Apolipoprotein E genotype is related to plasma levels of C-reactive protein and lipids and to longevity in nonagenarians

Summary Objective  Apolipoprotein E (APOE) genotype is a regulator of hepatic lipoprotein metabolisms and has been linked with longevity. The relationship between APOE genotype and plasma C‐reactive protein (CRP), which is produced by the liver during inflammation, has not been studied in nonagenari...

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Veröffentlicht in:Clinical endocrinology (Oxford) 2006-03, Vol.64 (3), p.265-270
Hauptverfasser: Rontu, Riikka, Ojala, Petri, Hervonen, Antti, Goebeler, Sirkka, Karhunen, Pekka J., Nikkilä, Matti, Kunnas, Tarja, Jylhä, Marja, Eklund, Carita, Hurme, Mikko, Lehtimäki, Terho
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Sprache:eng
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Zusammenfassung:Summary Objective  Apolipoprotein E (APOE) genotype is a regulator of hepatic lipoprotein metabolisms and has been linked with longevity. The relationship between APOE genotype and plasma C‐reactive protein (CRP), which is produced by the liver during inflammation, has not been studied in nonagenarians. The aim of the present study was to establish whether APOE genotype is related to plasma concentrations of CRP and lipids, or longevity among nonagenarians. Design and patients  This cross‐sectional study consisted of 291 Finnish nonagenarians and three previously described and genotyped control populations from the same area (i.e. newborns, 40‐year‐olds, and 70‐year‐olds). Results  In all nonagenarians and especially in women (P= 0.038), CRP level decreased linearly in the genotype order of ɛ2/2, ɛ2/3, ɛ3/3, ɛ2/4, ɛ3/4 and ɛ4/4. Total (P= 0.009) and low‐density lipoprotein (LDL) cholesterol (P = 0.076) levels, in turn, were increased in the ɛ4 allele carriers. In newborns, the ɛ4 frequency was 0.192, in 40‐year‐olds 0.181, in 70‐year‐olds 0.179 and in nonagenarians 0.095 (P < 0.0001). The decrease in the ɛ4 allele frequency in the elderly was more clearly seen in women than in men. Conclusions  APOEɛ4 allele seems to be associated with decreased inflammatory response as measured by CRP among nonagenarians. This finding may partly explain why some ɛ4 allele carriers can reach very old age despite increased risk of hypercholesterolaemia.
ISSN:0300-0664
1365-2265
DOI:10.1111/j.1365-2265.2006.02455.x