Advances in inflammatory bowel disease pathogenesis: linking host genetics and the microbiome

被引:337
|
作者
Knights, Dan [1 ,2 ,3 ]
Lassen, Kara G. [1 ,2 ]
Xavier, Ramnik J. [1 ,2 ,4 ,5 ]
机构
[1] Broad Inst Harvard & Massachusetts Inst Technol, Cambridge, MA USA
[2] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02114 USA
[3] Univ Minnesota, Dept Comp Sci & Engn, Minneapolis, MN USA
[4] Massachusetts Gen Hosp, Gastrointestinal Unit, Ctr Study Inflammatory Bowel Dis, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
关键词
INFLAMMATORY BOWEL DISEASE; GENETICS; INTESTINAL BACTERIA; CROHN'S DISEASE; ULCERATIVE COLITIS; GENOME-WIDE ASSOCIATION; INTESTINAL MICROBIOTA; SP NOV; SUSCEPTIBILITY; CELLS; NOD2; VARIANTS; PROMOTES; INDUCTION; BACTERIUM;
D O I
10.1136/gutjnl-2012-303954
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Studies of the genetics underlying inflammatory bowel diseases have increased our understanding of the pathways involved in both ulcerative colitis and Crohn's disease and focused attention on the role of the microbiome in these diseases. Full understanding of pathogenesis will require a comprehensive grasp of the delicate homeostasis between gut bacteria and the human host. In this review, we present current evidence of microbiome-gene interactions in the context of other known risk factors and mechanisms, and describe the next steps necessary to pair genetic variant and microbiome sequencing data from patient cohorts. We discuss the concept of dysbiosis, proposing that the functional composition of the gut microbiome may provide a more consistent definition of dysbiosis and may more readily provide evidence of genome-microbiome interactions in future exploratory studies.
引用
收藏
页码:1505 / 1510
页数:6
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