Recurrence risk estimation of acute intermittent porphyria based on analysis of porphobilinogen deaminase activity: A Bayesian approach
- 30 November 1984
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 19 (4) , 755-762
- https://doi.org/10.1002/ajmg.1320190415
Abstract
Red cell porphobilnogen deaminase is known to be an indicator of the carrier state for acute intermittent porphyria (AIP). This enzyme was assayed in three groups of individuals at least 15 years old: 105 affected individuals or obligate carriers, 234 unaffected first-degree relatives of patients, and 217 unrelated control persons. Analysis of the distribution of the control enzyme activities suggested presence of three commingled distributions. Also, the overlap between carrier-group and control-group values must be taken into account for genetic counseling of relatives whose enzyme activity lies within the overlap. A Bayesian approach is proposed to derive risks for these individuals, using the observed carrier and control distributions. The method is illustrated by deriving risks for a family from our sample.Keywords
This publication has 10 references indexed in Scilit:
- Genetic regulation of the red cell uroporphyrinogen-l-synthetase level in families with acute intermittent porphyriaClinical Genetics, 2008
- Increased erythrocyte uroporphyrinogen-I-synthetase, δ-aminolevulinic acid dehydratase and protoporphyrin in hemolytic anemiasThe American Journal of Medicine, 1977
- Skewness in Commingled DistributionsBiometrics, 1976
- DETECTION OF INTERMITTENT ACUTE PORPHYRIA TRAIT IN CHILDRENThe Lancet, 1976
- The spectrophotometric determination of uroporphyrinogen i synthetase activityClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- A Red Cell Enzyme Method for the Diagnosis of Acute Intermittent PorphyriaBlood, 1974
- A Microassay for Uroporphyrinogen I Synthase, One of Three Abnormal Enzyme Activities in Acute Intermittent Porphyria, and its Application to the Study of the Genetics of this DiseaseProceedings of the National Academy of Sciences, 1974
- Decreased Red Cell Uroporphyrinogen I Synthetase Activity in Intermittent Acute PorphyriaJournal of Clinical Investigation, 1972
- Intermittent Acute Porphyria — Demonstration of a Genetic Defect in Porphobilinogen MetabolismNew England Journal of Medicine, 1972