ARTHRITIS & RHEUMATISM
Vol. 64, No. 5, May 2012, pp 1388–1398
DOI 10.1002/art.33465
© 2012, American College of Rheumatology
Baseline Radiographic Damage, Elevated
Acute-Phase Reactant Levels, and Cigarette Smoking Status
Predict Spinal Radiographic Progression
in Early Axial Spondylarthritis
Denis Poddubnyy,
1
Hildrun Haibel,
1
Joachim Listing,
2
Elisabeth Ma ¨rker-Hermann,
3
Henning Zeidler,
4
Ju ¨rgen Braun,
5
Joachim Sieper,
1
and Martin Rudwaleit
6
Objective. To assess prospectively the rates and to
explore predictors of spinal radiographic progression
over 2 years in a cohort of patients with early axial
spondylarthritis (SpA).
Methods. Two hundred ten patients with axial
SpA from the German Spondyloarthritis Inception Co-
hort were selected for this analysis based on the avail-
ability of radiographs at baseline and after 2 years of
followup. Spinal radiographs were scored by 2 trained
readers in a blinded, randomly selected order according
to the modified Stoke Ankylosing Spondylitis Spine
Score (mSASSS). Spinal radiographic progression was
defined as worsening of the mean mSASSS by >2 units
over 2 years.
Results. Among the patients with axial SpA,
14.3% showed spinal radiographic progression after 2
years (20% of those with AS and 7.4% of those with
nonradiographic axial SpA). The following parameters
were independently associated with spinal radiographic
progression: presence of syndesmophytes at baseline
(odds ratio [OR] 6.29, P < 0.001), elevated levels of
markers of systemic inflammation (for the erythrocyte
sedimentation rate, OR 4.04, P 0.001; for C-reactive
protein level time-averaged over 2 years, OR 3.81, P
0.001), and cigarette smoking (OR 2.75, P 0.012).
These associations were confirmed by multivariate lo-
gistic regression analysis. No clear association with
spinal radiographic progression was observed for HLA–
B27 status, sex, age, disease duration, Bath Ankylosing
Spondylitis Disease Activity Index, Bath Ankylosing
Spondylitis Functional Index, presence of peripheral
arthritis, enthesitis, psoriasis, treatment with non-
steroidal antiinflammatory drugs, or treatment with
disease-modifying antirheumatic drugs at baseline.
Conclusion. The presence of radiographic damage
at baseline (syndesmophytes), elevated levels of acute-
phase reactants, and cigarette smoking were all inde-
pendently associated with spinal radiographic progres-
sion in patients with early axial SpA.
The term axial spondylarthritis (SpA) refers to
patients with radiographic sacroiliitis fulfilling the mod-
ified New York criteria for ankylosing spondylitis (AS)
(1) and patients with nonradiographic axial SpA (i.e.,
patients without definite radiographic changes in the
sacroiliac joints) (2). Both groups of patients can be
The German Spondyloarthritis Inception Cohort has been
supported by the German Federal Ministry of Education and Research
(BMBF) (grant FKZ 01G19946), as part of the German Competence
Network in Rheumatology. Because funding by BMBF was reduced
according to schedule in 2005 and discontinued in 2007, complemen-
tary financial support was obtained from Abbott, Amgen, Centocor,
Schering-Plough, and Wyeth. Since 2010, additional support has been
provided by the BMBF through the ANCYLOSS and ArthroMark
projects.
1
Denis Poddubnyy, MD, Hildrun Haibel, MD, Joachim
Sieper, MD: Charite ´ Universita ¨tsmedizin, Campus Benjamin Franklin,
Berlin, Germany;
2
Joachim Listing, PhD: German Rheumatism Re-
search Centre, Berlin, Germany;
3
Elisabeth Ma ¨rker-Hermann, MD:
Horst Schmidt Kliniken, Wiesbaden, Germany;
4
Henning Zeidler,
MD: Medizinische Hochschule Hannover, Hannover, Germany;
5
Ju ¨r-
gen Braun, MD: Rheumazentrum Ruhrgebiet, Herne, Germany;
6
Martin Rudwaleit, MD: Evangelisches Krankenhaus Hagen-Haspe,
Hagen, Germany.
Dr. Ma ¨rker-Hermann has received consulting fees, speaking
fees, and/or honoraria from Abbott, Wyeth, Roche, Chugai, MSD, and
Pfizer (less than $10,000 each). Dr. Braun has received consulting fees,
speaking fees, and/or honoraria from Abbott, MSD, Pfizer, and UCB
(less than $10,000 each). Dr. Rudwaleit has received consulting fees,
speaking fees, and/or honoraria from Abbott, Bristol-Myers Squibb,
MSD, Pfizer, and UCB (less than $10,000 each).
Address correspondence to Joachim Sieper, MD, Rheuma-
tology, Medical Department I, Charite ´ Universita ¨tsmedizin, Campus
Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
E-mail: joachim.sieper@charite.de.
Submitted for publication February 27, 2011; accepted in
revised form November 1, 2011.
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