Homozygous Familial Hypercholesterolemia Clinical Trial
Official title:
The Study of Gene Analysis and Treatment Optimization in Chinese Homozygous Familial Hypercholesterolemia
Identify new or novel genes which may impact on cholesterol level, and establish the relationship between those gene mutations with atherosclerosis, as well as responses to lipid-lowering drugs.
To better understand the genetics basis for LDL-C elevation and develop an optimized
lipid-lowering strategy, we propose to do the following studies:
1. To establish a China HoFH registry, and collect DNA and blood samples from all
available family members of each proband (pedigrees);
2. To detect gene mutations known to cause FH and identify family suitable for future
whole genome sequencing aimed to identify novel genes controlling cholesterol levels.
3.To establish the relationship between types of gene mutations and lipid and
atherosclerosis profile, as well as responses to lipid-lowering agents.
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Status | Clinical Trial | Phase | |
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Completed |
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