Literature DB >> 34811777

A conditional autoregressive model for genetic association analysis accounting for genetic heterogeneity.

Xiaoxi Shen1,2, Yalu Wen3, Yuehua Cui4, Qing Lu2.   

Abstract

Converging evidence from genetic studies and population genetics theory suggest that complex diseases are characterized by remarkable genetic heterogeneity, and individual rare mutations with different effects could collectively play an important role in human diseases. Many existing statistical models for association analysis assume homogeneous effects of genetic variants across all individuals, and could be subject to power loss in the presence of genetic heterogeneity. To consider possible heterogeneous genetic effects among individuals, we propose a conditional autoregressive model. In the proposed method, the genetic effect is considered as a random effect and a score test is developed to test the variance component of genetic random effect. Through simulations, we compare the type I error and power performance of the proposed method with those of the generalized genetic random field and the sequence kernel association test methods under different disease scenarios. We find that our method outperforms the other two methods when (i) the rare variants have the major contribution to the disease, or (ii) the genetic effects vary in different individuals or subgroups of individuals. Finally, we illustrate the new method by applying it to the whole genome sequencing data from the Alzheimer's Disease Neuroimaging Initiative.
© 2021 John Wiley & Sons Ltd.

Entities:  

Keywords:  genetic heterogeneity; score test

Mesh:

Year:  2021        PMID: 34811777      PMCID: PMC8792507          DOI: 10.1002/sim.9257

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  17 in total

1.  Genetic heterogeneity in human disease.

Authors:  Jon McClellan; Mary-Claire King
Journal:  Cell       Date:  2010-04-16       Impact factor: 41.582

2.  Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

Authors:  Bingshan Li; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2008-08-07       Impact factor: 11.025

3.  Rare-variant association testing for sequencing data with the sequence kernel association test.

Authors:  Michael C Wu; Seunggeun Lee; Tianxi Cai; Yun Li; Michael Boehnke; Xihong Lin
Journal:  Am J Hum Genet       Date:  2011-07-07       Impact factor: 11.025

4.  A powerful and adaptive association test for rare variants.

Authors:  Wei Pan; Junghi Kim; Yiwei Zhang; Xiaotong Shen; Peng Wei
Journal:  Genetics       Date:  2014-05-15       Impact factor: 4.562

5.  Shape differences of the brain ventricles in Alzheimer's disease.

Authors:  Luca Ferrarini; Walter M Palm; Hans Olofsen; Mark A van Buchem; Johan H C Reiber; Faiza Admiraal-Behloul
Journal:  Neuroimage       Date:  2006-07-12       Impact factor: 6.556

6.  A generalized genetic random field method for the genetic association analysis of sequencing data.

Authors:  Ming Li; Zihuai He; Min Zhang; Xiaowei Zhan; Changshuai Wei; Robert C Elston; Qing Lu
Journal:  Genet Epidemiol       Date:  2014-01-30       Impact factor: 2.135

7.  A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

Authors:  Stephan Morgenthaler; William G Thilly
Journal:  Mutat Res       Date:  2006-11-13       Impact factor: 2.433

8.  MRI of hippocampal volume loss in early Alzheimer's disease in relation to ApoE genotype and biomarkers.

Authors:  N Schuff; N Woerner; L Boreta; T Kornfield; L M Shaw; J Q Trojanowski; P M Thompson; C R Jack; M W Weiner
Journal:  Brain       Date:  2009-02-27       Impact factor: 13.501

Review 9.  Adult hippocampal neurogenesis and its role in Alzheimer's disease.

Authors:  Yangling Mu; Fred H Gage
Journal:  Mol Neurodegener       Date:  2011-12-22       Impact factor: 14.195

10.  A groupwise association test for rare mutations using a weighted sum statistic.

Authors:  Bo Eskerod Madsen; Sharon R Browning
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917

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