Literature DB >> 6846316

The use of life tables and survival analysis in testing genetic hypotheses, with an application to Alzheimer's disease.

G A Chase, M F Folstein, J C Breitner, T H Beaty, S G Self.   

Abstract

Because of the late onset of some neuropsychiatric disorders suspected to be under genetic influence, such as Alzheimer's disease, standard techniques for testing genetic hypotheses are difficult to apply to clinical data. The statistical aspects of life table methods and survival probability estimators which can be used to test such hypotheses have been neglected in the psychiatric literature. Two techniques of this kind, the Weinberg morbidity table and the Kaplan-Meier product limit estimator, are applied to real and simulated data. As estimators of lifetime incidence these methods yield roughly equivalent results for both types of data, although from a theoretical standpoint the original Weinberg estimator appears to suffer from logical defects. Parametric models may offer more definitive results, particularly when an estimator of segregation ratio is required. The clinical data in this report were gathered by interviewing relatives of Alzheimer's disease patients sampled through a nursing home survey in metropolitan Baltimore, Maryland during 1980.

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Year:  1983        PMID: 6846316     DOI: 10.1093/oxfordjournals.aje.a113581

Source DB:  PubMed          Journal:  Am J Epidemiol        ISSN: 0002-9262            Impact factor:   4.897


  9 in total

1.  Assessing familial aggregation of age at onset, by using estimating equations, with application to breast cancer.

Authors:  L Hsu; L P Zhao
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

2.  Gene-environment interaction: definitions and study designs.

Authors:  R Ottman
Journal:  Prev Med       Date:  1996 Nov-Dec       Impact factor: 4.018

3.  Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.

Authors:  P W Lunt; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

4.  Classification and genetic features of neonatal haemochromatosis: a study of 27 affected pedigrees and molecular analysis of genes implicated in iron metabolism.

Authors:  A L Kelly; P W Lunt; F Rodrigues; P J Berry; D M Flynn; P J McKiernan; D A Kelly; G Mieli-Vergani; T M Cox
Journal:  J Med Genet       Date:  2001-09       Impact factor: 6.318

Review 5.  How frailty models can be used for evaluating longevity limits: taking advantage of an interdisciplinary approach.

Authors:  A I Yashin; I A Iachine
Journal:  Demography       Date:  1997-02

6.  Estimating the probability for major gene Alzheimer disease.

Authors:  L A Farrer; L A Cupples
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

7.  A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.

Authors:  L A Lyons; R A Lewis; L C Strong; S Zuckerbrod; R E Ferrell
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

8.  Estimation of morbid risk and age at onset with missing information.

Authors:  L A Cupples; N Risch; L A Farrer; R H Myers
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

9.  Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy.

Authors:  S J Bale; A Chakravarti; M H Greene
Journal:  Am J Hum Genet       Date:  1986-02       Impact factor: 11.025

  9 in total

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