Publications by authors named "Akiko Yamagami"

Purpose: To investigate the usage status of biologics for the chronic treatment of optic neuritis including neuromyelitis optica spectrum disorders in Japan.

Design: Multicenter retrospective case series.

Methods: Patients diagnosed with anti-aquaporin 4 antibody (AQP4-Ab) positive optic neuritis and had been initiated on biologics (satralizumab, eculizumab, and inebilizumab) between January 2020 and August 2022 were identified at 30 facilities in Japan.

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Purpose: Myelin-oligodendrocyte glycoprotein antibody-positive optic neuritis (MOGON) is usually responsive to the steroid, but, for some patients, steroid pulse therapy alone may be inadequate. This study aimed to investigate the factors predicting the response to steroid pulse therapy in MOGON.

Methods: This study included 17 patients (24 eyes) with MOGON, who received single steroid pulse therapy as initial treatment.

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Article Synopsis
  • Leber's hereditary optic atrophy (LHON) is a genetic condition primarily affecting young males, caused by mutations in mitochondrial DNA that disrupt the electron transport chain, leading to vision loss.
  • The condition typically starts with vision impairment in one eye, quickly progressing to the other eye, resulting in very low visual acuity for many patients.
  • Differentiating LHON from other causes of optic neuritis involves various assessments, and collaboration between neurologists and ophthalmologists is vital for proper diagnosis and treatment.
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Article Synopsis
  • A study analyzed the clinical features of optic neuritis linked to anti-myelin oligodendrocyte glycoprotein antibodies (MOGON) in 31 patients, focusing on visual function and imaging results.
  • MOGON typically occurs in middle-aged individuals, presenting with symptoms like pain during eye movement and optic disc swelling.
  • MRI findings showed long lesions near the optic nerve sheath, with longer lesions correlating to poorer initial visual acuity; recurrent cases were associated with thinning of the retinal nerve fiber layer, emphasizing the need to minimize recurrences.
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Leber's hereditary optic neuropathy (LHON) is one of the hereditary optic neuropathies and is principally caused by three frequent mitochondria deoxyribonucleic acid (DNA) pathogenic variants (m.11778 G>A, m.3460 G>A, and m.

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A 29-year-old female with no family history presented with bilateral progressive blurred vision. Her symptoms appeared at 12-years-old and her visual acuity had since deteriorated from 0.6 to 0.

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Purpose: To study the spatial association of magnetic resonance imaging (MRI) contrast enhancement (CE) areas with visual field defect (VFD) asymmetry in initial cases of optic neuritis (ON) with altitudinal hemianopsia (AH) with reference to nonarteritic anterior ischemic optic neuropathy (NAION) with AH.

Study Design: Multicenter, cross-sectional study.

Methods: The present study comprised 19 ON patients and 20 NAION patients with AH who underwent orbital contrast fat-suppressed MRI.

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Herpes zoster ophthalmicus (HZO) presents a variety of ocular complications, most of which occur simultaneously as skin lesions. We report a case of HZO with delayed onset of multiple ocular complications. A 72-year-old man developed HZO, blepharitis, iritis, and conjunctivitis in the left eye, which resolved after topical ocular treatment and systemic acyclovir administration.

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Background: Leber hereditary optic neuropathy (LHON) is an acute or subacute optic neuropathy that mainly affects young males. The first nationwide epidemiological survey of LHON was conducted in 2014 in Japan, and LHON was officially designated as a rare intractable disease by the Japanese government in 2015. We conducted a second survey of the annual incidence of LHON in 2019, and estimated the total number of patients with LHON in Japan.

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Purpose: To evaluate the efficacy and safety of intravenous "freeze-dried sulfonated human normal immunoglobulin (GGS)" in patients with steroid-resistant optic neuritis (ON).

Study Design: Multicenter, prospective, double-blind, parallel-group, randomized controlled trial.

Methods: Patients with steroid-resistant acute ON were randomly assigned to receive either intravenous GGS (GGS group) or intravenous methylprednisolone (steroid pulse [SP] group).

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To compare the occurrence of disc hemorrhages (DH) and glaucoma progression in open-angle glaucoma (OAG) patients with different glaucomatous disc types. Prospective, hospital-based, observational cohort study. OAG patients examined between 2000 and 2005, whose discs were classified as typical myopic glaucomatous (MG), generalized enlargement of cup (GE), or focal glaucomatous (FG) disc type were included and followed for 5 years.

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To investigate the clinical characteristics and the effectiveness of maintenance therapy of anti-AQP4 antibody positive optic neuritis in Japanese patients, medical records from 69 patients (103 eyes) were retrospective reviewed. The status of relapse in patients who received maintenance therapy following acute therapy was compared with that before maintenance therapy in patients who started maintenance therapy ≥6 months after acute therapy. In Japan, anti-AQP4 antibody positive optic neuritis was characterized by older onset age and poor visual outcome.

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Purpose: To elucidate the clinical and epidemiologic characteristics of optic neuritis in Japan.

Design: Multicenter cross-sectional, observational cohort study.

Participants: A total of 531 cases of unilateral or bilateral noninfectious optic neuritis identified in 33 institutions nationwide in Japan.

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