Key result
Familial hypercholesterolaemia, high lifetime cholesterol burden, and elevated hs-CRP were significant independent predictors of increased arterial stiffness and carotid intima-media thickness.
Why the study?
Are lifetime cholesterol burden and hs-CRP levels associated with arterial stiffness and atherosclerosis in patients with familial hypercholesterolaemia?
Case-Control (n=52)
Are lifetime cholesterol burden and hs-CRP levels associated with arterial stiffness and atherosclerosis in patients with familial hypercholesterolaemia?
Lifetime cholesterol burden and systemic inflammation (hs-CRP) independently predict arterial stiffness and atherosclerosis in patients with familial hypercholesterolemia, emphasizing the need for early detection and treatment.
Answers are grounded in this paper and cite their sources.
Links lifetime cholesterol burden and hs-CRP to vascular changes in FH; hypothesis-generating, requires prospective validation before practice impact.
BACKGROUND: Familial hypercholesterolaemia (FH) is characterized by very high serum cholesterol and premature coronary atherosclerosis. Arterial stiffness and atherosclerosis are two major underlying pathophysiologies of arterial disease that are predictive of future cardiovascular events. The aims of this study were to quantify atherosclerosis and arterial stiffness and to evaluate their relationship with high sensitive C-reactive protein (hs-CRP) and the level of exposure to high serum cholesterol in FH patients. MATERIALS AND METHODS: We measured traditional risk factors, hs-CRP, intima-media thickness (IMT) of carotid artery, and brachial-ankle pulse wave velocity (baPWV) in 35 heterozygous FH subjects and 17 healthy control subjects. Cholesterol-year score (CYS) was calculated to estimate the lifetime cholesterol burden in FH subjects. RESULTS: FH subjects had significantly elevated total cholesterol, low-density lipoprotein cholesterol, and carotid IMT compared with those without mutations. Among FH patients, the baPWV and carotid IMT were higher in cases with high cholesterol burden than those without. Similarly, the baPWV and carotid IMT were also higher in cases with elevated hs-CRP (> 1 mg L(-1)) than those without. Multiple linear regression analysis demonstrated CYS and hs-CRP were significant independent predictors of baPWV and IMT in FH patients. CONCLUSIONS: Both high cholesterol burden and vascular inflammation are not only associated with atherosclerosis, but also contribute to the development of arterial stiffness in FH patients. Early detection of hypercholesterolaemia in FH patients is warranted to prevent the untoward pathophysiologies.
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Cheng et al. (2007) conducted a case-control in Familial hypercholesterolaemia (n=52). Familial hypercholesterolaemia, high cholesterol burden, and elevated hs-CRP vs. Healthy controls and FH patients with lower cholesterol burden or hs-CRP was evaluated on Brachial-ankle pulse wave velocity (baPWV) and carotid intima-media thickness (IMT). Familial hypercholesterolaemia, high lifetime cholesterol burden, and elevated hs-CRP were significant independent predictors of increased arterial stiffness and carotid intima-media thickness.
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