Integrated single-label liquid phase assay of APOE codons 112 and 158 and lipoprotein study in British Women

MR Abdollahi, PAI Guthrie, G Davey Smith, DA Lawlor, S Ebrahim, INM Day

Research output: Contribution to journalArticle (Academic Journal)

16 Citations (Scopus)

Abstract

Background: Apolipoprotein E (APOE) is an important element of lipid metabolism and, hence, cardiovascular disorders. APOE has 3 main allelic variants: 3, 4, and 2. Of these, 3 is the most common, followed by 4 and 2. The associations of these isoforms with cardiovascular disorders and Alzheimer disease have been widely studied in different populations. Most of the genotyping in these studies has been performed with gel-based methods, which have important limitations, particularly for large epidemiologic studies. We therefore developed an integrated "one-tube" liquid-phase assay. Methods: To measure APOE isoforms, we developed an integrated single-label liquid-phase fluorescence assay containing 2 PCR primers, 2 probes, and 2 quencher oligonucleotides. We used a 384-well LightTyper, but the assay would be generically applicable for use with any fluorescence detector with thermal ramp control. We validated this method and applied it in the British Women’s Heart and Health Study. Results: There were 4 melting peaks, at 41, 56, 61, and 69 °C, which generated 6 distinctive patterns representing genotypic combinations of 3, 4, and 2. The magnitude and direction of the associations found with total cholesterol, HDL-cholesterol, triglycerides, and estimated LDL-cholesterol were consistent with previous reports. Conclusion: The one-tube LightTyper assay presented here enables accurate, convenient, and economical genotyping of APOE and can be used for large epidemiologic studies.
Translated title of the contributionIntegrated single-label liquid phase assay of APOE codons 112 and 158 and lipoprotein study in British Women
Original languageEnglish
Pages (from-to)1420 - 1423
Number of pages4
JournalClinical Chemistry
Volume52(7)
DOIs
Publication statusPublished - Jul 2006

Bibliographical note

Publisher: American Association for Clinical Chemistry

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