Vitamin C Plasma Levels Associated with Inflammatory Biomarkers, CRP and RDW: Results from the NHANES 2003-2006 Surveys

被引:21
作者
Crook, Jennifer Marie [1 ]
Horgas, Ann L. [2 ]
Yoon, Saunjoo L. [2 ]
Grundmann, Oliver [3 ]
Johnson-Mallard, Versie [4 ]
机构
[1] Mayo Clin Florida, Ctr Hlth Equ & Community Engagement Res, Jacksonville, FL 32224 USA
[2] Univ Florida, Coll Nursing, Biobehav Nursing Sci, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Pharm, Entrepreneurial Programs Med Chem, Gainesville, FL 32610 USA
[4] Kent State Univ, Coll Nursing, Kent, OH 44240 USA
关键词
ascorbate; vitamin C; inflammation; CRP; RDW; SOCIOECONOMIC-STATUS; REACTIVE PROTEIN; INSIGHTS;
D O I
10.3390/nu14061254
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Although undisputed for its anti-inflammatory and immune system boosting properties, vitamin C remains an inconsistently investigated nutrient in the United States. However, subclinical inadequacies may partly explain increased inflammation and decreased immune function within the population. This secondary analysis cross-sectional study used the 2003-2006 NHANES surveys to identify more clearly the association between plasma vitamin C and clinical biomarkers of acute and chronic inflammation C-reactive protein (CRP) and red cell distribution width (RDW). From plasma vitamin C levels separated into five defined categories (deficiency, hypovitaminosis, inadequate, adequate, and saturating), ANOVA tests identified significant differences in means in all insufficient vitamin C categories (deficiency, hypovitaminosis, and inadequate) and both CRP and RDW in 7607 study participants. There were also statistically significant differences in means between sufficient plasma vitamin C levels (adequate and saturating categories) and CRP. Significant differences were not identified between adequate and saturating plasma vitamin C levels and RDW. Although inadequate levels of vitamin C may not exhibit overt signs or symptoms of deficiency, differences in mean levels identified between inflammatory biomarkers suggest a closer examination of those considered at risk for inflammatory-driven diseases. Likewise, the subclinical levels of inflammation presented in this study provide evidence to support ranges for further clinical inflammation surveillance.
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页数:9
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