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Abstract Number: 2009

Does Breastfeeding Influence the Presentation of  Juvenile Idiopathic Arthritis? Results From the Childhood Arthritis Prospective Study

Hannah Pickford1, Eileen Baildam2, Alice Chieng3, Joyce Davidson4, Helen E. Foster5, Janet Gardner-Medwin4, Lucy R. Wedderburn6, Wendy Thomson1 and Kimme L. Hyrich7, 1University of Manchester, Arthritis Research UK Epidemiology Unit, Manchester, United Kingdom, 2Alder Hey Children's Foundation NHS Trust, Liverpool, United Kingdom, 3Manchester Children's Hospital, Manchester, United Kingdom, 4Royal Hospital for Sick Children, Glasgow, United Kingdom, 5Institute Cellular Medicine, Musculoskeletal Research Group, Newcastle upon Tyne, United Kingdom, 6Rheumatology Unit , Institute of Child Health, University College London (UCL), London, United Kingdom, 7Manchester Academic Health Science Centre, Arthritis Research UK Epidemiology Unit, Manchester, United Kingdom

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: Juvenile Arthritis

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Session Information

Title: Pediatric Rheumatology - Clinical and Therapeutic Aspects: Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Diseases

Session Type: Abstract Submissions (ACR)

Background/Purpose: There is extensive research into the association between breastfeeding (BF) and the occurrence of autoimmune diseases, although results have been conflicting. Studies have suggested that BF may influence the presentation of juvenile idiopathic arthritis (JIA), with a higher prevalence of BF among children with polyarticular presentation. The aim of this analysis was to study the influence of BF on the presentation of JIA in a large prospective inception cohort of children with childhood-onset arthritis.

Methods: The Childhood Arthritis Prospective Study (CAPS) recruits children ≤ 16 years old with new onset (≥2 weeks) inflammatory arthritis from five tertiary hospitals in the United Kingdom. At presentation to pediatric rheumatology, a physician performs an examination and completes a Physician Global Assessment (PGA). Families also complete a Childhood Health Assessment Questionnaire (CHAQ) including a Parent General Evaluation (PGE) and pain visual analogue scale (VAS). Detailed demographic data is collected including age at onset, gender, ethnicity, and household factors including parental education and income. Families were also asked if the child was BF and for how long. Baseline characteristics were compared between those children who were and were not BF using descriptive statistics. The association between BF and a high CHAQ score (>0.75) at presentation were determined using multivariate logistic regression, adjusted for age at onset, symptom duration, ILAR subtype, hospital, ethnicity and socioeconomic status (SES). Using postcodes, SES was determined by calculating the Index of Multiple Deprivation score and categorised into three groups: low, medium and high.   

Results: 927 children (65% female) were included in the analysis: median age at onset 6.4 years. Overall, 54% were breastfed, although the majority for <6 months. BF children reported a lower median age at onset (5.7 vs 7.5 years; p<0.001), a lower CHAQ score, lower PGE and lower pain at baseline (see Table).There was a trend towards a higher proportion of BF children with rheumatoid factor negative polyarthritis but lesser enthesitis related and psoriatic arthritis. There was a statistically significant inverse association between BF and high CHAQ (OR 0.62, 95% CI 0.41, 0.95) which was no longer significant after adjustment (OR 0.66, 95% CI 0.41, 1.07).

Conclusion:  There is an association between breastfeeding and an earlier and less severe presentation of JIA, although this could be explained in part by socioeconomic factors. Further work to elucidate the association between breastfeeding and later presentation of autoimmune diseases is required.

 

Characteristic, median (IQR) or n(%)

Never Breastfed

Breastfed

p-value

n

424 (45.7)

503 (54.3)

Duration of breastfeeding (months)

–

3.6 (1.4, 6.9)

Age at onset of symptoms (years)

7.5 (3.4,10.7)

5.7 (2.0,10.1)

<0.001

Symptom duration (months)

5.4 (2.8, 12.1)

4.9 (2.4, 10.3)

0.308

Caucasian

394(92.9)

441(87.7)

0.008

ILAR Subtype

0.009

Systemic

23 (5.4)

26 (5.2)

Oligoarthritis

224 (52.8)

264 (52.5)

Polyarthritis RF negative

81 (19.1)

135 (26.8)

Polyarthritis RF positive

11 (2.6)

16 (3.2)

Enthesitis-related

34 (8.0)

18 (3.6)

Psoriatic

38 (9.0)

30 (6.0)

Undifferentiated

13 (3.1)

14 (2.8)

CHAQ  (n=677)

0.88 (0.25,1.63)

0.63 (0.13,1.25)

<0.001

Physician Global Assessment

31 (18, 54)

28 (15, 50)

0.057

Parent Global Evaluation

29 (6, 53)

18 (4, 45)

0.006

Pain  score

39 (10, 64)

23 (5, 50)

<0.001

Active joint count

2 (1, 5)

2 (1, 5)

0.747

Limited Joint Count

1 (1, 3)

1 (1, 3)

0.151

ESR, mm/hr

18 (6, 45)

21.5 (7, 53)

0.088

Hospital

<0.001

Liverpool

187 (44.1)

195 (38.8)

Manchester

86 (20.3)

88 (17.5)

Glasgow

68 (16.0)

71 (14.1)

Newcastle

31 (7.3)

20 (4.0)

London

52 (12.3)

129 (25.7)

Index of Multiple Deprivation Category (n=475)

<0.001

Low

28 (12.6)

61 (24.1)

Medium

93 (41.9)

123 (48.6)

High

101 (45.5)

69 (27.3)

 


Disclosure:

H. Pickford,
None;

E. Baildam,
None;

A. Chieng,
None;

J. Davidson,
None;

H. E. Foster,
None;

J. Gardner-Medwin,
None;

L. R. Wedderburn,
None;

W. Thomson,
None;

K. L. Hyrich,
None.

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