Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010;100 Suppl 1(Suppl 1):S97-105.
doi: 10.1016/j.ymgme.2010.01.014. Epub 2010 Feb 10.

Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium

Affiliations
Review

Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium

Jennifer Seminara et al. Mol Genet Metab. 2010.

Abstract

The Urea Cycle Disorders Consortium (UCDC) was created as part of a larger network established by the National Institutes of Health to study rare diseases. This paper reviews the UCDC's accomplishments over the first 6years, including how the Consortium was developed and organized, clinical research studies initiated, and the importance of creating partnerships with patient advocacy groups, philanthropic foundations and biotech and pharmaceutical companies.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest statement

None of the authors on this article have any relevant financial relationships with commercial interests.

Figures

Figure 1
Figure 1. The Urea Cycle Disorders Consortium (UCDC) within the context of the Rare Diseases Clinical Research Network (RDCRN)
DSMB-data safety and monitoring board; PRC-protocol review committee; CPAG-patient advocacy group; NUCDF-National Urea Cycle Disorders Foundation; DMCC-data monitoring and coordinating center.
Figure 2
Figure 2. UCDC Geographical Coverage
CHB-Children’s Hospital, Boston; YSM-Yale School of Medicine; MSSM-Mt Sinai School of Medicine; CHOP-Children’s Hospital of Philadelphia; CNMC-Children’s National Medical Center; VUMC-Vanderbilt University Medical Center; CWRU-Case Western Reserve University; UMN-University of Minnesota; TCH-The Children’s Hospital; BCM - Baylor College of Medicine; UCLA-University of California, Los Angeles; OHSU-Oregon Health Sciences University; UW-University of Washington (Seattle Children’s Hospital); HSC-Hospital for Sick Children, Toronto; UZH-University of Zurich Kinderspital
Figure 3
Figure 3
Organizational Structure of the Urea Cycle Disorders Consortium
Figure 4
Figure 4
The Urea Cycle
Figure 5
Figure 5
Actual Accrual vs. Expected Accrual per Longitudinal Study. Data current as of July 31, 2009. Target Enrollment to Date: 294; Enrolled to Date: 352
Figure 6
Figure 6
Hyperammonemic Episode Triggers (n=1084 episodes). Data current as of July 31, 2009
Figure 7
Figure 7
Self-reported developmental disabilities and psychiatric disorders in enrolled participants. Data current as of July 31, 2009
Figure 8
Figure 8
IQ of Adult Participants (17+) Experiencing Hyperammonemic (HA) Episodes vs. No Hyperammonemic Episodes (FSIQ – Full Scale IQ; VIQ – Verbal IQ; PIQ – Performance IQ)
Figure 9
Figure 9. Cognitive Range Across All Subjects Ages 3–16: Early vs. Late Onset and by Diagnosis*
*Includes estimated IQ scores for children unable to complete testing in their age range. Excludes lowest functioning children who were unable to complete the test battery in their age range.
Figure 10
Figure 10
Possible Age Effects on IQ

References

    1. Richesson RL, Young K, Lloyd J, Adams T, Guillette H, Malloy J, Krischer JP. An Automated Communication System in a Contact Registry for Persons with Rare Diseases: Tools for Retaining Potential Clinical Research Participants. AMIA Annu Symp Proc. 2007 Oct 11;:1094. - PubMed
    1. Brusilow S, Maestri NE. Urea cycle disorders: diagnosis, pathophysiology, therapy. In: Barness LA, DeVivo DC, Kaback MM, Morrow G, Oski FA, Rudolph AM, editors. Advances in Pediatrics. Vol. 43. Chicago: Mosby; 1996. p. 127. - PubMed
    1. Nagata N, Matsuda I, Oyanagi K. Estimated frequency of urea cycle enzymopathies in Japan. Am J Med Genet. 1991;39(2):228–229. - PubMed
    1. Tuchman M, Lee B, Lichter-Konecki U, Summar ML, Yudkoff M, Cederbaum SD, Kerr DS, Diaz GA, Seashore MR, Lee HS, McCarter RJ, Krischer JP, Batshaw ML the Urea Cycle Disorders Consortium of the Rare Diseases Clinical Research Network. Cross-sectional Multicenter Study of Patients with Urea Cycle Disorders in the United States. Mol Genet Metab Aug. 2008;94(4):397–402. - PMC - PubMed
    1. Krivitzky L, Babikian T, Lee HS, Thomas NH, Burk-Paull KL, Batshaw ML. Intellectual, Adaptive, and Behavioral Functioning in Children with Urea Cycle Disorders. Pediatr Res Jul. 2009;66(1):96–101. - PMC - PubMed

Publication types