研究者業績
基本情報
経歴
4-
2021年 - 現在
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2011年 - 2021年
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2006年 - 2011年
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2003年 - 2006年
学歴
2-
1993年4月 - 1997年3月
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1986年4月 - 1992年3月
論文
109-
Japanese journal of ophthalmology 69(1) 74-80 2025年1月PURPOSE: To investigate the incidence of postoperative macular hole (MH), visual acuity, and anatomical recovery in patients who underwent a non-fovea-sparing technique using a double-staining method for symptomatic myopic foveoschisis without pre-existing macular holes. STUDY DESIGN: A retrospective study. METHODS: We evaluated 39 eyes from 39 consecutive patients diagnosed with myopic foveoschisis from May 2017 to September 2022 at Fujita Health University Hospital. All patients underwent non-fovea-sparing internal limiting membrane peeling using a double-staining method and were monitored for 6 months postoperatively. Best-corrected visual acuity (BCVA) as measured by the logarithm of the minimum angle of resolution (logMAR), central retinal thickness (CRT), and the presence of foveoschisis were assessed using optical coherence tomography (OCT) preoperatively (pre) and at 1 month (1 M), 3 months (3 M), and 6 months (6 M) postoperatively. RESULTS: No cases of postoperative rhegmatogenous retinal detachment were observed. A postoperative MH developed in one eye. The mean logMAR values at pre, 1 M, 3 M, and 6 M were 0.38 ± 0.37, 0.23 ± 0.33, 0.18 ± 0.25, and 0.13 ± 0.29, respectively (all P < 0.001). The mean CRTs at pre, 1 M, 3 M, and 6 M were 384.6 ± 177.2, 262.2 ± 84.4, 200.3 ± 64.9, and 185.6 ± 61.0 μm, respectively (all P < 0.001). Foveoschisis was observed in all 39 eyes (100%) preoperatively and in 17 eyes (43.6%) at 1 M, nine eyes (34.6%) at 3 M, and zero eyes (0%) at 6 M postoperatively. CONCLUSION: The non-fovea-sparing double-staining technique was effective in treating myopic foveoschisis without MH, leading to significant improvements in both visual function and anatomical recovery. This method may be a promising surgical option for managing myopic foveoschisis.
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Scientific Reports 14(1) 2024年12月5日
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Retina 2024年11月13日Purpose: Retinal arterioles are attenuated in eyes with retinitis pigmentosa (RP), but dimensions such as lumen diameter (LD) and wall thickness (WT) have not been thoroughly investigated. This study aimed to determine the dimensions of reduced retinal arterioles in eyes with RP. Methods: The study included 66 patients with RP (66 eyes) and 36 control participants (36 eyes) for whom adaptive optics (AO) recordings of the retinal arteries were available. LD and WT were measured on the AO images. The correlations between arteriole dimensions and clinical parameters were determined. Results: The mean LD was significantly smaller in patients with RP than in controls, while the mean WT did not differ significantly. LD was significantly and positively correlated with the mean deviation (MD) of the Humphrey 10-2 field analyzer and ellipsoid zone (EZ) width. The WT and wall-to-lumen ratio were significantly and positively correlated with age and systolic blood pressure but not with MD and EZ width. Conclusion: Retinal arteriole dimensions were significantly correlated with retinal degeneration and systemic factors.
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Japanese journal of ophthalmology 68(6) 614-620 2024年11月PURPOSE: To assess the feasibility of swept-source optical coherence tomography angiography (SS-OCTA) to differentiate macular diseases, including nonpolypoidal macular neovascularization (MNV), polypoidal choroidal vasculopathy (PCV), type 3 MNV, and chronic central serous chorioretinopathy (CSC) without indocyanine green angiography (ICGA). STUDY DESIGN: Retrospective observational study. METHODS: This study examined 63 eyes of 63 patients with treatment-naive neovascular age-related macular degeneration (AMD), including 23 eyes with nonpolypoidal MNV, 17 eyes with PCV, and 1 eye with type 3 MNV and 22 eyes with chronic CSC. Two independent retina specialists, blinded to the clinical diagnosis, assessed each case of neovascular AMD and chronic CSC using only B-scan and en face images of SS-OCTA without referring to other examination outcomes. RESULTS: By SS-OCTA alone, 19 eyes were diagnosed with nonpolypoidal MNV, 17 eyes with PCV, 2 eyes with type 3 MNV, and 22 eyes with chronic CSC, indicating high sensitivity (82.6%, 94.1%, 100%, and 100%, respectively) and specificity (100%, 97.8%, 98.4%, and 100%, respectively); however, three eyes could not be diagnosed because of obscure images. The agreement of diagnosis with SS-OCTA alone was high between the two specialists (κ = 0.82). CONCLUSION: SS-OCTA showed high sensitivity and specificity in the differentiation of nonpolypoidal MNV, PCV, type 3 MNV, and chronic CSC. The differential criteria based on SS-OCTA could be a substitute for the ICGA-based diagnoses.
MISC
24-
Retina 39(9) e40-e41 2019年9月1日
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Retina 38(1) E1-E2 2018年1月1日
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AMERICAN JOURNAL OF OPHTHALMOLOGY 180 178-179 2017年8月
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ACTA OPHTHALMOLOGICA 95(4) E344-E345 2017年6月 査読有り
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PLOS ONE 12(5) e0176100 2017年5月 査読有り招待有り
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Japanese journal of ophthalmology : the official international journal of the Japanese Ophthalmological Society 61(3) 260-266 2017年5月
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OXIDATIVE MEDICINE AND CELLULAR LONGEVITY 9548767 2017年 査読有り
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OPHTHALMOLOGICA 237(2) 105-110 2017年 査読有り
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(12) . 2016年9月
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MEDICINE 95(39) e4978 2016年9月 査読有り
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Diminished density of cone photoreceptors in fovea of eyes with autosomal recessive bestrophinopathyINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(12) 2016年9月
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(9) OCT568-OCT574 2016年7月 査読有り
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 55(13) 2014年4月
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Japanese Journal of Ophthalmology 57(2) 233-238 2013年3月
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Retinal Cases and Brief Reports 4(2) 132-134 2010年3月
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RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 29(9) 1242-1248 2009年10月
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 49(8) 3551-3558 2008年8月
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 48(5) 2254-2259 2007年5月
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日本眼科学会雑誌 106(12) 737-756 2002年12月眼底に異常をみない先天停止性夜盲で網膜電図(ERG)のb波に選択的減弱がみられ,いわゆるnegative ERGを示す疾患は以前はSchubert-Bornschein型として一括されていた.著者等はそれを杆体系機能の有無により便宜上,完全型と不全型とに分類したが,この他にこの両者にはERG律動様小波や錐体系ERGに明確で普遍的な差がみられ,同一疾患のphenotypeの変化ではなく,異なった疾患の集合であるとの仮説を立てた.この仮説は近年分子遺伝学的に証明された.即ち,X染色体劣性遺伝の完全型はnyctalopin(NYX)に,不全型は網膜特異性のカルシウムチャンネルα1-subunitに繋がるCACNA1F遺伝子に変異が同定され,これにより両者は異なった疾患であることが証明された
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Japanese journal of ophthalmology 41(4) 255-259 1997年7月1日
書籍等出版物
2講演・口頭発表等
55-
17th APVRS Congress; Singapore 2024年11月23日
共同研究・競争的資金等の研究課題
16-
日本学術振興会 科学研究費助成事業 2019年4月 - 2022年3月
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日本学術振興会 科学研究費助成事業 2016年4月 - 2019年3月
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日本学術振興会 科学研究費助成事業 2015年4月 - 2018年3月
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日本学術振興会 科学研究費助成事業 2014年4月 - 2017年3月
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日本学術振興会 科学研究費助成事業 2013年4月 - 2016年3月