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Abstract Number: 2684

Association Between Anxiety and Depression and Rheumatoid Arthritis Outcome: Results from an Inception Early Rheumatoid Arthritis Cohort

Sizheng Zhao1,2, Samantha Hider3, Christopher Sparks2, Faith Matcham4, James Galloway5, Cristina Estrach1 and Nicola Goodson1,2, 1Department of Rheumatology, Aintree University Hospital, Liverpool, United Kingdom, 2Musculoskeletal Biology I, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, United Kingdom, 3Research Institute for Primary Care and Health Sciences, Keele University, Keele, United Kingdom, 4Psychological Medicine Clinical Academic Group, King's College London, London, United Kingdom, 5Academic Department of Rheumatology, King´s College London, London, United Kingdom

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Anxiety, depression and outcome measures, Early Rheumatoid Arthritis

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Session Information

Date: Tuesday, November 10, 2015

Title: Rheumatoid Arthritis - Clinical Aspects Poster Session III

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Anxiety and depression (A&D) are important comorbid conditions that affect patients with rheumatoid arthritis (RA). It is not known whether they impact on disease outcome in early RA (eRA). The aim of this study was to understand if A&D are: 1) associated with disease activity (DAS28) or disability at time of eRA diagnosis, 2) predictors of DAS28 and disability after 12 months of treatment.

Methods: An inception cohort of eRA patients was studied. At baseline, patients completed a detailed questionnaire recording self-rated quality of life (EQ5D) and disability (modified health assessment questionnaire (HAQ)). A categorical variable for level of anxiety and depression (A&D) was created from the EQ5D (0=none, 1=moderate, and 2=extreme levels of self-reported A&D). Disease activity (DAS28), DAS28 remission (<2.6), and HAQ were recorded at baseline and at 12 month review. Associations with A&D were explored: 1) at baseline using simple descriptive statistics, and 2) with 12-month outcomes using age and gender adjusted logistic regression.

Results: At baseline, 126 eRA patients had complete data. 36 (28.6%) patients reported moderate levels, and 14 (11.1%) extreme levels of A&D. Increasing A&D was significantly associated with elevated HAQ, and DAS28 at baseline (Table 1).

Age and gender adjusted logistic regression revealed that baseline A&D predicted a reduced likelihood of: 1) DAS28 remission (ORadj 0.38 [95%CI 0.18, 0.81]), and 2) good EULAR response (ORadj 0.41 [95%CI 0.13, 1.03]), at 12 months. No difference was observed in initial DMARD therapy. Baseline A&D was not significantly associated with mean change in DAS28 (ORadj 1.06 [95%CI 0.85, 1.32]), or minimal clinically significant improvement in HAQ (ORadj1.95 [95%CI 0.91, 4.20]). However, those reporting extreme level A&D at baseline were 5 times more likely to report HAQ above 1.0 at 12-months compared to without A&D  (ORadj 5.78 [95%CI 1.72, 19.52]).  

Conclusion: Anxiety and depression at diagnosis of eRA is a strong predictor of poor outcome (disease activity and disability) at 12 months. Whilst A&D predict reduced likelihood of good EULAR response, no significant associations were observed with absolute change in HAQ or DAS28 after 12 months of DMARD therapy. This suggests that patients with A&D may benefit from additional treatment, targeted to reduce A&D, combined with usual DMARD treatment in order to optimise outcomes.  Understanding the impact of confounding effect of anxiety and depression is important when assessing DMARD response in eRA.

Table 1 Disease characteristics at baseline by level of anxiety/depression.

 

Anxiety and depression

P-value

None (n=76)

Moderate (n=36)

Extreme (n=14)

Mean age (SD)

58 (15.0)

55.7 (16.9)

54.4 (16.2)

0.287

Female (%)

47 (61.8%)

30 (83.3%)

10 (71.4%)

0.031

Smoke (%)

23 (30%)

8 (22.2%)

4 (28.6%)

0.442

Obese (%)

19 (25.0%)

10 (27.8%)

4 (28.6%)

0.707

Rheumatoid factor positive (%)

48 (63.2%)

22 (61.1%)

11 (78.6%)

0.744

CCP positive (%)

50 (65.8%)

23 (63.9%)

8 (57.1%)

0.664

High CRP

(>14 [median])

36 (49.3%)

14 (40.0%)

9 (64.3%)

0.796

Median DAS28 [IQR]

4.8 [3.9, 5.5]

4.8 [4.3, 5.9]

6.4 [5.9, 7.4]

0.046*

High DAS28 (>5.1)

31 (40.8%)

13 (36.1%)

12 (85.7%)

0.309

Median HAQ [IQR]

0.75[0.25, 1.25]

1.25 [0.875, 1.5]

2.0 [1.125, 2.125]

0.000*

High HAQ (≥1.0)

30 (39.5%)

24 (66.7%)

11 (78.6%)

0.003

High TJC (>6)

34 (49.3%)

13 (44.8%)

9 (81.8%)

0.564

High SJC (>3)

26 (37.7%)

14 (48.3%)

7 (63.6%)

0.132

High ESR (>33)

40 (52.6%)

18 (50.0%)

9 (64.3%)

0.880

High Global VAS (>55)

35 (46.1%)

20 (55.6%)

12 (85.7%)

0.048

Initiated triple DMARD therapy

11 (14.5%)

7 (19.4%)

1 (7.1%%)

0.536

Table 2 Response at 12 months by level of anxiety/depression.

 

Anxiety and depression

P-value

None (n=76)

Moderate (n=36)

Extreme (n=14)

Median DAS28 at 1yr

2.3[1,7, 3.3]

3.0[2.1, 3.5]

3.5[2.0, 4.8]

0.046 *

DAS28 remission (<2.6)

47 (71.2%)

14 (21.2%)

5 (7.6%)

0.008

Good EULAR response

53 (69.7%)

19 (52.8%)

6 (42.9%)

0.025

Median change in DAS28 (from baseline)

2.2 [1.3, 3.1]

2.3 [1.0, 3.0]

2.7 [0.9, 4.7]

0.697

Median HAQ at 1yr

0.25 [0.0, 0.75]

0.5 [1.25, 1.0]

1.0[0.75, 2.0]

0.005 *

HAQ improvement (>0.25 above baseline)

39 (51.4%)

25(69.4%)

9(64.3%)

0.063

*Wilcoxon’s ranksum – any anxiety depression vs no anxiety depression


Disclosure: S. Zhao, None; S. Hider, None; C. Sparks, None; F. Matcham, None; J. Galloway, None; C. Estrach, None; N. Goodson, None.

To cite this abstract in AMA style:

Zhao S, Hider S, Sparks C, Matcham F, Galloway J, Estrach C, Goodson N. Association Between Anxiety and Depression and Rheumatoid Arthritis Outcome: Results from an Inception Early Rheumatoid Arthritis Cohort [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/association-between-anxiety-and-depression-and-rheumatoid-arthritis-outcome-results-from-an-inception-early-rheumatoid-arthritis-cohort/. Accessed .
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