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Sökning: (WFRF:(Peltonen Leena)) > USF1 gene variants ...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003831naa a2200481 4500
001oai:DiVA.org:uu-106228
003SwePub
008090617s2008 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1062282 URI
024a https://doi.org/10.1007/s00125-007-0892-92 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Auro, K.4 aut
2451 0a USF1 gene variants contribute to metabolic traits in men in a longitudinal 32-year follow-up study
264 c 2007-12-21
264 1b Springer Science and Business Media LLC,c 2008
338 a print2 rdacarrier
520 a 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.
653 a Cardiovascular diseases
653 a Epidemiology
653 a Genetics
653 a Lipids
653 a Metabolic syndrome
653 a Syndrome X
653 a MEDICINE
653 a MEDICIN
700a Kristiansson, K.4 aut
700a Zethelius, Björnu Uppsala universitet,Geriatrik4 aut0 (Swepub:uu)bjorzeth
700a Berne, Christianu Uppsala universitet,Institutionen för medicinska vetenskaper,Diabetes och endokrinologi4 aut0 (Swepub:uu)chber255
700a Lannfelt, Larsu Uppsala universitet,Geriatrik4 aut0 (Swepub:uu)lalan021
700a Taskinen, M-R.4 aut
700a Jauhiainen, M.4 aut
700a Perola, M.4 aut
700a Peltonen, Leena4 aut
700a Syvänen, Ann-Christineu Uppsala universitet,Institutionen för medicinska vetenskaper4 aut0 (Swepub:uu)anncsyva
710a Uppsala universitetb Geriatrik4 org
773t Diabetologiad : Springer Science and Business Media LLCg 51:3, s. 464-472q 51:3<464-472x 0012-186Xx 1432-0428
856u https://link.springer.com/content/pdf/10.1007%2Fs00125-007-0892-9.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-106228
8564 8u https://doi.org/10.1007/s00125-007-0892-9

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