Serum fibroblast growth factor 23, serum iron and bone mineral density in premenopausal women

dc.contributor.authorImel, Erik A.
dc.contributor.authorLiu, Ziyue
dc.contributor.authorMcQueen, Amie K.
dc.contributor.authorActon, Dena
dc.contributor.authorActon, Anthony
dc.contributor.authorPadgett, Leah R.
dc.contributor.authorPeacock, Munro
dc.contributor.authorEcons, Michael J.
dc.contributor.departmentDepartment of Medicine, IU School of Medicineen_US
dc.date.accessioned2017-08-14T17:55:35Z
dc.date.available2017-08-14T17:55:35Z
dc.date.issued2016-05
dc.description.abstractFibroblast growth factor 23 (FGF23) circulates as active protein and inactive fragments. Low iron status increases FGF23 gene expression, and iron deficiency is common. We hypothesized that in healthy premenopausal women, serum iron influences C-terminal and intact FGF23 concentrations, and that iron and FGF23 associate with bone mineral density (BMD). Serum iron, iron binding capacity, percent iron saturation, phosphorus, and other biochemistries were measured in stored fasting samples from healthy premenopausal white (n=1898) and black women (n=994), age 20-55years. Serum C-terminal and intact FGF23 were measured in a subset (1631 white and 296 black women). BMD was measured at the lumbar spine and femur neck. Serum phosphorus, calcium, alkaline phosphatase and creatinine were lower in white women than black women (p<0.001). Serum iron (p<0.0001) and intact FGF23 (p<0.01) were higher in white women. C-terminal FGF23 did not differ between races. Phosphorus correlated with intact FGF23 (white women, r=0.120, p<0.0001; black women r=0.163, p<0.01). However, phosphorus correlated with C-terminal FGF23 only in black women (r=0.157, p<0.01). Intact FGF23 did not correlate with iron. C-terminal FGF23 correlated inversely with iron (white women r=-0.134, p<0.0001; black women r=-0.188, p<0.01), having a steeper slope at iron <50mcg/dl than ≥50mcg/dl. Longitudinal changes in iron predicted changes in C-terminal FGF23. Spine BMD correlated with iron negatively (r=-0.076, p<0.01) in white women; femur neck BMD correlated with iron negatively (r=-0.119, p<0.0001) in black women. Both relationships were eliminated in weight-adjusted models. BMD did not correlate with FGF23. Serum iron did not relate to intact FGF23, but was inversely related to C-terminal FGF23. Intact FGF23 correlated with serum phosphorus. In weight-adjusted models, BMD was not related to intact FGF23, C-terminal FGF23 or iron. The influence of iron on FGF23 gene expression is not important in determining bone density in healthy premenopausal women.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationImel, E. A., Liu, Z., McQueen, A. K., Acton, D., Acton, A., Padgett, L. R., … Econs, M. J. (2016). Serum fibroblast growth factor 23, serum iron and bone mineral density in premenopausal women. Bone, 86, 98–105. http://doi.org/10.1016/j.bone.2016.03.005en_US
dc.identifier.urihttps://hdl.handle.net/1805/13819
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.bone.2016.03.005en_US
dc.relation.journalBoneen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectIronen_US
dc.subjectFibroblast growth factor 23en_US
dc.subjectFGF23en_US
dc.subjectBone mineral densityen_US
dc.subjectDXAen_US
dc.subjectPremenopausal womenen_US
dc.titleSerum fibroblast growth factor 23, serum iron and bone mineral density in premenopausal womenen_US
dc.typeArticleen_US
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