Eight-year follow-up of airway hyperresponsiveness in patients with primary Sjögren's syndrome

Autor: S. Valtysdottir, Bjorn Gudbjornsson, Dora Ludviksdottir, Hans Hedenström, Roger Hällgren
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Male
Longitudinal study
Respiratory Medicine and Allergy
Vital Capacity
lcsh:Medicine
Gastroenterology
Diffusion
0302 clinical medicine
follow-up
Body Size
Longitudinal Studies
Lung
Lung function
Methacholine Chloride
Lungmedicin och allergi
medicine.diagnostic_test
Follow up studies
General Medicine
Middle Aged
respiratory system
Respiratory Function Tests
medicine.anatomical_structure
Sjogren's Syndrome
Sjogren's syndrome
Female
Spirometry
medicine.medical_specialty
Airway hyperresponsiveness
Bronchial Provocation Tests
03 medical and health sciences
stomatognathic system
Internal medicine
medicine
Humans
In patient
Aged
030203 arthritis & rheumatology
business.industry
lcsh:R
lung function
Original Articles
eye diseases
respiratory tract diseases
stomatognathic diseases
030228 respiratory system
Sjögren’s syndrome
Immunology
Sjogren s
business
Follow-Up Studies
Zdroj: Upsala Journal of Medical Sciences
Upsala Journal of Medical Sciences, Vol 122, Iss 1, Pp 51-55 (2017)
Popis: Objective: To evaluate in a longitudinal study the influence of airway hyperresponsiveness (AHR) on lung function in patients with primary Sjogren's syndrome (pSS). Methods: Lung function was studied over an eight-year period in 15 patients who fulfilled the Copenhagen criteria for primary Sjogren's syndrome and who were covered in our earlier published study on AHR in patients with Sjogren's syndrome. Standard spirometry and measurements of lung volumes, diffusing capacity (DLCO), and AHR to methacholine were performed. Results: A significant decline over time was found in total lung capacity (TLC), vital capacity (VC), forced vital capacity (FVC), functional residual capacity (FRC), and expiratory midflows (FEF50). A sign of small airway obstruction (decrease in FEF50) at entry correlated with VC at follow-up (r = .8, P < .003), and the individual change in FEF50 during the observation period correlated with the individual change in VC (r = .6, P < .05). Six patients had increased AHR, and three of them had decreased DLCO. Six of the patients progressively reduced DLCO over time, and five of them had spirometric signs of increased small airway obstruction. Conclusions: During this eight-year follow-up we observed that one-third of the patients with pSS developed a significant reduction in lung function. Our findings suggest that small airways obstruction and AHR are associated with reduction of VC and development of impaired DLCO as a sign of interstitial lung disease in this group of patients.
Databáze: OpenAIRE