-
Je něco špatně v tomto záznamu ?
Evaluating the contribution of the cause of kidney disease to prognosis in CKD: results from the Study of Heart and Renal Protection (SHARP)
R. Haynes, N. Staplin, J. Emberson, WG. Herrington, C. Tomson, L. Agodoa, V. Tesar, A. Levin, D. Lewis, C. Reith, C. Baigent, MJ. Landray, . ,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, pozorovací studie, práce podpořená grantem
- MeSH
- chronická renální insuficience komplikace diagnóza etiologie MeSH
- chronické selhání ledvin epidemiologie mortalita terapie MeSH
- cystická onemocnění ledvin komplikace patofyziologie MeSH
- diabetické nefropatie komplikace patofyziologie MeSH
- dialýza ledvin MeSH
- glomerulonefritida komplikace patofyziologie MeSH
- hodnoty glomerulární filtrace fyziologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- následné studie MeSH
- prognóza MeSH
- rizikové faktory MeSH
- senioři MeSH
- transplantace ledvin MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
BACKGROUND: The relevance of the cause of kidney disease to prognosis among patients with chronic kidney disease is uncertain. STUDY DESIGN: Observational study. SETTINGS & PARTICIPANTS: 6,245 nondialysis participants in the Study of Heart and Renal Protection (SHARP). PREDICTOR: Baseline cause of kidney disease was categorized into 4 groups: cystic kidney disease, diabetic nephropathy, glomerulonephritis, and other recorded diagnoses. OUTCOMES: End-stage renal disease (ESRD; dialysis or transplantation) and death. RESULTS: During an average 4.7 years' follow-up, 2,080 participants progressed to ESRD, including 454 with cystic kidney disease (23% per year), 378 with glomerulonephritis (10% per year), 309 with diabetic nephropathy (12% per year), and 939 with other recorded diagnoses (8% per year). By comparison with patients with cystic kidney disease, other disease groups had substantially lower adjusted risks of ESRD (relative risks of 0.28 [95% CI, 0.24-0.32], 0.40 [95% CI, 0.34-0.47], and 0.29 [95% CI, 0.25-0.32] for glomerulonephritis, diabetic nephropathy, and other recorded diagnoses, respectively). Albuminuria and baseline estimated glomerular filtration rate were associated more weakly with risk of ESRD in patients with cystic kidney disease than the 3 other diagnostic categories (P for interaction, <0.001 and 0.01, respectively). Death before ESRD was uncommon in patients with cystic kidney disease, but was a major competing risk for participants with diabetic nephropathy, whose adjusted risk of death was 2-fold higher than that of the cystic kidney disease group (relative risk, 2.35 [95% CI, 1.73-3.18]). LIMITATIONS: Exclusion of patients with prior myocardial infarction or coronary revascularization. CONCLUSIONS: The cause of kidney disease has substantial prognostic implications. Other things being equal, patients with cystic kidney disease are at much higher risk of ESRD (and much lower risk of death before ESRD) than other patients. Patients with diabetic nephropathy are at particularly high risk of death prior to reaching ESRD.
1st Faculty of Medicine and General University Hospital Charles University Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15008208
- 003
- CZ-PrNML
- 005
- 20150310115831.0
- 007
- ta
- 008
- 150306s2014 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1053/j.ajkd.2013.12.013 $2 doi
- 035 __
- $a (PubMed)24613056
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Haynes, Richard $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 245 10
- $a Evaluating the contribution of the cause of kidney disease to prognosis in CKD: results from the Study of Heart and Renal Protection (SHARP) / $c R. Haynes, N. Staplin, J. Emberson, WG. Herrington, C. Tomson, L. Agodoa, V. Tesar, A. Levin, D. Lewis, C. Reith, C. Baigent, MJ. Landray, . ,
- 520 9_
- $a BACKGROUND: The relevance of the cause of kidney disease to prognosis among patients with chronic kidney disease is uncertain. STUDY DESIGN: Observational study. SETTINGS & PARTICIPANTS: 6,245 nondialysis participants in the Study of Heart and Renal Protection (SHARP). PREDICTOR: Baseline cause of kidney disease was categorized into 4 groups: cystic kidney disease, diabetic nephropathy, glomerulonephritis, and other recorded diagnoses. OUTCOMES: End-stage renal disease (ESRD; dialysis or transplantation) and death. RESULTS: During an average 4.7 years' follow-up, 2,080 participants progressed to ESRD, including 454 with cystic kidney disease (23% per year), 378 with glomerulonephritis (10% per year), 309 with diabetic nephropathy (12% per year), and 939 with other recorded diagnoses (8% per year). By comparison with patients with cystic kidney disease, other disease groups had substantially lower adjusted risks of ESRD (relative risks of 0.28 [95% CI, 0.24-0.32], 0.40 [95% CI, 0.34-0.47], and 0.29 [95% CI, 0.25-0.32] for glomerulonephritis, diabetic nephropathy, and other recorded diagnoses, respectively). Albuminuria and baseline estimated glomerular filtration rate were associated more weakly with risk of ESRD in patients with cystic kidney disease than the 3 other diagnostic categories (P for interaction, <0.001 and 0.01, respectively). Death before ESRD was uncommon in patients with cystic kidney disease, but was a major competing risk for participants with diabetic nephropathy, whose adjusted risk of death was 2-fold higher than that of the cystic kidney disease group (relative risk, 2.35 [95% CI, 1.73-3.18]). LIMITATIONS: Exclusion of patients with prior myocardial infarction or coronary revascularization. CONCLUSIONS: The cause of kidney disease has substantial prognostic implications. Other things being equal, patients with cystic kidney disease are at much higher risk of ESRD (and much lower risk of death before ESRD) than other patients. Patients with diabetic nephropathy are at particularly high risk of death prior to reaching ESRD.
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a diabetické nefropatie $x komplikace $x patofyziologie $7 D003928
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a hodnoty glomerulární filtrace $x fyziologie $7 D005919
- 650 _2
- $a glomerulonefritida $x komplikace $x patofyziologie $7 D005921
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a cystická onemocnění ledvin $x komplikace $x patofyziologie $7 D052177
- 650 _2
- $a chronické selhání ledvin $x epidemiologie $x mortalita $x terapie $7 D007676
- 650 _2
- $a transplantace ledvin $7 D016030
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a dialýza ledvin $7 D006435
- 650 _2
- $a chronická renální insuficience $x komplikace $x diagnóza $x etiologie $7 D051436
- 650 _2
- $a rizikové faktory $7 D012307
- 650 _2
- $a míra přežití $7 D015996
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a pozorovací studie $7 D064888
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Staplin, Natalie $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Emberson, Jonathan $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Herrington, William G $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Tomson, Charles $u North Bristol NHS Trust, Bristol, United Kingdom.
- 700 1_
- $a Agodoa, Lawrence $u National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD. $7 gn_A_00002217
- 700 1_
- $a Tesar, Vladimir $u First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
- 700 1_
- $a Levin, Adeera $u University of British Columbia, Vancouver, BC, Canada.
- 700 1_
- $a Lewis, David $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Reith, Christina $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Baigent, Colin $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
- 700 1_
- $a Landray, Martin J $u Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom. Electronic address: sharpclinical@ctsu.ox.ac.uk.
- 700 1_
- $a ,
- 773 0_
- $w MED00000258 $t American journal of kidney diseases the official journal of the National Kidney Foundation $x 1523-6838 $g Roč. 64, č. 1 (2014), s. 40-8
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24613056 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150306 $b ABA008
- 991 __
- $a 20150310120108 $b ABA008
- 999 __
- $a ok $b bmc $g 1065481 $s 891008
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 64 $c 1 $d 40-8 $i 1523-6838 $m American journal of kidney diseases $n Am J Kidney Dis $x MED00000258
- LZP __
- $a Pubmed-20150306