familial mediterranean fever/obesity

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Down-regulation of adiponectin in patients with familial Mediterranean fever during attack-free period.

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To evaluate the circulating levels of adipokines (leptin and adiponectin) and ghrelin in patients with familial Mediterranean fever (FMF) and also to assess the relationships between these molecules and disease-related parameters. Forty-eight FMF patients in attack-free period (31 men, [M], 17

Pseudotumor cerebri with familial Mediterranean fever.

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Pseudotumor cerebri (PC) is a condition that occurs predominantly in obese women, and long lists of putative causes and associations have been reported. We describe here the case of a woman in whom PC coexisted with familial Mediterranean fever (FMF). A review of the literature revealed no report of

The evaluation of cochlear functions in Familial Mediterranean Fever.

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Familial Mediterranean Fever (FMF) is a progressive disease characterized by chronic inflammation, which also has negative effects on cochlear functions and hearing levels. We investigated whether the cochlear functions and hearing levels of FMF patients were different than healthy controls and also

Is there a relationship between serum omentin level and acute phase response in patients with familial Mediterranean fever?

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Objectives: Familial Mediterranean fever (FMF) is an autoinflammatory disease characterized by frequent attacks and chronic inflammation. Subclinical inflammation continues during the attack-free period. Omentin is an anti-inflammatory

The effect of plasminogen activator inhibitor-1 -675 4G/5G polymorphism on familial Mediterranean fever (FMF) disease.

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Familial Mediterranean fever (FMF) is an autosomal recessive disease that is the most common of a rare group of disorders collectively termed familial hereditary periodic fever syndromes, also known as autoinflammatory syndromes. FMF is predominantly affecting people of Mediterranean descent and

Obesity is a significant susceptibility factor for idiopathic AA amyloidosis.

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BACKGROUND To investigate obesity as susceptibility factor in patients with idiopathic AA amyloidosis. METHODS Clinical, biochemical and genetic data were obtained from 146 patients with AA amyloidosis. Control groups comprised 40 patients with long-standing inflammatory diseases without AA

Colchicine Intolerance in FMF Patients and Primary Obstacles for Optimal Dosing

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Aim: Colchicine is the mainstay of treatment in FMF. However, in daily practice, it is not easy to maintain effective colchicine doses in substantial number of patients, due to its side effects. In this study, we aimed to investigate prevalence and risk factors for

Cardiovascular and metabolic risk factors in inherited autoinflammation.

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BACKGROUND The natural progression of metabolic abnormalities among patients with inherited autoinflammation is unclear. OBJECTIVE The objective of the study was to assess the cardiometabolic risk of participants with familial Mediterranean fever (FMF). METHODS This study included nationwide

Clinical spectrum of the pseudotumor cerebri in children: etiological, clinical features, treatment and prognosis.

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OBJECTIVE Pseudotumor cerebri (PTC) is a clinical condition characterized by signs and symptoms of increased intracranial pressure, such as headache and papilledema. Our aim was to investigate the etiological and clinical features of pseudotumor cerebri (PTC) in children. METHODS We performed a

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