Direct effect of the correction of acidosis on plasma parathyroid hormone concentrations, calcium and phosphate in hemodialysis patients: A prospective study

被引:24
作者
Movilli, E
Zani, R
Carli, O
Sangalli, L
Pola, A
Camerini, C
Scolari, F
Cancarini, GC
Maiorca, R
机构
[1] Univ Brescia, Div Nephrol, Spedali Civili, I-25123 Brescia, Italy
[2] Univ Brescia, Chair Nephrol, I-25123 Brescia, Italy
来源
NEPHRON | 2001年 / 87卷 / 03期
关键词
uremia; acidosis; dialysis; PTH; calcium; phosphate;
D O I
10.1159/000045923
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Metabolic acidosis contributes to renal osteodystrophy and together with hyperphosphatemia, hypocalcemia and altered vitamin D metabolism may result in increased levels of intact parathyroid hormone (iPTH) and metastatic calcifications. However, the impact of the correction of metabolic acidosis on iPTH levels and calcium-phosphate metabolism is still controversial. Study Design: The effects of the correction of metabolic acidosis on serum concentrations of iPTH, calcium (Ca), phosphate (PO4) and alkaline phosphatase were prospectively studied. Twelve uremic patients on maintenance hemodialysis (HD) for 49 months (median; range 6-243 months) with serum bicarbonate levels less than or equal to 20 mmol/l were studied before and after 3 months of oral sodium bicarbonate supplementation. Predialysis serum bicarbonate, arterial pH, ionized calcium, plasma sodium, plasma potassium, serum creatinine, hemoglobin, K-t/V, postdialysis body weight, predialysis systolic and diastolic blood pressure were also evaluated before and after correction. Results: Serum bicarbonate levels and arterial pH increased respectively from 19.3 +/- 0.6 to 24.4 +/- 1.2 mmol/l (p < 0.0001) and 7.34 <plus/minus> 0.03 to 7.40 +/- 0.02 (p < 0.001). iPTH levels decreased significantly from 399 <plus/minus> 475 to 305 +/- 353 pg/ml (p = 0.026). No changes in total serum Ca, plasma PO4, serum akaline phosphatase, K-t/V, serum creatinine, hemoglobin, body weight, predialysis systolic and diastolic blood pressures were observed. iCa decreased significantly. Conclusions: Our study demonstrates that the correction of metabolic acidosis in chronic HD patients reduces iPTH concentrations in HD patients with secondary hyperparathyroidism possibly by a direct effect on iPTH secretion. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:257 / 262
页数:6
相关论文
共 25 条
[1]   ACUTE METABOLIC-ACIDOSIS ENHANCES CIRCULATING PARATHYROID-HORMONE, WHICH CONTRIBUTES TO THE RENAL RESPONSE AGAINST ACIDOSIS IN THE RAT [J].
BICHARA, M ;
MERCIER, O ;
BORENSZTEIN, P ;
PAILLARD, M .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (02) :430-443
[2]   IMPORTANCE OF NUTRITION IN DIALYSIS PATIENTS [J].
BLAGG, CR .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1991, 17 (04) :458-461
[3]   Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study [J].
Block, GA ;
Hulbert-Shearon, TE ;
Levin, NW ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) :607-617
[4]   CLONING AND CHARACTERIZATION OF AN EXTRACELLULAR CA2+-SENSING RECEPTOR FROM BOVINE PARATHYROID [J].
BROWN, EM ;
GAMBA, G ;
RICCARDI, D ;
LOMBARDI, M ;
BUTTERS, R ;
KIFOR, O ;
SUN, A ;
HEDIGER, MA ;
LYTTON, J ;
HEBERT, SC .
NATURE, 1993, 366 (6455) :575-580
[5]  
BUSA WB, 1984, AM J PHYSIOL, V246, P409
[6]   THE CONTRIBUTION OF ACIDOSIS TO RENAL OSTEODYSTROPHY - DISCUSSION [J].
BUSHINSKY, DA ;
MADIAS, NE ;
HARRINGTON, JT ;
KING, A ;
LEMAY, S ;
PARKER, M .
KIDNEY INTERNATIONAL, 1995, 47 (06) :1816-1832
[7]  
BUSHINSKY DA, 1989, AM J PHYSIOL, V265, P836
[8]  
BUSHINSKY DA, 1995, AM J PHYSIOL, V264, P1364
[9]  
BUSHINSKY DA, 1989, REGULATION ACID BASE, P69
[10]   EFFECT OF ACUTE AND CHRONIC METABOLIC-ACIDOSIS ON SERUM IMMUNOREACTIVE PARATHYROID-HORMONE IN MAN [J].
COE, FL ;
FIRPO, JJ ;
HOLLANDSWORTH, DL ;
SEGIL, L ;
CANTERBURY, JM ;
REISS, E .
KIDNEY INTERNATIONAL, 1975, 8 (04) :262-273