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ABSTRACT: Objectives
To investigate changes in BMD in RA patients receiving 3-year biological/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARD) or conventional synthetic DMARD (csDMARD).Methods
Patients with RA were recruited from September 2014 until March 2019. Clinical characteristics, BMD and evidence of fragility fractures at enrolment were documented. Participants were treated according to the National Institute for Health and Care Excellence (NICE) guidelines over a 3-year observation period. Repeated BMD was measured at the end of the study period. Participants were grouped into those receiving b/tsDMARD or csDMARD and by propensity score matching (1:2).Results
A total of 388 participants completed the 3-year follow-up. After propensity score matchi
SUBMITTER: Chen JF
PROVIDER: S-EPMC7449814 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature