Patients and methods Patients All 150 patients from the original study were eligible to participate in the follow-up study. The inclusion and exclusion criteria for the baseline study have previously been described in detail [8]. In short, in each of three centres, general rheumatology clinics in Oslo (Norway), Truro (UK) and Amsterdam (The Netherlands), 50 female patients were consecutively enrolled. The patients included were 50–70 years old and fulfilled the American College of Rheumatology (formerly American Rheumatism

Association) 1987 revised classification criteria for RA. The disease duration of all patients was ≥5 years [9]. In total, 102 patients of the original cohort consented to a follow-up assessment (33 from Oslo, 34 from Truro and 35 GSK3235025 purchase from Amsterdam). The main reasons for not participating in the follow-up study were as follows: 15 moved away from the hospital area, five suffered mTOR inhibitor from severe co-morbidity, eight had died and 20 did not participate for unknown reasons or could not be contacted. The baseline characteristics of the 102 patients who had a follow-up measurement did not differ from the characteristics of all the 150 patients at baseline and of those

patients (n = 42) that dropped out (lowest p = 0.282; data not shown). Demographics and medical history Data at follow-up were collected from interviews, clinical examination, questionnaires and patient’s medical records and included height, weight, calcium intake, history of falls (number of falls during the last year and cause) and fractures (anatomical site

and cause), HMPL-504 manufacturer current and previous use of anti-osteoporotic [anti-resorptive therapy (ART) and hormone replacement therapy (HRT)] and disease-modifying anti-rheumatic drugs (DMARDs), and history of corticosteroid use (previous and current use, cumulative amount over the past 5 years, use of 7.5 mg for >6 months and number of months on corticosteroids). Physical disability was assessed by means of the Health Assessment Questionnaire (HAQ; 20 items, score range 0–3, with higher scores selleck kinase inhibitor indicating worse disability) [10]. Disease activity Measures of RA disease activity were assessed with visual analogue scales (0–100 mm) of pain and patient’s global disease activity; 28 tender and swollen joint counts, and acute phase reactants [the erythrocyte sedimentation rate (ESR; mm/h) and C-reactive protein (CRP; mg/L), both measured with standardised local measurement techniques]. The modified 28 joints disease activity score (DAS-28) was calculated according to published guidelines [11]. Joint scores were performed by experienced rheumatology nurses in Oslo and Truro and in Amsterdam by a physician (MV). The mean ESR and CRP were calculated based on all available measurements during the 5-year follow-up.