Performance of the systemic lupus erythematosus risk probability index in a cohort of undifferentiated connective tissue disease

Author:

Erden Abdulsamet1,Apaydın Hakan1ORCID,Fanouriakis Antonis23ORCID,Güven Serdar Can1,Armagan Berkan1,Akyüz Dağlı Pınar1,Konak Hatice Ecem1,Polat Bünyamin1,Atalar Ebru1,Esmer Serdar1,Karakaş Özlem1,Özdemir Bahar1,Eksin Mehmet Akif1,Omma Ahmet1,Kücüksahin Orhan4,Bertsias George K56,Boumpas Dimitrios T27

Affiliation:

1. Clinic of Rheumatology, Ankara City Hospital , Ankara, Turkey

2. Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens

3. Rheumatology, ‘Asklepieion’ General Hospital , Athens, Greece

4. Division of Rheumatology, Department of Internal Medicine, Ankara City Hospital, Yıldırım Beyazıt University , Ankara, Turkey

5. Rheumatology, Clinical Immunology and Allergy, University of Crete School of Medicine

6. Institute of Molecular Biology and Biotechnology, Foundation of Research and Technology—Hellas , Heraklion, Crete

7. Laboratory of Immune Regulation and Tolerance, Autoimmunity and Inflammation, Biomedical Research Foundation of the Academy of Athens , Athens, Greece

Abstract

Abstract Objectives We sought to evaluate the performance of the SLE Risk Probability Index (SLERPI) for identification of SLE in a large cohort of patients with UCTD. Methods The SLERPI was applied in a cohort of patients who met classification criteria for UCTD and did not fulfil any classification criteria for other defined CTD including SLE. Patients with a SLERPI score of >7 were ‘diagnosed’ as SLE. Patients diagnosed with SLE and those not were compared in terms of disease characteristics and index parameters. Results A total of 422 patients with UCTD were included in the study. Median (interquartile range) SLERPI was 4.25 (2.5) points, while 39 (9.2%) patients had a SLERPI score >7 and were diagnosed as SLE. Patients with younger age (P = 0.026) and presence of malar rash (P < 0.0001), mucosal ulcer (P < 0.0001), alopecia (P < 0.0001), ANA positivity (P < 0.0001), low C3 and C4 (P = 0.002), proteinuria >500 mg/24 h (P = 0.001), thrombocytopenia (P = 0.009) or autoimmune haemolytic anaemia (P < 0.0001) were more likely to fulfil criteria for SLE by the SLERPI. Conclusion SLERPI enabled a significant proportion of patients to be identified as SLE in our UCTD cohort. This new probability index may be useful for early identification of SLE among patients with signs of CTD without fulfilling any definite criteria set.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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