Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis
Diverticular disease is characterized by pouches (that is, diverticulae) due to weakness in the bowel wall, which can become infected and inflamed causing diverticulitis, with potentially severe complications. Here, we test 32.4 million sequence variants identified through whole-genome sequencing (W...
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Published in | Nature communications Vol. 8; no. 1; p. 15789 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
06.06.2017
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Diverticular disease is characterized by pouches (that is, diverticulae) due to weakness in the bowel wall, which can become infected and inflamed causing diverticulitis, with potentially severe complications. Here, we test 32.4 million sequence variants identified through whole-genome sequencing (WGS) of 15,220 Icelanders for association with diverticular disease (5,426 cases) and its more severe form diverticulitis (2,764 cases). Subsequently, 16 sequence variants are followed up in a diverticular disease sample from Denmark (5,970 cases, 3,020 controls). In the combined Icelandic and Danish data sets we observe significant association of intronic variants in
ARHGAP15
(Rho GTPase-activating protein 15; rs4662344-T:
P=
1.9 × 10
−18
, odds ratio (OR)=1.23) and
COLQ
(collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T:
P=
1.5 × 10
−10
, OR=0.87) with diverticular disease and in
FAM155A
(family with sequence similarity 155A; rs67153654-A:
P=
3.0 × 10
−11
, OR=0.82) with diverticulitis. These are the first loci shown to associate with diverticular disease in a genome-wide study.
A hallmark of diverticular disease is pouches in the bowel wall which can become infected and inflamed, causing the more severe diverticulitis. Here, the authors report the first genome-wide association study on these interconnected conditions and identify
ARHGAP15
,
COLQ
and
FAM155A
as novel risk loci. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms15789 |