Comparison of methods for determining renal function decline in early autosomal dominant polycystic kidney disease: the consortium of radiologic imaging studies of polycystic kidney disease cohort
- PMID: 16452494
- DOI: 10.1681/ASN.2005070697
Comparison of methods for determining renal function decline in early autosomal dominant polycystic kidney disease: the consortium of radiologic imaging studies of polycystic kidney disease cohort
Abstract
A decline in renal function suggests progression of chronic kidney disease. This can be determined by measured GFR (e.g., iothalamate clearance), serum creatinine (SCr)-based GFR estimates, or creatinine clearance. A cohort of 234 patients with autosomal dominant polycystic kidney disease and baseline creatinine clearance>70 ml/min were followed annually for four visits. Iothalamate clearance, SCr, and creatinine clearance were obtained at each visit. Estimated GFR (eGFR) was determined with the Modification of Diet in Renal Disease (MDRD) and Cockcroft-Gault equations. Renal function slopes had a mean residual SD of 10.7% by iothalamate clearance, 8.2% by MDRD equation, 7.7% by Cockcroft-Gault equation, and 14.8% by creatinine clearance. By each method, a decline in renal function (lowest quintile slope) was compared among baseline predictors. Hypertension was associated with a decline in iothalamate clearance (odds ratio [OR] 5.8; 95% confidence interval [CI] 2.3 to 14), eGFR (OR [MDRD] 2.0 [95% CI 1.0 to 4.2] or OR [Cockcroft-Gault] 1.9 [95% CI 0.9 to 3.9]), and creatinine clearance (OR 2.0; 95% CI 1.0 to 4.2). Each doubling of kidney volume at baseline was associated with a decline in iothalamate clearance (OR 2.4; 95% CI 1.5 to 3.7), eGFR (OR 1.7 [95% CI 1.1 to 2.6] or 2.1 [95% CI 1.4 to 3.3]), and creatinine clearance (OR 1.7; 95% CI 1.1 to 2.5). Predictor associations were strongest with measured GFR. Misclassification from changes in non-GFR factors (e.g., creatinine production, tubular secretion) conservatively biased associations with eGFR. Misclassification from method imprecision attenuated associations with creatinine clearance.
Similar articles
-
Are prediction equations for glomerular filtration rate useful for the long-term monitoring of type 2 diabetic patients?Nephrol Dial Transplant. 2006 Aug;21(8):2152-8. doi: 10.1093/ndt/gfl221. Epub 2006 May 15. Nephrol Dial Transplant. 2006. PMID: 16702203
-
Magnetic resonance measurements of renal blood flow and disease progression in autosomal dominant polycystic kidney disease.Clin J Am Soc Nephrol. 2007 Jan;2(1):112-20. doi: 10.2215/CJN.00910306. Epub 2006 Nov 2. Clin J Am Soc Nephrol. 2007. PMID: 17699395
-
Monitoring kidney function in type 2 diabetic patients with incipient and overt diabetic nephropathy.Diabetes Care. 2006 May;29(5):1024-30. doi: 10.2337/diacare.2951024. Diabetes Care. 2006. PMID: 16644632
-
Monitoring renal function and limitations of renal function tests.Semin Nucl Med. 2008 Jan;38(1):32-46. doi: 10.1053/j.semnuclmed.2007.09.003. Semin Nucl Med. 2008. PMID: 18096462 Review.
-
Evaluation of glomerular filtration rate and of albuminuria/proteinuria.J Nephrol. 2010 Mar-Apr;23(2):125-32. J Nephrol. 2010. PMID: 20213606 Review.
Cited by
-
Performance of glomerular filtration rate estimating equations in a community-based sample of Blacks and Whites: the multiethnic study of atherosclerosis.Nephrol Dial Transplant. 2018 Mar 1;33(3):417-425. doi: 10.1093/ndt/gfx042. Nephrol Dial Transplant. 2018. PMID: 28505377 Free PMC article.
-
Comparison of high glomerular filtration rate thresholds for identifying hyperfiltration.Nephrol Dial Transplant. 2020 Jun 1;35(6):1017-1026. doi: 10.1093/ndt/gfy332. Nephrol Dial Transplant. 2020. PMID: 30403810 Free PMC article.
-
Low-dose rapamycin (sirolimus) effects in autosomal dominant polycystic kidney disease: an open-label randomized controlled pilot study.Clin J Am Soc Nephrol. 2014 May;9(5):881-8. doi: 10.2215/CJN.02650313. Epub 2014 Apr 10. Clin J Am Soc Nephrol. 2014. PMID: 24721888 Free PMC article. Clinical Trial.
-
Interventions for preventing the progression of autosomal dominant polycystic kidney disease.Cochrane Database Syst Rev. 2024 Oct 2;10(10):CD010294. doi: 10.1002/14651858.CD010294.pub3. Cochrane Database Syst Rev. 2024. PMID: 39356039
-
Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume.Braz J Med Biol Res. 2014 Jul;47(7):584-93. doi: 10.1590/1414-431x20143584. Epub 2014 Jun 13. Braz J Med Biol Res. 2014. PMID: 24919173 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous