A case of hyperLp(a)aemia, associated with systemic lupus erythematosus, suffering from myocardial infarction and cerebral infarction

Jpn J Med. 1990 Jan-Feb;29(1):77-84. doi: 10.2169/internalmedicine1962.29.77.

Abstract

We describe a case of systemic lupus erythematosus (SLE) with nephrotic syndrome who suffered from myocardial infarction and cerebral infarction associated with hyperLp(a)aemia. The proband was an 18-year-old Japanese male who was found to have hypercholesterolemia and hyperLp(a)aemia, with a serum total cholesterol level of 361 mg/dl and a serum Lp(a) level of 197 mg/dl. His father and mother showed higher Lp(a)levels (26 and 56 mg/dl, respectively) than those in normals (18 +/- 0.6 mg/dl, mean +/- SE). Lp(a)glycoprotein phenotypes were examined. The proband had the phenotype S2/4, which is associated with high Lp(a) concentration. His parents had the phenotype S3/4 and S2/4. No cardiovascular diseases were noted in other members of his family. After treatment with CS-514, a competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase. Lp(a) levels decreased from 197 to 121 mg/dl, but still remained abnormally high. LDL apheresis using a Liposorber system was attempted in this patient. Total and LDL cholesterol levels decreased by 57 and 62%, respectively. Lp(a) levels decreased by 68%. These results suggest that LDL apheresis may be an alternative therapy in drug resistant hyperLp(a)aemia.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Angiography
  • Cerebral Infarction / complications*
  • Coronary Angiography
  • Female
  • Humans
  • Hypercholesterolemia / complications
  • Lipoprotein(a)
  • Lipoproteins / blood*
  • Lipoproteins / metabolism
  • Lupus Erythematosus, Systemic / complications*
  • Male
  • Myocardial Infarction / complications*
  • Pedigree
  • Phenotype

Substances

  • Lipoprotein(a)
  • Lipoproteins