Metabolismo Fosfocálcico Sociedad Uruguaya de Nefrología Grupo de Estudio del Metabolismo Fosfocálcico Sociedad Uruguaya de Nefrología Cátedra de Nefrología – Facultad de Medicina Montevideo – Uruguay
METABOLISMO FOSFOCALCICO (AÑO 1985) CALCIO n = 339 9 ± 1.3 mg/dl < 8 mg/dl 14 % 8 – 9 mg/dl 33 % 9.1 – 11 mg/dl 51% > 11 mg/dl 2%
METABOLISMO FOSFOCALCICO (AÑO 1985) FOSFORO n = 339 5.5 ± 1.4 mg/dl < 5.5 mg/dl 48% 5.5 – 7 mg/dl 40% > 7 mg/dl 12 %
METABOLISMO FOSFOCALCICO (AÑO 1985) PTH n = 339 8 – 1.2 9 % 1.3 – 5 46 % 5.1 – 10 25 % > 10 20 %
METABOLISMO FOSFOCALCICO (abril – octubre 2004) n = 2415 M: 59.6 % F: 40.4 % EDAD: 59.8 ± 16.9 años (2 – 94) Ca: 9.03 ± 0.79 mg/dl (5 – 11.5) P: 5.8 ± 1.6 mg/dl (1.3 – 11) FA: 272 ± 222 (15 – 2000) PTHi: 484 ± 533 pg/ml (2.3 – 4000)
METABOLISMO FOSFOCALCIO PAUTAS DOQI CALCIO: 8.4 - 9.5 mg/dl FOSFORO: 3.5 - 5.5 mg/dl • PTHi: 150 – 300 pg/ml
METABOLISMO FOSFOCALCICO (abril - octubre 2004) n = 2415 Calcio < 8.4 mg/dl 20.7 % 8.4 – 9.5 mg/dl 52.6 % > 9.5 mg/dl 26.8 % Fósforo < 3.5 mg/dl 5.5 % 3.5 – 5.5 mg/dl 39.8 % > 5.5 mg/dl 54.7 % PTHi > 150 pg/ml 29 % 150 – 300 pg/ml 21.6 % > 300 pg/ml 49.4 %
METABOLISMO FOSFOCALCICO (abril - octubre 2004)
Cannata et al* SUN PTHi < 150 47 % 29 % > 300 31 % 49.4 % 150 – 300 22 % 21.6 % > 300 31 % 49.4 % P > 5.5 49 % 54.7 % * Sólo 9.5% tenían Ca, P, PTHi y PxCa dentro del rango propuesto por las pautas K/DOQI (Cannata et al, JASN 14: 474A, 2003).
& Histomorfometría Osea. Universidad de Sao Paulo, Sao Paulo - Brasil Epidemiology of Renal Osteodystrophy in Uruguay Current indications of bone biopsies H. Caorsi*, I. Olaizola*, L. Labruna#, V. Jorgetti&, G. Acuña*, A. Petraglia*, L. Fajardo*, A. Alvarez*, P Ambrosoni*. * Grupo de estudio del metabolismo Fosfocálcico – Sociedad Uruguaya de Nefrología – Uruguay # Histomorfometría Osea. Instituto de Reumatología, Montevideo - Uruguay & Histomorfometría Osea. Universidad de Sao Paulo, Sao Paulo - Brasil
Bone Biopsies and Clinical Features of Patients 1985 – 2000 Aims To analyze the prevalence of the different types of bone disease over the time in dialysis patients in Uruguay. To determine current indication of bone biopsy in the diagnosis of renal osteodystrophy. Bone Biopsies and Clinical Features of Patients 1985 – 2000 167 Bone biopsies from hemodialysis symptomatic patients. 4% Diabetics. 93 Female; 74 Male. Age: 54 ± 13 years. Length of dialysis: 53 ± 33 months
Results Frequency of Different Histological Forms 1985 – 2000
a p < 0.001; b p < 0.01; c p < 0.05 Results Histological Diagnosis According to Year of Bone Biopsies 1985 – 2000 1985 - 1990 HD pts./year: 1187 n = 66 BB 1991 - 1996 HD pts./year: 1602 n = 84 BB 1997 - 2000 HD pts./year: 2254 n = 17 BB c b % Al in MF: 42.5 ± 47a % Al in MF : 20 ± 28a % Al in MF : 27 ± 18 a p < 0.001; b p < 0.01; c p < 0.05 % samples [Al]water: 88% (< 10 μg/l) 97% (< 2 μg/l)
Results Freqcuency of Adinamic Bone Disease with and without Aluminium Over the Time
Renal Osteodystrophy in Uruguay Bone Biopsy Registry iPTH levels pg/ml 1400 1300 1200 1100 1000 900 800 700 600 500 400 300 200 100 p < 0,001 OF OMa y ABDa
Conclusions Survival rates of patients on dialysis have increased with improve crescent of dialytic therapy, but the resultant increased duration of dialysis has led to rise in hyperparathyroidism. Our results show a significant increase in osteitis fibrosa in the last years. This can be explained by a longer time on dialysis of the patients. On the other hand, low turnover bone disease aluminium related (OM and ABD) decreased significantly, and we find that ABD without aluminium appears in the last period. The percentage of aluminium in the mineralization front in bone biopsies has diminished over the time. The modification of histological forms observed should be related to the improvement in the dialysis water treatment and the reduction of oral aluminium exposure.