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Published on: October 12, 2017
Lipoprotein(a) and cardiovascular disease in diabetic patients
1Department of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, Boston, MA 02115, USA.
Insights
Lipoprotein(a) (Lp[a]) may not increase cardiovascular disease (CVD) risk in diabetic patients, unlike in the general population. Further research is needed to confirm this differential effect of Lp[a] on CVD risk in diabetes.
Area of Science:
- Cardiovascular Science
- Metabolic Disorders
- Lipid Metabolism
Background:
- Lipoprotein(a) (Lp[a]) is implicated in cardiovascular disease (CVD) risk in the general population.
- Type 2 diabetes is associated with metabolic abnormalities and increased CVD risk.
- Previous studies show lower Lp[a] levels in diabetic patients, with inconsistent findings on Lp[a] and CVD risk.
Purpose of the Study:
- To investigate the role of Lp[a] in CVD risk specifically within diabetic patient cohorts.
- To clarify the potentially differential impact of Lp[a] on cardiovascular risk between diabetic patients and the general population.
Main Methods:
- Analysis of Lp[a]-related genetic markers in two diabetic cohorts.
- Review of existing epidemiological data on Lp[a] and CVD risk in diabetic populations.
Main Results:
- Lp[a]-related genetic markers did not predict CVD risk in the analyzed diabetic cohorts.
- Epidemiological studies on Lp[a] and CVD risk in diabetic patients have yielded inconsistent results.
Conclusions:
- Current evidence suggests Lp[a] may have a different role in cardiovascular risk for diabetic patients compared to the general population.
- Further prospective studies, Mendelian randomization, and functional studies are required to elucidate the causal relationship between Lp[a] and CVD in Type 2 diabetes.
Abstract:
Lipoprotein(a) (Lp[a]) is a LDL-like particle consisting of an ApoA moiety linked to one molecule of ApoB(100). Recent data from large-scale prospective studies and genetic association studies provide highly suggestive evidence for a potentially causal role of Lp(a) in affecting risk of cardiovascular disease (CVD) in general populations. Patients with Type 2 diabetes display clustered metabolic abnormalities and elevated risk of CVD. Lower plasma Lp(a) levels were observed in diabetic patients in several recent studies. Epidemiology studies of Lp(a) and CVD risk in diabetic patients generated inconsistent results. We recently found that Lp(a)-related genetic markers did not predict CVD in two diabetic cohorts. The current data suggest that Lp(a) may differentially affect cardiovascular risk in diabetic patients and in the general population. More prospective studies, Mendelian randomization analysis and functional studies are needed to clarify the causal relationship of Lp(a) and CVD in diabetic patients.
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