0 Evaluaciones
ID

46166

Descripción

Principal Investigator: Craig Wong, MD, MPH, University of New Mexico, Health Sciences Center and UNM Children's Hospital, Albuquerque, NM, USA MeSH: Kidney Diseases,Renal Insufficiency,Renal Insufficiency, Chronic https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000650 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 upload includes the genotype and baseline phenotype for the CKiD cohort. In brief the CKiD study is a prospective study of children with chronic kidney disease (CKD) between the ages of 1 year to 16 years of age and an estimated glomerular filtration rate (eGFR) by Schwartz equation between 30 and 75 ml/min per 1.73msup2/sup. Included in this upload are the phenotypic data for anemia traits utilized for the sub-study, "Role of Genetic Variation in the Anemia of Chronic Kidney Disease" (K24DK078737), with the RBC trait and anemia data pertaining to CKiD as well.

Link

dbGaP study=phs000650

Palabras clave

Versiones (2)
  1. 24/1/23 24/1/23 - Simon Heim
  2. 29/1/25 29/1/25 - Akane Nishihara
Titular de derechos de autor

Craig Wong, MD, MPH, University of New Mexico, Health Sciences Center and UNM Children's Hospital, Albuquerque, NM, USA

Subido en

29 de enero de 2025

DOI

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Licencia

Creative Commons BY 4.0
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    dbGaP phs000650 Genetic Factors Linked with Renal Progression (PediGFR) - CKiD

    Inglés

    Eligibility Criteria

    5 formularios  
    Inclusion and exclusion criteria
    Descripción

    Inclusion and exclusion criteria

    Alias
    UMLS CUI [1,1]
    C1512693
    UMLS CUI [1,2]
    C0680251
    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 are those who did not provide genetic consent, subject IDs whose genotyping did not pass quality control.
    Descripción

    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 are those who did not provide genetic consent, subject IDs whose genotyping did not pass quality control.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C3242136
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C1320549
    UMLS CUI [1,4]
    C0370003
    UMLS CUI [1,5]
    C0012854
    UMLS CUI [1,6]
    C4035953
    UMLS CUI [1,7]
    C0031437
    UMLS CUI [1,8]
    C0014792
    UMLS CUI [1,9]
    C0031437
    UMLS CUI [1,10]
    C0002871
    UMLS CUI [1,11]
    C0680251
    UMLS CUI [1,12]
    C2348585
    UMLS CUI [1,13]
    C1285573
    UMLS CUI [1,14]
    C0034378
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    Similar models

    Eligibility Criteria

    5 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Inclusion and exclusion criteria
    C1512693 (UMLS CUI [1,1])
    C0680251 (UMLS CUI [1,2])
    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 are those who did not provide genetic consent, subject IDs whose genotyping did not pass quality control.
    Item
    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 are those who did not provide genetic consent, subject IDs whose genotyping did not pass quality control.
    boolean
    C3242136 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C1320549 (UMLS CUI [1,3])
    C0370003 (UMLS CUI [1,4])
    C0012854 (UMLS CUI [1,5])
    C4035953 (UMLS CUI [1,6])
    C0031437 (UMLS CUI [1,7])
    C0014792 (UMLS CUI [1,8])
    C0031437 (UMLS CUI [1,9])
    C0002871 (UMLS CUI [1,10])
    C0680251 (UMLS CUI [1,11])
    C2348585 (UMLS CUI [1,12])
    C1285573 (UMLS CUI [1,13])
    C0034378 (UMLS CUI [1,14])
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