Serum CXCL-13 levels are associated with active neurological involvement in patients with systemic lupus erythematosus

<b>Background:</b> Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse systemic manifestations, including neuropsychiatric involvement (NPSLE), which can vary in severity and prognosis. Diagnosing NPSLE remains challenging, necessitating reliable diagnostic markers. CXCL13, a B-cell chemokine implicated in SLE, has garnered attention for its potential role in NPSLE.<b>Purpose:</b> This study aimed to assess serum CXCL-13 levels in NPSLE patients compared to SLE patients without neuropsychiatric symptoms and healthy controls.<b>Research Design:</b> All study groups were studied CXCL-13 levels from blood samples.<b>Study Sample:</b> One hundred twenty-five participants were categorized into four groups: SLE patients with active NPSLE (<i>n</i> = 6), SLE patients with inactive NPSLE (<i>n</i> = 26), SLE patients without NPSLE (<i>n</i> = 71), and healthy controls (<i>n</i> = 22).<b>Data Collection and Analyses:</b> Serum samples were collected at the time of enrollment and CXCL-13 levels were analysed by Enzyme Linked ImmunoSorbent Assay (ELISA) method.<b>Results:</b> Results indicated significantly elevated CXCL-13 levels in active NPSLE patients compared to other SLE patient groups and healthy controls (<i>p</i> < 0.001 for all). Patients with SLE, including those with inactive NPSLE or no history of NPSLE, had statistically significantly higher serum CXCL-13 levels compared to the control group (<i>p</i> < 0.001). Additionally, serum CXCL-13 levels positively correlated with disease activity assessed by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI).<b>Conclusion:</b> This study underscores the association between serum CXCL-13 levels and neuropsychiatric involvement in SLE, as well as their correlation with disease activity. Moreover, previous research suggesting a link between CXCL-13 levels and clinical activity in SLE further supports its potential as a diagnostic marker for NPSLE. Nevertheless, further investigations are warranted to validate the utility of CXCL-13 as a diagnostic tool for NPSLE and its role in disease management.

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Journal
Lupus
Published
2025-02-07
DOI
https://doi.org/10.1177/09612033251319405
Citations
2
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
3.34
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article

Serum CXCL-13 levels are associated with active neurological involvement in patients with systemic lupus erythematosus

Berna Göker, Burcugül Kaya, Hamit Küçük, Rıza Can Kardaş et al.
2 citations
Lupus
Systemic Lupus Erythematosus Research
3.34
article

Serum CXCL-13 levels are associated with active neurological involvement in patients with systemic lupus erythematosus

Berna Göker, Burcugül Kaya, Hamit Küçük, Rıza Can Kardaş, Abdurrahman Tufan, Mehmet Akif Öztürk, Hakan Babaoğlu, Hazan Karadeniz, İbrahim Vasi, Antonis Fanouriakis, Abdülsamet Erden, Rahime Duran, Derya Yıldırım, Handenur Koç Kanık
article en
2 citations

Abstract

<b>Background:</b> Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse systemic manifestations, including neuropsychiatric involvement (NPSLE), which can vary in severity and prognosis. Diagnosing NPSLE remains challenging, necessitating reliable diagnostic markers. CXCL13, a B-cell chemokine implicated in SLE, has garnered attention for its potential role in NPSLE.<b>Purpose:</b> This study aimed to assess serum CXCL-13 levels in NPSLE patients compared to SLE patients without neuropsychiatric symptoms and healthy controls.<b>Research Design:</b> All study groups were studied CXCL-13 levels from blood samples.<b>Study Sample:</b> One hundred twenty-five participants were categorized into four groups: SLE patients with active NPSLE (<i>n</i> = 6), SLE patients with inactive NPSLE (<i>n</i> = 26), SLE patients without NPSLE (<i>n</i> = 71), and healthy controls (<i>n</i> = 22).<b>Data Collection and Analyses:</b> Serum samples were collected at the time of enrollment and CXCL-13 levels were analysed by Enzyme Linked ImmunoSorbent Assay (ELISA) method.<b>Results:</b> Results indicated significantly elevated CXCL-13 levels in active NPSLE patients compared to other SLE patient groups and healthy controls (<i>p</i> < 0.001 for all). Patients with SLE, including those with inactive NPSLE or no history of NPSLE, had statistically significantly higher serum CXCL-13 levels compared to the control group (<i>p</i> < 0.001). Additionally, serum CXCL-13 levels positively correlated with disease activity assessed by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI).<b>Conclusion:</b> This study underscores the association between serum CXCL-13 levels and neuropsychiatric involvement in SLE, as well as their correlation with disease activity. Moreover, previous research suggesting a link between CXCL-13 levels and clinical activity in SLE further supports its potential as a diagnostic marker for NPSLE. Nevertheless, further investigations are warranted to validate the utility of CXCL-13 as a diagnostic tool for NPSLE and its role in disease management.

LupusVol. 34(3)
National and Kapodistrian University of Athens (GR), Memorial Ankara Hospital (TR), Gazi University (TR)
Good health and well-being
Openalex Percentile: Top 10%
Systemic Lupus Erythematosus Research
3.34
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