Publications by authors named "Sibel Yilmaz-Oner"

There are limited follow-up parameters for familial Mediterranean fever (FMF) related to disease severity and amyloidosis. Some hematological markers are emerging to assess inflammation. In this study, we hypothesized that some hematological parameters could be used to determine disease severity and amyloidosis in FMF.

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Introduction: Familial Mediterranean fever (FMF) is one of the common autoinflammatory diseases with multisystemic manifestation. Pleuritis is the only known pulmonary involvement of FMF; however, as far as we know, thoracic involvements in pleural, parenchymal, bronchial, and vascular structures have not been evaluated yet.

Method: We included 243 consecutive FMF patients who applied to our clinic within the last 5 years and were requested to have a thorax CT for any reason and 122 trauma patients without any comorbidity.

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Introduction: Exertional leg pain (ELP) and enthesitis are musculoskeletal findings in familial Mediterranean fever (FMF). They are not accepted as principal treatment targets. In this study, we assessed the effectiveness of treatments on ELP and enthesitis.

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Objective: To compare the clinical features, laboratory findings, and prognosis of Behçet's disease (BD) patients with and without Budd-Chiari syndrome (BCS).

Methods: This multicenter retrospective study investigated 61 (M/F: 41/20) patients with BD, having coexistent BCS, and 169 (M/F:100/69) BD patients as the control group without BCS from 22 different centers of Turkey diagnosed between 1990 and 2017.

Results: Of the total 61 BD patients with BCS, the onset of the first symptom and the median age of diagnosis were earlier in contrast to BD patients without BCS (p = 0.

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Introduction: Exertional leg pain (ELP) and enthesitis are musculoskeletal findings in familial Mediterranean fever (FMF). They are not accepted as principal treatment targets. In this study, we assessed the effectiveness of treatments on ELP and enthesitis.

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Article Synopsis
  • Familial Mediterranean fever (FMF) is a disease that can cause inflammation and pain in the body, and some FMF patients also show signs of enthesitis, which is pain where tendons and ligaments attach to bones.
  • In a study with 238 FMF patients, researchers found that 54 of them (about 23%) had enthesitis and these patients also experienced more severe symptoms and more frequent attacks than those without it.
  • The study suggests that enthesitis might indicate a more serious form of FMF and is often linked to other related problems, like joint pain and fever.
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Objective: To determine predictors and optimal duration of sustained remission (SR) in patients with rheumatoid arthritis (RA).

Methods: A total of 428 consecutive patients with RA visiting our clinic routinely between 2012 and 2013 were evaluated. Seventy seven of these patients in DAS28 remission were enrolled and followed up for 62.

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Objective: We have conducted this study to evaluate clinical and laboratory findings and to gather and evaluate information that would be useful in clinical practice, such as demographics, joint involvement patterns, laboratory anomalies, treatments applied, and responses obtained in patients diagnosed with gout.

Methods: In our study, the demographic, clinical, and laboratory characteristics of 94 patients diagnosed with gout were evaluated. The patients were re-evaluated with regard to their clinical and laboratory findings at the end of the 1 and 3 months, their responses to the treatment were observed, and where necessary, new treatment adjustments were made.

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Background/aim: The distribution of Mediterranean fever (MEFV) gene mutations in Turkish familial Mediterranean fever (FMF) patients varies according to geographic area of Turkey. There is a need for highly representative data for Turkish FMF patients. The aim of our study was to investigate the distribution of the common MEFV mutations in Turkish FMF patients in a nationwide, multicenter study.

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Rheumatoid nodules are the most common pulmonary manifestations of rheumatoid arthritis (RA) and are usually asymptomatic. In rare cases, they progress cavitary formation and cause severe clinical symptoms because of disease activity, infectious diseases, and other etiologies. The determination of clinical and histopathological features may be helpful for differential diagnosis in patients with RA with cavitary pulmonary nodules.

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Article Synopsis
  • The study looked at Familial Mediterranean fever (FMF), which is a disease where the body has improper inflammation, and focused on mutations in a specific part of the gene called exons.
  • Researchers checked data from over 2,200 FMF patients to see how different mutations affected their health.
  • They found that patients with mutations in exon 10 had worse symptoms than those with mutations in exon 2, meaning exon 10 mutations are associated with more severe cases of FMF.
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  • This study investigates the prevalence of inflammatory back pain (IBP), radiologic sacroiliitis, and spondyloarthritis (SpA) in patients with primary Sjögren's syndrome (SS), aiming to find a connection between these conditions.
  • Conducted with 85 primary SS patients and a control group of 100, results showed a significant occurrence of IBP and radiologic sacroiliitis in primary SS patients compared to controls.
  • The study concludes that IBP and sacroiliitis are more common in primary SS patients; however, it's unclear whether this is due to SpA coexisting with SS or if IBP is simply underdiagnosed in SS cases, suggesting further research is needed.
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Rheumatoid arthritis (RA) prevalence increases with age and old people are special patient population. The recognition of functional disability related to RA could be challenging in elderly patients because aging itself and potential co-morbid disease may also cause functional disability. In this study, we aimed to look at the correlation between disease activity and functional disability in elderly RA patients.

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Article Synopsis
  • The study investigates differences between early onset (≤20 years) and late onset (>20 years) Familial Mediterranean fever (FMF), focusing on patient demographics, clinical features, and genetic variations.
  • Out of 2,246 FMF patients in Turkey, 72.7% were in the early onset group, which experienced more severe symptoms and longer diagnosis delays, such as fever and arthritis.
  • Genetic analysis revealed that early onset patients had a higher prevalence of M694V mutations, suggesting this mutation may lead to more severe early disease manifestations.
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Objective: Approximately 30-45% of patients with familial Mediterranean fever (FMF) have been reported to have attacks despite colchicine treatment. Currently, data on the treatment of colchicine-unresponsive or colchicine-intolerant FMF patients are limited; the most promising alternatives seem to be anti-interleukin-1 (anti-IL-1) agents. Here we report our experience with the off-label use of anti-IL-1 agents in a large group of FMF patients.

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Article Synopsis
  • The study investigated the link between oral ulcer activity and medication adherence in 330 patients with Behçet's disease, focusing on gender differences.
  • Results showed that 66.4% of patients had active oral ulcers, with women exhibiting more ulcers if they had low medication adherence, unlike male patients where no significant link was found.
  • The findings suggest that low medication adherence is a critical factor in managing Behçet's disease, especially for female patients experiencing more severe oral ulcer activity.
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Gallstone (GS) formation is a multifactorial process and one of the associated factors is hyperinsulinemia. The aim of this cross-sectional study was to determine the association between size and count of gallstones, and insulin levels and resistance. The study group composed of 84 patients who have ultrasonographically confirmed gallstone(s).

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Objectives: Fatigue is a common symptom of chronic inflammatory diseases. The objective of this study was to investigate fatigue in patients with Behçet's syndrome (BS) and to examine the relationship between fatigue and disease activity, quality of life, anxiety and depression.

Methods: This is a cross-sectional study of 123 BS patients and 71 healthy controls in Turkey.

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Article Synopsis
  • The study focused on understanding the levels of certain substances (biomarkers) in the blood of patients with rheumatoid arthritis (RA) who are in remission, which means their symptoms are much better or gone.
  • It looked at 80 patients in remission and compared their biomarker levels to 80 healthy people to see any differences.
  • The results showed that even though patients were considered in remission, some of their biomarker levels were still higher than those of healthy individuals, suggesting that these levels could help doctors understand more about the patient's condition and whether they might get worse.
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A relationship between the presence of amyloidosis and SAA1 genotype has been shown in recent studies of (principally) familial Mediterranean fever patients. We found that the SAA1 rs12218 polymorphism was significantly more prevalent in ankylosing spondylitis patients with amyloidosis.

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Normal/increased pressure hydrocephaly is an unusual manifestation of systemic lupus erythematosus (SLE), and the pathogenesis is still unclear. We report the case of an 18-year-old white female with severe refractory renal and pulmonary involvement who developed stupor during intensive immunosuppressive treatment. Enlarged ventricles on imaging and increased intracranial pressure with the exclusion of infectious and hemorrhagic/thrombotic processes suggested increased pressure communicating hydrocephalus associated with SLE.

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The LupusQoL is a disease-specific health-related quality of life (HRQoL) measure for patients with lupus. We conducted this study to compare the efficiency of LupusQoL-TR (validated Turkish version of the LupusQoL questionnaire) with the 36-item Short-Form Health Survey (SF-36), a generic quality of life (QoL) scale, in Turkish patients with lupus. Both questionnaires were conducted at a single visit to the clinic.

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Objectives: The aim of our study was to evaluate quality of life (QoL) in patients with systemic lupus erythematosus (SLE) and assess the impact of disease activity and psychological distress on health-related quality of life (HRQoL) in Turkey.

Methods: The Medical Outcomes Study Short Form (SF) -36 was used in a cohort of 113 consecutive patients with SLE and 123 age- and gender-matched healthy subjects to measure HRQoL. Patients' disease activity was assessed with SLE disease activity index (SLEDAI) and psychological distress was evaluated by the Hospital Anxiety and Depression Scale (HADS) for all participants.

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Objectives: Leptin, is a fat tissue hormone which effects energy expenditure, food intake , hematopoiesis, osteogenesis, angiogenesis, reproductive and immune systems. We aimed to determine serum leptin levels and investigate the association between disease activity and other parameters in RA patients.

Methods: Patients with RA (n=106) as the study group, healthy controls (n=52) and osteoarthritis (OA) patients (n=37) as a control group were enrolled to the study.

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Objective: To investigate the effect of depression, anxiety, fatigue, and fibromyalgia (FM) on the remission status in patients with rheumatoid arthritis (RA), defined according to the 28-joint count Disease Activity Score (DAS28)-erythrocyte sedimentation rate (ESR) and the Boolean-based new American College of Rheumatology/European League Against Rheumatism remission criteria.

Methods: The subjects were patients with RA who participated in a hospital-based observational cohort. Patients who met the DAS28-ESR remission criteria at their latest visit were invited to participate in our study.

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