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Management of High and Very High-Risk Subjects with Familial Hypercholesterolemia: Results from an Observational
Ivo S Petrov1, Arman Sh Postadzhiyan2, Mariya P Tokmakova3
1Department of Angiology and Electrophysiology, City Clinic, Heart and Vascular Institute, Sofia, Bulgaria.
Insights
Familial hypercholesterolaemia (FH) management in Bulgaria shows low achievement of LDL-C targets. Improved early identification and physician education are crucial for better cardiovascular disease outcomes in FH patients.
Area of Science:
- Cardiology
- Genetics
- Public Health
Background:
- Familial hypercholesterolaemia (FH) is a genetic disorder leading to early atherosclerosis and cardiovascular disease (CVD).
- This study retrospectively analyzed FH patient characteristics and management in Bulgaria.
Purpose of the Study:
- To examine the clinical characteristics and management of FH subjects in Bulgaria.
- To assess the achievement of LDL-C targets in FH patients under current treatment protocols.
Main Methods:
- A 12-month retrospective observational study involving 12 cardiology sites in Bulgaria.
- Included 196 subjects meeting FH criteria, with baseline and 12-month LDL-C measurements and lipid-lowering therapy (LLT).
- Evaluated patient demographics, cardiovascular risk, and LLT regimens, including statins and ezetimibe.
Main Results:
- Mean age of FH subjects was 54.4 years, with 64.1% males; 26.8% were high-risk and 73.2% very high-risk for CVD.
- Mean LDL-C decreased from 5.6 mmol/L to 4.1 mmol/L over 12 months, but only 14.5% of high-risk and 5.0% of very high-risk subjects reached ESC/EAS targets.
- Most patients received statins (99.5%), with 38.6% on intensive statin therapy and 10% on combination therapy.
Conclusions:
- The majority of FH patients in Bulgaria do not achieve guideline-defined LDL-C targets.
- Early FH identification and enhanced physician education are recommended to improve patient management and reduce cardiovascular risk.
Background:
Familial hypercholesterolaemia (FH) is a genetic disorder causing accelerated atherosclerosis and premature cardiovascular disease (CVD). This retrospective observational study examined the clinical characteristics and management of FH subjects in Bulgaria over a 12-month period.
Materials And Methods:
Twelve cardiology sites participated in this study from May 2015 to May 2016. Eligible subjects had at least two routine low-density lipo-protein cholesterol (LDL C) measurements and a prescription for lipid-lowering therapy (LLT) at the start of the observation period. Mean values for gender, age and cardiovascular (CV) event history at baseline and LDL-C over time were estimated.
Results:
Of the 220 eligible subjects, 196 fulfilled the criteria for FH diagnosis: 27 definite, 94 probable and 75 possible. Mean age at enrolment was 54.4 years and 64.1% of subjects were male. Mean CV risk classification at baseline was 26.8% high-risk (HR) and 73.2% very high-risk (VHR). Mean LDL-C was 5.6 mmol/L at enrolment and 4.1 mmol/L at last observation visit (12 months). The ESC/EAS Guideline LDL-C targets (applicable at the time of the study) were achieved by 14.5% of HR and 5.0% of VHR subjects. Most subjects (n=219) received statins. One subject was statin intolerant (ezetimibe therapy). Intensive statin treatment (atorvastatin 40-80 mg/daily and rosuvastatin 20-40 mg/daily) was used in 38.6% of individuals during the observation period and 10% of subjects received combination therapy (statin plus ezetimibe or other LLT).
Conclusions:
Most subjects with FH do not reach the ESC/EAS defined LDL-C targets. Early identification and physician education may improve FH management.
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