Clinical Diagnosis of Acute Porphyria
Purpose
The purpose of this study is to test whether a focused questionnaire and laboratory tests can better define risk factors associated with possible genetic porphyria. The investigators hypothesize that the genetic carrier state of acute porphyria is distinctive enough that the Genetic Carrier Profile the investigators devise through this study will be useful in identifying carriers of genetic porphyria among the large population with undiagnosed abdominal pain.
Conditions
- Hereditary Coproporphyria (HCP)
- Acute Intermittent Porphyria (AIP)
- Variegate Porphyria (VP)
Eligibility
- Eligible Ages
- Over 15 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Be 15 years of age or older - Be a first-degree relative (child, sibling, parent, or grandparent) of an individual with genetically proven acute porphyria (AIP, HCP or VP) - Not have had any previous genetic testing for acute porphyria Group 2 Inclusion Criteria: - Be 15 years of age or older - Have a history of suggestive clinical features, such as abdominal, back or limb pain, recurrent nausea lasting days, reaction to medications, psychiatric history, or sun sensitivity. - An increase in urinary, fecal or serum porphobilinogen (PBG) and/or porphyrins Groups 1 and 2
Exclusion Criteria
- Have previously had genetic testing for acute porphyria - Have a history of "alarm" symptoms, such as anemia, unintentional weight loss, signs of GI (gastrointestinal) bleeding, or dysphagia (difficulty in swallowing). Follow Up Sub-Study (Group 3) Inclusion Criteria: - Have been seen by one of the Porphyria Consortium physicians/investigators 10 or more years prior to study initiation - Had a slight increase in porphyrins during the initial visit - Not given a diagnosis of porphyria at the time of the visit Follow Up Sub-Study (Group 3) Exclusion Criteria: - You have been seen by the Porphyria Consortium physician/investigator less than 10 years prior to study initiation.
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Group 1 | Group 1 will include subjects 15 years of age or older who are a first-degree relative (child, sibling, parent, or grandparent) of an individual with genetically proven acute porphyria (AIP, HCP or VP), and have not had any previous genetic testing for porphyria themselves. | |
| Group 2 (Not Yet Enrolling) | Group 2 will consist of subjects 15 years of age or older who have a history of clinical features suggestive of acute porphyria, such as such as abdominal, back or limb pain, recurrent nausea lasting days, reaction to medications, psychiatric history, or sun sensitivity, and an increase in urinary, fecal or serum porphobilinogen (PBG) and/or porphyrins. | |
| Group 3 | Subjects in Group 3 will participate in the "Follow Up Sub-Study." This group will include individuals who have been seen by one of the Porphyria Consortium physicians/investigators for suspicion of porphyria 10 or more years prior to study initiation, but were not given a diagnosis of porphyria at the time of their initial visit. |
More Details
- Status
- Completed
- Sponsor
- University of California, San Francisco
Study Contact
Detailed Description
The porphyrias are a group of genetic diseases caused by disturbances in the formation of heme, an essential component of hemoglobin and other proteins, leading to either acute (neurologic) and/or chronic (cutaneous) symptoms. Acute porphyria is often difficult to diagnose because symptoms may not be specific and, unless the patient is in an active attack, laboratory values typically may not be useful for diagnosing porphyria. The purpose of this study is to test whether a focused questionnaire and laboratory evaluation tool can better define risk factors associated with possible genetic porphyria. The goals of this study are: - To determine the presence and number of abnormal lab tests and porphyria-like symptoms in adult family members of the first person in a family who has been diagnosed with a disease of acute porphyria, 50% of whom are expected to carry the same genetic defect of the index case. - To devise a Genetic Carrie Profile that could be used to screen people in whom the diagnosis of porphyria is being considered. - To test the Profile in patients with symptoms suggestive of HCP and/or urine tests showing some elevation of porphyrins. - To explain other possible causes of minor increases in porphyrin levels in patients with recurrent abdominal pain who have not been diagnosed with porphyria