Genetic comorbidities in Parkinson's disease.

Genetic comorbidities in Parkinson's disease.
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DOI:
10.1093/hmg/ddt465
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发表时间:
2014-02-01
影响因子:
3.5
通讯作者:
United Kingdom Brain Expression Consortium (UKBEC)
United Kingdom Brain Expression Consortium (UKBEC)
中科院分区:
生物学2区
文献类型:
--
作者:
Nalls MA;Saad M;Noyce AJ;Keller MF;Schrag A;Bestwick JP;Traynor BJ;Gibbs JR;Hernandez DG;Cookson MR;Morris HR;Williams N;Gasser T;Heutink P;Wood N;Hardy J;Martinez M;Singleton AB;International Parkinson's Disease Genomics Consortium (IPDGC);Wellcome Trust Case Control Consortium 2 (WTCCC2);North American Brain Expression Consortium (NABEC);United Kingdom Brain Expression Consortium (UKBEC)

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帕金森病(PD)有许多已知的遗传风险因素。临床和流行病学研究表明存在可能与PD额外风险相关的中间因素。我们使用已知的与这些特定表型相关的全基因组关联研究(GWAS)位点构建了其他流行病学和临床因素的遗传风险特征,以在系统评价中估计遗传共病。我们根据与精神分裂症和克罗恩病相关的GWAS变异确定了与PD风险显著相关的遗传风险特征。调整与PD和精神分裂症或PD和克罗恩病相关的基因座附近的SNP的条件分析表明,与精神分裂症和PD相关的空间重叠基因座占大多数共享共病,而PD和克罗恩病共享的已知近端基因座之外的变异占其共享的遗传共病。我们研究了精神分裂症和克罗恩病基因座附近的脑甲基化和表达特征,以推断与遗传共病相关的变异体相关的脑功能变化。我们将我们的结果与流行病学文献的系统综述进行比较,而研究结果在一定程度上是不同的;边缘遗传关联证实了遗传和流行病学数据之间关联的方向性。我们发现PD和克罗恩病之间以及PD和精神分裂症之间存在很强的遗传定义水平的共病,相关变体可能在大脑中发生功能性后果。
Parkinson’s disease (PD) has a number of known genetic risk factors. Clinical and epidemiological studies have suggested the existence of intermediate factors that may be associated with additional risk of PD. We construct genetic risk profiles for additional epidemiological and clinical factors using known genome-wide association studies (GWAS) loci related to these specific phenotypes to estimate genetic comorbidity in a systematic review. We identify genetic risk profiles based on GWAS variants associated with schizophrenia and Crohn’s disease as significantly associated with risk of PD. Conditional analyses adjusting for SNPs near loci associated with PD and schizophrenia or PD and Crohn’s disease suggest that spatially overlapping loci associated with schizophrenia and PD account for most of the shared comorbidity, while variation outside of known proximal loci shared by PD and Crohn’s disease accounts for their shared genetic comorbidity. We examine brain methylation and expression signatures proximal to schizophrenia and Crohn’s disease loci to infer functional changes in the brain associated with the variants contributing to genetic comorbidity. We compare our results with a systematic review of epidemiological literature, while the findings are dissimilar to a degree; marginal genetic associations corroborate the directionality of associations across genetic and epidemiological data. We show a strong genetically defined level of comorbidity between PD and Crohn’s disease as well as between PD and schizophrenia, with likely functional consequences of associated variants occurring in brain.
DOI: 10.1371/journal.pgen.1001283
发表时间: 2011-01-27
期刊: PLoS genetics
影响因子: 4.5
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Festen EA;Goyette P;Green T;Boucher G;Beauchamp C;Trynka G;Dubois PC;Lagacé C;Stokkers PC;Hommes DW;Barisani D;Palmieri O;Annese V;van Heel DA;Weersma RK;Daly MJ;Wijmenga C;Rioux JD
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发表时间: 2011-02-22
期刊: Circulation
影响因子: 37.8
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通讯作者: Chasman DI
DOI: 10.1038/nature10405
发表时间: 2011-09-11
期刊: NATURE
影响因子: 64.8
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发表时间: 2010-12
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影响因子: 30.8
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影响因子: 56.9
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