Literature DB >> 6459987

Comparison of mathematical models for the maternal age dependence of Down's syndrome rates.

S H Lamson, E B Hook.   

Abstract

The maternal age dependence of Down's syndrome rates was analyzed by two mathematical models, a discontinuous (DS) slope model which fits different exponential equations to different parts of the 20-49 age interval and a CPE model which fits a function that is the sum of a constant and exponential term over this whole 20-49 range. The CPE model had been considered but rejected by Penrose, who preferred models postulating changes with age assuming either a power function X10, where X is age or a Poisson model in which accumulation of 17 events was the assumed threshold for the occurrence of Down's syndrome. However, subsequent analyses indicated that the two models preferred by Penrose did not fit recent data sets as well as the DS or CPE model. Here we report analyses of broadened power and Poisson models in which n (the postulated number of independent events) can vary. Five data sets are analyzed. For the power models the range of the optimal n is 11 to 13; for the Poisson it is 17 to 25. The DS, Poisson, and power models each give the best fit to one data set; the CPE, to two sets. No particular model is clearly preferable. It appears unlikely that, with a data set from any single available source, a specific etiologic hypothesis for the maternal age dependence of Down's syndrome can be clearly inferred by the use of these or similar regression models.

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Year:  1981        PMID: 6459987     DOI: 10.1007/bf00283670

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  8 in total

1.  Frequency of Down syndrome in livebirths by single-year maternal age interval: results of a Massachusetts study.

Authors:  E B Hook; J J Fabia
Journal:  Teratology       Date:  1978-06

2.  Estimated rates of Down syndrome in live births by one year maternal age intervals for mothers aged 20-49 in a New York State study-implications of the risk figures for genetic counseling and cost-benefit analysis of prenatal diagnosis programs.

Authors:  E B Hook; G M Chambers
Journal:  Birth Defects Orig Artic Ser       Date:  1977

3.  Down syndrome in live births by single year maternal age interval in a Swedish study: comparison with results from a New York State study.

Authors:  E B Hook; A Lindsjö
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025

4.  Maternal age and Down syndrome: age-specific incidence rates by single-year intervals.

Authors:  B K Trimble; P A Baird
Journal:  Am J Med Genet       Date:  1978

5.  Is routine prenatal karyotyping indicated in pregnancies of very young women?

Authors:  H Zellweger; J Simpson
Journal:  J Pediatr       Date:  1973-04       Impact factor: 4.406

6.  A simple function for maternal-age-specific rates of Down syndrome in the 20-to-49-year age range and its biological implications.

Authors:  S H Lamson; E B Hook
Journal:  Am J Hum Genet       Date:  1980-09       Impact factor: 11.025

7.  Rates of Down's syndrome at the upper extreme of maternal age--absence of a "leveling" effect and evidence for artifacts resulting from analyses of rates by five-year maternal age intervals.

Authors:  E B Hook; S H Lamson
Journal:  Am J Epidemiol       Date:  1980-01       Impact factor: 4.897

8.  Down's syndrome in South Australia.

Authors:  G R Sutherland; S R Clisby; G Bloor; R F Carter
Journal:  Med J Aust       Date:  1979-07-28       Impact factor: 7.738

  8 in total
  5 in total

1.  Epidemiology of Down syndrome in South Australia, 1960-89.

Authors:  A J Staples; G R Sutherland; E A Haan; S Clisby
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

2.  An analysis of paternal age and 47,+21 in 35,000 new prenatal cytogenetic diagnosis data from the New York State Chromosome Registry: no significant effect.

Authors:  P K Cross; E B Hook
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

3.  Paternal age and Down's syndrome genotypes diagnosed prenatally: no association in New York state data.

Authors:  E B Hook; P K Cross
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  An aetiological study of 290 XXY males, with special reference to the role of paternal age.

Authors:  A D Carothers; S Collyer; R De Mey; I Johnstone
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  The frequency of 47,+21,47,+18, and 47,+13 at the uppermost extremes of maternal ages: results on 56,094 fetuses studied prenatally and comparisons with data on livebirths.

Authors:  E B Hook; P K Cross; R R Regal
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

  5 in total

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