How is it used?
Lp(a) is not currently routinely ordered. It may be ordered along with other
lipid tests to selectively screen for risk factors for coronary artery disease (CAD) and cerebral vascular disease. Lp(a) and several other emerging cardiac risk markers (such as
Apo B,
hs-CRP,
Apo A, and
homocysteine levels) are ordered on patients who have a strong family history of premature coronary artery disease.
Some doctors may also order these tests on patients with existing heart or vascular disease, especially those who have normal or only mildly elevated lipids. Since about 50% of the people who have heart attacks have normal cholesterol levels, doctors are starting to look at other factors that may have an influence on heart disease. It is thought that elevated Lp(a) levels can exacerbate other heart and vascular disease processes.
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When is it ordered?
Lp(a) may be ordered, along with other
lipid tests, when you have a family history of premature coronary artery disease and when your doctor suspects a familial hypercholesterolemia. He may also order an Lp(a) level when you have had a
stroke or
heart attack but have normal or only mildly elevated lipids.
In rare cases, an Lp(a) level may be ordered on a post menopausal woman to see if elevations in Lp(a) (tied to decreasing estrogen levels) have significantly increased her risk of developing CAD.
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What does the test result mean?
Lp(a) levels are genetically determined and remain relatively constant over an individual's lifetime. They are not affected by lifestyle changes or by most drugs.
High Lp(a) levels may increase a person's risk for developing coronary artery disease and cerebral vascular disease and can occur in patients with a normal lipid profile. Elevated levels of Lp(a) are thought to work independently, to add to any underlying heart or vascular disease processes. Other conditions that may cause elevated levels of Lp(a) include:
Low levels of Lp(a) do not appear to cause problems.
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Is there anything else I should know?
Lp(a) levels are not routinely ordered tests. A National Cholesterol Education Program (NCEP) guideline, the “Adult Treatment Panel III” (pg. II-21,
available in PDF) acknowledged the possible usefulness of Lp(a) and other emerging cardiac risk tests like Lp(a), but it did not recommend them for widespread screening. The National Academy of Clinical Biochemistry (NACB) guidelines for emerging biomarkers of
cardiovascular disease and
stroke also recommend testing for individuals with a strong family history of premature risk of CVD or those with intermediate cardiovascular risk but not for general screening.
This is partially due to the fact that Lp(a) levels are genetically determined and difficult to change. Niacin and estrogen (for postmenopausal women) have been shown to lower Lp(a) levels a small amount, but their effect appears to be short term, and it is not known if lowering Lp(a) levels actually lowers risk. Experts are currently not recommending drug treatments for elevated Lp(a) levels, but some are suggesting that patients with elevated Lp(a) levels should be especially vigilant about lowering their low-density lipoprotein (LDL – the “bad” cholesterol) levels, which may help lower their overall risk.
In general, lipids should not be measured during a fever or major infection, within four weeks of an acute
myocardial infarction (heart attack), a stroke, or major surgery, right after excessive alcohol intake, with severely uncontrolled diabetes, when a woman is pregnant, or during rapid weight loss.
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