Familial hypercholesterolaemia: summary of NICE guidanceBMJ 2008; 337 doi: https://doi.org/10.1136/bmj.a1095 (Published 27 August 2008) Cite this as: BMJ 2008;337:a1095
All rapid responses
The NICE guidelines for familial
hypercholesterolaemia (FH) are based on the commonly accepted view that early
coronary heart disease in FH is caused by high cholesterol.1 Several
observations indicate that it is not that simple.
First, studies including only people with FH
have shown that both the prevalence and future cardiovascular disease are
independent on their blood cholesterol level;2-7 in one of the
studies mean cholesterol was even lowest in those who had coronary heart
In accordance, cholesterol lowering by ileal
surpass8 or by non-statin drugs9 has no effect in FH, indicating
that the small effect obtained with the statins is due to their pleiotropic
effects. Most likely, it is their effect on the coagulation system,10-12
as some of the strongest risk factors in FH are high fibrinogen, high factor VIII,13 and high
prothrombin,7 because people with FH may have other genetic
aberrations as well.7 This interpretation fits well with the fact
that atherosclerosis in FH is mainly located to arteries that are exposed to
mechanical forces, while premature atherosclerosis is absent in the cerebral
arteries, even in homozygous FH.14,15
more surprising is that according to the The Simon Broome FH Register Group,
the mean life expectancy in FH is as long as for other people; more die from
CHD at a young age, but fewer die from cancer and other diseases later in life.16
These calculations were based on a selection of FH people with close relatives,
who had died early, and the authors therefore assumed that the prognosis would
have been even better for unselected individuals. Also, before 1900 their life
expectancy was longer than for the general population,17 probably
because high cholesterol protects against infectious diseases,18 the
commonest cause of death at that time.
a more appropriate management of FH might be to evaluate the coagulation system
and to find appropriate means to correct possible abnormalities. People with FH
without such abnormalities should also be told that their high cholesterol is
an advantage. The peace of mind following this information should probably be
more beneficial for the prevention of CHD than any cholesterol lowering
1. Wierzbicki AS, Humphries SE, Minhas R; Guideline Development Group.
Familial hypercholesterolaemia: summary of NICE guidance.BMJ 2008;337:a1095
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familial hypercholesterolemia. Long-term follow-up of 96 patients. Arteriosclerosis
3. Hill JS, Hayden MR, Frohlich J, Pritchard PH. Genetic and
environmental factors affecting the incidence of coronary artery disease in
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disease in heterozygous familial hypercholesterolemia patients with the same
LDL receptor gene mutation. Circulation 1995; 92:290-5.
Ajubi N, van Asten WN, Stalenhoef AF. The prevalence of
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Rodriguez G, Bertolini S, Nobili F,
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Neil HA, Hawkins MM, Durrington PN,
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Competing interests: No competing interests