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                  <mods:namePart>Llauradó, Gemma</mods:namePart>
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                  <mods:namePart>Megía, Ana</mods:namePart>
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                  <mods:namePart>Cano, Albert</mods:namePart>
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                  <mods:namePart>Giménez-Palop, Olga</mods:namePart>
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                  <mods:namePart>Simón, Inmaculada</mods:namePart>
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                  <mods:namePart>González-Sastre, Montserrat</mods:namePart>
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                  <mods:namePart>Berlanga Escalera, Eugenio</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Fernández-Veledo, Sonia</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Vendrell, Joan</mods:namePart>
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               <mods:name>
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                  <mods:namePart>González Clemente, José Miguel</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Universitat Autònoma de Barcelona</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2015</mods:dateIssued>
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               <mods:abstract>To investigate the usefulness of Fibroblast Growth Factor 23 (FGF-23) and vitamin D as possible biomarkers of pre-clinical atherosclerosis, assessed as arterial stiffness (AS), in a group of subjects with type 1 diabetes (T1DM) and no previous cardiovascular events. 68 T1DM patients and 68 age- and sex-matched controls were evaluated for 1) age, sex, diabetes duration, physical activity, smoking, alcohol intake, BMI, blood pressure, fasting plasma glucose, HbA, estimated glomerular filtration rate (eGFR) and lipid profile; 2) microvascular complications; 3) blood concentrations of FGF-23 and mineral metabolism parameters (calcium, phosphate, parathyroid hormone (PTH) and 25-hydroxy-vitamin D (25(OH)D)); 4) AS, assessed as aortic pulse wave velocity (aPWV); and 5) low-grade inflammation (hsCRP, IL-6, sTNFαR1, sTNFαR2) and endothelial dysfunction (ED) markers (ICAM-1, VCAM-1, E-Selectin). Patients with T1DM had higher aPWV compared with controls (p&lt;0.001), but they did not present differences in 25(OH)D (70.3(50.4-86.2)nmol/L vs. 70.7(59.7-83.0)nmol/L; p = 0.462) and in FGF-23 plasma concentrations (70.1(38.4-151.9)RU/mL vs. 77.6(51.8-113.9)RU/mL; p = 0.329). In T1DM patients, higher concentrations of FGF-23 were positively associated with aPWV after adjusting for eGFR and classical cardiovascular risk factors (model 1: ß = 0.202, p = 0.026), other mineral metabolism parameters (model 2: ß = 0.214, p = 0.015), microvascular complications, low-grade inflammation and ED markers (model 3: ß = 0.170, p = 0.045). Lower 25(OH)D concentrations were also associated with higher aPWV after adjusting for all the above-mentioned factors (model 3: ß = -0.241, p = 0.015). We conclude that both FGF-23 plasma concentrations (positively) and 25(OH)D serum concentrations (negatively) are associated with AS in patients with T1DM and no previous cardiovascular events.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
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                  <mods:title>FGF-23/Vitamin D Axis in Type 1 Diabetes : The Potential Role of Mineral Metabolism in Arterial Stiffness</mods:title>
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