Publications by authors named "Seolhee Baek"

Background And Purpose: This study evaluated the diagnostic utility of an anti-signal-recognition particle 54 (anti-SRP54) antibody-based enzyme-linked immunosorbent assay (ELISA) as well as the clinical, serological, and pathological characteristics of patients with SRP immune-mediated necrotizing myopathy (IMNM).

Methods: We evaluated 87 patients with idiopathic inflammatory myopathy and 107 healthy participants between January 2002 and December 2023. The sensitivity and specificity of the ELISA for anti-SRP54 antibodies were assessed, and the clinical profiles of patients with anti-SRP54 antibodies were determined.

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  • Researchers studied the quality of life (QOL) of patients with a condition called MOGAD and compared it to another condition called AQP4-IgG positive NMOSD.
  • They found that the overall QOL was similar between both groups, but many patients in both groups struggled with sleep, pain, and feelings of sadness.
  • The study suggests that both conditions need more focus on improving sleep and mental health to help patients feel better overall.
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  • Neuromyelitis optica spectrum disorder (NMOSD) is a central nervous system disease that differs from multiple sclerosis by the presence of anti-aquaporin 4 antibodies (AQP4-ab) and occasionally other non-organ-specific autoantibodies.
  • A study involving 158 NMOSD patients collected data on various autoantibodies and analyzed their impact on clinical characteristics and disability levels.
  • Results indicated that the rheumatoid factor (RF) was significantly associated with higher disability levels; RF, age at onset, and annual relapse rate (ARR) emerged as key predictors for severe disability in NMOSD patients.
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  • The study focuses on the clinical features and treatment outcomes of idiopathic intracranial hypertension (IIH) specifically in Korean patients, as there is limited data on this in Asian populations.
  • A total of 59 patients were analyzed, with a majority being women and only a portion classified as obese; various headache types were reported, with chronic and episodic migraines being the most common.
  • Treatment results showed that after 3-6 months, intracranial pressure normalized in 25% of patients, and over half experienced significant headache improvement, indicating a positive response to medical management overall.
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  • During the COVID-19 pandemic, patients with myasthenia gravis (MG) faced greater risks, including higher mortality rates compared to the general public due to respiratory issues and immunotherapy.
  • A study in South Korea analyzed 92 MG patients who contracted COVID-19, focusing on the differences in clinical outcomes between those vaccinated and unvaccinated.
  • Results showed that unvaccinated patients had significantly higher hospitalization rates, ICU admissions, and deterioration of MG compared to vaccinated patients, highlighting the importance of vaccination in this vulnerable population.
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  • This study investigates autonomic dysfunction in early Parkinson's disease (PD) patients who are not on medication and do not experience orthostatic hypotension (OH), focusing on the effects of the Valsalva maneuver (VM).
  • Researchers analyzed data from 61 drug-naïve PD patients and 20 controls, assessing various VM parameters like changes in systolic blood pressure and heart rate to identify differences in autonomic function.
  • The findings indicate that early PD patients have significantly lower sympathetic function, as indicated by decreased blood pressure changes, suggesting that sympathetic dysfunction might be an early sign of autonomic issues in PD.
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Background: Optic neuritis (ON) prognosis is influenced by various factors including attack severity, underlying aetiologies, treatments and consequences of previous episodes. This study, conducted on a large cohort of first ON episodes, aimed to identify unique prognostic factors for each ON subtype, while excluding any potential influence from pre-existing sequelae.

Methods: Patients experiencing their first ON episodes, with complete aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein (MOG) antibody testing, and clinical data for applying multiple sclerosis (MS) diagnostic criteria, were enrolled.

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Background: Appropriate evaluation and management of dysphagia are essential in neurological disorders. However, there is currently a lack of a simple yet reliable method for dysphagia evaluation.

Aim: This study aimed to investigate the usefulness of new dynamic M-mode ultrasonography (US) parameters of suprahyoid muscle (SHM) to evaluate dysphagia.

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  • The study focuses on anti-myelin-associated glycoprotein (MAG) neuropathy, a condition that doesn't respond well to traditional immunotherapy, emphasizing the need to evaluate different treatments and develop better biomarkers for managing the disease.
  • A total of 91 patients with high anti-MAG antibody levels were recruited, with 68 analyzed for treatment outcomes; zanubrutinib showed the highest treatment response (50%), followed by rituximab (36.4%), while corticosteroids and other therapies showed lower effectiveness.
  • Findings suggest nerve conduction study (NCS) metrics, particularly the end CMAP amplitudes, can serve as effective objective markers for tracking disease progression and predicting flare-ups in patients
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Background: Serum levels of neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) reflect the disease activity and disability in central nervous system (CNS) demyelinating diseases. However, the clinical significance of NfL and GFAP in idiopathic transverse myelitis (iTM), an inflammatory spinal cord disease with unknown underlying causes, remains unclear. This study aimed to investigate NfL and GFAP levels in iTM and their association with the clinical parameters compared with those in TM with disease-specific antibodies such as anti-aquaporin 4 or myelin oligodendrocyte glycoprotein antibodies (sTM).

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Background: The clinical implications of myelin oligodendrocyte glycoprotein autoantibodies (MOG-Abs) are increasing. Establishing MOG-Ab assays is essential for effectively treating patients with MOG-Abs. We established an in-house cell-based assay (CBA) to detect MOG-Abs to identify correlations with patients' clinical characteristics.

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The need for developing a simple and effective assessment tool for muscle mass has been increasing in a rapidly aging society. This study aimed to evaluate the feasibility of the surface electromyography (sEMG) parameters for estimating muscle mass. Overall, 212 healthy volunteers participated in this study.

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Background: Standard autonomic testing includes a 10-minute head-up tilt table test to detect orthostatic hypotension. Although this test can detect delayed orthostatic hypotension (dOH) between 3 and 10 minutes of standing, it cannot detect late-onset dOH after 10 minutes of standing.

Methods: To determine whether Valsalva maneuver responses can identify patients who would require prolonged head-up tilt table test to diagnose late-onset dOH; patients with immediate orthostatic hypotension (onset <3 minutes; n=176), early-onset dOH (onset between 3 and 10 minutes; n=68), and late-onset dOH (onset >10 minutes; n=32) were retrospectively compared with controls (n=114) with normal head-up tilt table test and composite autonomic scoring scale score of 0.

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The measurement of skeletal muscle mass is essential for the diagnosis of sarcopenia. Muscle ultrasonography has emerged as a useful tool for evaluating sarcopenia because it can be used to assess muscle quality and quantity. This study investigated whether muscle ultrasonography is effective for estimating appendicular skeletal muscle mass (ASM) and screening for sarcopenia.

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  • * It involved a retrospective analysis of 160 patients, ultimately narrowing down to 89 AChR Ab-negative MG patients, finding that 24.7% tested positive for anti-MuSK antibodies via ELISA, showing high agreement with other testing methods.
  • * The findings suggest that while CBA is more sensitive for detecting anti-MuSK antibodies, ELISA may still have valuable diagnostic applications, especially when distinguishing between MuSK MG and conditions with similar symptoms, like motor neuron disease.
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Ophthalmoplegia is the diagnostic hallmark of anti-GQ1b antibody syndrome. This study aimed to define the patterns of acute comitant strabismus in patients with anti-GQ1b antibody syndromes. We retrospectively analyzed the ocular motor findings in 84 patients with anti-GQ1b antibody-associated ophthalmoplegia during the acute phases.

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Introduction: Hemifacial spasm (HFS) is an involuntary intermittent twitching of the facial muscles. Medical and surgical treatments can be considered for HFS. Among medical treatments, clonazepam is a benzodiazepine used to treat epilepsy, psychiatric symptoms, and movement disorders.

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Background: Handgrip strength (HGS), an indicator of overall muscle strength, is a key component in sarcopenia diagnosis. Although exercise is an effective strategy to prevent sarcopenia, the most appropriate exercise type targeting sarcopenia needs to be established. This study aimed to investigate the relationship between the physical activity (PA) patterns and HGS.

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Step length is a critical hallmark of health status. However, few studies have investigated the modifiable factors that may affect step length. An exploratory, cross-sectional study was performed to evaluate the surface electromyography (sEMG) and body impedance analysis (BIA) parameters, combined with individual demographic data, to predict the individual step length using the GAITRite® system.

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•VKH is an idiopathic autoimmune disease presenting with uveomeningeal syndrome.•Granulomatous uveitis and serious retinal detachments are the most common findings of VKH.•VKH can masquerade as IIH by presenting with severe headache and optic disc edema.

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We describe acute vestibular syndrome in a 48-year-old woman with breast cancer who was finally found to have anti-Ma2-associated encephalitis. Although the initial diagnosis was vestibular neuritis elsewhere, progression of symptoms and additional findings of bilateral ptosis and circumlimbal injections, vertical saccadic slowing, and impaired convergence led to a suspicion of a rostral midbrain lesion and final diagnosis. The patient's symptoms and ocular motor signs improved markedly after administration of IV methylprednisolone and oral tacrolimus.

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