Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study

ObjectiveDepression is a potential risk factor for developing IBD. This association may be related to GI symptoms occurring before diagnosis. We aimed to determine whether depression, adjusted for pre-existing GI symptoms, is associated with subsequent IBD.DesignWe conducted a nested case–control st...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gut 2021-09, Vol.70 (9), p.1642-1648
Hauptverfasser: Blackwell, Jonathan, Saxena, Sonia, Petersen, Irene, Hotopf, Matthew, Creese, Hanna, Bottle, Alex, Alexakis, Christopher, Pollok, Richard C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1648
container_issue 9
container_start_page 1642
container_title Gut
container_volume 70
creator Blackwell, Jonathan
Saxena, Sonia
Petersen, Irene
Hotopf, Matthew
Creese, Hanna
Bottle, Alex
Alexakis, Christopher
Pollok, Richard C
description ObjectiveDepression is a potential risk factor for developing IBD. This association may be related to GI symptoms occurring before diagnosis. We aimed to determine whether depression, adjusted for pre-existing GI symptoms, is associated with subsequent IBD.DesignWe conducted a nested case–control study using the Clinical Practice Research Datalink identifying incident cases of UC and Crohn’s disease (CD) from 1998 to 2016. Controls without IBD were matched for age and sex. We measured exposure to prevalent depression 4.5–5.5 years before IBD diagnosis. We created two sub-groups with prevalent depression based on whether individuals had reported GI symptoms before the onset of depression. We used conditional logistic regression to derive ORs for the risk of IBD depending on depression status.ResultsWe identified 10 829 UC cases, 4531 CD cases and 15 360 controls. There was an excess of prevalent depression 5 years before IBD diagnosis relative to controls (UC: 3.7% vs 2.7%, CD 3.7% vs 2.9%). Individuals with GI symptoms prior to the diagnosis of depression had increased adjusted risks of developing UC and CD compared with those without depression (UC: OR 1.47, 95% CI 1.21 to 1.79; CD: OR 1.41, 95% CI 1.04 to 1.92). Individuals with depression alone had similar risks of UC and CD to those without depression (UC: OR 1.13, 95% CI 0.99 to 1.29; CD: OR 1.12, 95% CI 0.91 to 1.38).ConclusionsDepression, in the absence of prior GI symptoms, is not associated with subsequent development of IBD. However, depression with GI symptoms should prompt investigation for IBD.
doi_str_mv 10.1136/gutjnl-2020-322308
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2455172077</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2455172077</sourcerecordid><originalsourceid>FETCH-LOGICAL-b413t-43475d8a2b5bd9418c8ec7380cc7d008cdf9f850b374c63331205f377977fc343</originalsourceid><addsrcrecordid>eNqNkcuKFTEQhoMozvHoC7iQgBs37eTaSbuT8QoDbnQdcmvtQ7rT5jLDWQjzDvOGPok59OjC1UCgqPDVX_XzA_Aco9cY0_78ey2HJXQEEdRRQiiSD8AOs162TsqHYIcQFh0XbDgDT3I-IISkHPBjcEYpRkOP8A78eufX5HOe4gKn03PT1eSqDhle_4gwV5P9z-qXEo7Q-Ssf4tqgMeh51iWmIzTx2gfopux19m-ghmtca9ClCXamfTm4-Fxasa35fXNr41JSDDCX6o5PwaOxrfLP7uoefPvw_uvFp-7yy8fPF28vO8MwLR2jTHAnNTHcuIFhaaW3gkpkrXDNlHXjMEqODBXM9rS5I4iPVIhBiNFSRvfg1aa7ptjc5KLmKVsfgl58rFkRxjkWBAnR0Jf_oYdY09KuU4RzOdBetAV7QDbKpphz8qNa0zTrdFQYqVM4agtHncJRWzht6MWddDWzd_9G_qbRgG4DzHy4j-AfbyidEQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2558936733</pqid></control><display><type>article</type><title>Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study</title><source>MEDLINE</source><source>PubMed Central</source><creator>Blackwell, Jonathan ; Saxena, Sonia ; Petersen, Irene ; Hotopf, Matthew ; Creese, Hanna ; Bottle, Alex ; Alexakis, Christopher ; Pollok, Richard C</creator><creatorcontrib>Blackwell, Jonathan ; Saxena, Sonia ; Petersen, Irene ; Hotopf, Matthew ; Creese, Hanna ; Bottle, Alex ; Alexakis, Christopher ; Pollok, Richard C ; POP-IBD study group</creatorcontrib><description>ObjectiveDepression is a potential risk factor for developing IBD. This association may be related to GI symptoms occurring before diagnosis. We aimed to determine whether depression, adjusted for pre-existing GI symptoms, is associated with subsequent IBD.DesignWe conducted a nested case–control study using the Clinical Practice Research Datalink identifying incident cases of UC and Crohn’s disease (CD) from 1998 to 2016. Controls without IBD were matched for age and sex. We measured exposure to prevalent depression 4.5–5.5 years before IBD diagnosis. We created two sub-groups with prevalent depression based on whether individuals had reported GI symptoms before the onset of depression. We used conditional logistic regression to derive ORs for the risk of IBD depending on depression status.ResultsWe identified 10 829 UC cases, 4531 CD cases and 15 360 controls. There was an excess of prevalent depression 5 years before IBD diagnosis relative to controls (UC: 3.7% vs 2.7%, CD 3.7% vs 2.9%). Individuals with GI symptoms prior to the diagnosis of depression had increased adjusted risks of developing UC and CD compared with those without depression (UC: OR 1.47, 95% CI 1.21 to 1.79; CD: OR 1.41, 95% CI 1.04 to 1.92). Individuals with depression alone had similar risks of UC and CD to those without depression (UC: OR 1.13, 95% CI 0.99 to 1.29; CD: OR 1.12, 95% CI 0.91 to 1.38).ConclusionsDepression, in the absence of prior GI symptoms, is not associated with subsequent development of IBD. However, depression with GI symptoms should prompt investigation for IBD.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2020-322308</identifier><identifier>PMID: 33109601</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Adolescent ; Adult ; Antidepressants ; Case-Control Studies ; Clinical medicine ; Codes ; Colitis, Ulcerative - etiology ; Colitis, Ulcerative - psychology ; Crohn Disease - etiology ; Crohn Disease - psychology ; Crohn's disease ; Depression - complications ; Diagnosis ; Female ; Gastroenterology ; Humans ; Hypotheses ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - etiology ; Inflammatory Bowel Diseases - psychology ; Male ; Mental depression ; Population ; Population-based studies ; Primary care ; Risk Factors ; Socioeconomic factors ; Statistical analysis ; Young Adult</subject><ispartof>Gut, 2021-09, Vol.70 (9), p.1642-1648</ispartof><rights>Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b413t-43475d8a2b5bd9418c8ec7380cc7d008cdf9f850b374c63331205f377977fc343</citedby><cites>FETCH-LOGICAL-b413t-43475d8a2b5bd9418c8ec7380cc7d008cdf9f850b374c63331205f377977fc343</cites><orcidid>0000-0002-3980-4466 ; 0000-0001-9978-2011 ; 0000-0003-3787-2083 ; 0000-0002-5487-0752 ; 0000-0003-4278-3720 ; 0000-0003-0431-7753 ; 0000-0001-6452-6763 ; 0000-0002-0037-7524</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33109601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blackwell, Jonathan</creatorcontrib><creatorcontrib>Saxena, Sonia</creatorcontrib><creatorcontrib>Petersen, Irene</creatorcontrib><creatorcontrib>Hotopf, Matthew</creatorcontrib><creatorcontrib>Creese, Hanna</creatorcontrib><creatorcontrib>Bottle, Alex</creatorcontrib><creatorcontrib>Alexakis, Christopher</creatorcontrib><creatorcontrib>Pollok, Richard C</creatorcontrib><creatorcontrib>POP-IBD study group</creatorcontrib><title>Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study</title><title>Gut</title><addtitle>Gut</addtitle><description>ObjectiveDepression is a potential risk factor for developing IBD. This association may be related to GI symptoms occurring before diagnosis. We aimed to determine whether depression, adjusted for pre-existing GI symptoms, is associated with subsequent IBD.DesignWe conducted a nested case–control study using the Clinical Practice Research Datalink identifying incident cases of UC and Crohn’s disease (CD) from 1998 to 2016. Controls without IBD were matched for age and sex. We measured exposure to prevalent depression 4.5–5.5 years before IBD diagnosis. We created two sub-groups with prevalent depression based on whether individuals had reported GI symptoms before the onset of depression. We used conditional logistic regression to derive ORs for the risk of IBD depending on depression status.ResultsWe identified 10 829 UC cases, 4531 CD cases and 15 360 controls. There was an excess of prevalent depression 5 years before IBD diagnosis relative to controls (UC: 3.7% vs 2.7%, CD 3.7% vs 2.9%). Individuals with GI symptoms prior to the diagnosis of depression had increased adjusted risks of developing UC and CD compared with those without depression (UC: OR 1.47, 95% CI 1.21 to 1.79; CD: OR 1.41, 95% CI 1.04 to 1.92). Individuals with depression alone had similar risks of UC and CD to those without depression (UC: OR 1.13, 95% CI 0.99 to 1.29; CD: OR 1.12, 95% CI 0.91 to 1.38).ConclusionsDepression, in the absence of prior GI symptoms, is not associated with subsequent development of IBD. However, depression with GI symptoms should prompt investigation for IBD.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antidepressants</subject><subject>Case-Control Studies</subject><subject>Clinical medicine</subject><subject>Codes</subject><subject>Colitis, Ulcerative - etiology</subject><subject>Colitis, Ulcerative - psychology</subject><subject>Crohn Disease - etiology</subject><subject>Crohn Disease - psychology</subject><subject>Crohn's disease</subject><subject>Depression - complications</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory Bowel Diseases - etiology</subject><subject>Inflammatory Bowel Diseases - psychology</subject><subject>Male</subject><subject>Mental depression</subject><subject>Population</subject><subject>Population-based studies</subject><subject>Primary care</subject><subject>Risk Factors</subject><subject>Socioeconomic factors</subject><subject>Statistical analysis</subject><subject>Young Adult</subject><issn>0017-5749</issn><issn>1468-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkcuKFTEQhoMozvHoC7iQgBs37eTaSbuT8QoDbnQdcmvtQ7rT5jLDWQjzDvOGPok59OjC1UCgqPDVX_XzA_Aco9cY0_78ey2HJXQEEdRRQiiSD8AOs162TsqHYIcQFh0XbDgDT3I-IISkHPBjcEYpRkOP8A78eufX5HOe4gKn03PT1eSqDhle_4gwV5P9z-qXEo7Q-Ssf4tqgMeh51iWmIzTx2gfopux19m-ghmtca9ClCXamfTm4-Fxasa35fXNr41JSDDCX6o5PwaOxrfLP7uoefPvw_uvFp-7yy8fPF28vO8MwLR2jTHAnNTHcuIFhaaW3gkpkrXDNlHXjMEqODBXM9rS5I4iPVIhBiNFSRvfg1aa7ptjc5KLmKVsfgl58rFkRxjkWBAnR0Jf_oYdY09KuU4RzOdBetAV7QDbKpphz8qNa0zTrdFQYqVM4agtHncJRWzht6MWddDWzd_9G_qbRgG4DzHy4j-AfbyidEQ</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Blackwell, Jonathan</creator><creator>Saxena, Sonia</creator><creator>Petersen, Irene</creator><creator>Hotopf, Matthew</creator><creator>Creese, Hanna</creator><creator>Bottle, Alex</creator><creator>Alexakis, Christopher</creator><creator>Pollok, Richard C</creator><general>BMJ Publishing Group LTD</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3980-4466</orcidid><orcidid>https://orcid.org/0000-0001-9978-2011</orcidid><orcidid>https://orcid.org/0000-0003-3787-2083</orcidid><orcidid>https://orcid.org/0000-0002-5487-0752</orcidid><orcidid>https://orcid.org/0000-0003-4278-3720</orcidid><orcidid>https://orcid.org/0000-0003-0431-7753</orcidid><orcidid>https://orcid.org/0000-0001-6452-6763</orcidid><orcidid>https://orcid.org/0000-0002-0037-7524</orcidid></search><sort><creationdate>202109</creationdate><title>Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study</title><author>Blackwell, Jonathan ; Saxena, Sonia ; Petersen, Irene ; Hotopf, Matthew ; Creese, Hanna ; Bottle, Alex ; Alexakis, Christopher ; Pollok, Richard C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b413t-43475d8a2b5bd9418c8ec7380cc7d008cdf9f850b374c63331205f377977fc343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antidepressants</topic><topic>Case-Control Studies</topic><topic>Clinical medicine</topic><topic>Codes</topic><topic>Colitis, Ulcerative - etiology</topic><topic>Colitis, Ulcerative - psychology</topic><topic>Crohn Disease - etiology</topic><topic>Crohn Disease - psychology</topic><topic>Crohn's disease</topic><topic>Depression - complications</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Gastroenterology</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Inflammatory Bowel Diseases - etiology</topic><topic>Inflammatory Bowel Diseases - psychology</topic><topic>Male</topic><topic>Mental depression</topic><topic>Population</topic><topic>Population-based studies</topic><topic>Primary care</topic><topic>Risk Factors</topic><topic>Socioeconomic factors</topic><topic>Statistical analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blackwell, Jonathan</creatorcontrib><creatorcontrib>Saxena, Sonia</creatorcontrib><creatorcontrib>Petersen, Irene</creatorcontrib><creatorcontrib>Hotopf, Matthew</creatorcontrib><creatorcontrib>Creese, Hanna</creatorcontrib><creatorcontrib>Bottle, Alex</creatorcontrib><creatorcontrib>Alexakis, Christopher</creatorcontrib><creatorcontrib>Pollok, Richard C</creatorcontrib><creatorcontrib>POP-IBD study group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blackwell, Jonathan</au><au>Saxena, Sonia</au><au>Petersen, Irene</au><au>Hotopf, Matthew</au><au>Creese, Hanna</au><au>Bottle, Alex</au><au>Alexakis, Christopher</au><au>Pollok, Richard C</au><aucorp>POP-IBD study group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>2021-09</date><risdate>2021</risdate><volume>70</volume><issue>9</issue><spage>1642</spage><epage>1648</epage><pages>1642-1648</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><abstract>ObjectiveDepression is a potential risk factor for developing IBD. This association may be related to GI symptoms occurring before diagnosis. We aimed to determine whether depression, adjusted for pre-existing GI symptoms, is associated with subsequent IBD.DesignWe conducted a nested case–control study using the Clinical Practice Research Datalink identifying incident cases of UC and Crohn’s disease (CD) from 1998 to 2016. Controls without IBD were matched for age and sex. We measured exposure to prevalent depression 4.5–5.5 years before IBD diagnosis. We created two sub-groups with prevalent depression based on whether individuals had reported GI symptoms before the onset of depression. We used conditional logistic regression to derive ORs for the risk of IBD depending on depression status.ResultsWe identified 10 829 UC cases, 4531 CD cases and 15 360 controls. There was an excess of prevalent depression 5 years before IBD diagnosis relative to controls (UC: 3.7% vs 2.7%, CD 3.7% vs 2.9%). Individuals with GI symptoms prior to the diagnosis of depression had increased adjusted risks of developing UC and CD compared with those without depression (UC: OR 1.47, 95% CI 1.21 to 1.79; CD: OR 1.41, 95% CI 1.04 to 1.92). Individuals with depression alone had similar risks of UC and CD to those without depression (UC: OR 1.13, 95% CI 0.99 to 1.29; CD: OR 1.12, 95% CI 0.91 to 1.38).ConclusionsDepression, in the absence of prior GI symptoms, is not associated with subsequent development of IBD. However, depression with GI symptoms should prompt investigation for IBD.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>33109601</pmid><doi>10.1136/gutjnl-2020-322308</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-3980-4466</orcidid><orcidid>https://orcid.org/0000-0001-9978-2011</orcidid><orcidid>https://orcid.org/0000-0003-3787-2083</orcidid><orcidid>https://orcid.org/0000-0002-5487-0752</orcidid><orcidid>https://orcid.org/0000-0003-4278-3720</orcidid><orcidid>https://orcid.org/0000-0003-0431-7753</orcidid><orcidid>https://orcid.org/0000-0001-6452-6763</orcidid><orcidid>https://orcid.org/0000-0002-0037-7524</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0017-5749
ispartof Gut, 2021-09, Vol.70 (9), p.1642-1648
issn 0017-5749
1468-3288
language eng
recordid cdi_proquest_miscellaneous_2455172077
source MEDLINE; PubMed Central
subjects Adolescent
Adult
Antidepressants
Case-Control Studies
Clinical medicine
Codes
Colitis, Ulcerative - etiology
Colitis, Ulcerative - psychology
Crohn Disease - etiology
Crohn Disease - psychology
Crohn's disease
Depression - complications
Diagnosis
Female
Gastroenterology
Humans
Hypotheses
Inflammatory bowel disease
Inflammatory bowel diseases
Inflammatory Bowel Diseases - etiology
Inflammatory Bowel Diseases - psychology
Male
Mental depression
Population
Population-based studies
Primary care
Risk Factors
Socioeconomic factors
Statistical analysis
Young Adult
title Depression in individuals who subsequently develop inflammatory bowel disease: a population-based nested case–control study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T11%3A02%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Depression%20in%20individuals%20who%20subsequently%20develop%20inflammatory%20bowel%20disease:%20a%20population-based%20nested%20case%E2%80%93control%20study&rft.jtitle=Gut&rft.au=Blackwell,%20Jonathan&rft.aucorp=POP-IBD%20study%20group&rft.date=2021-09&rft.volume=70&rft.issue=9&rft.spage=1642&rft.epage=1648&rft.pages=1642-1648&rft.issn=0017-5749&rft.eissn=1468-3288&rft_id=info:doi/10.1136/gutjnl-2020-322308&rft_dat=%3Cproquest_cross%3E2455172077%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2558936733&rft_id=info:pmid/33109601&rfr_iscdi=true