Seminars in arthritis and rheumatism · 2025
Circulating biomarkers and detection of pulmonary diseases in patients with systemic lupus erythematosus: A systematic review and meta-analysis of observational studies.
СтатьяСистематический обзорМетаанализНазвание и аннотация: Перевод в очереди
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Langkilde Henrik Zachar, Davidsen Jesper Rømhild, Harders Stefan Markus Walbom, Patabendige Sanjeewa, Nilsson Christine, Svenungsson Elisabet, Touma Zahi, Fløjborg Sille, Christensen Robin, Voss Anne
Аннотация
BACKGROUND: Pulmonary diseases (PD) in systemic lupus erythematosus (SLE) are common and cover several entities. Diagnosing PD in SLE is often challenging, why reliable biomarkers are warranted. Several studies have explored the relationship between circulating biomarkers (CB) and detection of PD in SLE, but with conflicting results.
OBJECTIVE: To investigate evidence supporting associations between CB and PD in SLE through a systematic literature review of observational studies.
METHOD: We searched MEDLINE and EMBASE for studies addressing potential associations between CB and PD in SLE. Afterwards forward- and backward citation search was performed. Internal validity and risk of bias were addressed with Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) and Outcome Reporting Bias in Trials (ORBIT). Association between CB and PD across studies were investigated through meta-analyses and individual studies were summarized in tables.
RESULTS: We identified 13,504 references; of these, 24 studies were eligible, including 1883 patients and 43 different CB. In individual studies 21 different CB were significantly associated with PD. Meta-analyses resulted in 10 associations of potential clinical significance between PD or PD-related outcomes and five CB (anti-double stranded DNA antibodies, anti-Ribonucleoprotein antibodies, anti-Smith antibodies, CC motif Ligand 21, and Interferon Gamma Inducible Protein 10).
CONCLUSION: Through meta-analyses we identified CB that were significantly associated with PD in SLE including anti-dsDNA. Furthermore, anti-dsDNA, anti-Sm, anti-RNP, and CCL21 were associated with reduced pulmonary function in SLE. The results were rated with very low certainty of evidence, why they are hypothesis generating. Further studies addressing associations are needed.
OBJECTIVE: To investigate evidence supporting associations between CB and PD in SLE through a systematic literature review of observational studies.
METHOD: We searched MEDLINE and EMBASE for studies addressing potential associations between CB and PD in SLE. Afterwards forward- and backward citation search was performed. Internal validity and risk of bias were addressed with Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) and Outcome Reporting Bias in Trials (ORBIT). Association between CB and PD across studies were investigated through meta-analyses and individual studies were summarized in tables.
RESULTS: We identified 13,504 references; of these, 24 studies were eligible, including 1883 patients and 43 different CB. In individual studies 21 different CB were significantly associated with PD. Meta-analyses resulted in 10 associations of potential clinical significance between PD or PD-related outcomes and five CB (anti-double stranded DNA antibodies, anti-Ribonucleoprotein antibodies, anti-Smith antibodies, CC motif Ligand 21, and Interferon Gamma Inducible Protein 10).
CONCLUSION: Through meta-analyses we identified CB that were significantly associated with PD in SLE including anti-dsDNA. Furthermore, anti-dsDNA, anti-Sm, anti-RNP, and CCL21 were associated with reduced pulmonary function in SLE. The results were rated with very low certainty of evidence, why they are hypothesis generating. Further studies addressing associations are needed.