Literature DB >> 12911554

Renal structure in early autosomal-dominant polycystic kidney disease (ADPKD): The Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease (CRISP) cohort.

Arlene B Chapman1, Lisa M Guay-Woodford, Jared J Grantham, Vicente E Torres, Kyongtae T Bae, Deborah A Baumgarten, Philip J Kenney, Bernard F King, James F Glockner, Louis H Wetzel, Marijn E Brummer, W Charles O'Neill, Michelle L Robbin, William M Bennett, Saulo Klahr, Gladys H Hirschman, Paul L Kimmel, Paul A Thompson, J Philip Miller.   

Abstract

BACKGROUND: Autosomal-dominant polycystic kidney disease (ADPKD) is characterized by gradual renal enlargement and cyst growth prior to loss of renal function. Standard radiographic imaging has not provided the resolution and accuracy necessary to detect small changes in renal volume or to reliably measure renal cyst volumes. The Consortium for Radiologic Imaging Studies in Polycystic Kidney Disease (CRISP) is longitudinally observing ADPKD individuals using high-resolution magnetic resonance (MR) imaging to determine if change in renal and cyst volumes can be detected over a short period of time, and if they correlate with decline in renal function early in disease.
METHODS: Standardization studies were conducted in phantoms and four subjects at each participating clinical center. After, in the full-scale protocol, healthy ADPKD individuals 15 to 45 years old with creatinine clearance>70 mL/min underwent standardized MR renal imaging, renal iothalamate clearance, comprehensive clinical evaluation, and determination of 24-hour urinary albumin and electrolyte excretion. Stereology was used from T1-weighted images to quantify renal volume, and region-growing thresholding was used from T2-weighted images to determine cyst volume. Renal structures were evaluated in relation to demographic, clinical, and biochemical variables using means/medians, standard deviations, and Pearson correlations.
RESULTS: Reliability coefficients for MR renal and cyst volume measurements in phantoms were 99.9% and 89.2%, respectively. In the full-scale protocol, 241 ADPKD individuals (145 women and 96 men) were enrolled. Total renal, cyst, and % cyst volume were significantly greater in each decade group. Hypertensive individuals demonstrated greater renal, cyst, and % cyst volume than normotensive subjects. Age-adjusted renal (r = -0.31, P < 0.0001), cyst (r = -0.36, P < 0.0001), and % cyst volume (r = -0.35, P < 0.0001) were inversely related to glomerular filtration rate (GFR). Age-adjusted renal volume (r = 0.42, P < 0.0001), cystic (r = 0.39, P < 0.0001, and % cyst volume (r = 0.41, P < 0.0001) were related with urinary albumin excretion.
CONCLUSION: MR measures of renal and cyst volume are reliable and accurate in patients with ADPKD. ADPKD is characterized by significant cystic involvement that increases with age. Structure (renal and cyst volume) and function (GFR) are inversely related and directly related with the presence of hypertension and urinary albumin excretion in individuals with normal renal function.

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Year:  2003        PMID: 12911554     DOI: 10.1046/j.1523-1755.2003.00185.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  142 in total

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Authors:  Shobha Ratnam; Surya M Nauli
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Authors:  G Canaud; B Knebelmann; P C Harris; F Vrtovsnik; J-M Correas; N Pallet; C M Heyer; E Letavernier; F Bienaimé; E Thervet; F Martinez; F Terzi; C Legendre
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Authors:  William E Sweeney; Ellis D Avner
Journal:  Pediatr Nephrol       Date:  2010-10-29       Impact factor: 3.714

5.  The association of serum angiogenic growth factors with renal structure and function in patients with adult autosomal dominant polycystic kidney disease.

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Journal:  Int Urol Nephrol       Date:  2018-04-13       Impact factor: 2.370

6.  Development and validation of GFR-estimating equations using diabetes, transplant and weight.

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Journal:  Nephrol Dial Transplant       Date:  2009-09-30       Impact factor: 5.992

7.  3DUS as an alternative to MRI for measuring renal volume in children with autosomal dominant polycystic kidney disease.

Authors:  Luc Breysem; Stéphanie De Rechter; Frederik De Keyzer; Maria Helena Smet; Bert Bammens; Maria Van Dyck; Maarten Hofmans; Raymond Oyen; Elena Levtchenko; Djalila Mekahli
Journal:  Pediatr Nephrol       Date:  2018-01-06       Impact factor: 3.714

8.  Validation of a Metabolite Panel for a More Accurate Estimation of Glomerular Filtration Rate Using Quantitative LC-MS/MS.

Authors:  Tiffany A Freed; Josef Coresh; Lesley A Inker; Douglas R Toal; Regis Perichon; Jingsha Chen; Kelli D Goodman; Qibo Zhang; Jessie K Conner; Deirdre M Hauser; Kate E T Vroom; Maria L Oyaski; Jacob E Wulff; Gudný Eiríksdóttir; Vilmundur Gudnason; Vicente E Torres; Lisa A Ford; Andrew S Levey
Journal:  Clin Chem       Date:  2019-01-15       Impact factor: 8.327

9.  Effect of pioglitazone on survival and renal function in a mouse model of polycystic kidney disease.

Authors:  K L Raphael; K A Strait; P K Stricklett; B C Baird; K Piontek; G G Germino; D E Kohan
Journal:  Am J Nephrol       Date:  2009-09-24       Impact factor: 3.754

10.  Segmentation of individual renal cysts from MR images in patients with autosomal dominant polycystic kidney disease.

Authors:  Kyungsoo Bae; Bumwoo Park; Hongliang Sun; Jinhong Wang; Cheng Tao; Arlene B Chapman; Vicente E Torres; Jared J Grantham; Michal Mrug; William M Bennett; Michael F Flessner; Doug P Landsittel; Kyongtae T Bae
Journal:  Clin J Am Soc Nephrol       Date:  2013-03-21       Impact factor: 8.237

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