High plasma phosphate as a risk factor for decline in renal function and mortality in pre-dialysis patients
Background. Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study...
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Published in | Nephrology, dialysis, transplantation Vol. 22; no. 10; pp. 2909 - 2916 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Oxford University Press
01.10.2007
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
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Abstract | Background. Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study was to determine the association of plasma phosphate with renal function loss and mortality in CKD stage IV–V pre-dialysis patients with GFR <20 ml/min/1.73 m2. Methods. Incident pre-dialysis patients were included between 1999 and 2001 in the multi-centre PREPARE study, and followed until 2003 or death. Rate of decline in renal function for each patient was calculated by linear regression using the Modification of Diet in Renal Disease (MDRD) formula to estimate GFR (eGFR). Results. A total of 448 patients were included [mean (SD) age 60 (15) years, eGFR 13 (5.4) ml/min/1.73 m2, decline in renal function 0.38 (0.95) ml/min/month]. Phosphate concentration at baseline was 4.71 (1.16) mg/dl, calcium 9.25 (0.77) mg/dl and calcium–phosphate product 43.5 (10.9) mg2/dl2. For each mg/dl higher phosphate concentration, the mean (95% CI) decline in renal function increased with 0.154 (0.071–0.237) ml/min/month. After adjustment, this association remained [β 0.178 (0.082–0.275)]. Seven percent of the patients died. Crude mortality risk was 1.25 (0.85–1.84) per mg/dl increase in phosphate, which increased to 1.62 (1.02–2.59) after adjustment. Conclusions. High plasma phosphate is an independent risk factor for a more rapid decline in renal function and a higher mortality during the pre-dialysis phase. Plasma phosphate within the normal range is likely of vital importance in pre-dialysis patients. |
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AbstractList | Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study was to determine the association of plasma phosphate with renal function loss and mortality in CKD stage IV-V pre-dialysis patients with GFR <20 ml/min/1.73 m(2).
Incident pre-dialysis patients were included between 1999 and 2001 in the multi-centre PREPARE study, and followed until 2003 or death. Rate of decline in renal function for each patient was calculated by linear regression using the Modification of Diet in Renal Disease (MDRD) formula to estimate GFR (eGFR).
A total of 448 patients were included [mean (SD) age 60 (15) years, eGFR 13 (5.4) ml/min/1.73 m(2), decline in renal function 0.38 (0.95) ml/min/month]. Phosphate concentration at baseline was 4.71 (1.16) mg/dl, calcium 9.25 (0.77) mg/dl and calcium-phosphate product 43.5 (10.9) mg(2)/dl(2). For each mg/dl higher phosphate concentration, the mean (95% CI) decline in renal function increased with 0.154 (0.071-0.237) ml/min/month. After adjustment, this association remained [beta 0.178 (0.082-0.275)]. Seven percent of the patients died. Crude mortality risk was 1.25 (0.85-1.84) per mg/dl increase in phosphate, which increased to 1.62 (1.02-2.59) after adjustment.
High plasma phosphate is an independent risk factor for a more rapid decline in renal function and a higher mortality during the pre-dialysis phase. Plasma phosphate within the normal range is likely of vital importance in pre-dialysis patients. BACKGROUNDHyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study was to determine the association of plasma phosphate with renal function loss and mortality in CKD stage IV-V pre-dialysis patients with GFR <20 ml/min/1.73 m(2).METHODSIncident pre-dialysis patients were included between 1999 and 2001 in the multi-centre PREPARE study, and followed until 2003 or death. Rate of decline in renal function for each patient was calculated by linear regression using the Modification of Diet in Renal Disease (MDRD) formula to estimate GFR (eGFR).RESULTSA total of 448 patients were included [mean (SD) age 60 (15) years, eGFR 13 (5.4) ml/min/1.73 m(2), decline in renal function 0.38 (0.95) ml/min/month]. Phosphate concentration at baseline was 4.71 (1.16) mg/dl, calcium 9.25 (0.77) mg/dl and calcium-phosphate product 43.5 (10.9) mg(2)/dl(2). For each mg/dl higher phosphate concentration, the mean (95% CI) decline in renal function increased with 0.154 (0.071-0.237) ml/min/month. After adjustment, this association remained [beta 0.178 (0.082-0.275)]. Seven percent of the patients died. Crude mortality risk was 1.25 (0.85-1.84) per mg/dl increase in phosphate, which increased to 1.62 (1.02-2.59) after adjustment.CONCLUSIONSHigh plasma phosphate is an independent risk factor for a more rapid decline in renal function and a higher mortality during the pre-dialysis phase. Plasma phosphate within the normal range is likely of vital importance in pre-dialysis patients. Background. Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study was to determine the association of plasma phosphate with renal function loss and mortality in CKD stage IV–V pre-dialysis patients with GFR <20 ml/min/1.73 m2. Methods. Incident pre-dialysis patients were included between 1999 and 2001 in the multi-centre PREPARE study, and followed until 2003 or death. Rate of decline in renal function for each patient was calculated by linear regression using the Modification of Diet in Renal Disease (MDRD) formula to estimate GFR (eGFR). Results. A total of 448 patients were included [mean (SD) age 60 (15) years, eGFR 13 (5.4) ml/min/1.73 m2, decline in renal function 0.38 (0.95) ml/min/month]. Phosphate concentration at baseline was 4.71 (1.16) mg/dl, calcium 9.25 (0.77) mg/dl and calcium–phosphate product 43.5 (10.9) mg2/dl2. For each mg/dl higher phosphate concentration, the mean (95% CI) decline in renal function increased with 0.154 (0.071–0.237) ml/min/month. After adjustment, this association remained [β 0.178 (0.082–0.275)]. Seven percent of the patients died. Crude mortality risk was 1.25 (0.85–1.84) per mg/dl increase in phosphate, which increased to 1.62 (1.02–2.59) after adjustment. Conclusions. High plasma phosphate is an independent risk factor for a more rapid decline in renal function and a higher mortality during the pre-dialysis phase. Plasma phosphate within the normal range is likely of vital importance in pre-dialysis patients. Background. Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal studies, elevated plasma phosphate has been shown to be associated with an accelerated decline in renal function. The aim of this study was to determine the association of plasma phosphate with renal function loss and mortality in CKD stage IV-V pre-dialysis patients with GFR <20 ml/min/1.73 m2. Methods. Incident pre-dialysis patients were included between 1999 and 2001 in the multi-centre PREPARE study, and followed until 2003 or death. Rate of decline in renal function for each patient was calculated by linear regression using the Modification of Diet in Renal Disease (MDRD) formula to estimate GFR (eGFR). Results. A total of 448 patients were included [mean (SD) age 60 (15) years, eGFR 13 (5.4) ml/min/1.73 m2, decline in renal function 0.38 (0.95) ml/min/month]. Phosphate concentration at baseline was 4.71 (1.16) mg/dl, calcium 9.25 (0.77) mg/dl and calcium-phosphate product 43.5 (10.9) mg2/dl2. For each mg/dl higher phosphate concentration, the mean (95% CI) decline in renal function increased with 0.154 (0.071-0.237) ml/min/month. After adjustment, this association remained [β 0.178 (0.082-0.275)]. Seven percent of the patients died. Crude mortality risk was 1.25 (0.85-1.84) per mg/dl increase in phosphate, which increased to 1.62 (1.02-2.59) after adjustment. Conclusions. High plasma phosphate is an independent risk factor for a more rapid decline in renal function and a higher mortality during the pre-dialysis phase. Plasma phosphate within the normal range is likely of vital importance in pre-dialysis patients. |
Author | Sijpkens, Yvo W. Krediet, Raymond T. Boeschoten, Elisabeth W. Dekker, Friedo W. Beetz, Ivo Noordzij, Marlies Grootendorst, Diana C. van Manen, Jeannette G. Huisman, Roel M. Voormolen, Nora |
Author_xml | – sequence: 1 givenname: Nora surname: Voormolen fullname: Voormolen, Nora organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 2 givenname: Marlies surname: Noordzij fullname: Noordzij, Marlies organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 3 givenname: Diana C. surname: Grootendorst fullname: Grootendorst, Diana C. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 4 givenname: Ivo surname: Beetz fullname: Beetz, Ivo organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 5 givenname: Yvo W. surname: Sijpkens fullname: Sijpkens, Yvo W. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 6 givenname: Jeannette G. surname: van Manen fullname: van Manen, Jeannette G. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 7 givenname: Elisabeth W. surname: Boeschoten fullname: Boeschoten, Elisabeth W. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 8 givenname: Roel M. surname: Huisman fullname: Huisman, Roel M. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 9 givenname: Raymond T. surname: Krediet fullname: Krediet, Raymond T. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands – sequence: 10 givenname: Friedo W. surname: Dekker fullname: Dekker, Friedo W. organization: Department of Clinical Epidemiology, Leiden University Medical Center, 2Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam, 3Department of Nephrology, Leiden University Medical Center, Leiden, 4Hans Mak Institute, Naarden, 5Department of Nephrology, University Medical Center Groningen, Groningen, 6Department of Nephrology, Academic Medical Center, Amsterdam and 7the PREPARE study group consists of: P. Gerlag, Maxima Medical Centre, Veldhoven; C.J. Doorenbos, Deventer Ziekenhuizen, Deventer; K. Jie, Groene Hart Hospital, Gouda; A. Schrander-van der Meer, Rijnland Ziekenhuis, Leiderdorp; C. Verburgh, Kennemer Gasthuis, Haarlem, The Netherlands |
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Keywords | decline: mortality renal function serum phosphate CKD Kidney disease Human Phosphates Urinary system disease Renal function Hemodialysis Mortality Extrarenal dialysis Risk factor Renal failure Dialysis |
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Snippet | Background. Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in... Hyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in animal... BACKGROUNDHyperphosphataemia is associated with increased mortality in patients with chronic kidney disease (CKD) stage IV or on dialysis. Furthermore, in... |
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SubjectTerms | Aged Algorithms Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences CKD decline: mortality Emergency and intensive care: renal failure. Dialysis management Female Glomerular Filtration Rate Humans Hyperphosphatemia - complications Hyperphosphatemia - diagnosis Intensive care medicine Kidney - metabolism Kidney - pathology Kidney Failure, Chronic - complications Kidney Failure, Chronic - metabolism Kidney Failure, Chronic - mortality Male Medical sciences Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Phosphates - blood Regression Analysis Renal Dialysis - methods Renal failure renal function Risk Factors serum phosphate Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Treatment Outcome |
Title | High plasma phosphate as a risk factor for decline in renal function and mortality in pre-dialysis patients |
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