TY - JOUR T1 - Lack of activation of renal functional reserve predicts the risk of significant renal involvement in systemic sclerosis JF - Annals of the Rheumatic Diseases JO - Ann Rheum Dis SP - 1963 LP - 1967 DO - 10.1136/ard.2011.152892 VL - 70 IS - 11 AU - Riccardo Livi AU - Serena Guiducci AU - Federico Perfetto AU - Gabriele Ciuti AU - Elisa Grifoni AU - Letizia Conforti AU - Felice Galluccio AU - Alberto Moggi Pignone AU - Marco Matucci Cerinic Y1 - 2011/11/01 UR - http://ard.bmj.com/content/70/11/1963.abstract N2 - Objective To evaluate if defective activation of renal functional reserve (RFR) in systemic sclerosis (SSc) without clinical signs of renal involvement predicts the risk of developing clinically relevant renal damage. Methods Twenty-eight normotensive SSc patients with normal renal function and no urinary abnormalities were submitted to an intravenous amino acid load to activate RFR. Nineteen patients (six with diffuse cutaneous SSc (dcSSc)) had an RFR activation defect, while nine (two with dcSSc) showed normal RFR. All patients were followed up for 5 years, with periodic evaluation of renal function, urinary protein excretion and systemic blood pressure (BP). Results At admission, patients with normal RFR had lower BP than those with abnormal RFR; no age, disease duration or creatinine clearance (CCr) differences were found. Five years later, patients with abnormal RFR showed, with respect to basal values, a significantly higher CCr reduction than patients with normal RFR (mean percent decrease 15.4±9.5 vs 2.6±3.8, p<0.001). Among patients with abnormal RFR, 13 (68.4%) showed a CCr reduction of ≥2 ml/min/year, with a final CCr of ≤70 ml/min in eight cases; two patients developed microalbuminuria and 10 grade 1 or 2 systemic hypertension. Significant CCr reduction rates were found in eight patients with high BP and in five patients who remained normotensive. No patient with normal RFR had proteinuria or high BP during follow-up. Conclusions Lack of RFR activation is an early sign of renal involvement in SSc, and is a harbinger of an increased risk of developing renal insufficiency and systemic hypertension. ER -