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Apolipoproteins (apoproteins) and LPL variation in Mennonite populations of Kansas and Nebraska

Bibliographic Data

ID17701403
AuthorsDarío Alfredo Demarchi (0000-0003-3782-8269, Universidad Nacional de Córdoba, corresponding author), M J Mosher (0000-0002-2497-5369, University of North Carolina at Chapel Hill), M H Crawford (0000-0001-7103-2278, University of Kansas)
Year2005
Volume17
Issue5
Pages593-600
Publication date2005-01-01
Open AccessYes
TypeARTICLE
VenueAmerican Journal of Human Biology (JOURNAL)
Journal identifiersISSN: 1042-0533 • E-ISSN: 1520-6300
PublisherWiley (PUBLISHER • GB)
DOI10.1002/ajhb.20425
PMID16136540
OpenAlexW1980502434
LanguageEN
Citations received3
References cited20

Apoproteins (also known as apolipoproteins) have been studied extensively because of their role in lipid transport, association between specific genotypes and elevated serum lipid levels, and increased risk of heart disease. There is considerable genetic variation in the geographic distributions of these markers, with a north-south cline of the APOE*4 allele observed in Europe by Lucotte et al. ([1997] Hum Biol 69:253-262). This study compares the frequencies of seven APO (APOA1 -75 bp, APOA1 +83 bp, APOB Ins/Del, APOB XbaI, APOC3 SstI, and APOE) and LPL loci in Mennonite populations from Kansas and Nebraska. In total, 277 individuals were sampled from Goessel, Meridian, Garden View, and Lone Tree in 2002-2004. In addition, DNA samples that were collected in 1981 from Henderson, Nebraska, were genotyped for the seven APO and LPL loci. Of the seven APO and LPL loci tested, only one locus, APOB XbaI, departed significantly from Hardy-Weinberg equilibrium, with an unexpected excess of observed heterozygotes. The frequencies of the several APO loci are unique among the Mennonites, separating them from other European populations. A bidimensional scaling representation of Reynold's co-ancestry distances based on allelic frequencies of the seven APO and LPL markers in five Mennonite congregations fails to represent schematically the known patterns of fission. It is unclear whether the observed patterns are due to selection operating on these loci or whether genetic drift, small populations sizes, or a lack of statistical power of these biallelic loci distort the observed genetic relationship among congregations

Allele · Allele frequency · Apolipoprotein B · Apolipoprotein E · Biology · Cholesterol · Gene · Genetic variation · Hum · Population · Cancer, Lipids, and Metabolism · Demography · Diabetes, Cardiovascular Risks, and Lipoproteins · Genetic Associations and Epidemiology · Medicine · Endocrinology · Genetics · Internal Medicine

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    Phillip E Melton, M J Mosher et al.•Human Biology•2010

  • Paternal Genetic Structure in Contemporary Mennonite Communities from the American Midwest

    Beaty Beaty, Mosher Mosher et al.•Human Biology•2016

  • Patterns of DNA Methylation across the Leptin Core Promoter in Four Diverse Asian and North American Populations

    Mosher Mosher, Phillip E Melton et al.•Human Biology•2016

  • Estimation of the Coancestry Coefficient

    Open Access•John Reynolds, B S Weir et al.•Genetics•1983

  • Performing the Exact Test of Hardy-Weinberg Proportion for Multiple Alleles

    Sun‐Wei Guo, Sun Wei Guo et al.•Biometrics•1992

  • Kin‐structured migration

    Open Access•Alan G Fix•American Journal of Human Biology•2004

Citations per year0.19
Citation span2010 - 2016 (7)
Highly citedNo

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