» Articles » PMID: 3225821

A Simple Method for Calculating Risks Before DNA Analysis

Overview
Journal J Med Genet
Specialty Genetics
Date 1988 Oct 1
PMID 3225821
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Calculation of carrier risk of an X linked disease may be performed on a small computer after DNA analysis, but a method for rapid hand estimation of the risk is still useful for a quick check of the results and weighing the relative importance of each element of information, such as the determination of a haplotype. Each risk estimation is a function of a prior risk and the product of likelihood ratios and these terms are derived themselves from parameters such as fitness or the relative mutation rate in male and female gametes. Even if it is often difficult to have strong experimental estimation of these variables, the existence of a normal father or grandfather must be considered whenever male fitness is not null. The likelihood ratio for a woman for not being a carrier, when her father is not affected and her mother has herself a likelihood R for not having the mutated gene, may be expressed as the ratio 2R/(CmR + 1), with Cm being a function of male fitness and relative mutation rate. Cm represents the odds ratio for the mother of a carrier not to be a carrier, given that the father of the known carrier is not affected. This formula can be used recurrently and reduces to 2R/(R + 1) in lethal X linked disease. When likelihood ratios are expressed as an algebraic function, maximum values are easily determined, hence fixing the limits of DNA analysis.

Citing Articles

Germinal mosaicism and risk calculation in X-linked diseases.

Jeanpierre M Am J Hum Genet. 1992; 50(5):960-7.

PMID: 1570845 PMC: 1682604.

References
1.
EMERY A . Carrier detection in sex-linked muscular dystrophy. J Genet Hum. 1965; 14(4):318-29. View

2.
Maag U, Gold R . A simple combinatorial method for calculating genetic risks. Clin Genet. 1975; 7(5):361-7. DOI: 10.1111/j.1399-0004.1975.tb00343.x. View

3.
EMERY A, Holloway S . Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy. Hum Hered. 1977; 27(2):118-26. DOI: 10.1159/000152860. View

4.
EMERY A . Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis. Br Med Bull. 1980; 36(2):117-22. DOI: 10.1093/oxfordjournals.bmb.a071624. View

5.
Lathrop G, Lalouel J . Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet. 1984; 36(2):460-5. PMC: 1684427. View