Guidelines
Guidelines recommend Lp(a) testing for risk reclassification in intermediate-risk patients, a review of Lp(a)'s cardiovascular and non-cardiac disease associations (Curr Med Chem 2017)
Original title: Lipoprotein (a) and Cardiovascular Risk: The Show Must go on
This narrative review by Katsiki, Al-Rasadi and Mikhailidis surveys Lp(a) as an independent, moderate predictor of coronary heart disease (CHD) prevalence and severity, linked to established and emerging cardiovascular risk factors including age, sex, ethnicity, smoking, dyslipidaemia, hypertension, obesity, type 2 diabetes, alcohol use, arterial stiffness and hyperuricaemia. Beyond CHD, Lp(a) has also been associated with non-cardiac vascular disease and conditions carrying elevated cardiovascular risk, including chronic kidney disease, metabolic syndrome, non-alcoholic fatty liver disease, erectile dysfunction, obstructive sleep apnoea, inflammatory bowel disease and HIV infection. Several guidelines recommend using Lp(a) to redefine vascular risk, particularly in asymptomatic individuals at intermediate or high cardiovascular risk or with a family history of premature CHD, though a standardised measurement method and selective potent Lp(a)-lowering therapies are still needed before large randomised trials can establish whether lowering Lp(a) reduces cardiovascular events.
Original abstract
Lipoprotein (a) [Lp(a)] is an independent but moderate, predictor for coronary heart disease (CHD) prevalence and severity. Several established and emerging cardiovascular (CV) risk factors including age, gender, ethnicity, smoking, dyslipidemia, hypertension, obesity, type 2 diabetes mellitus, alcohol consumption, arterial stiffness and hyperuricemia have been linked to Lp(a) metabolism. Apart from CHD, Lp(a) has been also associated with non-cardiac vascular diseases and diseases associated with increased CV risk such as chronic kidney disease, metabolic syndrome, non-alcoholic fatty liver disease, erectile dysfunction, obstructive sleep apnea syndrome, inflammatory bowel diseases and human immunodeficiency virus infection. The above data are discussed in the present narrative review. Several guidelines suggest the clinical use of Lp(a) in (re)defining vascular risk, especially in asymptomatic individuals at intermediate or high CV risk and those with a family history of premature CHD. By improving individuals risk stratification, Lp(a) may contribute to a better secondary prevention strategy. However, there is still a need to establish a standardized method to measure Lp(a) as well as selective potent therapies for lowering Lp(a). This will support conducting large randomized trials in order to establish whether lowering circulating Lp(a) levels will result in a significant reduction in CV events.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.