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Sökning: onr:"swepub:oai:DiVA.org:uu-106228" > USF1 gene variants ...

USF1 gene variants contribute to metabolic traits in men in a longitudinal 32-year follow-up study

Auro, K. (författare)
Kristiansson, K. (författare)
Zethelius, Björn (författare)
Uppsala universitet,Geriatrik
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Berne, Christian (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper,Diabetes och endokrinologi
Lannfelt, Lars (författare)
Uppsala universitet,Geriatrik
Taskinen, M-R. (författare)
Jauhiainen, M. (författare)
Perola, M. (författare)
Peltonen, Leena (författare)
Syvänen, Ann-Christine (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper
visa färre...
 (creator_code:org_t)
2007-12-21
2008
Engelska.
Ingår i: Diabetologia. - : Springer Science and Business Media LLC. - 0012-186X .- 1432-0428. ; 51:3, s. 464-472
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • AIMS/HYPOTHESIS: Genetic variants of upstream transcription factor 1 (USF1) have previously been associated with dyslipidaemias in family studies. Our aim was to further address the role of USF1 in metabolic syndrome and cardiovascular traits at the population level in a large Swedish male cohort (n=2,322) with multiple measurements for risk factors during 32 years of follow-up. METHODS: Participants, born in 1920-1924, were examined at 50, 60, 70 and 77 years of age. The follow-up period for cardiovascular events was 1970-2002. We genotyped three haplotype tagging polymorphisms capturing the major allelic variants of USF1. RESULTS: SNP rs2774279 was associated with the metabolic syndrome. The minor allele of rs2774279 was less common among individuals with metabolic syndrome than among healthy controls [p=0.0029 when metabolic syndrome was defined according to the National Cholesterol Education Program Adult Treatment Panel III; p=0.0073 when defined according to the International Diabetes Federation (IDF)]. The minor allele of rs2774279 was also associated with lower BMI, lower fasting glucose values and higher HDL-cholesterol concentrations in longitudinal analyses. With SNP rs2073658, a borderline association with metabolic syndrome was observed (p=0.036, IDF), the minor allele being the risk-increasing allele. The minor allele of rs2073658 also associated with higher total and LDL-cholesterol, apolipoprotein B-100 and lipoprotein(a) concentrations in longitudinal analyses. Importantly, these trends with respect to the allelic variants prevailed throughout the follow-up time of three decades. CONCLUSIONS/INTERPRETATION: Our results suggest that USF1 variants associate with the metabolic syndrome at population level and influence the cardiovascular risk factors throughout adulthood in a consistent, longitudinal manner.

Nyckelord

Cardiovascular diseases
Epidemiology
Genetics
Lipids
Metabolic syndrome
Syndrome X
MEDICINE
MEDICIN

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