scholarly journals Neutrophil-lymphocyte ratio in children with familial Mediterranean fever: original article

2015 ◽  
Vol 2 (1) ◽  
pp. 20-23 ◽  
Author(s):  
Fatma Duksal ◽  
Demet Alaygut ◽  
Ahmet Sami Guven ◽  
Mahmut Ekici ◽  
Mehmet Burhan Oflaz ◽  
...  
2014 ◽  
Vol 29 (1) ◽  
pp. 80-83 ◽  
Author(s):  
Mehmet Celikbilek ◽  
Serkan Dogan ◽  
Lutfi Akyol ◽  
Elif Borekci ◽  
Gokmen Zararsiz ◽  
...  

Inflammation ◽  
2013 ◽  
Vol 36 (6) ◽  
pp. 1357-1362 ◽  
Author(s):  
Ahmet Ahsen ◽  
Memnune Sena Ulu ◽  
Seref Yuksel ◽  
Kasım Demir ◽  
Mukremin Uysal ◽  
...  

2021 ◽  
Author(s):  
Esra Nagehan Akyol Onder ◽  
Fethi Sirri Cam ◽  
Pelin Ertan

Abstract Background Familial Mediterranean Fever (FMF), which is characterised by recurrent episodes of fever with serositis, is associated with ongoing inflammation without clinical findings during attack-free periods, leading to amyloidosis, the most important complication of FMF. The objective of this study was to investigate the C-reactive protein/albumin ratio (CAR) as a marker to identify subclinical inflammation in symptom-free FMF children and compare the CAR with other systemic inflammatory markers such as mean platelet volume (MPV), red cell distribution width (RDW), neutrophil/lymphocyte ratio (NLR) and platelet/lymphocyte ratio (PLR). Material and Methods We included 100 patients and 70 healthy subjects. Hospital records were obtained to collect data on laboratory findings and genetic mutations. Results We found that the CAR levels of our FMF patients were significantly higher than those of the control group. We also evaluated that the CAR values had a higher area-under-the-curve value than the other systemic inflammation parameters including CRP, MPV, RDW, NLR, PLR based on Receiver-Operating Characteristics (ROC) analysis. Conclusion It is important to identify subclinical inflammation in FMF patients with simple, reliable, easily accessible markers to avoid amyloidosis. Although the CAR might be used to assess subclinical inflammation in paediatric FMF patients, the prognostic value of CAR is not superior to CRP. Merging CRP and albumin into a single index thus provides no additional benefit in detecting subclinical inflammation in FMF.


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