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Abstract Number: 1053

Co-Morbidity Is Associated with Disease Severity in Early Rheumatoid Arthritis

Christopher Sparks1, Aleena Abdullah2, Steven Zhao3, Cristina Estrach3 and Nicola Goodson1, 1Musculoskeletal Biology1, University of Liverpool, Liverpool, United Kingdom, 2Musculoskeletal biology1, University of Liverpool, Liverpool, United Kingdom, 3Rheumatology, University Hospital Aintree, Liverpool, United Kingdom

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Comorbidity, Disability and rheumatoid arthritis (RA), Disease Activity

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Session Information

Title: Epidemiology and Public Health (ACR): Rheumatoid Arthritis and Systemic Lupus Erythematosus Outcomes

Session Type: Abstract Submissions (ACR)

Background/Purpose

Co-morbidity has been shown to increase length of hospital stay and mortality in hospitalised patients. However, in early rheumatoid arthritis (eRA) co-morbidity may confound treatment response and affect disease severity measures (disease activity scores (DAS28) and health assessment questionnaire (HAQ)).

The study aims were to assess:

1) Whether self reported comorbidity correlates with baseline DAS28 & HAQ in an eRA cohort? 

2) Does co-morbidity burden predict DAS28 remission and HAQ after 1yr of treatment?

Methods:

At time of eRA diagnosis, patients completed a modified validated self-reported 14 item comorbidity questionnaire (1). Each co-morbidity item scores 1 point (maximum score 14). Use of treatment or associated impairment contributes to a weighted co-morbidity score (Maximum score 36). The number of comorbidity items were divided into 3 categories: low≤1, medium=2 , & and high ≥3. Correlation between co-morbidity number and weighted score and DAS28 and modified mHAQ were assessed at baseline using Spearman’s rank correlation.

Logistic regression (adjusting for age, gender, smoking, obesity, & seropositive status) were used to explore whether baseline co-morbidity:1) number & 2) weighted score, predicted 1yr DAS28 remission & high HAQ (defined as >1).

Results

147 eRA patients, with symptom duration less than 12 months, mean age 58.1yrs & 67% female, had complete baseline and 1yr data. All were treated with synthetic DMARDS following a treat to target regime.

At baseline, comorbid disease was reported by 107 (72.8%) with median number of 1 [ IQR 0, 3] comorbid conditions in addition to RA.  The median weighted co-morbidity score was 2 [ IQR 0, 3]. Patients reporting ≥2 co-morbidities had higher prevalence of high HAQ>1 and DAS28> 5.1. Modest correlation was observed between the number of co-morbidities and 1)DAS28- rho 0.23, (p<0.05) and 2)HAQ- rho 0.31(p<0.01).

After 1 year, 77 (52.4%) achieved DAS28 <2.6 and 28 (19.1%) had HAQ score >1. Reporting 2 or more co-morbidities was associated with reduced rates of DAS28 remission and high HAQ score at 1 year (table 1). Increasing numbers of co-morbidity and use of the co-morbidity weighted scores did not increase the strength of association.

 

Table1:- Predictors of disease severity after 1 year

DAS28<2.6

1 year HAQ >1

Comorbidity

 

n

ORadj (95%CI)

ORadj  (95%CI)

Number

0-1 (ref)

90

1.0

1.0

2

23

0.35 (0.13, 0.94)

2.16 (0.63, 7.31)

>=3

34

0.46 (0.19, 1.56)

5.16 (1.64, 16.24)

 

Weighted

0-1 (ref)

58

1.0

1.0

2-3

44

1.31  (0.57, 3.03)

2.48 (0.79, 7.77)

>=4

45

0.30 (0.12, 0.74)

4.11 (1.26, 13.3)

Conclusion

Self reported comorbid disease burden predicts disease activity and level of disability in an eRA cohort after 1 year of treatment. Weighting co-morbidity for severity and function do not increase the strength of association with 1 year outcomes in early RA. Adjusting for the confounding effects of co-morbidity is important when assessing response to treatment. Use of self reported co-morbidity questionnaires appear to be an acceptable method of quantifying co-morbidity in routine rheumatology outpatient departments.

1)      Sangha O, et al. The Self-Administered comorbidity questionnaire:A New Method to Assess Comorbidity for Clinical and Health Services Research.  Arthritis Rheum 2003;49:156-63.


Disclosure:

C. Sparks,
None;

A. Abdullah,
None;

S. Zhao,
None;

C. Estrach,
None;

N. Goodson,
None.

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