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Published on: September 15, 2018
Risk of fatal stroke in patients with treated familial hypercholesterolemia: a prospective registry study
R R Huxley1, M H Hawkins, S E Humphries
1Division Public Health and Primary Health Care, Institute of Health Sciences, University of Oxford, Oxford, UK.
Insights
Patients with treated familial hypercholesterolemia show no increased risk of fatal stroke. However, untreated individuals may face higher risks, aligning with familial hypercholesterolemia being a panvascular disease.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Epidemiology
Background:
- Familial hypercholesterolemia (FH) is known to affect carotid atherosclerosis.
- The stroke risk in treated FH patients remains uncertain.
Purpose of the Study:
- To determine the risk of fatal stroke in patients with treated familial hypercholesterolemia.
Main Methods:
- A prospective cohort study of 2871 patients with FH in the UK (1980-1998).
- Follow-up for 22,992 person-years, calculating mortality rates and standardized mortality ratios (SMRs).
Main Results:
- A total of 169 deaths occurred, with 9 (5.3%) attributed to stroke.
- The stroke mortality rate was 0.39 per 1000 person-years.
- The SMR for fatal stroke was not significantly different from the general population (SMR=79).
Conclusions:
- Treated familial hypercholesterolemia patients do not appear to have an elevated risk of fatal stroke.
- Untreated FH individuals might be at increased risk, supporting FH as a panvascular condition.
Background And Purpose:
Although it is recognized that in heterozygous familial hypercholesterolemia, large extracranial carotid vessels are affected by atherosclerosis, the risk of fatal stroke after treatment with cholesterol-lowering therapy remains uncertain. The goal of this study was to determine the risk of fatal stroke in patients with treated familial hypercholesterolemia.
Methods:
A cohort of 1405 men and 1466 women with definite or possible heterozygous familial hypercholesterolemia was recruited from 21 outpatient lipid clinics in the United Kingdom. Patients were followed up prospectively from 1980 to 1998 for 22 992 person-years for a median duration of 7.9 years (interquartile range, 4.9 to 12.0 years). The mortality rate was calculated, and the standardized mortality ratio for men and women 20 to 79 years of age was derived from the ratio of the observed deaths to the number expected in the general population of England and Wales (standardized mortality ratio=100 for the standard population).
Results:
A total of 169 deaths occurred; 9 (5.3%) were a result of stroke. The mortality rate from stroke was 0.39 per 1000 person-years (95% confidence interval, 0.18 to 0.74), and the standardized mortality ratio for fatal stroke was nonsignificantly lower than in the general population (79; 95% CI, 36 to 150).
Conclusions:
The results suggest that patients with treated familial hypercholesterolemia are not at increased risk of fatal stroke. However, the possibility cannot be excluded that untreated individuals are at increased risk, which would be consistent with the evidence that familial hypercholesterolemia is a panvascular disease.
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