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Study Description

The Pediatric Investigation for Genetic Factors Associated with Renal Progression (PediGFR) (RO1-DK082394) is an international collaborative study among three large prospective cohort studies of children with chronic kidney disease. The participating parent cohort studies are the "Chronic Kidney Disease in Children (CKiD)", the "Effect of Strict Blood Pressure Control and ACE Inhibition on CRF Progression in Pediatric Patients (ESCAPE)", and the "Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C)" study. In these cohorts, pediatric subjects with CKD have been prospectively followed with standardized measurements for renal progression.

The current version of the dbGaP data upload includes the genotype and baseline phenotype for the ESCAPE Trial cohort. In brief, the ESCAPE Trial is a prospective study on the effect of strict blood pressure control and ACE inhibition in children with chronic kidney disease (CKD) between the ages of 3 to 18 years of age and an estimated glomerular filtration rate (eGFR) by Schwartz equation between 15 and 75 ml/min per 1.73m2.

Authorized Access
Publicly Available Data
  Link to other NCBI resources related to this study
Study Inclusion/Exclusion Criteria

Inclusion Criteria:

  • Age 3-18 years
  • Moderate state of renal failure (creatinine clearance 15 - 75 ml / min / 1.73 m2)
  • Mean arterial blood pressure (ABPM) > 50.percentile and/or antihypertensive treatment
  • Written informed consent

Exclusion Criteria:

  • Unstable clinical condition (vomiting, anorexia, etc) or superimposed important disease
  • Unilateral or bilateral renal artery stenosis
  • Urological surgery possibly affecting renal function expected during study period
  • Insufficient compliance with prescribed antihypertensive medication during the run-in period
  • Secondary renal diseases such as lupus, amyloidosis and primary hyperoxaluria, and patients treated with immunosuppressive agents (including corticosteroids)
  • Severe primary cardiac disease, hepatic insufficiency and malabsorption syndrome
  • Erythropoietin or growth hormone therapy with a duration of less than 3 months prior to run-in period
  • Pregnancy

The PediGFR utilized de-identified data from subjects who had consented for genetic testing, provided a sample of DNA, and who had data available for the renal trait phenotype as well and RBC trait and anemia phenotype. Exclusions from the total ESCAPE Trial cohort are those who did not provide genetic consent or subjects IDs whose genotyping did not pass quality control.

Molecular Data
TypeSourcePlatformNumber of Oligos/SNPsSNP Batch IdComment
Whole Genome Genotyping Illumina HumanOmni2.5-Quad N/A N/A
Study History

The PediGFR study is an international collaborative study designed to determine the gene loci associated with renal progression in children. Genotyping of the US-based CKiD cohort occurred prior to the genotyping of the European cohorts (ESCAPE and 4C). The genotyping and phenotyping data for CKiD cohort have been released by dbGap as the first wave of PediGFR data, which also include the anemia data of an ancillary study (K24DK078737) under PI Susan Furth: "The Role of Genetic Variation in the Anemia of Chronic Kidney Disease", that utilized the genotyping data of CKiD. Subsequent dbGaP upload will include the anemia data for the ESCAPE trial.

Selected Publications
Diseases/Traits Related to Study (MeSH terms)
Authorized Data Access Requests
Study Attribution
  • Principal Investigators
    • Craig Wong, MD, MPH. University of New Mexico Health Sciences Center and UNM Children's Hospital.
    • Franz Schaefer, MD. Center for Pediatrics and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany.
  • Funding Source
    • R01DKO82394. National Institutes of Health, Bethesda, MD, USA.