Genetic analysis of atopy and asthma as quantitative traits and ordered polychotomies

Traits related to atopy and asthma were defined in a random cohort of 131 families with three or more children. Correlation analysis provides no evidence of imprinting, maternal effect, or a major role of environment shared by sibs. Commingling analysis favours more than one distribution, the upper one being common for asthma and very common for atopy. Segregation analysis of rank‐transformed variables provides only equivocal evidence of major genes against a polygenic background but suggests that such genes (if present) are individually common and not of large effect. Segregation analysis under a two‐locus model gives consistent results with minimal distributional assumptions. To enter combined segregation analysis we favour a restricted model in which the major locus is additive on the liability scale and the pseudopolygenic modifier locus accounts for at least half the genetic variance. Total IgE and bronchial reactivity are proposed for meta‐analysis of atopy and asthma respectively. Genetic analysis of complex inheritance is discussed and it is shown that allelic association with random loci is not a feasible approach.

[1]  D. Strachan,et al.  Self-reported prevalence of asthma symptoms in children in Australia, England, Germany and New Zealand: an international comparison using the ISAAC protocol. , 1993, The European respiratory journal.

[2]  G. P. Herbison,et al.  Atopy in childhood. III. Relationship with pulmonary function and airway responsiveness , 1993, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[3]  P. van Eerdewegh,et al.  Alzheimer's disease: A piscatorial trek , 1993, Genetic epidemiology.

[4]  R. Elston,et al.  Statistical validity of the Haseman‐Elston sib‐pair test in small samples , 1993, Genetic epidemiology.

[5]  M. Babron,et al.  Linkage detection by the Affected‐Pedigree‐Member method: What is really tested? , 1993, Genetic epidemiology.

[6]  G. Lathrop,et al.  Maternal inheritance of atopic IgE responsiveness on chromosome 11 q , 1992, The Lancet.

[7]  N. Pearce,et al.  Comparison of a video questionnaire * with the IUATLD written questionnaire for measuring asthma prevalence , 1992, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[8]  N Risch,et al.  Model misspecification and multipoint linkage analysis. , 1992, Human heredity.

[9]  N. Morton,et al.  Genetic epidemiology of complex phenotypes , 1991, Annals of human genetics.

[10]  C. Sing,et al.  Evidence that a single gene with gender- and age-dependent effects influences systolic blood pressure determination in a population-based sample. , 1991, American journal of human genetics.

[11]  S. Holgate,et al.  Effect of atopy on the natural history of symptoms, peak expiratory flow, and bronchial responsiveness in 7- and 8-year-old children with cough and wheeze. A 12-month longitudinal study [published errarum appears in Am Rev Respir Dis 1992 Aug;146(2):540]. , 1991, The American review of respiratory disease.

[12]  N Poisson,et al.  Validity and repeatability of the IUATLD (1984) Bronchial Symptoms Questionnaire: an international comparison. , 1989, The European respiratory journal.

[13]  D. Rao,et al.  Equivalence of the mixed and regressive models for genetic analysis. I. Continuous traits , 1989, Genetic epidemiology.

[14]  E. Lander,et al.  The appropriate threshold for declaring linkage when allowing sex-specific recombination rates. , 1988, American journal of human genetics.

[15]  N. Morton,et al.  Alternative bioassays of kinship between loci. , 1988, American journal of human genetics.

[16]  T. Beaty,et al.  Inheritance of total serum IgE (basal levels) in man. , 1987, American journal of human genetics.

[17]  N. Morton,et al.  Combined analysis of genetic segregation and linkage under an oligogenic model. , 1984, Computers and biomedical research, an international journal.

[18]  G. Bonney,et al.  On the statistical determination of major gene mechanisms in continuous human traits: regressive models. , 1984, American journal of medical genetics.

[19]  A. Woolcock,et al.  Rapid method for measurement of bronchial responsiveness. , 1983, Thorax.

[20]  N. Morton,et al.  Immunoglobulin E revisited. , 1980, American journal of human genetics.

[21]  N E Morton,et al.  A genetic study of immunoglobulin E. , 1978, American journal of human genetics.

[22]  N E Morton,et al.  Skewness in commingled distributions. , 1976, Biometrics.

[23]  H. Akaike A new look at the statistical model identification , 1974 .

[24]  N. Morton,et al.  Relation between homozygous viability and average dominance in Drosophila melanogaster. , 1968, Genetics.