High prolidase levels in patients with Familial Mediterranean Fever (FMF)

Author:

Bayram Meliha1,Derin Mehmet Emin2,Doğan Halef Okan3,Asan Gökmen1,Şahin Mehtap3,Şahin Ali2

Affiliation:

1. Department of Internal Medicine , Cumhuriyet University , Faculty of Medicine , Sivas , Turkey

2. Department of Internal Medicine – Rheumatology , Cumhuriyet University , Faculty of Medicine , Sivas , Turkey

3. Department of Biochemistry , Cumhuriyet University , Faculty of Medicine , Sivas , Turkey

Abstract

Abstract Introduction. Familial Mediterranean Fever (FMF) is an autoinflammatory disease. Prolidase is a specific imidodipeptidase that plays a role in collagen degradation, and an important role in inflammation and wound healing. Hypoxia-inducible factor-1α (HIF-1) is an important protein in the regulation of immunological response, hemostasis, vascularization. The aim of the study was to compare serum prolidase and HIF-1α levels in patients with FMF in attack-free period and healthy control group. Methods. Between August 2017 and December 2017, sixty patients diagnosed with FMF according to the criteria of the Tel-hashomer and admitted to Sivas Cumhuriyet University Medical Faculty, Internal Medicine Rheumatology Department and sixty healthy volunteers were enrolled in the study. Results. Median serum prolidase levels were 72.1 (25.1–114.9) ng/ml in FMF group and 30.7 (21.3–86.2) ng/mL in healthy control (HC) group (p = 0.018). ROC analysis showed that the sensitivity was 65% and the specificity was 68.3% at serum prolidase levels 54.03 ng/mL (p < 0.05). The median serum levels of HIF-1α in the FMF group was 482.0 (292.0–3967.0) pg/mL and 632.0 (362.0–927.0) pg/mL in the HC group (p > 0.05). There was no significant correlation between laboratory findings, sex, age, and prolidase (p > 0.05). Conclusion. Serum prolidase enzyme levels in FMF patients with attack-free period were significantly higher than in the HC group. However, the role of prolidase and HIF1-α in the FMF disease needs to be clarified with more extensive and comprehensive studies.

Publisher

Walter de Gruyter GmbH

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