin-treated FH patients versus healthy controls.
- To investigate the impact of statin therapy on cardiovascular risk markers in FH.
Main Methods:
- Endothelial function assessed using the Endo-PAT® system to measure reactive hyperemia index (RHI).
- Analyzed 27 inflammatory biomarkers and standard laboratory tests from fasting blood samples.
- Included 14 FH patients on statins and 11 healthy control participants.
Main Results:
- No significant differences in age, weight, blood pressure, or BMI between FH and control groups.
- Similar endothelial function (RHI) and levels of various inflammatory markers (TNF-α, IL-1β, IL-6, hs-CRP, etc.) were observed.
- Lipid profiles, apolipoproteins, homocysteine, HbA1c, platelets, and fibrinogen also showed no significant intergroup differences.
Conclusions:
- Statin treatment in FH patients did not result in statistically significant differences in endothelial function or inflammatory biomarkers compared to healthy controls.
- Assessed endothelial function and inflammatory status appear normalized in FH patients on statins.
Background:
Familial hypercholesterolemia (FH) is associated with an increased risk of premature atherosclerosis. Central in this aspect is enhanced inflammation and endothelial dysfunction.
Objective:
We sought to examine inflammatory cytokines and endothelial dysfunction in patients with FH treated with statins (n = 14) compared with healthy control patients (n = 11).
Methods:
Endothelial function was evaluated by the use of the Endo-PAT® system which measured mean reactive hyperemia index. Fasting blood samples were drawn, and 27 biomarkers in addition to standard laboratory tests were analyzed.
Results:
There were no statistically significant differences between the FH group and the control group regarding age, weight, blood pressure, or body mass index. Endothelial function given as RHI was 1.58 and 1.93 (P = NS) in the control and FH groups, respectively. There were no differences between the groups in tumor necrosis factor-alpha, interleukin (IL-1) beta, IL-1 receptor antagonist, IL-6, IL-10, monocyte chemoattractant protein 1, high-sensitivity C-reactive protein, or any of the other inflammatory markers tested. Furthermore, no significant differences between the groups in high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, apolipoprotein A, apolipoprotein B, lipoprotein (a), homocysteine, HbA(₁c), platelets, and fibrinogen were found.
Conclusion:
Endothelial function assessed by reactive hyperemia index-peripheral arterial tonometry or inflammatory state assessed by soluble inflammatory biomarkers were not different in FH patients on statins compared with healthy control patients.
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