About: The association between uncarboxylated matrix Gla protein and lipoprotein-associated phospholipase A2     Goto   Sponge   NotDistinct   Permalink

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  • Lipoprotein-associated phospholipase A2 (Lp-PLA2) is independently associated with cardiovascular risk, probably via inflammatory activity in sclerotic plaque. We speculated whether Lp-PLA2 has a role in the aetiology of vascular calcifications, estimated from circulating uncarboxylated matrix Gla protein (MGP) species and whether we could find a potential interaction of Lp-PLA2 and MGP in terms of mortality. MATERIALS AND METHODS: We examined 798 patients (mean age 65.1 years) with stable vascular disease and followed them in a prospective study. Both, desphospho-uncarboxylated and total MGP (dp-ucMGP or t-ucMGP) were quantified by pre-commercial ELISA assays, developed by VitaK (Maastricht, The Netherland) RESULTS: Lp-PLA2 activity was independently positively associated with desphospho-uncarboxylated MGP (dp-ucMGP) [beta coeff=0.098, p=0.006]. 1SD of Lp-PLA2 activity was associated with 37% increased risk (p=0.001) of elevated dp-ucMGP (≥977pmol/L, top quartile). In the Cox proportional hazard model adjusted for conventional risk factors, the patients in the highest quartile of dp-ucMGP or lowest quintile of total-uncarboxylated ucMGP (<2660nmol/L) had higher risk of all-cause mortality [HRR 2.79 (95% CI 1.97-3.94) and HRR 1.69 (95% CI 1.18-2.42), respectively]. We observed no effect of high Lp-PLA2 activity (≥195nmol/min/mL) on total mortality. CONCLUSIONS: We assume that Lp-PLA2 is involved in vascular calcification and that dp-ucMGP is a more appropriate biomarker of residual risk than Lp-PLA2 itself.
  • Lipoprotein-associated phospholipase A2 (Lp-PLA2) is independently associated with cardiovascular risk, probably via inflammatory activity in sclerotic plaque. We speculated whether Lp-PLA2 has a role in the aetiology of vascular calcifications, estimated from circulating uncarboxylated matrix Gla protein (MGP) species and whether we could find a potential interaction of Lp-PLA2 and MGP in terms of mortality. MATERIALS AND METHODS: We examined 798 patients (mean age 65.1 years) with stable vascular disease and followed them in a prospective study. Both, desphospho-uncarboxylated and total MGP (dp-ucMGP or t-ucMGP) were quantified by pre-commercial ELISA assays, developed by VitaK (Maastricht, The Netherland) RESULTS: Lp-PLA2 activity was independently positively associated with desphospho-uncarboxylated MGP (dp-ucMGP) [beta coeff=0.098, p=0.006]. 1SD of Lp-PLA2 activity was associated with 37% increased risk (p=0.001) of elevated dp-ucMGP (≥977pmol/L, top quartile). In the Cox proportional hazard model adjusted for conventional risk factors, the patients in the highest quartile of dp-ucMGP or lowest quintile of total-uncarboxylated ucMGP (<2660nmol/L) had higher risk of all-cause mortality [HRR 2.79 (95% CI 1.97-3.94) and HRR 1.69 (95% CI 1.18-2.42), respectively]. We observed no effect of high Lp-PLA2 activity (≥195nmol/min/mL) on total mortality. CONCLUSIONS: We assume that Lp-PLA2 is involved in vascular calcification and that dp-ucMGP is a more appropriate biomarker of residual risk than Lp-PLA2 itself. (en)
Title
  • The association between uncarboxylated matrix Gla protein and lipoprotein-associated phospholipase A2
  • The association between uncarboxylated matrix Gla protein and lipoprotein-associated phospholipase A2 (en)
skos:prefLabel
  • The association between uncarboxylated matrix Gla protein and lipoprotein-associated phospholipase A2
  • The association between uncarboxylated matrix Gla protein and lipoprotein-associated phospholipase A2 (en)
skos:notation
  • RIV/00159816:_____/15:00061248!RIV15-MSM-00159816
http://linked.open...avai/riv/aktivita
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  • P(ED1.100/02/0123)
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  • 1
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  • 36
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  • RIV/00159816:_____/15:00061248
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  • Stroke; Mortality risk; Matrix Gla protein; Lipoprotein-associated phospholipaseA(2); Euroaspire; Coronary heart disease (en)
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  • IE - Irsko
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  • [1FBD491B2DCD]
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  • Maturitas
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  • 80
http://linked.open...iv/tvurceVysledku
  • Bruthans, J.
  • Cífková, Renata
  • Filipovský, J.
  • Seidlerová, J.
  • Wohlfahrt, Peter
  • Mayer, O.
  • Vaněk, J.
  • Trefil, L.
  • Drummen, N.E.A.
  • Kielbergerová, L.
  • Knapen, M.H.J
  • Vermeer, C.
http://linked.open...ain/vavai/riv/wos
  • 000348013900013
issn
  • 0378-5122
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.maturitas.2014.10.003
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