Cited by 23Advanced Glycation End Products researchRheumatoid Arthritis Research and TherapiesGlycosylation and Glycoproteins Research

Increased serum concentrations of N ɛ -carboxymethyllysine are related to the presence and the severity of rheumatoid arthritis

Knani, Ines, Bouzidi, Hassan, Zrour, Saoussen, Bergaoui, Naceur, Hammami, Mohamed, Kerkeni, Mohsen·2018·Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

Abstract

Background There are limited data regarding the contribution of advanced glycation end products in the presence of rheumatoid arthritis. We investigated whether serum N ɛ -carboxymethyllysine and pentosidine were related to the presence and the severity of rheumatoid arthritis. Methods Eighty patients with rheumatoid arthritis and 30 control subjects were included in a cross-sectional study. The severity of rheumatoid arthritis was assessed using the disease activity score for 28 joints. Serum N ɛ -carboxymethyllysine and pentosidine were measured by enzyme-linked immunosorbent assay. Results Serum N ɛ -carboxymethyllysine and pentosidine concentrations were significantly higher in patients with rheumatoid arthritis vs. control subjects ( P ɛ -carboxymethyllysine and pentosidine concentrations were significantly higher in rheumatoid arthritis patients with high disease activity vs. rheumatoid arthritis patients with moderate disease activity ( P ɛ -carboxymethyllysine was independently associated with the presence of rheumatoid arthritis (OR = 1.21, 95% CI: 1.05-1.39, P = 0.006). Furthermore, in a multivariate stepwise regression analysis, N ɛ -carboxymethyllysine was independently correlated with disease activity score for 28 joints (standardized β = 0.43, P = 0.001). Conclusion Serum N ɛ -carboxymethyllysine and pentosidine were increased during rheumatoid arthritis, and N ɛ -carboxymethyllysine was independently associated with the presence and the severity of rheumatoid a…

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Crossref · 10.1177/0004563217733500

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References 38 · Cited by 23

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
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine
Published
2017-11-03
Volume
55
Issue
4
Pages
430-436
ISSN
  • 0004-5632 (ISSN-L)
  • 1758-1001
OpenAlex
W2808791865
Cited by
23
References
38
Citations by year
2026: 4 · 2025: 1 · 2024: 4 · 2023: 3 · 2021: 4 · 2020: 3 · 2019: 2 · 2018: 2
FWCI
1.59
Type
journal article
Language
en
Open access
closed
Locations
  • Annals of Clinical Biochemistry International Journal of Laboratory Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
Keywords
rheumatoid arthritis, carboxymethyllysine, pentosidine, advanced glycation end products, serum biomarkers, disease activity, DAS28, disease severity
MeSH terms
Adult, Arginine, Arthritis, Rheumatoid, Cross-Sectional Studies, Enzyme-Linked Immunosorbent Assay, Female, Humans, Lysine, Male, Middle Aged, Severity of Illness Index, Biomarkers, Case-Control Studies

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