Steroids in Ankylosing Spondylitis
Systemic corticosteroids should be strongly avoided for axial disease in ankylosing spondylitis, while local corticosteroid injections may be used selectively for peripheral manifestations. 1
Systemic Corticosteroids: Not Recommended
The use of systemic glucocorticoids for axial disease is not supported by evidence and is strongly recommended against. 1 This represents a Grade A recommendation from both ASAS/EULAR and ACR/SAA/SPARTAN guidelines, despite being based on very low quality evidence—the strength of the recommendation reflects the lack of efficacy data combined with well-established risks. 1
The rationale for avoiding systemic steroids is multifactorial:
- No demonstrated efficacy: There are no controlled trials showing benefit for axial symptoms, which constitute the primary disease manifestation in AS. 1
- Significant comorbidity burden: Patients with AS already face increased risks of osteoporosis and cardiovascular disease—two conditions that systemic corticosteroids directly worsen. 1, 2
- Bone health concerns: Corticosteroids decrease bone formation and increase bone resorption through effects on calcium regulation and osteoblast inhibition, particularly problematic given that AS patients already have elevated osteoporosis risk. 2
- Metabolic complications: The FDA label for prednisone explicitly warns about glucose intolerance, sodium retention with edema, and cardiovascular effects—all relevant to the AS population. 2
Local Corticosteroid Injections: Conditionally Recommended
Corticosteroid injections directed to the local site of musculoskeletal inflammation may be considered for specific peripheral manifestations. 1
Appropriate Use Cases:
- Isolated active sacroiliitis despite NSAIDs: Conditionally recommend locally administered parenteral glucocorticoids (very low quality evidence). 1
- Active peripheral arthritis with stable axial disease despite NSAIDs: Conditionally recommend intra-articular glucocorticoids. 1
- Active enthesitis with stable axial disease despite NSAIDs: Conditionally recommend local glucocorticoids. 1
Critical Safety Caveat:
Peri-tendon injections of Achilles, patellar, and quadriceps tendons must be avoided due to rupture risk. 1, 3 This represents a specific contraindication even when local steroid therapy is otherwise appropriate. 3
Small RCTs have demonstrated level Ib evidence for efficacy of intra-articular or periarticular corticosteroid injections for sacroiliac joint pain, though no studies exist for peripheral arthritis or enthesitis specifically in AS. 1
Recommended Treatment Algorithm
First-line therapy: NSAIDs (including COX-2 inhibitors) for pain and stiffness, with continuous treatment preferred over on-demand use for persistently active disease. 1
Second-line for axial disease: Anti-TNF therapy for persistently high disease activity despite conventional treatments—not systemic corticosteroids. 1
For peripheral manifestations only: Consider local corticosteroid injections to specific inflamed sites (avoiding peri-tendon areas), while sulfasalazine may be added for peripheral arthritis. 1
Comorbidity management: Given the increased cardiovascular and osteoporosis risk in AS, rheumatologists must actively screen for and manage these conditions rather than adding systemic corticosteroids that would exacerbate both. 1
Common Pitfalls
Do not use oral corticosteroids as a bridge to biologic therapy—this practice lacks evidence and exposes patients to unnecessary risks. 1 The guidelines explicitly state there is no evidence to support obligatory DMARD use before anti-TNF therapy, and the same principle applies to corticosteroids. 1
Do not inject corticosteroids into or around the Achilles tendon insertion—this carries significant rupture risk even when treating legitimate enthesitis. 1, 3
Do not overlook the osteoporosis risk—if systemic corticosteroids are used for any reason (such as extra-articular manifestations managed by other specialists), bone protection strategies including calcium, vitamin D, bisphosphonates, and weight-bearing exercise must be implemented for any patient anticipated to receive ≥5 mg prednisone equivalent for ≥3 months. 2