<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kronzer VL</submitter><funding>NHLBI NIH HHS</funding><funding>NIAMS NIH HHS</funding><pagination>358-364</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8977280</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>49(4)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>We aimed to determine whether specific respiratory tract diseases are associated with increased rheumatoid arthritis (RA) risk.&lt;h4>Methods&lt;/h4>This case-control study within the Mass General Brigham Biobank matched newly diagnosed RA cases to 3 controls on age, sex, and electronic health record history. We identified RA using a validated algorithm and confirmed by medical record review. Respiratory tract disease exposure required 1 inpatient or 2 outpatient codes at least 2 years before the index date of RA clinical diagnosis or matched date. Logistic regression models calculated ORs for RA with 95% CIs, adjusting for confounders. We then stratified by serostatus ("seropositive" was positive rheumatoid factor and/or anticitrullinated protein antibodies) and smoking.&lt;h4>Results&lt;/h4>We identified 741 RA cases and 2223 controls (both median age 55, 76% female). Acute sinusitis (OR 1.61, 95% CI 1.05-2.45), chronic sinusitis (OR 2.16, 95% CI 1.39-3.35), and asthma (OR 1.39, 95% CI 1.03-1.87) were associated with increased risk of RA. Acute respiratory tract disease burden during the preindex exposure period was also associated with increased RA risk (OR 1.30 per 10 codes, 95% CI 1.08-1.55). Acute pharyngitis was associated with seronegative (OR 1.68, 95% CI 1.02-2.74) but not seropositive RA; chronic rhinitis/pharyngitis was associated with seropositive (OR 2.46, 95% CI 1.01-5.99) but not seronegative RA. Respiratory tract diseases tended towards higher associations in smokers, especially > 10 pack-years (OR 1.52, 95% CI 1.02-2.27, &lt;i>P&lt;/i> = 0.10 for interaction).&lt;h4>Conclusion&lt;/h4>Acute and chronic sinusitis, pharyngitis, and acute respiratory burden increased RA risk. The mucosal paradigm of RA pathogenesis may involve the upper respiratory tract.</pubmed_abstract><journal>The Journal of rheumatology</journal><pubmed_title>Association of Sinusitis and Upper Respiratory Tract Diseases With Incident Rheumatoid Arthritis: A Case-control Study.</pubmed_title><pmcid>PMC8977280</pmcid><funding_grant_id>R03 HL148484</funding_grant_id><funding_grant_id>K23 AR069688</funding_grant_id><funding_grant_id>P30 AR072577</funding_grant_id><funding_grant_id>L30 AR066953</funding_grant_id><funding_grant_id>P30 AR070253</funding_grant_id><funding_grant_id>R03 AR075886</funding_grant_id><pubmed_authors>Sparks JA</pubmed_authors><pubmed_authors>Doyle TJ</pubmed_authors><pubmed_authors>Crowson CS</pubmed_authors><pubmed_authors>Vassallo R</pubmed_authors><pubmed_authors>Davis JM</pubmed_authors><pubmed_authors>Losina E</pubmed_authors><pubmed_authors>Kronzer VL</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Zaccardelli A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of Sinusitis and Upper Respiratory Tract Diseases With Incident Rheumatoid Arthritis: A Case-control Study.</name><description>&lt;h4>Objective&lt;/h4>We aimed to determine whether specific respiratory tract diseases are associated with increased rheumatoid arthritis (RA) risk.&lt;h4>Methods&lt;/h4>This case-control study within the Mass General Brigham Biobank matched newly diagnosed RA cases to 3 controls on age, sex, and electronic health record history. We identified RA using a validated algorithm and confirmed by medical record review. Respiratory tract disease exposure required 1 inpatient or 2 outpatient codes at least 2 years before the index date of RA clinical diagnosis or matched date. Logistic regression models calculated ORs for RA with 95% CIs, adjusting for confounders. We then stratified by serostatus ("seropositive" was positive rheumatoid factor and/or anticitrullinated protein antibodies) and smoking.&lt;h4>Results&lt;/h4>We identified 741 RA cases and 2223 controls (both median age 55, 76% female). Acute sinusitis (OR 1.61, 95% CI 1.05-2.45), chronic sinusitis (OR 2.16, 95% CI 1.39-3.35), and asthma (OR 1.39, 95% CI 1.03-1.87) were associated with increased risk of RA. Acute respiratory tract disease burden during the preindex exposure period was also associated with increased RA risk (OR 1.30 per 10 codes, 95% CI 1.08-1.55). Acute pharyngitis was associated with seronegative (OR 1.68, 95% CI 1.02-2.74) but not seropositive RA; chronic rhinitis/pharyngitis was associated with seropositive (OR 2.46, 95% CI 1.01-5.99) but not seronegative RA. Respiratory tract diseases tended towards higher associations in smokers, especially > 10 pack-years (OR 1.52, 95% CI 1.02-2.27, &lt;i>P&lt;/i> = 0.10 for interaction).&lt;h4>Conclusion&lt;/h4>Acute and chronic sinusitis, pharyngitis, and acute respiratory burden increased RA risk. The mucosal paradigm of RA pathogenesis may involve the upper respiratory tract.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-22T11:46:39.985Z</modification><creation>2025-04-06T00:07:27.784Z</creation></dates><accession>S-EPMC8977280</accession><cross_references><pubmed>34654732</pubmed><doi>10.3899/jrheum.210580</doi></cross_references></HashMap>