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 inNephrology, dialysis, transplantation Vol. 22; no. 10; pp. 2909 - 2916
Main Authors Voormolen, Nora, Noordzij, Marlies, Grootendorst, Diana C., Beetz, Ivo, Sijpkens, Yvo W., van Manen, Jeannette G., Boeschoten, Elisabeth W., Huisman, Roel M., Krediet, Raymond T., Dekker, Friedo W.
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.10.2007
Oxford Publishing Limited (England)
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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.
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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Issue 10
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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PublicationTitle Nephrology, dialysis, transplantation
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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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