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Association between dietary factors and plasma fetuin-A concentrations in the general population

Authors

  • K. Nimptsch
  • J. Janke
  • T. Pischon
  • J. Linseisen

Journal

  • British Journal of Nutrition

Citation

  • Br J Nutr 114 (8): 1278-1285

Abstract

  • Circulating fetuin-A, a novel marker for hepatic fat accumulation, has been related to a higher risk of type 2 diabetes and cardiovascular diseases in a growing number of prospective studies. However, little is known about dietary determinants of fetuin-A concentrations in the general population. Therefore, we aimed to investigate the association between dietary intake of energy, energy-providing nutrients, alcohol and major food groups and plasma fetuin-A concentrations in the Bavarian Food Consumption Survey II. Dietary intake was assessed by three 24-h dietary recalls, and plasma concentrations of fetuin-A were measured in 558 adults (18-81 years). After multivariable adjustment for lifestyle factors and body fatness, higher energy intake was nonsignificantly associated with higher fetuin-A concentrations (per 2092 kJ/d (500 kcal/d) 3.7 microg/ml, 95 % CI -0.5, 7.8 microg/ml). There was no clear association between energy-providing nutrients and fetuin-A concentrations. Higher alcohol intake was associated with lower fetuin-A concentrations (P trend 0.003): mean fetuin-A concentrations were 324 (95 % CI 313, 335) microg/ml in non-drinkers, and with 293 (95 % CI 281, 306) microg/ml significantly lower in participants who drank >/=30 g alcohol per d. Mean fetuin-A concentrations decreased across quintiles of milk and dairy product intake (lowest quintile 319 (95 % CI 309, 330) microg/ml; highest quintile 304 (95 % CI 293, 314) microg/ml; P trend 0.03), and each 150-g increment in milk/dairy products per d was associated with 5.6 (95 % CI -9.6, -1.5) microg/ml lower fetuin-A. Dietary intakes of vegetables, meat or fish were not associated with fetuin-A concentrations. Because of the preventive potential of our findings, further exploration is warranted.


DOI

doi:10.1017/S0007114515002639