Evidence map›Paper›PMID 31353421›Full record

ArticleClinical rheumatology2019

The longitudinal effect of biologic use on patient outcomes (disease activity, function, and disease severity) within a rheumatoid arthritis registry.

Nancy A Shadick, Nicole M Gerlanc, Michelle L Frits, Bradley S Stolshek, Brenna L Brady, Christine Iannaccone, David Collier, Jing Cui, Alex Mutebi, Michael E Weinblatt

Registry-linked trialOpen access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01793103 (Brigham and Women's Rheumatoid Arthritis Sequential Study), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01793103 active not recruitingnot on this map

Brigham and Women's Rheumatoid Arthritis Sequential Study

Typeobservational_patient_registrySponsorBrigham and Women's HospitalRan2003 to 2028Enrolled1,598ConditionsRheumatoid Arthritis
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Nancy A ShadickBrigham and Women's Hospital, 60 Fenwood Road, Boston, MA, 02115, USA. nshadick@bwh.harvard.edu.ORCID http://orcid.org/0000-0003-3953-845X
Nicole M GerlancHealth Analytics, LLC, Columbia, MD, USA.
Michelle L FritsBrigham and Women's Hospital, 60 Fenwood Road, Boston, MA, 02115, USA.
Bradley S StolshekAmgen Inc., Thousand Oaks, CA, USA.
Brenna L BradyHealth Analytics, LLC, Columbia, MD, USA.
Christine IannacconeBrigham and Women's Hospital, 60 Fenwood Road, Boston, MA, 02115, USA.
David CollierAmgen Inc., Thousand Oaks, CA, USA.
Jing CuiBrigham and Women's Hospital, 60 Fenwood Road, Boston, MA, 02115, USA.
Alex MutebiAmgen Inc., Thousand Oaks, CA, USA.
Michael E WeinblattBrigham and Women's Hospital, 60 Fenwood Road, Boston, MA, 02115, USA.
Brigham and Women's Hospital · USAmgen (United States) · USTruven Health Analytics (United States) · US

Funding

Amgen (US) NA
6 · The paper itself

Abstract

introductionBiologics effectively manage symptoms and disease activity in rheumatoid arthritis (RA), but their long-term effects remain unclear.

methodLongitudinal data were examined from the Brigham and Women's Rheumatoid Arthritis Sequential Study (BRASS) registry. Linear regression modeled the effect of biologic exposure on changes in disease activity (Disease Activity Score-28 with C-reactive protein [DAS28-CRP]), functional status (modified Health Assessment Questionnaire [mHAQ]), and RA severity (Routine Assessment of Patient Index Data [RAPID3]). Biologic exposure was the ratio of time on a biologic relative to time participating in the BRASS cohort.

resultsThe analysis included 1395 RA patients, 82.3% female, with 6783 unique study visits from 2003 to 2015. At the patient's first visit, mean (SD) age was 56.3 (14.2) years and mean (SD) duration of RA was 12.7 (11.9) years. Average follow-up duration was 5.59 years (range, 1-13). Over time, DAS28-CRP, mHAQ, and RAPID3 scores decreased as the biologic exposure ratio increased. In repeated measures regression models, increased biologic exposure was significantly associated with decreased DAS28-CRP score (β = - 0.647; P < 0.001), decreased mHAQ score (β = - 0.096; P < 0.001), and decreased RAPID3 score (β = - 0.724; P < 0.001) during follow-up. Methotrexate use at baseline predicted decreased DAS28-CRP, mHAQ, and RAPID3 scores during follow-up. Biologic use at baseline predicted increased DAS28-CRP or mHAQ during follow-up.

conclusionsIncreased biologic exposure is associated with decreased disease activity, function impairment, and RA severity. Future studies should examine whether earlier initiation of biologics improves patient outcomes in RA.

trial registrationClinicalTrials.gov , NCT01793103 Key Points • Biologics effectively manage symptoms and disease activity in rheumatoid arthritis (RA), but their long-term effects remain unclear. • In this analysis of longitudinal annual population samples of 1395 RA patients in the Brigham and Women's Rheumatoid Arthritis Sequential Study (BRASS) registry, disease activity, function, and severity scores improved as time on biologic therapy increased. • In repeated measures regression models, time on biologic therapy was a significant predictor of improved outcomes for disease activity, function, and RA severity. • Further studies should examine whether earlier initiation of biologics limits the long-term effect of inflammation on RA outcomes.

Indexed as

RegistriesAdultAgedAntirheumatic AgentsArthritis, RheumatoidBiological ProductsFemaleHumansLinear ModelsMaleMiddle AgedSeverity of Illness IndexTreatment OutcomeAntirheumatic AgentsBiological ProductsBiologicsDisease activityExposureFunctionRheumatoid arthritisSeverity

Identifiers

PMID31353421
OpenAlexW2964974546

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.