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Published on: October 12, 2017
Lipoprotein(a) and Family History Predict Cardiovascular Disease Risk
Anurag Mehta1, Salim S Virani2, Colby R Ayers3
1Emory Clinical Cardiovascular Research Institute, Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia. Electronic address: https://twitter.com/amehta_09.
Insights
Elevated lipoprotein(a) (Lp[a]) and family history (FHx) of coronary heart disease (CHD) independently increase cardiovascular risk. Combining Lp[a] testing with FHx assessment improves risk prediction and guides prevention strategies.
Area of Science:
- Cardiology
- Genetics
- Preventive Medicine
Background:
- Elevated lipoprotein(a) (Lp[a]) and family history (FHx) of coronary heart disease (CHD) are known cardiovascular risk factors.
- Lp[a] testing is often performed in individuals with a FHx of CHD.
Purpose of the Study:
- To investigate the independent and combined associations of Lp[a] and FHx with atherosclerotic cardiovascular disease (ASCVD) and CHD in asymptomatic individuals.
- To evaluate the utility of combining Lp[a] and FHx for cardiovascular risk assessment.
Main Methods:
- Two cohorts (ARIC and DHS) with plasma Lp[a] measurements and FHx ascertainment were analyzed.
- Elevated Lp[a] was defined as the highest race-specific quintile.
- Cox regression models adjusted for cardiovascular risk factors were used to determine associations.
Main Results:
- Both FHx and elevated Lp[a] were independently associated with increased ASCVD risk.
- Individuals with both elevated Lp[a] and FHx exhibited the highest ASCVD risk (HR: 1.43).
- The combination of elevated Lp[a] and FHx significantly improved risk reclassification and discrimination for ASCVD and CHD compared to either marker alone.
Conclusions:
- Elevated Lp[a] and FHx have independent and additive joint associations with cardiovascular risk.
- Concurrent assessment of Lp[a] and FHx can enhance cardiovascular risk prediction.
- Combining Lp[a] and FHx may aid in guiding primary prevention therapy decisions.
Background:
Elevated lipoprotein(a) (Lp[a]) and family history (FHx) of coronary heart disease (CHD) are individually associated with cardiovascular risk, and Lp(a) is commonly measured in those with FHx.
Objectives:
The aim of this study was to determine independent and joint associations of Lp(a) and FHx with atherosclerotic cardiovascular disease (ASCVD) and CHD among asymptomatic subjects.
Methods:
Plasma Lp(a) was measured and FHx was ascertained in 2 cohorts. Elevated Lp(a) was defined as the highest race-specific quintile. Independent and joint associations of Lp(a) and FHx with cardiovascular risk were determined using Cox regression models adjusted for cardiovascular risk factors.
Results:
Among 12,149 ARIC (Atherosclerosis Risk In Communities) participants (54 years, 56% women, 23% black, 44% with FHx), 3,114 ASCVD events were observed during 21 years of follow-up. FHx and elevated Lp(a) were independently associated with ASCVD (hazard ratio [HR]: 1.17; 95% confidence interval [CI]: 1.09 to 1.26, and HR: 1.25; 95% CI: 1.12 to 1.40, respectively), and no Lp(a)-by-FHx interaction was noted (p = 0.75). Compared with subjects without FHx and nonelevated Lp(a), those with either elevated Lp(a) or FHx were at a higher ASCVD risk, while those with both had the highest risk (HR: 1.43; 95% CI: 1.27 to 1.62). Similar findings were observed for CHD risk in ARIC, in analyses stratified by premature FHx, and in an independent cohort, the DHS (Dallas Heart Study). Presence of both elevated Lp(a) and FHx resulted in greater improvement in ASCVD and CHD risk reclassification and discrimination indexes than either marker alone.
Conclusions:
Elevated plasma Lp(a) and FHx have independent and additive joint associations with cardiovascular risk and may be useful concurrently for guiding primary prevention therapy decisions.
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