TY - JOUR
T1 - Vitamin K and vitamin D status
T2 - Associations with inflammatory markers in the Framingham offspring study
AU - Shea, M. Kyla
AU - Booth, Sarah L.
AU - Massaro, Joseph M.
AU - Jacques, Paul F.
AU - D'Agostino, Ralph B.
AU - Dawson-Hughes, Bess
AU - Ordovas, José M.
AU - O'Donnell, Christopher J.
AU - Kathiresan, Sekar
AU - Keaney, John F.
AU - Vasan, Ramachandran S.
AU - Benjamin, Emelia J.
PY - 2008/2
Y1 - 2008/2
N2 - In vitro data suggest protective roles for vitamins K and D in inflammation. To examine associations between vitamins K and D and inflammation in vivo, the authors used multiple linear regression analyses, adjusted for age, sex, body mass index, triglyceride concentrations, use of aspirin, use of lipid-lowering medication, season, menopausal status, and hormone replacement therapy. Participants were from the Framingham Offspring Study (1997-2001; n = 1,381; mean age = 59 years; 52% women). Vitamin K status, measured by plasma phylloquinone concentration and phylloquinone intake, was inversely associated with circulating inflammatory markers as a group and with several individual inflammatory biomarkers (p < 0.01). Percentage of undercarboxylated osteocalcin, a functional measure of vitamin K status, was not associated with overall inflammation but was associated with C-reactive protein (p < 0.01). Although plasma 25-hydroxyvitamin D was inversely associated with urinary isoprostane concentration, an indicator of oxidative stress (p < 0.01), overall associations between vitamin D status and inflammation were inconsistent. The observation that high vitamin K status was associated with lower concentrations of inflammatory markers suggests that a possible protective role for vitamin K in inflammation merits further investigation.
AB - In vitro data suggest protective roles for vitamins K and D in inflammation. To examine associations between vitamins K and D and inflammation in vivo, the authors used multiple linear regression analyses, adjusted for age, sex, body mass index, triglyceride concentrations, use of aspirin, use of lipid-lowering medication, season, menopausal status, and hormone replacement therapy. Participants were from the Framingham Offspring Study (1997-2001; n = 1,381; mean age = 59 years; 52% women). Vitamin K status, measured by plasma phylloquinone concentration and phylloquinone intake, was inversely associated with circulating inflammatory markers as a group and with several individual inflammatory biomarkers (p < 0.01). Percentage of undercarboxylated osteocalcin, a functional measure of vitamin K status, was not associated with overall inflammation but was associated with C-reactive protein (p < 0.01). Although plasma 25-hydroxyvitamin D was inversely associated with urinary isoprostane concentration, an indicator of oxidative stress (p < 0.01), overall associations between vitamin D status and inflammation were inconsistent. The observation that high vitamin K status was associated with lower concentrations of inflammatory markers suggests that a possible protective role for vitamin K in inflammation merits further investigation.
KW - Inflammation
KW - Vitamin D
KW - Vitamin K
UR - https://www.scopus.com/pages/publications/38849189427
UR - https://www.scopus.com/pages/publications/38849189427#tab=citedBy
U2 - 10.1093/aje/kwm306
DO - 10.1093/aje/kwm306
M3 - Article
C2 - 18006902
AN - SCOPUS:38849189427
SN - 0002-9262
VL - 167
SP - 313
EP - 320
JO - American journal of epidemiology
JF - American journal of epidemiology
IS - 3
ER -