Summary
A statistical test of polygenic inheritance (TPI) against the alternative of a rare major gene is presented. It is designed for a random sample of quantitative observations on index cases and siblings of those index cases (probands) selected on the basis of the observed measurements of these probands. The test focuses on an increase of the variance of siblings of probands over its value under polygenic inheritance, such an increase being expected in the presence of a major gene producing a shift of the quantitative observations. Certain data on lipids are then analyzed by this test. A major gene can tentatively be confirmed for triglycerides but not for cholesterol. In addition, the values of all index cases are subjected to an analysis of a mixture of normal distributions (NOCOMP computer program), resulting in a significant second component for triglycerides but not for cholesterol. For both TPI and NOCOMP, the exponent in a power transformation is estimated by maximum likelihood simultaneously with all other parameters, so that these analysis methods are robust against a wide range of skewness in the data, which is demonstrated by manipulation of the observations and their reanalyis.
Similar content being viewed by others
References
Berg, K., Heiberg, A.: Confirmation of linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism. In: Winnipeg Conference, (1977): Fourth International Workshop on Human Gene Mapping. Birth Defects: Original Article Series (in press) 1979. The National Foundation, New York
Boman, H., Ott, J., Hazzard, W. R., Albers, J. J., Cooper, M. N., Motulsky, A. G.: Familial hyperlipidemia in 95 randomly ascertained hyperlipidemic men. Clin. Genet. 13, 108 (1978)
Box, G. E. P., Cox, D. R.: An analysis of transformations. J. Roy. Statist. Soc. 26B, 211–252 (1964)
Cannings, C., Thompson, E. A.: Ascertainment in the sequential sampling, of pedigrees. Clin. Genet. 12, 208–212 (1977)
Elandt-Johnson, R. C.: Probability models and statistical methods in genetics. New York: Wiley 1971
Elston, R. C., Namboodiri, K. K., Go, R. C. P., Siervogel, R. M., Glueck, C. J.: Possible linkage between essential familial hypercholesterolemia and third complement component (C3). In: Baltimore Conference (1975): Third International Workshop on Human Gene Mapping. Birth Defects: Original Article Series, XII: 7, 1976. The National Foundation, New York
Fain, P. R.: Characteristics of simple sibship variance tests for the detection of major loci and application to height, weight and spatial performance. Ann. Hum. Genet. 42, 109–120 (1977)
Fain, P. R., Ott, J.: Heterogeneity of within-sibship, variance as a test of the major gene hypothesis. (Abstract.) In: International Congress Series no. 397, p. 180. Amsterdam: Excerpta Medica 1977
Felsenstein, J.: Estimation of number of loci controlling variation in a quantitative character. (Abstract.) Genetics 74, s78 (1973)
Fredrickson, D. R., Goldstein, J. L., Brown, M. S.: The familial hyperlipoproteinemias. In: The metabolic basis of inherited disease, 4th ed., Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S. (eds.). New York: McGraw-Hill 1978
Goldstein, J. L., Schrott, H. G., Hazzard, W. R., Bierman, E. L., Motulsky, A. G.: Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. J. Clin. Invest. 52, 1544–1568 (1973)
Harris, H., Whittaker, M., Lehmann, H., Silk, E.: The pseudocholinesterase variants. Esterase levels and dibucaine numbers in families selected through suxamethonium sensitive individuals. Acta Genet. 10, 1–16 (1960)
Hasselblad, V.: Estimation of parameters for a mixture of normal distributions. Technometrics 8, 431–444 (1966)
Lange, K., Westlake, J., Spence, M. A.: Extensions to pedigree analysis. III. Variance components by the scoring method. Ann. Hum. Genet. 39, 485–491 (1976)
Mérat, P.: Distributions de fréquences interprétation du déterminisme génétique des caractères quantitatifs et recherche, de “gènes majeurs”. Biometrics 24, 277–293 (1968)
Morton N. E., Rao, D. C.: Causal analysis of family resemblance. In: Genetic analysis of common diseases and applications to predictive factors in coronary disease, Sing, C. F., Skolnick, M. (eds.), pp. 431–452. New York: Alan R. Liss 1979
Morton, N. E., MacLean, C. J., Kagan, A., Gulbrandsen, C. L., Rhoads, G. G., Yee, S., Lew, R.: Comingling in distributions of lipids and related variables. Am. J. Hum. Genet. 29, 52–59 (1977)
Motulsky, A. G.: The genetics of abnormal drug responses. Ann. NY Acad. Sci. 123, 167–177 (1965)
Namboodiri, K. K., Elston, R. C., Glueck, C. J., Fallat, R., Buncher, C. R., Tsang, R.: Bivariate analyses of cholesterol and triglyceride levels in families in which probands have type IIb lipoprotein phenotype. Am. J. Hum. Genet. 27, 454–471 (1975)
Ott, J.: Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis. Ann. Hum. Genet. 40, 443–454 (1977)
Ott, J.: Comment in: Genetic epidemiology, Morton, N. E., Chung, C. (eds.) p. 235. New York: Academic Press 1978a
Ott, J.: Ascertainment in the Seattle lipid studies. In: Genetic analysis of common diseases and applications to predictive factors in coronary disease. Sing, C. F., Skolnick, M. (eds.), pp. 383–388. New York: Alan R. Liss 1979
Ott, J., Schrott, H. G., Goldstein, J. L., Hazzard, W. R., Allen, F. H. Jr., Falk, C. T., Motulsky, A. G.: Linkage studies in a large kindred with familial hypercholesterolemia. Am. J. Hum. Genet. 26, 598–603 (1974)
Penrose, L. S.: Effects of, additive genes at many loci compared with those of a set of alleles at one locus in parent-child and sib correlations. Ann. Hum. Genet. 33, 15–21 (1969)
Rao, C. R.: Linear statistical inference and its applications. New York: Wiley 1973
Schrott, H. G., Goldstein, J. L., Hazzard, W. R., McGoodwin, M. M., Motulsky, A. G.: Familial hypercholesterolemia in a large kindred: evidence for a monogenic mechanism. Ann. Intern. Med. 76, 711–720 (1972)
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Ott, J. Detection of rare major genes in lipid levels. Hum Genet 51, 79–91 (1979). https://doi.org/10.1007/BF00278296
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00278296