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Meta-Analysis
. 2024 Sep 4;24(1):207.
doi: 10.1007/s10238-024-01478-x.

Diagnostic accuracy of the neutrophil-to-lymphocyte ratio and the platelet-to-lymphocyte ratio in rheumatoid arthritis: a systematic review and meta-analysis

Affiliations
Meta-Analysis

Diagnostic accuracy of the neutrophil-to-lymphocyte ratio and the platelet-to-lymphocyte ratio in rheumatoid arthritis: a systematic review and meta-analysis

Arduino A Mangoni et al. Clin Exp Med. .

Abstract

Existing challenges with the early diagnosis of rheumatoid arthritis (RA) and active disease, mainly by non-rheumatologists, have prompted the search for novel biomarkers. Elevations in indices derived from blood cell counts, e.g., the neutrophil-to-lymphocyte ratio (NLR) and the platelet-to-lymphocyte ratio (PLR), have been reported in RA patients. However, their diagnostic accuracy has not been comprehensively assessed. Therefore, we conducted a systematic review and meta-analysis of studies reporting the sensitivity and specificity of the NLR and PLR, obtained by receiver operating characteristic (ROC) curve analysis, for the presence of RA and active disease. We searched electronic databases from inception to 15 March 2024 and assessed the risk of bias using the JBI Critical Appraisal Checklist (PROSPERO registration number: CRD42024533546). In 15 studies, the NLR exhibited acceptable accuracy for the presence of RA (area under the curve, AUC = 0.76, 95% CI 0.72 to 0.80) and active disease (AUC = 0.70, 95% CI 0.66 to 0.74). The PLR exhibited good accuracy for the presence of RA (AUC = 0.80, 95% CI 0.76 to 0.83). There were insufficient studies to assess the accuracy of the PLR for the presence of active disease. Our systematic review and meta-analysis suggests that the NLR and the PLR are promising biomarkers of RA (NLR and PLR) and active disease (NLR). Further research is required to investigate whether the NLR and PLR can significantly enhance the capacity to diagnose RA and active disease in clinical practice.

Keywords: Active disease; Diagnostic accuracy; Lymphocyte ratio; Neutrophil; Platelet; Rheumatoid arthritis; To.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Flow chart of study selection
Fig. 2
Fig. 2
Forest plot of the pooled estimates of sensitivity and specificity of the neutrophil-to-lymphocyte ratio for the presence of rheumatoid arthritis
Fig. 3
Fig. 3
Summary receiver operating characteristics curve with 95% confidence region and prediction region of the neutrophil-to-lymphocyte ratio for the presence of rheumatoid arthritis
Fig. 4
Fig. 4
Fagan’s nomogram of the neutrophil-to-lymphocyte ratio for the presence of rheumatoid arthritis
Fig. 5
Fig. 5
Forest plot of the pooled estimates of sensitivity and specificity of the neutrophil-to-lymphocyte ratio for the presence of active disease
Fig. 6
Fig. 6
Summary receiver operating characteristics curve with 95% confidence region and prediction region of the neutrophil-to-lymphocyte ratio for the presence of active disease
Fig. 7
Fig. 7
Fagan’s nomogram of the neutrophil-to-lymphocyte ratio for the presence of active disease
Fig. 8
Fig. 8
Forest plot of the pooled estimates of sensitivity and specificity of the platelet-to-lymphocyte ratio for the presence of rheumatoid arthritis
Fig. 9
Fig. 9
Summary receiver operating characteristics curve with 95% confidence region and prediction region of the platelet-to-lymphocyte ratio for the presence of rheumatoid arthritis
Fig. 10
Fig. 10
Fagan’s nomogram of the neutrophil-to-lymphocyte ratio for the presence of rheumatoid arthritis

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