Consumption of red meat and whole-grain bread in relation to biomarkers of obesity, inflammation, glucose metabolism and oxidative stress
Blood Glucose
Male
610
Medicine (miscellaneous)
Body Mass Index
03 medical and health sciences
Animals
Humans
Life Style
Glycated Hemoglobin
Inflammation
2. Zero hunger
0303 health sciences
Nutrition and Dietetics
Cholesterol, HDL
Alanine Transaminase
Original Contribution
Bread
Diet
3. Good health
C-Reactive Protein
Cross-Sectional Studies
Cardiovascular Diseases
Cattle
Female
Adiponectin
Edible Grain
Biomarkers
DOI:
10.1007/s00394-012-0340-6
Publication Date:
2012-03-17T06:41:23Z
AUTHORS (8)
ABSTRACT
To examine the association of red meat and whole-grain bread consumption with plasma levels of biomarkers related to glucose metabolism, oxidative stress, inflammation and obesity.Our cross-sectional study was based on 2,198 men and women who were selected as a sub-cohort for an investigation of biological predictors of diabetes and cardiovascular diseases from the European Prospective Investigation into Cancer and Nutrition-Potsdam study. Circulating levels of glycated hemoglobin, adiponectin, hs-CRP, gamma-glutamyltransferase, alanine-aminotransferase, fetuin-A, HDL-cholesterol and triglycerides were measured from random blood samples. Diet and lifestyle data were assessed by questionnaires, and anthropometric data were measured.After multivariable adjustment, higher consumption of whole-grain bread was significantly (P trend <0.05) associated with lower levels of GGT, ALT and hs-CRP, whereas higher consumption of red meat was significantly associated with higher levels of GGT and hs-CRP when adjusted for potential confounding factors related to lifestyle and diet. Further adjustment for body mass index and waist circumference attenuated the association between red meat and hs-CRP (P = 0.19).The results of this study suggest that high consumption of whole-grain bread is related to lower levels of GGT, ALT and hs-CRP, whereas high consumption of red meat is associated with higher circulating levels of GGT and hs-CRP.
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CITATIONS (179)
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