Literature DB >> 19429595

Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study.

X Li, K L Monda, H H H Göring, K Haack, S A Cole, V P Diego, L Almasy, S Laston, B V Howard, N M Shara, E T Lee, L G Best, R R Fabsitz, J W MacCluer, Kari E North.   

Abstract

BACKGROUND: Recent studies have identified chromosomal regions linked to variation in high density lipoprotein cholesterol (HDL-C), apolipoprotein A-1 (apo A-1) and triglyceride (TG), although results have been inconsistent and previous studies of American Indian populations are limited.
OBJECTIVE: In an attempt to localise quantitative trait loci (QTLs) influencing HDL-C, apo A-1 and TG, we conducted genome-wide linkage scans of subjects of the Strong Heart Family Study.
METHODS: We implemented analyses in 3484 men and women aged 18 years or older, at three study centres.
RESULTS: With adjustment for age, sex and centre, we detected a QTL influencing both HDL-C (logarithm of odds (LOD) = 4.4, genome-wide p = 0.001) and apo A-1 (LOD = 3.2, genome-wide p = 0.020) nearest marker D6S289 at 6p23 in the Arizona sample. Another QTL influencing apo A-1 was found nearest marker D9S287 at 9q22.2 (LOD = 3.0, genome-wide p = 0.033) in the North and South Dakotas. We detected a QTL influencing TG nearest marker D15S153 at 15q22.31 (LOD = 4.5 in the overall sample and LOD = 3.8 in the Dakotas sample, genome-wide p = 0.0044) and when additionally adjusted for waist, current smoking, current alcohol, current oestrogen, lipid treatment, impaired fasting glucose, and diabetes, nearest marker D10S217 at 10q26.2 (LOD = 3.7, genome-wide p = 0.0058) in the Arizona population.
CONCLUSIONS: The replication of QTLs in regions of the genome that harbour well known candidate genes suggest that chromosomes 6p, 9q and 15q warrant further investigation with fine mapping for causative polymorphisms in American Indians.

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Year:  2009        PMID: 19429595      PMCID: PMC3388907          DOI: 10.1136/jmg.2008.063891

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  45 in total

1.  Fasting insulin and obesity-related phenotypes are linked to chromosome 2p: the Strong Heart Family Study.

Authors:  Vincent P Diego; Harald H H Göring; Shelley A Cole; Laura Almasy; Thomas D Dyer; John Blangero; Ravindranath Duggirala; Sandra Laston; Charlotte Wenger; Teresa Cantu; Bennett Dyke; Kari North; Theodore Schurr; Lyle G Best; Richard B Devereux; Richard R Fabsitz; Barbara V Howard; Jean W MacCluer
Journal:  Diabetes       Date:  2006-06       Impact factor: 9.461

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Authors:  Chin-Fu Hsiao; Yen-Feng Chiu; Fu-Tien Chiang; Low-Tone Ho; Wen-Jane Lee; Yi-Jen Hung; Yii-Der I Chen; Timothy A Donlon; Eric Jorgenson; David Curb; Neil Risch; Chao A Hsiung
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Journal:  Circulation       Date:  2007-12-17       Impact factor: 29.690

9.  Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.

Authors:  Jaspal S Kooner; John C Chambers; Carlos A Aguilar-Salinas; David A Hinds; Craig L Hyde; Gregory R Warnes; Francisco J Gómez Pérez; Kelly A Frazer; Paul Elliott; James Scott; Patrice M Milos; David R Cox; John F Thompson
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Journal:  Nat Genet       Date:  2008-01-13       Impact factor: 38.330

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Journal:  Ann Hum Genet       Date:  2011-05       Impact factor: 1.670

2.  Genetic loci for blood lipid levels identified by linkage and association analyses in Caribbean Hispanics.

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3.  Linkage and association analysis of obesity traits reveals novel loci and interactions with dietary n-3 fatty acids in an Alaska Native (Yup'ik) population.

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7.  Direct and indirect genetic effects on triglycerides through omics and correlated phenotypes.

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