Evidence map›Paper›PMID 40677467›Full record

ArticleCureus2025

Comparative Efficacy and Safety of Thalidomide and Sulfasalazine in Moderate to Severe Ankylosing Spondylitis: A Real-World Study From Bangladesh.

A F M Mahbubul Alam, Mohammad Abul Kalam Azad, M Masudul Hassan, Sajeda Islam, Md Nazrul Islam, Minhaj Rahim Choudhury, Syed Atiqul Haq

Abstract read
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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

A F M Mahbubul AlamRheumatology, Mymensingh Medical College, Mymensingh, BGD.
Mohammad Abul Kalam AzadRheumatology, Bangladesh Medical University, Dhaka, BGD.
M Masudul HassanRheumatology, Bangladesh Medical University, Dhaka, BGD.
Sajeda IslamPhysical Medicine and Rehabilitation, Mugda Medical College, Dhaka, BGD.
Md Nazrul IslamRheumatology, Bangabandhu Sheikh Mujib Medical University, Dhaka, BGD.
Minhaj Rahim ChoudhuryRheumatology, Bangladesh Medical University, Dhaka, BGD.
Syed Atiqul HaqRheumatology, Green Life Center for Rheumatic Care and Research, Dhaka, BGD.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe present study aimed to determine the efficacy and safety of thalidomide compared to sulfasalazine (SSZ) in moderate to severe cases of ankylosing spondylitis (AS) in Bangladesh.

methodsThis experimental study was conducted from January 2017 to December 2018 in the Department of Rheumatology, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh. The experimental study included 93 adult patients with moderate to severe AS (47 received thalidomide, and 46 received SSZ). Change in disease status was considered an efficacy endpoint, while the prevalence of adverse events was considered a safety endpoint.

resultsThalidomide showed better efficacy compared to SSZ in terms of disease activity index (Bath Ankylosing Spondylitis Disease Activity Index) (2.84 vs. 4.49, p < 0.001). Secondary endpoints such as functional index (Bath Ankylosing Spondylitis Functional Index) (2.32 vs. 3.34, p = 0.021), patients' global assessment (2.92 vs. 4.11, p < 0.001), physician global assessment (2.67 vs. 3.60, p < 0.001), spinal pain score (2.52 vs. 3.31, p = 0.025), swollen joint count (0.05 vs. 0.40, p < 0.001), morning stiffness (2.08 vs. 3.27, p < 0.001), erythrocyte sedimentation rate (28.17 mm vs. 34.25 mm, p = 0.023), and C-reactive protein (9.57 mg/l vs. 21.34 mg/l, p = 0.027) were also better in the thalidomide group. Moreover, a significantly higher number of patients achieved 40% improvement in the thalidomide group compared to the SSZ group (90% vs. 10%, p < 0.001). Pedal edema was the most common adverse event (16, 46%) in the thalidomide group, followed by somnolence (13, 37%), drowsiness (12, 34%), dry mouth (11, 31%), and skin rash (11, 31%). On the other hand, anorexia (17, 48%), headache (15, 43%), and gastric irritation (10, 28%) were common adverse events in the SSZ group.

conclusionDespite a few mild side effects, thalidomide is effective and safe in comparison with SSZ for treating patients with moderate to severe AS for short-term assessment.

Indexed as

ankylosing spondylitisback painspondyloarthritissulfasalazinethalidomide

Identifiers

PMID40677467
PMCPMC12269721

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.