Publications by authors named "Vegh E"

Introduction: Erdheim-Chester disease (ECD) is a rare disease that belongs to the group of Dendritic and histiocytic neoplasms. Only 2000 cases have been reported worldwide. It can present with a wide range of symptoms, making a differential diagnosis especially difficult.

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  • - Cardiovascular issues are common in patients with rheumatoid arthritis (RA) and ankylosing spondylitis (AS), and natural autoantibodies (nAAbs) play a role in inflammation and atherosclerosis linked to these conditions.
  • - A study involving 53 patients treated with anti-TNF therapies over a year found improvements in vascular function and stabilization of vascular thickness, while also noting changes in nAAb levels.
  • - The research suggests that nAAbs may independently affect autoimmunity and vascular health in biologic-treated patients, highlighting a complex relationship between arthritis, inflammation, and cardiovascular risks.
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Motivation: Zooarchaeology by Mass Spectrometry (ZooMS) is a palaeoproteomics method for the taxonomic determination of collagen, which traditionally involves challenging manual spectra analysis with limitations in quantitative results. As the ZooMS reference database expands, a faster and reproducible identification tool is necessary. Here we present SpecieScan, an open-access algorithm for automating taxa identification from raw MALDI-ToF mass spectrometry (MS) data.

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In our present study, we aimed to assess the effects of anti-TNF therapy on periodontal condition in a mixed cohort of patients with rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Moreover, we wished to determine whether the baseline dental condition of these patients would affect response to biological therapy. A cohort of 24 arthritis patients was consecutively recruited before starting anti-TNFα therapy.

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  • The study investigates how 12 months of tofacitinib treatment affects the Renin-Angiotensin-Aldosterone system (RAAS) in rheumatoid arthritis patients, particularly focusing on angiotensin converting enzyme (ACE) and ACE2 levels.
  • Twenty-six RA patients completed the study, revealing that tofacitinib treatment significantly increased serum ACE levels and the ACE/ACE2 ratio after one year, while ACE2 activity only showed a temporary increase at six months.
  • The results suggest a link between baseline inflammation, disease duration, and specific biomarkers (like rheumatoid factor) with changes in the ACE/ACE2 ratio during the treatment period.
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  • The study aimed to assess the effects of tofacitinib therapy on angiogenic factors and vascular health in patients with rheumatoid arthritis (RA).
  • Over one year, 26 RA patients treated with tofacitinib showed significant reductions in certain inflammatory cytokines and growth factors, indicating a potential decrease in synovial and aortic inflammation.
  • The findings suggest that after one year of treatment, certain biomarkers like NT-proBNP and CathK may indicate vascular health, linking them to blood vessel function in RA patients.
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  • This study investigates how tofacitinib, a JAK inhibitor, impacts metabolic changes associated with rheumatoid arthritis (RA) over one year, focusing on arginine and methionine levels and their connection to inflammation and cardiovascular health.
  • Thirty RA patients were monitored for inflammatory markers, vascular function, and various amino acid levels before and after treatment, revealing significant decreases in inflammatory markers but no major changes in vascular function.
  • After 12 months, higher doses of tofacitinib increased certain amino acids like L-arginine and methionine, with mixed correlations noted between these amino acids and inflammation, but no overall improvement in vascular function metrics was observed.
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  • JAK inhibitor tofacitinib, used for treating rheumatoid arthritis (RA), shows a complex impact on lipids and metabolic markers related to cardiovascular health over a one-year period.
  • In a study involving 30 RA patients, several lipid and adipokine levels were monitored, revealing significant changes in certain markers like TC, HDL, LDL, and TSP-1, while others remained stable.
  • The study found correlations between metabolic indicators, clinical markers, and vascular functions, suggesting that tofacitinib therapy influences CV risk factors and highlights the need for comprehensive evaluations in RA patients.
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Postmortem chemical transformation of bone bioapatite can take place during early diagenesis, resulting in a more thermodynamically stable mineral phase. This paper examines the impact of a one year postmortem interval on unburnt and burnt bone's structural and chemical alterations. This question is of importance for the reconstruction of funerary practices involving cremation in the archaeological record, as well as forensic anthropological investigations.

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Introduction: Angiotensin-converting enzyme (ACE) and ACE2 have been implicated in the regulation of vascular physiology. Elevated synovial and decreased or normal ACE or ACE2 levels have been found in rheumatoid arthritis (RA). Very little is known about the effects of tumor necrosis factor α (TNF-α) inhibition on ACE or ACE2 homeostasis.

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Background: Cardiovascular (CV) morbidity, mortality, and metabolic syndrome are associated with rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Here, lipids and other metabolic markers in relation to vascular function and clinical markers were evaluated in RA and AS patients undergoing one-year anti-TNF therapy.

Patients And Methods: Fifty-three patients including 36 RA patients treated with either etanercept (ETN) or certolizumab pegol (CZP) and 17 AS patients treated with ETN were included in a 12-month follow-up study.

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Cardiovascular (CV) disease and osteoporosis (OP) have been associated with rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Bone and vascular biomarkers and parameters along with the effect of 1-year anti-TNF therapy on these markers were assessed in order to determine correlations between vascular pathophysiology and bone metabolism in RA and AS. Thirty-six patients treated with etanercept or certolizumab pegol and 17 AS patients treated with ETN were included in a 12-month follow-up study.

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Introduction: Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) are associated with osteoporosis. There have not been many peripheral quantitative computed tomography (QCT) studies in patients receiving biologics. We assessed volumetric and areal bone mineral density (BMD) by forearm QCT and dual-energy X-ray absorptiometry (DXA), respectively in addition to laboratory biomarkers in these arthritides.

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Periodontal disease (PD) can be an important precipitating factor in the production of citrullinated proteins. Its importance is emphasized, but it is not the only way to produce citrullinated proteins. The aim of the current study was to determine the periodontal conditions and the salivary citrullinated protein content in patients with rheumatoid arthritis (RA) compared to healthy controls.

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Disordered lysosomal/autophagy pathways initiate and drive pancreatitis, but the underlying mechanisms and links to disease pathology are poorly understood. Here, we show that the mannose-6-phosphate (M6P) pathway of hydrolase delivery to lysosomes critically regulates pancreatic acinar cell cholesterol metabolism. Ablation of the Gnptab gene encoding a key enzyme in the M6P pathway disrupted acinar cell cholesterol turnover, causing accumulation of nonesterified cholesterol in lysosomes/autolysosomes, its depletion in the plasma membrane, and upregulation of cholesterol synthesis and uptake.

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Background: The outcome of rheumatoid arthritis (RA) should be determined early. Rapid radiological progression (RRP) is > or = 5 units increase according to the van der Heijde-Sharp score within a year. The risk of RRP can be estimated by a matrix model using non-radiographic indicators, such as C-reactive protein (CRP), rheumatoid factor (RF) and swollen joint count (SJC).

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Unlabelled: Janus kinase (JAK) inhibitors are used to treat rheumatoid arthritis (RA). We assessed the effects of tofacitinib on bone density and bone markers in association with clinical and laboratory parameters in RA. Tofacitinib stabilized bone density and resulted in a positive balance of bone turnover.

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Objective: Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) have been associated with cardiovascular disease. The treatment of arthritis by tumor necrosis factor-α (TNF-α) inhibitors may decrease the serum concentrations of vascular biomarkers. We determined circulating levels of oxidized low-density lipoprotein (oxLDL)/β glycoprotein I (β-GPI) complexes, antibodies to 60 kDa heat shock protein (anti-Hsp60), soluble urokinase plasminogen activator receptor (suPAR), and B-type natriuretic peptide (BNP) fragment in sera of RA and AS patients undergoing anti-TNF treatment.

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Increased cardiovascular (CV) morbidity and mortality have been found in rheumatoid arthritis (RA). Tumour necrosis factor α (TNF-α) inhibitors may improve vascular function. In the first part of this study, we determined microcirculation during postoocclusive reactive hyperemia (PORH) representing endothelial function.

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Accelerated atherosclerosis, increased cardiovascular morbidity and mortality have been associated with rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Vascular function, clinical and laboratory markers and the effects of anti-TNF therapy were assessed in arthritides. Fifty-three 53 patients including 36 RA patients treated with either etanercept (ETN) or certolizumab pegol and 17 AS patients treated with ETN were included in a 12-month follow-up study.

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Objective: We wished to determine bone alterations in systemic sclerosis (SSc) patients by conventional densitometry (DXA), peripheral quantitative computed tomography (pQCT), and bone biomarkers.

Methods: We included 44 SSc patients and 33 age-matched healthy controls. Lumbar spine and femoral neck bone mineral density (BMD) was assessed by DXA.

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Objectives: Rheumatoid arthritis (RA) and ankylosing spondylitis (AS) have been associated with generalized and localized bone loss. We conducted a comprehensive study using imaging (dual-energy X-ray absorptiometry, DXA) and laboratory biomarkers in order to determine bone health and to study the effects of anti-tumor necrosis factor (TNF) biologics in RA and AS.

Patients And Methods: Thirty-six RA and 17 AS patients undergoing 1-year etanercept (ETN) or certolizumab-pegol (CZP) therapy were studied.

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