Apolipoprotein E allele distribution in trisomy 13, 18, and 21 conceptuses in a Hungarian population

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Reports documented a higher frequency of apolipoprotein E (apoE) allele ε4 among mothers of children diagnosed with Down syndrome. We studied the prevalence of apoE alleles among 56 conceptuses with trisomy 13, trisomy 18 or trisomy 21. The presence of the 3 most common apoE alleles (ε2, ε3, ε4) was determined by polymerase chain reaction-restriction fragment length polymorphism, and trisomy status was detected by fluorescent polymerase chain reaction followed by DNA fragment analysis and by conventional cytologic methods. We found no significant difference in the distribution of apoE alleles in the group of trisomy 21 fetuses compared with samples from healthy blood donors. The odds of having trisomy 18 for the apoE ε4 group was 3-fold as high as for apoE ε3 allele compared with the healthy control group. Furthermore, a statistically significant association was found for those with trisomy 18 and apoE ε4, while for those with trisomy 13 and apoE ε4, the test showed no significant association. The observed apoE allele ε3 frequencies among patients with Down syndrome and healthy control subjects may help explain and support previous work that did not find high rates of atherosclerosis among these persons. The role of apoE alleles in the development of trisomies needs further study.

Original languageEnglish
Pages (from-to)535-538
Number of pages4
JournalAmerican Journal of Clinical Pathology
Volume113
Issue number4
DOIs
Publication statusPublished - Jan 1 2000

Keywords

  • Apolipoprotein E
  • Fluorescent polymerase chain reaction
  • Trisomy 13
  • Trisomy 18
  • Trisomy 21

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Fingerprint Dive into the research topics of 'Apolipoprotein E allele distribution in trisomy 13, 18, and 21 conceptuses in a Hungarian population'. Together they form a unique fingerprint.

  • Cite this