Publications by authors named "Eugene Krustev"

Article Synopsis
  • Cranial neuropathies (CN) are a rare manifestation of neuropsychiatric lupus, and the study investigates the association of anti-KIF20B antibodies as a possible biomarker for this condition within a large cohort of SLE patients.
  • The research involved 795 patients from a larger cohort, revealing that 29.8% were positive for anti-KIF20B, with a significantly higher positivity rate (70%) in those with CN compared to those without (29.3%).
  • Findings suggest that anti-KIF20B positivity is linked to CN in SLE patients, indicating its potential as a biomarker, though further research is required to confirm these results.
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Introduction: Systemic lupus erythematosus (SLE) is characterized by autoantibody expression and aberrant autoreactive B cells contribute to disease progression; therefore, B cell inhibition has been an attractive target for novel therapies. However, after more than two decades of research and over 40 randomized clinical trials, only one such therapy, belimumab, has been approved for use in SLE.

Areas Covered: In this review, we discuss the evidence for B cell-targeted therapies in SLE and lupus nephritis.

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Article Synopsis
  • Researchers have found that α-1-Antitrypsin (AAT) shows potential in protecting cartilage and reducing inflammation and pain in models of rheumatoid arthritis.
  • AAT treatment led to improved gene expression related to cartilage health and reduced detrimental gene expression in arthritic joints.
  • The study suggests that AAT may serve as a promising new therapy to alleviate pain and promote cartilage repair in arthritis patients.
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Background Knee joint injections and aspirations are essential procedures for medical students, residents, and primary care physicians to master. Simulation-based training has been shown to improve learner confidence and performance scores in knee joint injections. Current knee joint simulators are expensive, ranging from hundreds to thousands of dollars.

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  • Mediators like neutrophil elastase are linked to joint pain in osteoarthritis (OA) and inflammation caused by injury or irritation.
  • In a study using male mice, researchers injected monoiodoacetate (MIA) into knee joints to simulate OA and observed the effects of neutrophil elastase and proteinase-activated receptor-2 (PAR2) on joint inflammation and pain over 14 days.
  • Results showed that MIA increased neutrophil elastase activity and joint pain early on, with treatments targeting neutrophil elastase and PAR2 leading to improvements in inflammation and nerve damage.
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Background: The endocannabinoid system has been shown to reduce inflammatory flares and pain in rodent models of arthritis. A limitation of endocannabinoids is that they are rapidly denatured by hydrolysing enzymes such as fatty acid amide hydrolase (FAAH) which renders them physiologically inert. Osteoarthritis (OA) is primarily a degenerative joint disease; however, it can incorporate mild inflammation and peripheral neuropathy.

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Smoke inhalation-associated lung injuries (SI-ALI) present multiple challenges to the rural emergency department, and they require timely and appropriate management to prevent significant mortality and morbidity. In this report, we outline an adaptable simulation of an SI-ALI patient that is designed for use in a rural emergency department. The aim of this simulation is to better equip clinicians and emergency department staff who may encounter SI-ALI in rural settings.

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Article Synopsis
  • Neurogenic inflammation is a local inflammatory response influenced by neuropeptide release in various organs, affecting leukocyte behavior in the knee joint's microcirculation.
  • The study shows that stimulating the saphenous nerve can alter leukocyte rolling in the synovial microcirculation, with the frequency of stimulation playing a critical role.
  • Pre-treatment with specific antagonists suggests that endocannabinoids are involved in modulating this inflammatory response, highlighting their potential therapeutic role in managing inflammation.
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While acute inflammation is a natural physiological response to tissue injury or infection, chronic inflammation is maladaptive and engenders a considerable amount of adverse pain. The chemical mediators responsible for tissue inflammation act on nociceptive nerve endings to lower neuronal excitation threshold and sensitize afferent firing rate leading to the development of allodynia and hyperalgesia, respectively. Animal models have aided in our understanding of the pathophysiological mechanisms responsible for the generation of chronic inflammatory pain and allowed us to identify and validate numerous analgesic drug candidates.

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There are over 100 different types of arthritis and each can differ greatly in their aetiology and pathophysiology; however, one characteristic that is common to all arthritic conditions is joint pain. Musculoskeletal pain is the leading cause of disability in the world, and the number one reason arthritis patients visit their primary care physician. Despite the prevalence and burden of arthritis pain, current analgesics lack sufficient efficacy and are plagued by multiple adverse side effects.

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Introduction: During the progression of rheumatoid arthritis (RA), there are frequent but intermittent flares in which the joint becomes acutely inflamed and painful. Although a number of drug therapies are currently used to treat RA, their effectiveness is variable and side effects are common. Endocannabinoids have the potential to ameliorate joint pain and inflammation, but these beneficial effects are limited by their rapid degradation.

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