Genetic and environmental pathways to complex diseases

被引:54
作者
Gohlke, Julia M. [1 ]
Thomas, Reuben [1 ]
Zhang, Yonqing [2 ]
Rosenstein, Michael C. [3 ]
Davis, Allan P. [3 ]
Murphy, Cynthia [3 ]
Becker, Kevin G. [2 ]
Mattingly, Carolyn J. [3 ]
Portier, Christopher J. [1 ]
机构
[1] Natl Inst Environm Hlth Sci, Environm Syst Biol Grp, Mol Toxicol Lab, Res Triangle Pk, NC 27709 USA
[2] NIA, Gene Express & Genom Unit, NIH, Baltimore, MD 21224 USA
[3] Mt Desert Isl Biol Lab, Dept Bioinformat, Salsbury Cove, ME 04672 USA
关键词
SYSTEMATIC METAANALYSES; EXPRESSION PROFILES; RETINOIC ACID; INFLAMMATION; OBESITY; RISK; ASSOCIATION; DIFFERENTIATION; SCHIZOPHRENIA; ATORVASTATIN;
D O I
10.1186/1752-0509-3-46
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Pathogenesis of complex diseases involves the integration of genetic and environmental factors over time, making it particularly difficult to tease apart relationships between phenotype, genotype, and environmental factors using traditional experimental approaches. Results: Using gene-centered databases, we have developed a network of complex diseases and environmental factors through the identification of key molecular pathways associated with both genetic and environmental contributions. Comparison with known chemical disease relationships and analysis of transcriptional regulation from gene expression datasets for several environmental factors and phenotypes clustered in a metabolic syndrome and neuropsychiatric subnetwork supports our network hypotheses. This analysis identifies natural and synthetic retinoids, antipsychotic medications, Omega 3 fatty acids, and pyrethroid pesticides as potential environmental modulators of metabolic syndrome phenotypes through PPAR and adipocytokine signaling and organophosphate pesticides as potential environmental modulators of neuropsychiatric phenotypes. Conclusion: Identification of key regulatory pathways that integrate genetic and environmental modulators define disease associated targets that will allow for efficient screening of large numbers of environmental factors, screening that could set priorities for further research and guide public health decisions.
引用
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页数:15
相关论文
共 77 条
[1]   Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database [J].
Allen, Nicole C. ;
Bagade, Sachin ;
McQueen, Matthew B. ;
Ioannidis, John P. A. ;
Kavvoura, Fotini K. ;
Khoury, Muin J. ;
Tanzi, Rudolph E. ;
Bertram, Lars .
NATURE GENETICS, 2008, 40 (07) :827-834
[2]  
[Anonymous], 2007, FOOD NUTR PHYS ACT P
[3]   Opinion - Mendelian disorders deserve more attention [J].
Antonarakis, SE ;
Beckmann, JS .
NATURE REVIEWS GENETICS, 2006, 7 (04) :277-282
[4]  
Aragon A, 2004, ALCOHOL CLIN EXP RES, V28, p43A
[5]  
BAGADE S, 2008, ALZHEIMER RES FORUM
[6]   Efficacy and safety of a new HMG-CoA reductase inhibitor, atorvastatin, in patients with hypertriglyceridemia [J].
BakkerArkema, RG ;
Davidson, MH ;
Goldstein, RJ ;
Davignon, J ;
Isaacsohn, JL ;
Weiss, SR ;
Keilson, LM ;
Brown, WV ;
Miller, VT ;
Shurzinske, LJ ;
Black, DM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (02) :128-133
[7]   Obesity and related metabolic abnormalities during antipsychotic drug administration: Mechanisms, management and research perspectives [J].
Baptista, T ;
Kin, NMKNY ;
Beaulieu, S ;
de Baptista, EA .
PHARMACOPSYCHIATRY, 2002, 35 (06) :205-219
[8]  
Bastard JP, 2006, EUR CYTOKINE NETW, V17, P4
[9]  
Becker KG, 2004, NAT GENET, V36, P431, DOI 10.1038/ng0504-431
[10]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300