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Summary

at San Francisco, California and other locations
study started
estimated completion:
D. Montgomery Bissell

Description

Summary

The objective of this protocol is to conduct a longitudinal multidisciplinary investigation of the human porphyrias including the natural history, morbidity, pregnancy outcomes, and mortality in people with these disorders.

Details

The porphyrias are a group of rare metabolic diseases that may present in childhood or adult life and are due to deficiencies of enzymes in the heme biosynthetic pathway. The most common manifestations are related to accumulation of intermediates in the pathway and usually occur as acute neurological attacks, or cutaneous photosensitivity. Multiple mutations have been identified in each of the porphyrias. The risk of disability or death from these disorders is significant, in part because diagnosis is often delayed due to lack of adoption of diagnostic testing in clinical practice. Moreover, the natural history of these disorders is not well described and it is not known what determines differences in outcomes. New therapies are needed. For existing therapies, high-quality evidence on short and long term efficacy and safety is generally lacking. Therefore, the purpose of this long-term follow-up study of a large group of patients with the various porphyrias is to provide a better understanding of the natural history of these disorders, as affected by available therapies, and to aid in developing new forms of treatment.

The Office of Rare Diseases (ORD) of the National Institutes of Health (NIH) established a Rare Diseases Clinical Research Network (RDCRN) in collaboration with other NIH Institutes and currently has funded 19 rare diseases clinical research consortia and one Data Management and Coordinating Center. The Porphyrias Consortium was created as part of the RDCRN, to study the human porphyrias. The Porphyrias Consortium is a consortium of the academic institutions listed in the participating institutions table. All Centers in the Porphyrias Consortium are participating in the Longitudinal Study of the Porphyrias. Additional centers may be added if funding is available.

The initial objective of this protocol is to assemble a well-documented group of patients with confirmed diagnoses of specific porphyrias for clinical, biochemical, and genetic studies. The long-term objective is to conduct a longitudinal investigation of the natural history, complications, and therapeutic outcomes in people with acute and cutaneous porphyria.

Keywords

Acute Porphyrias Cutaneous Porphyrias porphyria acute intermittent coproporphyria variegate erythropoietic protoporphyria hepatoerythropoietic cutanea tarda AIP HCP VP ADP ALAD PCT HEP CEP EPP XLP

Eligibility

You can join if…

  • Individuals with a documented diagnosis of a porphyria.
  • For each type of porphyria, the inclusion criteria are based on
  • clinical features;
  • biochemical findings, as documented by laboratory reports (or copies) of porphyria-specific testing performed after 1980 (Absolute values are preferred for diagnostic biochemical thresholds. Fold increases in comparison to an upper(or lower) limit of normal (ULN or LLN) are also acceptable, but are complicated by considerable variation between laboratories in normal limits. Equivocal biochemical measurements may require confirmation by a consortium reference laboratory;)
  • molecular findings documenting the identification of a mutation in a porphyria-related gene.
  • In addition, an individual or a parent or guardian must be willing to give written informed consent or assent, as appropriate.
  • Provision is made for enrolling relatives who may not have symptoms but have biochemical or molecular documentation of a porphyria, or in the case of recessive disorders carry a disease-related mutation.

You CAN'T join if...

  • Cases with elevations of porphyrins in urine, plasma or erythrocytes due to other diseases (i.e. secondary porphyrinuria or porphyrinemia), such as liver and bone marrow diseases;
  • Patients with a prior diagnosis of porphyria that cannot be documented by review of existing medical records or repeat biochemical or DNA testing.

Locations

  • University of Utah accepting new patients
    Salt Lake City, Utah, 84132, United States
  • University of Washington accepting new patients
    Seattle, Washington, 98195, United States
  • University of Texas Medical Branch accepting new patients
    Galveston, Texas, 77555, United States
  • University of Alabama, Birmingham accepting new patients
    Birmingham, Alabama, 35294, United States
  • Cleveland Clinic terminated
    Cleveland, Ohio, 44195, United States
  • Carolinas Medical Center and HealthCare System terminated
    Charlotte, North Carolina, 28203, United States
  • Wake Forest University Health Sciences accepting new patients
    Winston-Salem, North Carolina, 27106, United States
  • University of Miami accepting new patients
    Miami, Florida, 33136, United States
  • Icahn School of Medicine at Mount Sinai accepting new patients
    New York, New York, 10029, United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Icahn School of Medicine at Mount Sinai
Links
Website for the Rare Diseases Clinical Research Network (RDCRN) Porphyrias Consortium (PC)
ID
NCT01561157
Lead Scientist
D. Montgomery Bissell
Study Type
Observational
Last Updated
August 1, 2017
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