Methylglyoxal: A Relevant Marker of Disease Activity in Patients with Rheumatoid Arthritis
Open accessAbstract
Background . The contribution of methylglyoxal (MGO) and soluble receptor for advanced glycation end products (sRAGE) in the presence of rheumatoid arthritis (RA) is still unknown. We investigated whether serum MGO and sRAGE were related to the presence of disease activity in RA. Methods . 80 patients with RA and 30 control subjects were included in a cross-sectional study. The severity of RA was assessed using the disease activity score for 28 joints (DAS28). Serum MGO and sRAGE were measured by ELISA. Results . Serum MGO levels were significantly higher in patients with RA versus control subjects ( P < 0.001 ) and were increased in RA patients with higher disease activity versus RA patients with moderate disease activity ( P = 0.019 ). Serum sRAGE concentrations were significantly decreased in RA patients with higher disease activity versus RA patients with moderate disease activity and versus control subjects ( P = 0.004 ; P = 0.002 , resp.). A multiple logistic regression analysis demonstrated that MGO was independently associated with the presence of activity disease in RA (OR = 1.17, 95% CI: 1.02–1.31, P = 0.01 ). Conclusion . Serum MGO and sRAGE levels are inversely related to the activity of RA, and MGO is independently associated with a higher disease activity of RA.
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Serum pentosidine levels were higher in RA patients (n = 80) than in controls (n = 30), measured by ELISA.
“| RA | Serum | Control subjects (n = 30) vs. RA patients (n = 80) | ELISA | Higher CML and pentosidine levels in RA patients | [237,238] |”
From Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases (2021) · cites this paper as [238]
The Discussion says that CML and pentosidine were increased in RA, citing the authors’ earlier work. This paper studied 80 RA patients and 30 controls, but its Methods specify ELISA measurements of MGO and sRAGE, not pentosidine. It therefore does not establish that pentosidine was measured by ELISA or was higher in this particular cohort. (LLM, conf=0.88)
Experimental — accuracy not yet measuredSerum CML levels were higher in RA patients (n = 80) than in controls (n = 30), measured by ELISA.
“| RA | Serum | Control subjects (n = 30) vs. RA patients (n = 80) | ELISA | Higher CML and pentosidine levels in RA patients | [237,238] |”
From Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases (2021) · cites this paper as [238]
The Discussion reports that CML levels were increased in RA, citing the authors’ earlier work. But this paper’s Methods and Results describe ELISA measurements of MGO and sRAGE—not CML—in its 80 RA patients and 30 controls. It therefore does not establish the claimed CML measurement for that cohort. (LLM, conf=0.88)
Experimental — accuracy not yet measured
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- Authors
- Knani, I., Bouzidi, H., Zrour, S., Bergaoui, N., Hammami, M., & Kerkeni, M.
- Affiliations
- University of Monastir (TN)
- Laboratory of Biochemistry, University Hospital Tahar Sfar, Mahdia, Tunisia
- Hospital Fatuma Bourguiba Monastir (TN)
- Corresponding author
- Kerkeni, Mohsen
- Venue
- Disease Markers
- Publisher
- Wiley
- Published
- 2018
- Volume
- 2018
- Pages
- 1-6
- ISSN
- 0278-0240 (ISSN-L)
- 1875-8630
- PMC
- PMC5828101
- OpenAlex
- W2788508712
- Cited by
- 25
- References
- 43
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 2 · 2023: 5 · 2022: 5 · 2021: 4 · 2020: 3 · 2019: 2 · 2018: 1
- FWCI
- 1.94
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Disease Markers (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- University of Monastir
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
- Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
- Keywords
- methylglyoxal, rheumatoid arthritis, disease activity, soluble receptor for advanced glycation end products, serum biomarkers, DAS28, advanced glycation end products
- MeSH terms
- Adult, Arthritis, Rheumatoid, Cross-Sectional Studies, Female, Humans, Male, Middle Aged, Pyruvaldehyde, Severity of Illness Index, Biomarkers, Logistic Models, Glycation End Products, Advanced
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