Genetic contribution to motility disorders of the upper gastrointestinal tract

doi:10.4291/wjgp.v4.i4.65

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Nov 15, 2013 (publication date) through Jul 22, 2024

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World Journal of Gastrointestinal Pathophysiology

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2150-5330

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastrointest Pathophysiol. Nov 15, 2013; 4(4): 65-73
Published online Nov 15, 2013. doi: 10.4291/wjgp.v4.i4.65

Table 3 Overview of genetic association studies in post-infectious dyspepsia

Protein (gene)	Polymorphism	Finding	Ref.
MIF	-173C	Risk factor for EPS	[56]
IL17	-7488T	Risk factor for EPS	[56]
COX-1	T1676C	Risk factor for EPS	[57]
NPS-R	rs2609234, rs6972158, and rs1379928	No association	[58]

IL: Interleukin; COX-1: Cyclooxygenase-1; EPS: Encapsulating peritoneal sclerosis; MIF: Macrophage migration inhibitory factor.

Citation: Sarnelli G, D’Alessandro A, Pesce M, Palumbo I, Cuomo R. Genetic contribution to motility disorders of the upper gastrointestinal tract. World J Gastrointest Pathophysiol 2013; 4(4): 65-73
URL: https://www.wjgnet.com/2150-5330/full/v4/i4/65.htm
DOI: https://dx.doi.org/10.4291/wjgp.v4.i4.65