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Familial Hypercholesterolaemia in the Malaysian Community: Prevalence, Under-Detection and Under-Treatment
Yung-An Chua1, Aimi Zafira Razman1, Anis Safura Ramli1,2
1Institute of Pathology, Laboratory and Forensic Medicine (I-PPerForM), Universiti Teknologi MARA, Sungai Buloh.
Insights
Familial hypercholesterolaemia (FH) is common in Malaysia, with a prevalence of 1:100. Most FH patients are under-detected and do not reach treatment targets, increasing coronary artery disease risk.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Public Health
Background:
- Familial hypercholesterolaemia (FH) is a prevalent autosomal dominant lipid disorder causing severe hypercholesterolaemia.
- Early intervention in FH can mitigate the risk of premature coronary artery disease (CAD).
- Data on FH prevalence, detection, and treatment control in Malaysia are limited.
Purpose of the Study:
- To determine the prevalence of FH in the Malaysian community.
- To assess the detection rates and treatment control of FH patients.
- To highlight the need for improved public health strategies for FH management.
Main Methods:
- A community-based study involving 5130 participants across Malaysia.
- Collection of blood samples for lipid profiles and glucose levels.
- Clinical screening for FH using the Dutch Lipid Clinic Network Criteria, including family history and physical examination for xanthomata and corneal arcus.
Main Results:
- The prevalence of clinically diagnosed FH was found to be 1:100 (55 out of 5130 participants).
- An estimated 320,000 individuals in Malaysia have FH, with a detection rate of only 0.5%.
- Despite prescription of lipid-lowering medications to over half of potential FH patients, none achieved the target LDL-c levels.
Conclusions:
- The prevalence of FH in Malaysia is higher than in many global populations.
- FH patients in Malaysia are significantly under-detected and undertreated, failing to meet therapeutic LDL-c targets.
- Enhanced public health initiatives are crucial for early FH detection and effective treatment to prevent premature CAD.
Aim:
Familial hypercholesterolaemia (FH) is the most common autosomal dominant lipid disorder, leading to severe hypercholesterolaemia. Early detection and treatment with lipid-lowering medications may reduce the risk of premature coronary artery disease in FH patients. However, there is scarcity of data on FH prevalence, detection rate, treatment and control with lipid-lowering therapy in the Malaysian community.
Methods:
Community participants (n=5130) were recruited from all states in Malaysia. Blood samples were collected for lipid profiles and glucose analyses. Personal and family medical histories were collected by means of assisted questionnaire. Physical examination for tendon xanthomata and premature corneal arcus were conducted on-site. FH were clinically screened using Dutch Lipid Clinic Network Criteria.
Results:
Out of 5130 recruited community participants, 55 patients were clinically categorised as potential (Definite and Probable) FH, making the prevalence FH among the community as 1:100. Based on current total population of Malaysia (32 million), the estimated number of FH patients in Malaysia is 320,000, while the detection rates are estimated as 0.5%. Lipid-lowering medications were prescribed to 54.5% and 30.5% of potential and possible FH patients, respectively, but none of them achieved the therapeutic LDL-c target.
Conclusion:
Clinically diagnosed FH prevalence in Malaysian population is much higher than most of the populations in the world. At community level, FH patients are clinically under-detected, with majority of them not achieving target LDL-c level for high-risk patients. Therefore, public health measures are warranted for early detection and treatment, to enhance opportunities for premature CAD prevention.
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