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Lipoprotein (a) and coronary heart disease among women: beyond a cholesterol carrier?
Iris Shai1, Eric B Rimm, Susan E Hankinson
1Department of Nutrition, Harvard School of Public Health, Boston, MA 02115, USA. ishai@hsph.harvard.edu
Insights
High lipoprotein(a) [Lp(a)] levels significantly increase the risk of coronary heart disease (CHD) events in women. This finding suggests Lp(a) may play a role in thrombosis and inflammation, impacting cardiovascular health.
Area of Science:
- Cardiovascular Science
- Biochemistry
- Epidemiology
Background:
- Lipoprotein(a) [Lp(a)], due to its structural similarity to plasminogen, is implicated in thrombosis and inflammation.
- Assessing Lp(a)'s role in coronary heart disease (CHD) requires assays unaffected by plasminogen-like repeats.
Purpose of the Study:
- To evaluate the association between lipoprotein(a) [Lp(a)] levels and the risk of coronary heart disease (CHD) events in women.
- To investigate the combined effects of Lp(a) with fibrinogen and C-reactive protein on CHD risk.
Main Methods:
- Analysis of data from 32,826 women in the Nurses' Health Study with 8 years of follow-up.
- Case-control comparison using 228 CHD events and matched controls.
- Multivariable logistic regression adjusted for various cardiovascular risk factors.
Main Results:
- Elevated Lp(a) levels (≥30 mg/dL) were associated with a 1.9-fold increased odds ratio for CHD events (95% CI: 1.3-3.0).
- High Lp(a) combined with high fibrinogen showed a 3.2-fold increased odds ratio for CHD (95% CI: 1.6-6.5).
- High Lp(a) combined with high C-reactive protein showed a 3.67-fold increased odds ratio for CHD (95% CI: 2.03-6.64).
Conclusions:
- Lipoprotein(a) levels above 30 mg/dL are linked to a doubled risk of CHD events in women.
- These findings suggest a potential role for Lp(a) in the mechanisms of thrombosis and inflammation contributing to CHD.
Aims:
With its homology with plasminogen, lipoprotein(a) [Lp(a)] may be related to thrombosis and inflammation. We assessed the role of Lp(a) in coronary heart diseases (CHD) by a recently developed assay that is not affected by the plasminogen-like Kringle-type-2 repeats.
Methods And Results:
Of 32 826 women from the Nurses' Health Study, who provided blood at baseline, we documented 228 CHD events during 8 years of follow-up. Each case was compared with two matched controls. In a multivariable model adjusted for body mass index, family history, hypertension, diabetes, post-menopausal hormone use, physical activity, blood drawing characteristics, and alcohol intake, the odd ratio (OR) for Lp(a) levels > or =30 mg/dL was 1.9(95% CI: 1.3-3.0) when compared with those with Lp(a)<30 mg/dL. Women with high levels of both Lp(a) (> or =30 mg/dL) and fibrinogen (> or =400 mg/dL) had an OR of 3.2(95% CI: 1.6-6.5) for CHD, when compared with the combination of low levels (P interaction=0.05). Women with high levels of both Lp(a) and C-reactive protein (> or =3 mg/L) had an OR of 3.67(95% CI: 2.03-6.64) for CHD, when compared with the combination of low levels (P interaction=0.06).
Conclusion:
Lp(a) levels >30 mg/dL are associated with twice the risk of CHD events among women and may be related to thrombosis and inflammation.
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