@article{10902/31408, year = {2013}, url = {https://hdl.handle.net/10902/31408}, abstract = {Introduction: To investigate how markers of β-cell secretion (proinsulin-processing metabolites) are expressed in rheumatoid arthritis (RA) patients and their potential relation with the insulin resistance (IR) observed in these patients. Methods: The 101 RA patients and 99 nondiabetic sex- and age-matched controls were included. IR by homeostatic model assessment (HOMA2), and β-cell secretion, as measured by insulin, split and intact proinsulin, and C-peptide levels were determined for both groups. Multiple regression analysis was performed to compare IR between groups and to explore the interrelations between RA features, proinsulin metabolites, and IR. Data were adjusted for glucocorticoids intake and for IR classic risk factors. Results: Compared with controls, RA patients showed higher HOMA-IR (β coef., 0.40 (95% CI, 0.20 to 0.59); P = 0.00). When data were adjusted for glucocorticoids intake, noncorticosteroid patients maintained a higher IR index (β, 0.14 (0.05 to 0.24); P = 0.00). Impaired insulin processing in RA patients was detected by the onset of elevated split proinsulin levels (β, 0.70 pmol/L (0.38 to 1.02); P = 0.00). These data remained significant also when adjusted for prednisone intake (b, 0.19 (0.00 to 0.36) pmol/L; P = 0.04). Split proinsulin-to-C-peptide ratios were higher in RA patients undergoing corticosteroid therapy (b, 0.25 (0.12 to 0.38); P = 0.03) and were nearly significant in comparison between noncorticosteroids patients and controls (b, 0.16 (-0.02 to 0.34); P = 0.08). Interestingly, the impact of HOMA-IR on the ratio of intact proinsulin to C-peptide was higher in controls compared with patients (b, 6.23 (1.41 to 11.06) versus 0.43 (-0.86 to 1.71); P = 0.03). Conclusions: b-Cell function is impaired in nondiabetic and in RA patients not taking corticoids by a mechanism that seems to be, at least in part, independent of IR.}, organization = {This work was supported by a grant from the Fundación Española de Reumatología to I. F-A. and by a grant from the Spanish Ministry of Health (Fondo de Investigaciones Sanitarias) to F.D-G. [FIS 09/02209]. The authors are indebted to the entire staff of the Rheumatology Service of Hospital Universitario de Canarias and especially to Drs. Vanesa Hernández-Harnández, Esmeralda Delgado-Frias, and Maria Angeles Gantes, and to Mrs. Rodríguez-Vargas for their steadfast support.}, publisher = {BioMed Central}, publisher = {Arthritis Research & Therapy, 2013, 15(1), R17}, title = {Impaired beta cell function is present in nondiabetic rheumatoid arthritis patients}, author = {Ferraz-Amaro, Iván and García-Dopico, José A. and Medina-Vega, Lilian and González-Gay Mantecón, Miguel Ángel and Díaz-González, Federico}, }