Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study

Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current stu...

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Published inFrontiers in genetics Vol. 13; p. 928944
Main Authors Shi, Yue, Feng, Sijia, Yan, Mengdie, Wei, Shuyan, Yang, Kejia, Feng, Yue
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 19.08.2022
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Online AccessGet full text
ISSN1664-8021
1664-8021
DOI10.3389/fgene.2022.928944

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Abstract Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19–1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05–1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16–1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83–0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97–1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92–1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.
AbstractList Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19–1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05–1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16–1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83–0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97–1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92–1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.
Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19-1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05-1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16-1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83-0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97-1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92-1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19-1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05-1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16-1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83-0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97-1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92-1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.
Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR).Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP.Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19–1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05–1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16–1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83–0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97–1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92–1.02, p = 0.172).Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.
Author Shi, Yue
Feng, Sijia
Wei, Shuyan
Feng, Yue
Yan, Mengdie
Yang, Kejia
AuthorAffiliation Chengdu University of Traditional Chinese Medicine , Chengdu , China
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Cites_doi 10.1093/ije/dyw088
10.1093/ije/dyx028
10.1093/hmg/ddu328
10.1016/S0140-6736(17)32448-0
10.1038/540S97a
10.1053/j.gastro.2020.05.016
10.1038/s41588-018-0099-7
10.14309/ajg.0000000000001834
10.1034/j.1600-065x.2002.19002.x
10.1053/j.gastro.2021.07.042
10.3390/nu12051420
10.1093/ije/dyw220
10.1136/bmj.k601
10.3109/00365521.2015.1041152
10.1038/nature11582
10.1016/j.cgh.2017.06.037
10.1038/ng.998
10.1111/jgh.14872
10.1097/01.mib.0000164195.75207.1e
10.1053/j.gastro.2004.01.063
10.1053/j.gastro.2020.06.098
10.1038/nrgastro.2015.136
10.1002/gepi.21758
10.1111/apt.12373
10.3748/wjg.v20.i17.4846
10.17235/reed.2019.5535/2018
10.3389/fgene.2021.631061
10.1002/gepi.21965
10.1007/s12664-019-00970-7
10.1093/ije/dyr036
10.1038/ng.3359
10.1053/j.gastro.2020.05.011
10.1093/ije/dyv080
10.1016/S0140-6736(17)31796-8
10.1097/01.mib.0000161308.65951.db
10.1097/MCG.0000000000001033
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Edited by: Farren Briggs, Case Western Reserve University, United States
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Reviewed by: Nastaran Asri, Shahid Beheshti University of Medical Sciences, Iran
This article was submitted to Applied Genetic Epidemiology, a section of the journal Frontiers in Genetics
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References Mårild (B23) 2022
Burgess (B5) 2011; 40
Lazarus (B14) 2002; 190
Davies (B7) 2018; 362
Singh (B30) 2018; 16
Mak (B21) 2020; 35
Rönnblom (B28) 2015; 50
Jostins (B12) 2012; 491
Hartwig (B10) 2016; 45
Rogler (B27) 2021; 161
Lebwohl (B16) 2018; 391
Liu (B17) 2015; 47
Loftus (B19) 2004; 126
Bowden (B3); 45
Bowden (B1) 2015; 44
Trynka (B32) 2011; 43
Kang (B13) 2013; 38
Pascual (B25) 2014; 20
Lundin (B20) 2015; 12
Pinto-Sanchez (B26) 2020; 159
Shah (B29) 2019; 53
Hodson (B11) 2016; 540
Zhang (B36) 2021; 12
Ng (B24) 2017; 390
Lebwohl (B15) 2021; 160
Manceñido Marcos (B22) 2020; 112
Swerdlow (B31) 2016; 45
Burgess (B4) 2013; 37
Lo (B18) 2020; 159
Yang (B35) 2005; 11
Bowden (B2); 40
Davey Smith (B6) 2014; 23
García-Santisteban (B9) 2020; 12
Tursi (B33) 2005; 11
Dhawan (B8) 2019; 38
Verbanck (B34) 2018; 50
References_xml – volume: 45
  start-page: 1600
  year: 2016
  ident: B31
  article-title: Selecting instruments for mendelian randomization in the wake of genome-wide association studies
  publication-title: Int. J. Epidemiol.
  doi: 10.1093/ije/dyw088
– volume: 45
  start-page: 1717
  year: 2016
  ident: B10
  article-title: Two-sample mendelian randomization: Avoiding the downsides of a powerful, widely applicable but potentially fallible technique
  publication-title: Int. J. Epidemiol.
  doi: 10.1093/ije/dyx028
– volume: 23
  start-page: R89
  year: 2014
  ident: B6
  article-title: Mendelian randomization: Genetic anchors for causal inference in epidemiological studies
  publication-title: Hum. Mol. Genet.
  doi: 10.1093/hmg/ddu328
– volume: 390
  start-page: 2769
  year: 2017
  ident: B24
  article-title: Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: A systematic review of population-based studies
  publication-title: Lancet (London, Engl.
  doi: 10.1016/S0140-6736(17)32448-0
– volume: 540
  start-page: S97
  year: 2016
  ident: B11
  article-title: Inflammatory bowel disease
  publication-title: Nature
  doi: 10.1038/540S97a
– volume: 159
  start-page: 884
  year: 2020
  ident: B26
  article-title: Association between inflammatory bowel diseases and celiac disease: A systematic review and meta-analysis
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2020.05.016
– volume: 50
  start-page: 693
  year: 2018
  ident: B34
  article-title: Detection of widespread horizontal pleiotropy in causal relationships inferred from mendelian randomization between complex traits and diseases
  publication-title: Nat. Genet.
  doi: 10.1038/s41588-018-0099-7
– year: 2022
  ident: B23
  article-title: Association of celiac disease and inflammatory bowel disease: A nationwide register-based cohort study
  publication-title: Am. J. Gastroenterol.
  doi: 10.14309/ajg.0000000000001834
– volume: 190
  start-page: 9
  year: 2002
  ident: B14
  article-title: Single nucleotide polymorphisms in innate immunity genes: Abundant variation and potential role in complex human disease
  publication-title: Immunol. Rev.
  doi: 10.1034/j.1600-065x.2002.19002.x
– volume: 161
  start-page: 1118
  year: 2021
  ident: B27
  article-title: Extraintestinal manifestations of inflammatory bowel disease: Current concepts, treatment, and implications for disease management
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2021.07.042
– volume: 12
  start-page: E1420
  year: 2020
  ident: B9
  article-title: A two-sample mendelian randomization analysis investigates associations between gut microbiota and celiac disease
  publication-title: Nutrients
  doi: 10.3390/nu12051420
– volume: 45
  start-page: 1961
  ident: B3
  article-title: Assessing the suitability of summary data for two-sample mendelian randomization analyses using MR-egger regression: The role of the I2 statistic
  publication-title: Int. J. Epidemiol.
  doi: 10.1093/ije/dyw220
– volume: 362
  start-page: k601
  year: 2018
  ident: B7
  article-title: Reading mendelian randomisation studies: A guide, glossary, and checklist for clinicians
  publication-title: BMJ
  doi: 10.1136/bmj.k601
– volume: 50
  start-page: 1234
  year: 2015
  ident: B28
  article-title: Celiac disease, collagenous sprue and microscopic colitis in IBD. observations from a population-based cohort of IBD (ICURE)
  publication-title: Scand. J. Gastroenterol.
  doi: 10.3109/00365521.2015.1041152
– volume: 491
  start-page: 119
  year: 2012
  ident: B12
  article-title: Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
  publication-title: Nature
  doi: 10.1038/nature11582
– volume: 16
  start-page: 823
  year: 2018
  ident: B30
  article-title: Global prevalence of celiac disease: Systematic review and meta-analysis
  publication-title: Clin. Gastroenterol. Hepatol.
  doi: 10.1016/j.cgh.2017.06.037
– volume: 43
  start-page: 1193
  year: 2011
  ident: B32
  article-title: Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
  publication-title: Nat. Genet.
  doi: 10.1038/ng.998
– volume: 35
  start-page: 380
  year: 2020
  ident: B21
  article-title: The epidemiology of inflammatory bowel disease: East meets west
  publication-title: J. Gastroenterol. Hepatol.
  doi: 10.1111/jgh.14872
– volume: 11
  start-page: 662
  year: 2005
  ident: B33
  article-title: High prevalence of celiac disease among patients affected by Crohn’s disease
  publication-title: Inflamm. Bowel Dis.
  doi: 10.1097/01.mib.0000164195.75207.1e
– volume: 126
  start-page: 1504
  year: 2004
  ident: B19
  article-title: Clinical epidemiology of inflammatory bowel disease: Incidence, prevalence, and environmental influences
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2004.01.063
– volume: 160
  start-page: 63
  year: 2021
  ident: B15
  article-title: Epidemiology, presentation, and diagnosis of celiac disease
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2020.06.098
– volume: 12
  start-page: 507
  year: 2015
  ident: B20
  article-title: Coeliac disease and autoimmune disease-genetic overlap and screening
  publication-title: Nat. Rev. Gastroenterol. Hepatol.
  doi: 10.1038/nrgastro.2015.136
– volume: 37
  start-page: 658
  year: 2013
  ident: B4
  article-title: Mendelian randomization analysis with multiple genetic variants using summarized data
  publication-title: Genet. Epidemiol.
  doi: 10.1002/gepi.21758
– volume: 38
  start-page: 226
  year: 2013
  ident: B13
  article-title: Systematic review: Worldwide variation in the frequency of coeliac disease and changes over time
  publication-title: Aliment. Pharmacol. Ther.
  doi: 10.1111/apt.12373
– volume: 20
  start-page: 4846
  year: 2014
  ident: B25
  article-title: Inflammatory bowel disease and celiac disease: Overlaps and differences
  publication-title: World J. Gastroenterol.
  doi: 10.3748/wjg.v20.i17.4846
– volume: 112
  start-page: 7
  year: 2020
  ident: B22
  article-title: the association between de novo inflammatory bowel disease and celiac disease
  publication-title: Rev. Esp. Enferm. Dig.
  doi: 10.17235/reed.2019.5535/2018
– volume: 12
  start-page: 631061
  year: 2021
  ident: B36
  article-title: Assessment of causal direction between gut microbiota and inflammatory bowel disease: A mendelian randomization analysis
  publication-title: Front. Genet.
  doi: 10.3389/fgene.2021.631061
– volume: 40
  start-page: 304
  ident: B2
  article-title: Consistent estimation in mendelian randomization with some invalid instruments using a weighted median estimator
  publication-title: Genet. Epidemiol.
  doi: 10.1002/gepi.21965
– volume: 38
  start-page: 185
  year: 2019
  ident: B8
  article-title: Celiac disease in the east and the west: Bridging the gaps between the guidelines and their implementation in daily practice is mandatory
  publication-title: Indian J. Gastroenterol.
  doi: 10.1007/s12664-019-00970-7
– volume: 40
  start-page: 755
  year: 2011
  ident: B5
  article-title: Avoiding bias from weak instruments in mendelian randomization studies
  publication-title: Int. J. Epidemiol.
  doi: 10.1093/ije/dyr036
– volume: 47
  start-page: 979
  year: 2015
  ident: B17
  article-title: Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
  publication-title: Nat. Genet.
  doi: 10.1038/ng.3359
– volume: 159
  start-page: 873
  year: 2020
  ident: B18
  article-title: Dietary inflammatory potential and risk of Crohn’s disease and ulcerative colitis
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2020.05.011
– volume: 44
  start-page: 512
  year: 2015
  ident: B1
  article-title: Mendelian randomization with invalid instruments: Effect estimation and bias detection through egger regression
  publication-title: Int. J. Epidemiol.
  doi: 10.1093/ije/dyv080
– volume: 391
  start-page: 70
  year: 2018
  ident: B16
  article-title: Coeliac disease
  publication-title: Lancet (London, Engl.
  doi: 10.1016/S0140-6736(17)31796-8
– volume: 11
  start-page: 528
  year: 2005
  ident: B35
  article-title: Inflammatory bowel disease in patients with celiac disease
  publication-title: Inflamm. Bowel Dis.
  doi: 10.1097/01.mib.0000161308.65951.db
– volume: 53
  start-page: 514
  year: 2019
  ident: B29
  article-title: Link between celiac disease and inflammatory bowel disease
  publication-title: J. Clin. Gastroenterol.
  doi: 10.1097/MCG.0000000000001033
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Snippet Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD)...
Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn's disease (CD)...
Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD)...
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SubjectTerms celiac disease
Crohn’s disease
Genetics
inflammatory bowel disease
Mendelian randomization
ulcerative colitis
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Title Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
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