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Chronic rhinosinusitis associated with chronic bronchitis in a five-year follow-up: the Telemark study

BMC Pulmonary Medicine volume 22, Article number: 406 (2022) Cite this article

Abstract

Background

Chronic rhinosinusitis (CRS) is associated with generalised airway inflammation. Few studies have addressed the relationship between CRS and chronic bronchitis (CB).

Methods

This prospective study over a five-year period aims to investigate the risk of developing CB in subjects reporting CRS at the beginning of the study. A random sample of 7393 adult subjects from Telemark County, Norway, answered a comprehensive respiratory questionnaire in 2013 and then 5 years later in 2018. Subjects reporting CB in 2013 were excluded from the analyses. New cases of CB in 2018 were analysed in relation to having CRS in 2013 or not.

Results

The prevalence of new-onset CB in 2018 in the group that reported CRS in 2013 was 11.8%. There was a significant increase in the odds of having CB in 2018 in subjects who reported CRS in 2013 (OR 3.8, 95% CI 2.65–5.40), adjusted for age, sex, BMI, smoking and asthma.

Conclusion

In this large population sample, CRS was associated with increased odds of developing CB during a five-year follow-up. Physicians should be aware of chronic bronchitis in patients with CRS.

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Background

Chronic rhinosinusitis (CRS) is a prevalent, multifactorial upper airway disease affecting up to 12% of the adult population worldwide [1]. CRS is characterised by mucosal inflammation in the nose and paranasal sinuses, causing symptoms of nasal obstruction and discharge, loss of smell, facial pain, malaise resulting in sleep impairment and poor quality of life [2]. CRS has been strongly associated with asthma in both epidemiological and clinical studies [3, 4]. CRS has also been linked to chronic obstructive pulmonary disease (COPD), but there are still only a few studies [3, 5, 6].

Chronic bronchitis (CB) is a long-term inflammatory disease in the lower airways which involves a productive cough, impaired quality of life [7], an increased decline in lung function [8, 9], a higher risk of cardiovascular disease [10] and increased mortality [10]. The worldwide prevalence of CB is estimated to be 6.4% [11]. In the Nordic countries, the prevalence of CB is reported to be 4.6% in Norway and 7.2% in Sweden respectively [12, 13]. Since both CRS and CB are characterised by inflammation in the airway mucosa and have similar co-morbidities and risk factors such as smoking [12, 14] and occupational exposure [15,16,17], it is of great interest to further investigate the potential relationship between these diseases.

Few studies have previously investigated the association between upper airway inflammation and CB [18, 19]. In a large, population-based study from Sweden, Montnémery et al. showed, using a cross-sectional design, that nasal symptoms were more common in subjects with CB, but they did not use the European Position paper on Rhinosinusitis and Nasal polyps (EPOS) definition of CRS, since this definition was not established at the time. Further, in a small clinical trial, Håkansson et al. subsequently reported that CRS with nasal polyps was associated with CB [18].

To our knowledge, the present study is the first prospective study to assess CRS based on the EPOS definition and the risk of developing CB in a large, randomised population. Additionally, we analysed sex, age, body mass index (BMI), smoking and asthma as possible confounders for developing CB.

Methods

Study population

The Telemark Study is a prospective longitudinal study of a random sample from the general population of Telemark County, Norway, designed to evaluate airway diseases in relation to various risk factors such as occupational exposure, lifestyle factors and smoking status. The study has previously been described in detail [20]. Briefly, in 2013, a random sample of 50,000 subjects living in Telemark County in southeastern Norway, aged 16–50, was drawn from the Norwegian population register and a questionnaire was sent out by mail. The response rate after two reminders was 33% (n = 16,099). A total of 7952 subjects answered the questionnaire both in 2013 and 5 years later in 2018. The vast majority of the subjects were Caucasians. No clinical examination by a physician were performed.

Study design

The present study evaluates the risk of developing CB during a five-year observation period between 2013 and 2018 in relation to having CRS in 2013. All subjects reporting CB in 2013 and subjects who did not answer the questions on CRS in 2013 or 2018 were excluded. A total of 7393 subjects were included in this study. CRS in relation to CB adjusted for potential confounders, such as age, sex, BMI, smoking and asthma, was calculated. All variables and their definitions included in this study are shown in Table 1. A schematic description of the study design is shown in Fig. 1.

Table 1 Baseline demographic data and clinical characteristics in 2013
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Fig. 1
figure 1

Study flow chart

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Outcomes

Chronic bronchitis was defined as the positive answer to all three questions, 1, “Do you usually cough up phlegm or have mucus in the lungs that is hard to get up? 2. Do you cough up or bring up phlegm in this way nearly every day for at least 3 months each year? 3. Have you had periods with similar symptoms for at least two consecutive years? [21, 22].

EPOS guideline is a widely accepted consensus document. The EPOS guidelines have a validated definition of CRS for epidemiological studies used in this study [2]. CRS was defined as the presence of two or more CRS cardinal symptoms for ≥12 weeks, of which one must be either nasal blockage/obstruction/congestion or nasal discharge (anterior/posterior nasal drip), called “major symptom”, and/or additional symptoms, such as facial pain/pressure and/or a reduction in or the loss of smell, called “minor symptom”. All subjects giving a positive answer to at least two major symptoms and/or one major and one minor symptom were defined as having CRS. Clinical studies of chronic rhinosinusitis (CRS) recommend the performance of a clinical examination by a physician, including an endoscopic examination of the nose and a CT scan of the nose and sinuses. The specific questions defining CRS is seen in Fig. 2.

Fig. 2
figure 2

Questions defining chronic rhinosinusitis

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In a sub-analysis, we explored whether there was a relationship between the number of CRS cardinal symptoms reported and the likelihood of developing CB during the five-year observation period. Subjects who reported CRS cardinal symptoms without complying with the definition of CRS according to the EPOS criteria were categorised as “CRS-related symptoms” (for example, one or two minor symptoms). Subjects fulfilling the minimum criteria for CRS were categorised as “CRS” and, finally, subjects who reported more cardinal symptoms than the minimum criteria for CRS were categorised as “CRS+” (for example, two major and two minor symptoms).

Asthma was defined as a positive answer to the question “Have you ever been diagnosed with asthma by a physician?”

Smoking status was defined and categorised as current smoker, past and never smokers, based on the following questions: “Do you smoke daily (applies even if you only smoke a few cigarettes, cigars, or pipe daily)?” and/or “Do you smoke only occasionally (not daily, but weekends, party smoking or the like)” was categorised as “current smokers”. “Have you smoked in the past?” was categorised as “past smoker”. “Never smokers” answered no to all of the questions mentioned above.

The study was approved by the Regional Committee for Medical and Health Research Ethics in Norway (2012/1665/REK Sør-Øst D) and written informed consent was obtained from all the subjects before study inclusion.

Statistics

Analyses were performed with the SAS statistical software version 9.4 (SAS Institute Inc., Cary, NC, USA). Chi-square tests were used for categorical variables and the Cochran-Armitage trend test was used for unadjusted trend analysis. Multivariable logistic regression models were used to calculate odds ratios and 95% confidence intervals. P-values of < 0.05 were considered statistically significant.

Results

Study population characteristics

The study population comprises a total of 7393 individuals, all of whom answered the CRS questions in both 2013 and 2018. The prevalence of CRS in the study population was 6.6% in 2013. The median age of the study population in 2013 was 41 years (IQR, 17–50; Table 1). In 2013, both current smoking and asthma were more common in the CRS group (24.2% vs. 19.7%) and (21.3% vs. 8.6%) respectively (Table 1). At follow-up in 2018, 255 subjects reported new-onset CB (Fig.1).

The risk of developing CB when having CRS

The prevalence of new-onset CB in 2018 in the group that reported CRS in 2013 was 11.8% (Table 2). There was a significant increase in the odds of having CB in 2018 in subjects who reported CRS in 2013 (OR 3.8, 95% CI 2.65–5.40), adjusted for age, sex, BMI, smoking and asthma compared with subjects who did not report CRS. In the sub-analysis of the relationship between the number of CRS cardinal symptoms and the likelihood of developing CB, the prevalence of CB increased with each category, CRS-related symptoms, CRS and CRS+ (p < 0.01; Fig.3). In the logistic regression analysis, the odds were approximately seven times higher in the CRS+ group compared with not reporting any of the CRS cardinal symptoms (OR 7.33, 95% CI 4.58–11.73; Fig. 4). Age (p = 0.02), BMI (p = 0.003), smoking (p = 0.009) and asthma (p < 0.001) but not sex (p = 0.6) were regarded as confounders for CB in the regression analysis.

Table 2 Chronic rhinosinusitis (CRS) in 2013 and its relationship to chronic bronchitis (CB) in 2018
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Fig. 3
figure 3

Percentage of subjects with CRS-related symptoms (CRS cardinal symptoms without fulfilling the definition for CRS), CRS and CRS+ (more CRS cardinal symptoms than the minimum criteria for CRS) in relation to chronic bronchitis (CB). Cochran-Armitage trend test p < 0.01

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Fig. 4
figure 4

Odds ratio (OR) for developing chronic bronchitis (CB) in relation to CRS-related symptoms (CRS cardinal symptoms without fulfilling the definition for CRS), CRS and CRS+ (more CRS cardinal symptoms than the minimum criteria for CRS) adjusted for age, sex, BMI, smoking and asthma

Full size image

Discussion

In this prospective, longitudinal, population-based study, 7393 randomly selected subjects from Telemark, Norway, were followed for 5 years. Having CRS was associated with an increased risk of developing CB during the five-year observation period and, in the multiple regression model adjusted for age, sex, BMI, asthma and smoking, CRS remained a risk factor for developing CB. Moreover, for every additional CRS cardinal symptom reported, the risk of having CB increased. An increased number of reported CRS cardinal symptoms could indicate more severe CRS. Subjects in the CRS+ group reported the most CRS cardinal symptoms and had an odds ratio of developing CB that was seven times higher than subjects not reporting any CRS cardinal symptoms at all. In line with other studies, age, BMI, smoking and asthma were also related to CB [12, 23, 24]. In a small Danish clinical study from 2014, Hakansson et al. [18] reported that CB is more common in CRS patients with nasal polyps compared with controls (42.5% vs. 9.5%, p < 0.01). In 2000, Montnémery et al. [19] found an association between CB and upper airway symptoms in a Swedish cross-sectional, population-based study. However, they used a different definition of CB and did not follow the EPOS definition of CRS, since it was not established at the time [2]. To the best of our knowledge, this is the first prospective study to assess upper respiratory symptoms and self-reported CRS based on the EPOS definition and the risk of developing CB in a large, random population sample.

CRS and CB share several risk factors, such as tobacco smoking and occupational exposure [15, 17, 25,26,27]. The main risk factor for developing CB is tobacco smoking and the cumulative 30-year incidence of CB in current smokers has been reported at 42%, compared with 12% in never-smokers [8], which is in line with our findings. Furthermore, both CRS and CB are associated with asthma [3, 28]. In this study, we adjusted the analyses for asthma and smoking and the relationship remained the same. One hypothesis that could explain the association between CRS and CB is that patients with CRS develop a compromised “gatekeeper” function in the upper airway and less protection of the lower airways because of the ongoing sino-nasal inflammation. This impaired gatekeeper function could expose the lower airways to an excess of unconditioned inhaled air and make the lower airways more susceptible to developing chronic bronchitis. Another possible hypothesis is a systemic spread of inflammation via the bone marrow to both the upper and lower airways through the blood stream, as has been suggested in the well-established relationship between allergic rhinitis and asthma [29, 30]. There is also evidence of an association between CRS and COPD [5, 6, 31, 32]. Even though CB is often associated with COPD, CB is a primary disease entity that often co-exists with COPD and is also considered a phenotype of COPD. This study highlights the importance of conducting further clinical studies investigating a causal relationship between ongoing upper and lower airway inflammation in subjects with CRS and CB.

The Telemark Study is a large, prospective, population-based study of an unselected population. Another strength is the prospective study design, which makes it possible to study the development of CB. Furthermore, the study population is representative, with a prevalence of asthma close to the EU estimate at 8.2% in adults. In the study population, 20% reported to be current smokers which is slightly higher compared to 16% of the general population in Norway in 2013, but that estimate is from all citizens aged 16–74 (Statistics, Norway). In this study, the response rate was 33%. The potential causes and effects of non-response in the Telemark Study were investigated in 2016 by Abrahamsen et al. [20]. They concluded that the estimates for asthma and several respiratory symptoms including a productive cough were valid.

The fact that this study is based on questionnaire data made it possible to address a large population-based cohort. The CRS definition used here is based on the EPOS recommendations for epidemiological, questionnaire-based studies. However, in the absence of a clinical examination of the nose and/or CT scan of the sinuses, it is not possible to exclude the possibility that the CRS cardinal symptoms have origins other than nasal mucosal inflammation, such as structural obstruction of the nose (nasal septal deviation, turbinate hypertrophy) or facial pressure or pain (migraine) etc. In questionnaire-based studies, there is also a risk of recall bias. This questionnaire-based study did not include data on all shown associations with CB and CRS. For instance, CRS is related to allergic rhinitis and CRS with nasal polyps has been associated with genetic factors [33]. It is also important to acknowledge that both CRS and CB can develop and resolve over time. Both CRS and CB are chronic respiratory diseases with a substantial impact on daily life and health-related quality of life for many patients. It is important that clinicians are aware of the close association between upper and lower airway inflammation beyond asthma and allergic rhinitis and more studies are needed to examine possible mechanisms and improved treatments.

Conclusion

To our knowledge, this is the first large, prospective, population-based study reporting an increased odds of developing CB in subjects with CRS during a five-year observation period. Physicians should be aware of chronic bronchitis in patients with CRS.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available because of privacy policy regulations, but they are available from the corresponding author in response to a reasonable request.

Abbreviations

BMI:

Body Mass Index

CRS:

Chronic rhinosinusitis

CB:

Chronic bronchitis

COPD:

Chronic obstructive pulmonary disease

EPOS:

European position paper on rhinosinusitis and nasal polyposis

References

  1. Fokkens WJ, Lund VJ, Hopkins C, Hellings PW, Kern R, Reitsma S, Toppila-Salmi S, Bernal-Sprekelsen M, Mullol J, Alobid I, et al. European position paper on rhinosinusitis and nasal polyps 2020. Rhinology. 2020;58:1–464.

    Article  PubMed  Google Scholar 

  2. Fokkens WJ, Lund VJ, Mullol J, Bachert C, Alobid I, Baroody F, Cohen N, Cervin A, Douglas R, Gevaert P, et al: European Position Paper on Rhinosinusitis and Nasal Polyps 2012. Rhinol Suppl 2012:3 p preceding table of contents, 1–298.

  3. Khan A, Vandeplas G, Huynh TMT, Joish VN, Mannent L, Tomassen P, Van Zele T, Cardell LO, Arebro J, Olze H, et al. The global allergy and asthma European network GALEN rhinosinusitis cohort: a large European cross-sectional study of chronic rhinosinusitis patients with and without nasal polyps. Rhinology. 2019;57:32–42.

    Article  CAS  PubMed  Google Scholar 

  4. Rajan JP, Wineinger NE, Stevenson DD, White AA. Prevalence of aspirin-exacerbated respiratory disease among asthmatic patients: a meta-analysis of the literature. J Allergy Clin Immunol. 2015;135:676–81 e671.

    Article  CAS  PubMed  Google Scholar 

  5. Arndal E, Sorensen AL, Lapperre TS, Said N, Trampedach C, Aanaes K, Alanin MC, Christensen KB, Backer V, von Buchwald C. Chronic rhinosinusitis in COPD: a prevalent but unrecognized comorbidity impacting health related quality of life. Respir Med. 2020;171:106092.

    Article  PubMed  Google Scholar 

  6. Bergqvist J, Andersson A, Schioler L, Olin AC, Murgia N, Bove M, Janson C, Abramson MJ, Leynaert B, Nowak D, et al. Non-infectious rhinitis is more strongly associated with early-rather than late-onset of COPD: data from the European Community respiratory health survey (ECRHS). Eur Arch Otorhinolaryngol. 2020;277:1353–9.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Kanervisto M, Saarelainen S, Vasankari T, Jousilahti P, Heistaro S, Heliovaara M, Luukkaala T, Paavilainen E. COPD, chronic bronchitis and capacity for day-to-day activities: negative impact of illness on the health-related quality of life. Chron Respir Dis. 2010;7:207–15.

    Article  PubMed  Google Scholar 

  8. Pelkonen M, Notkola IL, Nissinen A, Tukiainen H, Koskela H. Thirty-year cumulative incidence of chronic bronchitis and COPD in relation to 30-year pulmonary function and 40-year mortality: a follow-up in middle-aged rural men. Chest. 2006;130:1129–37.

    Article  PubMed  Google Scholar 

  9. Guerra S, Sherrill DL, Venker C, Ceccato CM, Halonen M, Martinez FD. Chronic bronchitis before age 50 years predicts incident airflow limitation and mortality risk. Thorax. 2009;64:894–900.

    Article  CAS  PubMed  Google Scholar 

  10. Puddu PE, Menotti A, Kromhout D, Kafatos A, Tolonen H. Chronic bronchitis in the 50-year follow-up of the European cohorts of the seven countries study: prevalence, mortality and association with cardiovascular diseases. Respir Med. 2021;181:106385.

    Article  PubMed  Google Scholar 

  11. Halbert RJ, Natoli JL, Gano A, Badamgarav E, Buist AS, Mannino DM. Global burden of COPD: systematic review and meta-analysis. Eur Respir J. 2006;28:523–32.

    Article  CAS  PubMed  Google Scholar 

  12. Axelsson M, Ekerljung L, Eriksson J, Hagstad S, Ronmark E, Lotvall J, Lundback B. Chronic bronchitis in West Sweden - a matter of smoking and social class. Eur Clin Respir J. 2016;3:30319.

    Article  PubMed  Google Scholar 

  13. Leivseth L, Nilsen TI, Mai XM, Johnsen R, Langhammer A. Lung function and respiratory symptoms in association with mortality: the HUNT study. COPD. 2014;11:59–80.

    Article  PubMed  Google Scholar 

  14. Hutson K, Clark A, Hopkins C, Ahmed S, Kumar N, Carrie S, Erskine S, Sunkaraneni V, Philpott C, Group C. Evaluation of smoking as a modifying factor in chronic rhinosinusitis. JAMA Otolaryngol Head Neck Surg. 2021;147:159–65.

    Article  Google Scholar 

  15. Clarhed UKE, Johansson H, Veel Svendsen M, Toren K, Moller AK, Hellgren J. Occupational exposure and the risk of new-onset chronic rhinosinusitis aeuro a prospective study 2013-2018. Rhinology. 2020;58:597–604.

    CAS  PubMed  Google Scholar 

  16. Lytras T, Kogevinas M, Kromhout H, Carsin AE, Anto JM, Bentouhami H, Weyler J, Heinrich J, Nowak D, Urrutia I, et al. Occupational exposures and incidence of chronic bronchitis and related symptoms over two decades: the European Community respiratory health survey. Occup Environ Med. 2019;76:222–9.

    Article  PubMed  Google Scholar 

  17. Thilsing T, Rasmussen J, Lange B, Kjeldsen AD, Al-Kalemji A, Baelum J. Chronic rhinosinusitis and occupational risk factors among 20- to 75-year-old Danes-a GA(2) LEN-based study. Am J Ind Med. 2012;55:1037–43.

    Article  PubMed  Google Scholar 

  18. Hakansson K, Thomsen SF, Konge L, Mortensen J, Backer V, von Buchwald C. A comparative and descriptive study of asthma in chronic rhinosinusitis with nasal polyps. Am J Rhinol Allergy. 2014;28:383–7.

    Article  PubMed  Google Scholar 

  19. Montnemery P, Svensson C, Adelroth E, Lofdahl CG, Andersson M, Greiff L, Persson CG. Prevalence of nasal symptoms and their relation to self-reported asthma and chronic bronchitis/emphysema. Eur Respir J. 2001;17:596–603.

    Article  CAS  PubMed  Google Scholar 

  20. Abrahamsen R, Svendsen MV, Henneberger PK, Gundersen GF, Toren K, Kongerud J, Fell AK. Non-response in a cross-sectional study of respiratory health in Norway. BMJ Open. 2016;6:e009912.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Definition and classification of chronic bronchitis for clinical and epidemiological purposes. A report to the Medical Research Council by their committee on the Aetiology of chronic bronchitis. Lancet. 1965;1:775–9.

  22. Global Strategy for the Diagnosis, Management and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease (GOLD) [http://www.goldcopd.org/.]

  23. Guerra S, Sherrill DL, Bobadilla A, Martinez FD, Barbee RA. The relation of body mass index to asthma, chronic bronchitis, and emphysema. Chest. 2002;122:1256–63.

    Article  PubMed  Google Scholar 

  24. Woodruff PG, van den Berge M, Boucher RC, Brightling C, Burchard EG, Christenson SA, Han MK, Holtzman MJ, Kraft M, Lynch DA, et al. American Thoracic Society/National Heart, Lung, and Blood Institute asthma-chronic obstructive pulmonary disease overlap workshop report. Am J Respir Crit Care Med. 2017;196:375–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Doney B, Hnizdo E, Graziani M, Kullman G, Burchfiel C, Baron S, Fujishiro K, Enright P, Hankinson JL, Stukovsky KH, et al. Occupational risk factors for COPD phenotypes in the multi-ethnic study of atherosclerosis (MESA) lung study. COPD. 2014;11:368–80.

    Article  PubMed  Google Scholar 

  26. Ehrlich RI, White N, Norman R, Laubscher R, Steyn K, Lombard C, Bradshaw D. Predictors of chronic bronchitis in south African adults. Int J Tuberc Lung Dis. 2004;8:369–76.

    CAS  PubMed  Google Scholar 

  27. LeVan TD, Koh WP, Lee HP, Koh D, Yu MC, London SJ. Vapor, dust, and smoke exposure in relation to adult-onset asthma and chronic respiratory symptoms: the Singapore Chinese health study. Am J Epidemiol. 2006;163:1118–28.

    Article  PubMed  Google Scholar 

  28. Mejza F, Gnatiuc L, Buist AS, Vollmer WM, Lamprecht B, Obaseki DO, Nastalek P, Nizankowska-Mogilnicka E, Burney PGJ. Collaborators B, collaborators Bs: prevalence and burden of chronic bronchitis symptoms: results from the BOLD study. Eur Respir J. 2017;50.

  29. Denburg JA, Keith PK. Eosinophil progenitors in airway diseases: clinical implications. Chest. 2008;134:1037–43.

    Article  CAS  PubMed  Google Scholar 

  30. Brozek JL, Bousquet J, Agache I, Agarwal A, Bachert C, Bosnic-Anticevich S, Brignardello-Petersen R, Canonica GW, Casale T, Chavannes NH, et al. Allergic rhinitis and its impact on asthma (ARIA) guidelines-2016 revision. J Allergy Clin Immunol. 2017;140:950–8.

    Article  PubMed  Google Scholar 

  31. Hurst JR, Wilkinson TM, Donaldson GC, Wedzicha JA. Upper airway symptoms and quality of life in chronic obstructive pulmonary disease (COPD). Respir Med. 2004;98:767–70.

    Article  PubMed  Google Scholar 

  32. Hens G, Vanaudenaerde BM, Bullens DM, Piessens M, Decramer M, Dupont LJ, Ceuppens JL, Hellings PW. Sinonasal pathology in nonallergic asthma and COPD: 'united airway disease' beyond the scope of allergy. Allergy. 2008;63:261–7.

    Article  CAS  PubMed  Google Scholar 

  33. Bohman A, Oscarsson M, Holmberg K, Johansson L, Millqvist E, Nasic S, Torinsson-Naluai A, Bende M. Heredity of nasal polyps. Rhinology. 2015;53:25–8.

    Article  PubMed  Google Scholar 

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Acknowledgments

The authors would like to thank the Department of Occupational and Environmental Medicine, Telemark Hospital, Norway, for funding and the performance of data collection and handling. We would also like to thank the Department of Occupational and Environmental Medicine, Sahlgrenska University Hospital, Sweden, for its contribution to retrieving and filing data. Furthermore, we wish to thank Gølin Finckenhagen Gundersen and Nikola Zivadinovic, who collected the data at the Department of Occupational and Environmental Medicine, Skien, Norway.

Funding

Open access funding provided by University of Gothenburg. Open access funding provided by the University of Gothenburg, the Swedish Research Council for Health, Working Life and Welfare, the ALF Agreement relating to the research and education of doctors (state funding), the Gothenburg Medical Society.

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Authors and Affiliations

  1. Department of Otorhinolaryngology, Head & Neck Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden

    Joel Bergqvist & Johan Hellgren

  2. Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

    Joel Bergqvist, Mogens Bove & Johan Hellgren

  3. Department of ENT & Oral Maxillofacial Surgery, NU Hospital Group, Trollhättan, Sweden

    Mogens Bove

  4. COPD Center, Department of Respiratory Medicine and Allergology, Sahlgrenska University Hospital, Gothenburg, Sweden

    Anders Andersson

  5. COPD Center, Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

    Anders Andersson

  6. Occupational and Environmental Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

    Linus Schiöler

  7. Department of Occupational and Environmental Medicine, Telemark Hospital, Skien, Norway

    Geir Klepaker, Regine Abrahamsen & Anne Kristin M. Fell

  8. Department of Community Medicine and Global Health, Institute of Health and Society, University of Oslo, Oslo, Norway

    Anne Kristin M. Fell

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Contributions

JB, AA, LS, MB, JH contributed to the conceptualisation and study design. JB, AA, LS, JH analysed the data. JB, AA, LS, MB, AKF, JH interpreted the data. All the authors contributed to drafting the article or revising it critically for important intellectual content and gave their final approval of the version to be published. All the authors take responsibility for the integrity of the data and accuracy of the data analysis. All the authors have read and approved the final manuscript.

Corresponding author

Correspondence to Joel Bergqvist.

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Ethics approval and consent to participate

The study was approved by the Regional Committee for Medical and Health Research Ethics in Norway (2012/1665/REK Sør-Øst D) and written informed consent was obtained from all subjects prior to study inclusion. All methods in this study were performed in accordance with the relevant guidelines and regulations.

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Not applicable.

Competing interests

JB, AA, LS, MB, GK, RA, AKF, JH report no competing interests.

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Bergqvist, J., Bove, M., Andersson, A. et al. Chronic rhinosinusitis associated with chronic bronchitis in a five-year follow-up: the Telemark study. BMC Pulm Med 22, 406 (2022). https://doi.org/10.1186/s12890-022-02203-8

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BMC Pulmonary Medicine

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