ACR Meeting Abstracts

ACR Meeting Abstracts

Abstract Number: 589

Smoking, Alcohol Intake and Body Mass Index in Prediction of Disease Activity over Time in Early Axial Spondyloarthritis – Results from the SPondyloArthritis Caught Early (SPACE) Cohort

Sofia Exarchou 1, Carl Turesson1, Ulf Lindström 2, Roberta Ramonda 3, Robert B.M. Landewé 4, Hanne Dagfinrud 5, Floris van Gaalen 6, Désirée van der Heijde 6 and Lennart Jacobsson 7, 1Lund University, Malmö, Sweden, 2University of Gothenburg, Gothenburg, Sweden, 3University of Padova, Padova, Italy, 4Amsterdam University Medical Center, Amsterdam, Netherlands, 5University of Oslo, Oslo, Norway, 6Leiden University Medical Center, Leiden, Netherlands, 7Dept of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Sweden,, Gothenburg, Sweden

Meeting: 2019 ACR/ARP Annual Meeting

Keywords:

Session Information

Date: Sunday, November 10, 2019

Title: Spondyloarthritis Including Psoriatic Arthritis – Clinical Poster I: Axial Spondyloarthritis, Clinical Features

Session Type: Poster Session (Sunday)

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

Background/Purpose: In ankylosing spondylitis (AS), smokers have been found to have both higher disease activity and greater syndesmophyte progression, and a higher body mass index (BMI) has been associated with disease activity in cross sectional studies of both late and early disease. In established AS, alcohol consumption (AC) was associated with lower disease activity. However, little is known about the longitudinal effect on disease activity of such modifiable life-style factors, and very few studies have been performed in early axial spondylarthritis (axSPA). Our aim was therefore to study the relation of baseline smoking, BMI and AC with disease activity over time in early axSPA.

Methods: Data from the SPondyloArthritis Caught Early cohort, which includes patients with chronic back pain for ≥3 months, ≤2 years and onset < 45 years, were used to predict disease activity, measured as ASDAS, during the first year of follow-up. ASDAS was recorded at baseline (inclusion), after 3 and 12 months. Patients included in the analyses had a definite diagnosis of axSPA (physician’s level of confidence regarding SpA-diagnosis ≥7 on a 0-10 scale). Exposures measured at baseline were categorized as follows; BMI (normal < 25, overweight 25-29.9, obese > 30 kg/m2), smoking history (never, previous, current) and AC (none, 1-2, 3-5, ≥6 units of alcohol/week). Differences in ASDAS over 1 year by BMI category, smoking status and AC at baseline were estimated using mixed linear regression models, taking into account repeated measures of ASDAS.

Results: Of the 344 included subjects, the mean age at inclusion was 30 years and 49% were men. ASDAS decreased over the year of study with 0.58 in men and 0.46 in women. Obesity was more common in women whereas smoking and increased AC were more frequent in men (Table 1).

In age-adjusted models obesity in women (compared to normal BMI), but not in men, was associated with on average 0.58 (95% CL: 0.26, 0.90) higher ASDAS. The highest category of AC (≥6 units/week, compared to no AC) in women was associated with -0.54 (95% CL: -1.04, -0.04) lower ASDAS; and current smoking (compared to never smoking) in men with 0.32 (95% CL: 0.01, 0.63) higher ASDAS (Table 1).

In multivariate analyses including age, BMI-category, smoking history and AC the point estimates were overall similar, albeit the difference between current smokers and non-smokers in men did not reach statistical significance (Table 1).

Conclusion: Current smoking, AC and BMI, representing modifiable life style factors, were associated with disease activity over time in patients with early axSPA, with modest estimated differences and different patterns in women and men. Further analyses will explore to what extent residual confounding may explain these associations.


Table_ACR_abstract_2019_SPACE_ASDAS_final

Table 1.

Disclosure: S. Exarchou, None; C. Turesson, None; U. Lindström, None; R. Ramonda, None; R. Landewé, Abbott, 2, 5, 8, Abbott, Amgen, Bristol-Myers Squibb, Centocor, Merck, Pfizer, Roche, Schering-Plough, UCB, Wyeth, 8, Abbott, Amgen, Centocor, Novartis, Pfizer, Roche, Schering-Plough, UCB, Wyeth, 2, AbbVie, 5, Abbvie, 5, 8, AbbVie, Ablynx, Amgen, Astra-Zeneca, Bristol-Myers Squibb, Centocor, GSK, Novartis, Merck, Pfizer, Roche, Schering- Plough, UCB, Wyeth, 5, Ablynx, 5, Amgen, 2, 5, 8, AstraZeneca, 5, BMS, 5, 8, Bristol Myers Squibb, 5, 8, Bristol-Myers Squibb, 5, Celgene, 5, 8, Centocor, 2, 5, 8, Director of Rheumatology Consultancy BV, which is a registered company under Dutch law, 6, Eli Lilly, 5, 8, Eli Lilly and Company, 5, Eli-Lilly, 5, 8, Galapagos, 5, 8, Gilead, 5, 8, GlaxoSmithKline, 5, Glaxo-Smith-Kline, 5, 8, Janssen, 5, 8, Merck, 5, 8, MSD, 5, 8, Novartis, 5, 8, Pfizer, 5, 8, Rheumatology bv, 4, Rheumatology Consultancy BV, 9, Roche, 2, 5, 8, Schering-Plough, 2, 5, 8, UCB, 5, 8, UCB Pharma, 2, 5, 8, Wyeth, 2, 5, 8; H. Dagfinrud, None; F. van Gaalen, None; D. van der Heijde, AbbVie, 5, AbbVie, Amgen, Astellas, AstraZeneca, BMS, 5, Amgen, 5, Astellas, 5, 9, Astellas Pharma, 5, AstraZeneca, 5, BMS, 5, Boehringer Ingelheim, 5, Boehringer Ingelheim, Celgene, Daiichi, Eli-Lilly, Galapagos, Gilead, GSK, Janssen, Merck, Novartis, Pfizer, Regeneron, Roche, Sanofi, Takeda, UCB, 5, Boehringer-Ingelheim, 5, Bristol-Myers Squibb, 5, Celgene, 5, Daiichi, 5, 9, Daiichi Sankyo, 5, Director of Imaging Rheumatology, 6, Director of Imaging Rheumatology bv, 9, Eli Lilly, 5, Eli Lilly and Company, 5, Eli-Lilly, 5, Galapagos, 5, Gilead, 5, Gilead Sciences, Inc., 5, GlaxoSmithKline, 5, Glaxo-Smith-Kline, 5, GSK, 5, 8, Imaging Rheumatology bv, 9, Imaging Rheumatology BV, 9, Imaging Rheumatology bv., 9, Janssen, 5, 8, Janssen Pharmaceutica, 5, Merck, 5, 8, Novartis, 5, 8, Pfizer, 5, 8, Pfizer Inc, 5, Regeneron, 5, 8, Rheumatology bv, 4, 9, Roche, 5, 8, Sanofi, 5, 8, Takeda, 5, 8, Takeda Pharmaceutical Company, 5, UCB, 5, 8, UCB Pharma, 5; L. Jacobsson, None.

To cite this abstract in AMA style:

Exarchou S, Turesson C, Lindström U, Ramonda R, Landewé R, Dagfinrud H, van Gaalen F, van der Heijde D, Jacobsson L. Smoking, Alcohol Intake and Body Mass Index in Prediction of Disease Activity over Time in Early Axial Spondyloarthritis – Results from the SPondyloArthritis Caught Early (SPACE) Cohort [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/smoking-alcohol-intake-and-body-mass-index-in-prediction-of-disease-activity-over-time-in-early-axial-spondyloarthritis-results-from-the-spondyloarthritis-caught-early-space-cohort/. Accessed .

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