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Reduced serum lipoprotein(a) levels in patients with primary biliary cirrhosis

W L Gregory1, F L Game, M Farrer

  • 1Department of Pharmacological Sciences, University of Newcastle upon Tyne, Medical School, UK.

Atherosclerosis
|January 1, 1994
PubMed

Insights

Primary biliary cirrhosis (PBC) patients have lower lipoprotein(a) (Lp(a)) levels than healthy individuals. This reduction in Lp(a) may contribute to a lower incidence of coronary heart disease (CHD) in PBC patients.

Area of Science:

  • Cardiovascular Medicine
  • Hepatology
  • Biochemistry

Background:

  • Elevated lipoprotein(a) (Lp(a)) is an independent risk factor for coronary heart disease (CHD).
  • Primary biliary cirrhosis (PBC) is associated with high serum cholesterol, a known CHD risk factor.
  • Paradoxically, PBC patients exhibit a lower than expected incidence of CHD.

Purpose of the Study:

  • To investigate the hypothesis that reduced serum Lp(a) levels in PBC patients may explain their lower CHD incidence.
  • To compare Lp(a) levels in PBC patients, non-PBC liver disease patients, and healthy controls.

Main Methods:

  • Fasting blood samples were collected from 42 PBC patients, 39 non-PBC liver disease patients, and 432 community controls.
  • Serum analysis included total cholesterol, triglycerides, HDL cholesterol, apolipoproteins A1 and B.
  • Lp(a) levels were quantified using an enzyme-linked immunosorbent assay (ELISA).

Main Results:

  • PBC patients showed significantly lower Lp(a) concentrations compared to healthy controls (median 28.5 mg/l vs. 75.0 mg/l, P < 0.005).
  • Non-PBC liver disease patients also had reduced Lp(a) levels compared to controls (median 52.0 mg/l, P = 0.001).
  • Significant negative correlations were observed between Lp(a) and bilirubin levels in both PBC and non-PBC liver disease groups.

Conclusions:

  • This study demonstrates reduced Lp(a) levels in PBC patients.
  • Lower Lp(a) may be a contributing factor to the potential cardioprotective effect observed in PBC patients, despite elevated LDL cholesterol.
  • Further research is warranted to elucidate the mechanisms behind this association.

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