Calcium, phosphate, and parathyroid hormone levels in combination and as a function of dialysis duration predict mortality: Evidence for the complexity of the association between mineral metabolism and outcomes

被引:289
作者
Stevens, LA
Djurdjev, O
Cardew, S
Cameron, EC
Levin, A
机构
[1] Tufts Univ New England Med Ctr, Div Nephrol, Boston, MA 02111 USA
[2] Univ British Columbia, Dept Med, Div Nephrol, Vancouver, BC, Canada
[3] Univ British Columbia, CHEOS, Vancouver, BC, Canada
[4] Univ British Columbia, Sch Med, Vancouver, BC, Canada
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2004年 / 15卷 / 03期
关键词
D O I
10.1097/01.ASN.0000113243.24155.2F
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
Current literature suggests associations between abnormal mineral metabolism (MM) to cardiovascular disease in dialysis populations, with conflicting results. MM physiology is complex; therefore, it was hypothesized that constellations of MM parameters, reflecting this complexity, would be predictive of mortality and that this effect would be modified by dialysis duration (DD). Prevalent dialysis patients in British Columbia, Canada, who had measurements of calcium (Ca), phosphate (Pi), and parathyroid hormone (iPTH) between January and March 2000 were followed prospectively until December 2002. Statistical analysis included Cox proportional hazard models with Ca, Pi, and iPTH alone and in combination as explanatory variables; analyses were stratified by DD. The 515 patients included in this analysis represent British Columbia and Canadian dialysis populations: 69% were on hemodialysis, mean age was 60 +/- 17 yr, 40% were female, and 34% had diabetes. Mean Ca and Pi values were 2.32 +/- 0.22 mmol/L and 1.68 +/- 0.59 mmol/L, respectively, and median iPTH was 15.8 pmol/L (25th to 75th percentile: 6.9 to 37.3 pmol/L). Serum Pi, after adjusting for demographic, dialysis type and adequacy, hemoglobin, and albumin, independently predicted mortality (risk ratio [RR], 1.56 per 1 mmol/L; 95% confidence interval [CI], 1.15 to 2.12; P = 0.004). When combinations of parameters were modeled (overall P = 0.003), the combinations of high serum Pi and Ca with high iPTH (RR, 3.7 1; 95% CI, 1.53 to 9.03; P = 0.004) and low iPTH (RR, 4.30; 95% CI, 2.01 to 9.22; P < 0.001) had highest risks for mortality as compared with the combination of high iPTH with normal serum Ca and Pi that had the lowest mortality and was used as index category. These effects varied across different strata of DD. This analysis demonstrates the importance of examining combinations of MM parameters as opposed to single variables alone and the effect of DD. In so doing, the complex interaction of time and MM can begin to be understand. Further exploration is required.
引用
收藏
页码:770 / 779
页数:10
相关论文
共 40 条
  • [1] Hyperphosphatemia aggravates cardiac fibrosis and microvascular disease in experimental uremia
    Amann, K
    Törnig, J
    Kugel, B
    Gross, ML
    Tyralla, K
    El-Shakmak, A
    Szabo, A
    Ritz, E
    [J]. KIDNEY INTERNATIONAL, 2003, 63 (04) : 1296 - 1301
  • [2] Importance of low serum intact parathyroid hormone as a predictor of mortality in hemodialysis and peritoneal dialysis patients: 14 years of prospective observation
    Avram, MM
    Mittman, N
    Myint, MM
    Fein, P
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (06) : 1351 - 1357
  • [3] Effect of hyperparathyroidism on arterial distensibility in renal transplant recipients
    Barenbrock, M
    Hausberg, M
    Kosch, R
    Kisters, K
    Hoeks, APG
    Rahn, KH
    [J]. KIDNEY INTERNATIONAL, 1998, 54 (01) : 210 - 215
  • [4] Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study
    Block, GA
    Hulbert-Shearon, TE
    Levin, NW
    Port, FK
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) : 607 - 617
  • [5] Electron beam computed tomography in the evaluation of cardiac calcifications in chronic dialysis patients
    Braun, J
    Oldendorf, M
    Moshage, W
    Heidler, R
    Zeitler, E
    Luft, FC
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (03) : 394 - 401
  • [6] Phosphorus and uremic serum up-regulate osteopontin expression in vascular smooth muscle cells
    Chen, NX
    O'Neill, KD
    Duan, D
    Moe, SM
    [J]. KIDNEY INTERNATIONAL, 2002, 62 (05) : 1724 - 1731
  • [7] Davies MR, 2002, J AM SOC NEPHROL, V13, p59A
  • [8] Pathophysiological mechanisms of vascular calcification in end-stage renal disease
    Davies, MR
    Hruska, KA
    [J]. KIDNEY INTERNATIONAL, 2001, 60 (02) : 472 - 479
  • [9] Clinical epidemiology of cardiovascular disease in chronic renal disease
    Foley, RN
    Parfrey, PS
    Sarnak, MJ
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (05) : S112 - S119
  • [10] Ganesh SK, 2001, J AM SOC NEPHROL, V12, P2131, DOI 10.1681/ASN.V12102131