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Abstract Number: 2508

Obese Axial Spondyloarthropathy Patients Have Worse Disease Outcomes

Gillian Fitzgerald1, Phil Gallagher2, Catherine Sullivan3, Killian O Rourke4, Claire Sheehy5, Frances Stafford6, Carmel Silke7, Muhammad Haroon8, Ronan Mullan9, Sandy Fraser10, Grainne Murphy11, Shawn Chavrimootoo12, Oliver FitzGerald13 and Finbar O' Shea1, 1Rheumatology, St James's Hospital, Dublin 8, Ireland, 2St. Vincent's University Hospital, Department of Rheumatology, Dublin, Ireland, 3Rheumatology, UCHG Ireland, Galway, Ireland, 4Rheumatology, Midlands Regional Hospital, Tullamore, Co Offaly, Ireland, 5Rheumatology, University Hospital Waterford, Waterford, Ireland, 6Rheumatology, Blackrock Clinic, Co Dublin, Ireland, 7Rheumatology, Sligo University Hospital, Sligo, Ireland, 8Rheumatology, Kerry General Hospital, Co Kerry, Ireland, 9Department of Rheumatology, Tallaght Hospital, TCD, Dublin 24, Ireland, 10Department of Rheumatology, University Hospitals Limerick, Ireland, Limerick, Ireland, 11Rheumatology, Cork University Hospital, Cork, Ireland, 12Rheumatology, Our Lady's Hospital, Co Meath, Ireland, 13St. Vincent's University Hospital, Department of Rheumatology. UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: axial spondyloarthritis and obesity, Disease Activity

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Session Information

Date: Tuesday, November 7, 2017

Title: Spondyloarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment Poster III: Outcomes, Outcome Measures, and Comorbidities

Session Type: ACR Poster Session C

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

Background/Purpose:

Obesity is a worldwide public health concern, due to its association with morbidity and mortality. Existing literature looking at obesity in axial spondyloarthropathy (axSpA) is sparse, but indicates increased BMI is prevalent. The impact of obesity on disease outcome is less well known. We aimed to determine the prevalence of obesity in a large axSpA cohort and describe its association with disease outcomes.

Methods:

Ankylosing Spondylitis Registry of Ireland (ASRI) provided the cohort for this study. The objectives of ASRI are to provide descriptive epidemiological data on the Irish axSpA population. A standardised clinical assessment is performed on each patient. Structured interviews provide patient-reported data. Weight is recorded in kilograms (kg) and height in centimetres (cm). BMI is categorised per the World Health Organisation criteria: normal weight <25 kg/m2, overweight 25-29.9 kg/m2 and obese ≥ 30 kg/m2. Statistical analysis is performed using SPSS.

Results:

As of June 2017, 683 patients have been enrolled: 77% (n=526) male, mean age 45.9 ± 12.4 years, mean disease duration 19±12.2 years, mean delay to diagnosis 8.6±8.1 years, 78.8% fulfil modified New York criteria. Mean BASDAI is 3.9±2.5, BASMI is 3.6 ± 2.5, BASFI is 3.6± 2.7 and HAQ is 0.52 ±0.52.

Mean BMI in this cohort is 27.8±5.3 kg/m2: 1.1% (n=7) underweight, 31.6% (n=205) normal BMI, 38.9% (n=252) overweight, 28.4% (n=184) obese. Overall, 67.3% are overweight or obese: these patients are significantly older, have longer disease duration and more comorbidities, especially hypertension and hyperlipidaemia, than normal weight patients. Obese patients have significantly higher disease activity and worse physical function, spinal mobility and quality of life than both normal weight and overweight patients (table 1). The prevalence of smoking is lower in obese patients than normal weight patients. In univariable linear regression, BMI and obesity are associated with higher BASDAI, ASQoL, BASMI, BASFI and HAQ scores (table 2). In multivariable regression analysis, obesity remains an independent predictor of higher disease activity and worse function.

Conclusion:

Over two thirds of this axSpA cohort are overweight or obese. Higher BMI and obesity independently predicts worse disease outcomes. Strategies should be put in place to actively reduce axSpA patient’s BMI.

Table 1: Patient characteristics stratified according to BMI categories. Values are mean (±SD) or n (%).

Characteristic

Normal weight n=212

Overweight n=252

Obese n=184

Age, years

41.6 (±12.3)

47.4 (±11.8)*

48.7 (±11.8)*

Male

156 (73.6%)

202 (80.2%)

143 (77.3%)

Disease duration, years

16.5 (±11.2)

20.1 (±11.9)*

20.6 (±12.9)*

HLA B-27 positive

151 (95%)

177 (93.2%)

116 (89.9%)

BMI, kg/m2

22.6 (±1.7)

27.3 (±1.4)

34.4 (±4.5)

ASQoL (0-18)

6 (±5.5)

6 (±5.5)

8 (±5.4)* †

HAQ (0-3)

0.47 (±0.5)

0.57 (±0.5)

0.68 (±0.57)* †

BASDAI (0-10)

3.7 (±2.5)

3.8 (±2.4)

4.5 (±2.3)* †

BASFI (0-10)

2.9 (±2.5)

3.6 (±2.6)*

4.6 (±2.6)* †

BASMI (0-10)

3 (±2.3)

3.5 (±2.5)

4.6 (±2.5)* †

Uveitis

76 (35.8%)

88 (34.9%)

67 (36.4%)

Psoriasis

33 (15.6%)

49 (19.4%)

39 (21.2%)

Inflammatory bowel disease

17 (8%)

30 (11.9%)

14 (7.6%)

Hypertension

19 (9%)

53 (21%)* †

71 (38.6%) *†

Hyperlipidaemia

15 (7.1%)

40 (15.9%)* †

56 (30.4%)* †

Diabetes

3 (1.4%)

11 (4.4%)

15 (8.2%)*

Current smoker

81 (38.2%)

78 (31%)

33 (17.9%)* †

Current alcohol intake

160 (75.5%)

189 (75%)

116 (63%)* †

Biologic use

155 (73.1%)

182 (72.2%)

129 (70.1%)

NSAID use

113 (53.3%)

109 (43.3%)

106 (57.6%) †

*p value <0.05 compared to BMI <25 kg/m2; † p value <0.05 compared to BMI 25-30 kg/m2.

Table 2: Linear regression analysis of association between BMI and obesity with clinical outcome.

Dependent variable

Predicting variable

Univariable analysis, B (95% CI)

P

Multivariable analysis, B (95% CI)

P

BASDAI

BMI

0.089 (0.01-0.08)

0.02

0.07 (0-0.07)

0.1

Obesity

0.13 (0.29-1.1)

<0.01

0.13 (0.25-1.1)

<0.01

ASQoL

BMI

0.14 (0.07-0.23)

<0.01

 

0.14 (0.06-0.23)

<0.01

Obesity

0.16 (1.1-2.9)

<0.01

0.17 (1.14-3.08)

<0.01

BASMI

BMI

0.26 (0.09-0.16)

<0.01

0.17 (0.05-0.11)

<0.01

Obesity

0.22 (0.8-1.63)

<0.01

0.18 (0.62-1.38)

<0.01

BASFI

BMI

0.24 (0.08-.16)

<0.01

0.17 (0.05-0.12)

<0.01

Obesity

0.21 (0.78-1.66)

<0.01

0.17 (0.58-1.45)

<0.01

HAQ

BMI

0.14 (0.01-0.02)

<0.01

0.1 (0-0.02)

0.02

Obesity

0.16 (0.1-0.28)

<0.01

-0.15 (0.09-0.27)

<0.01

 


Disclosure: G. Fitzgerald, Abbvie, 9; P. Gallagher, None; C. Sullivan, None; K. O Rourke, None; C. Sheehy, None; F. Stafford, None; C. Silke, None; M. Haroon, None; R. Mullan, None; S. Fraser, None; G. Murphy, None; S. Chavrimootoo, None; O. FitzGerald, Pfizer, Abbvie, BMS, Novartis, UCB, Janssen, Celgene and Lilly, 2; F. O' Shea, None.

To cite this abstract in AMA style:

Fitzgerald G, Gallagher P, Sullivan C, O Rourke K, Sheehy C, Stafford F, Silke C, Haroon M, Mullan R, Fraser S, Murphy G, Chavrimootoo S, FitzGerald O, O' Shea F. Obese Axial Spondyloarthropathy Patients Have Worse Disease Outcomes [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/obese-axial-spondyloarthropathy-patients-have-worse-disease-outcomes/. Accessed .
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