Abstract

BackgroundIncreased iron stores are associated with increased risk of type 2 diabetes, however, the mechanisms underlying these associations are poorly understood. Because a reduction of circulating osteocalcin levels after iron overload have been demonstrated in cell cultures, and osteocalcin is related to glucose and insulin metabolism, the iron-induced osteocalcin reductions could contribute to explain the role of iron metabolism in the development of type 2 diabetes mellitus.ObjectiveTo analyzed the associations between serum total and uncarboxylated osteocalcin and adiponectin concentrations with serum ferritin and soluble transferrin receptor (sTfR) in elderly subjects.DesignWe evaluated a total of 423 subjects from the PREDIMED cohort in a population-based cross-sectional analysis. Extensive clinical, nutritional and laboratory measurements, including total and uncarboxylated osteocalcin, adiponectin, ferritin and sTfR were recorded.ResultsSerum ferritin was positively correlated with increased glucose and insulin circulating levels but also with HOMA-IR, and was inversely associated with total osteocalcin and adiponectin. A regression analysis revealed that serum ferritin and transferrin receptor levels were significantly associated with a decrease in total and uncarboxylated osteocalcin. Serum sTfR levels were associated with lower uncarboxylated osteocalcin levels in the whole-study subjects and remained significant only in the IFG (impaired fasting glucose) individuals.ConclusionsWe described, for the first time, an inverse association between serum ferritin and sTfR with osteocalcin and extend previous results on adiponectin, thus supporting that factors related to iron metabolism could contribute to the insulin resistance and the development of type 2 diabetes mellitus.Trial RegistrationControlled-Trials.com ISRCTN35739639 <ISRCTN35739639>.

Highlights

  • Iron is an essential mineral for humans is potentially hazardous in excess amounts

  • A regression analysis revealed that serum ferritin and transferrin receptor levels were significantly associated with a decrease in total and uncarboxylated osteocalcin

  • Serum soluble transferrin receptor (sTfR) levels were associated with lower uncarboxylated osteocalcin levels in the whole-study subjects and remained significant only in the impaired fasting glucose (IFG) individuals

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Summary

Introduction

Iron is an essential mineral for humans is potentially hazardous in excess amounts. Excessive iron stores in patients with hereditary hemochromatosis (HH) have been causally related with the development of type 2 diabetes mellitus (T2DM) [1]. Moderately increased iron stores are associated with hyperglycemia and hyperinsulinemia, or an increased risk of type 2 diabetes mellitus in apparently healthy subjects [2,3,4,5]. These findings have been confirmed in a recent meta-analysis of five prospective epidemiologic studies, giving a pooled RR of 1.63 for type 2 diabetes mellitus in subjects with the highest levels of ferritin [6]. Because a reduction of circulating osteocalcin levels after iron overload have been demonstrated in cell cultures, and osteocalcin is related to glucose and insulin metabolism, the ironinduced osteocalcin reductions could contribute to explain the role of iron metabolism in the development of type 2 diabetes mellitus

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