2024/10/07 更新

写真a

ムトウ レイコ
武藤 玲子
MUTO Reiko
所属
大学院医学系研究科 腎不全システム治療学寄附講座 特任助教
職名
特任助教
外部リンク

学位 1

  1. 博士 (医学) ( 2022年3月   名古屋大学 ) 

研究キーワード 1

  1. Radiomics, 腎臓, 性差, 分子

研究分野 3

  1. ライフサイエンス / 腎臓内科学

  2. ライフサイエンス / 腎臓内科学

  3. 情報通信 / 生命、健康、医療情報学

所属学協会 6

  1. 日本分子生物学会

    2013年4月 - 現在

  2. 日本透析学会

    2013年4月 - 現在

  3. 日本腎臓学会

    2013年4月 - 現在

  4. 日本透析学会

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  5. 日本腎臓学会

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  6. 日本分子生物学会

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受賞 9

  1. 第8回TSUBASA PROJECT賞

    2023年12月   日本透析医学会   性差に着目した透析患者胸部X線画像の解析

  2. 第8回TSUBASA PROJECT賞

    2023年12月   日本透析医学会   性差に着目した透析患者胸部X線画像の解析

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  3. 優秀演題賞 (研修医指導)

    2019年10月   日本内科学会東海地方会  

  4. 優秀演題賞 (研修医指導)

    2019年10月   日本内科学会東海地方会  

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  5. Developmental Biology Travel Grant to 2016 Marine Biological Laboratory Embryology Course, Woods Hole, USA

    2016年8月   Developmental Biology  

  6. Developmental Biology Travel Grant to 2016 Marine Biological Laboratory Embryology Course, Woods Hole, USA

    2016年8月  

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  7. 岡田節人基金若手研究者海外交流助成

    2016年5月   日本発生生物学会  

  8. 岡田節人基金若手研究者海外交流助成

    2016年5月   日本発生生物学会  

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  9. Resident award

    2011年10月   日本呼吸器学会東海地方学会  

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論文 7

  1. Efficacy of On-line Hemodiafiltration for Rhabdomyolysis Presenting with Acute Kidney Injury Due to Unexpected Drug Abuse 査読有り

    Sato, N; Inagaki, K; Takanashi, M; Muto, R; Kato, N; Maruyama, S; Akahori, T

    INTERNAL MEDICINE   62 巻 ( 19 ) 頁: 2865 - 2870   2023年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:一般社団法人 日本内科学会  

    Myoglobin is a well-known cause of acute kidney injury (AKI) due to rhabdomyolysis. However, whether or not removing serum myoglobin by on-line hemodiafiltration (OHDF) improves the kidney function remains unclear. We herein report a patient with a history of methamphetamine abuse who developed AKI due to rhabdomyolysis. A urinalysis and blood collection results obtained before and after OHDF demonstrated that OHDF improved the kidney function by removing a large amount of serum myoglobin rather than via urinary excretion. In conclusion, OHDF may prevent AKI progression effectively when the urine volume is insufficient.

    DOI: 10.2169/internalmedicine.1107-22

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  2. IgA-dominant glomerulonephritis with DNAJB9-negative fibrillar polytypic immunoglobulin deposits in the subepithelium 査読有り

    Muto, R; Maeda, K; Fukui, S; Saito, S; Kato, N; Kosugi, T; Shimizu, A; Maruyama, S

    CEN CASE REPORTS   12 巻 ( 3 ) 頁: 323 - 328   2023年8月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CEN Case Reports  

    Fibrillary glomerulonephritis (FGN), a rare disease is pathologically characterized by glomerular fibril accumulation ranging from 12 to 24 nm in diameter with negative Congo red staining. Recently, the identification of DnaJ homolog subfamily B member 9 (DNAJB9) as a highly sensitive and specific marker for FGN has revolutionized diagnosis of this disease. However, few recent studies have reported DNAJB9-negative glomerulonephritis with fibrillar deposits. As such, it remains unclear whether DNAJB9-negative cases can be considered equivalent to FGN. Here, we report the case of a 70-year-old woman who developed renal impairment and nephrotic-range proteinuria. Renal biopsy and pathological examination revealed focal glomerulonephritis with fibrocellular crescents. Immunofluorescence microscopy showed IgA-dominant deposition of polytypic IgG in the glomerulus. Electron microscopy revealed hump-like subepithelial electron dense deposits with fibrils of 15–25 nm in diameter. These findings were consistent with FGN; thus, Congo red and direct fast scarlet (DFS) staining, and immunohistochemistry for DNAJB9 were performed. In addition to negative Congo red/DFS/DNAJB9 staining, laser microdissection (LMD) and liquid chromatography-tandem mass spectrometry (LC–MS/MS) resulted negative for DNAJB9, which is a highly sensitive and specific marker for FGN. The patient’s renal function further declined, prompting administration of rituximab weekly for 2 weeks, similar to the treatment for FGN. This is a unique case of IgA-dominant glomerulonephritis with DNAJB9-negative fibrillar polytypic immunoglobulin deposits in the subepithelium, unlike previous DNAJB9-negative cases. Thus, DNAJB9-negative cases diagnosed based on accurate electron microscopic evaluation must be gathered, and LMD and LC–MS/MS must be used to analyze the organized fibrillar deposits to reveal the disease entity.

    DOI: 10.1007/s13730-022-00759-2

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  3. Recurrent Cerebrovascular Complications under Enzyme Replacement Therapy in a Patient with Fabry Disease on Peritoneal Dialysis 査読有り

    Muto, R; Suzuki, Y; Shimizu, H; Yasuda, K; Ishimoto, T; Maruyama, S; Ito, Y; Mizuno, M

    INTERNAL MEDICINE   62 巻 ( 4 ) 頁: 565 - 569   2023年2月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:一般社団法人 日本内科学会  

    Fabry disease is an X-linked lysosomal storage disorder due to mutations in the alpha-galactosidase A gene, which leads to the accumulation of globotriaosylceramide in various organs. In Fabry disease with endstage renal disease (ESRD), cerebrovascular events are lethal, even with enzyme replacement therapy (ERT). However, the utility of biomarkers to evaluate the ERT response is unclear. We herein report a case of recurrent cerebrovascular complications under ERT in a Fabry disease patient, progressing to ESRD on peritoneal dialysis. Further studies are warranted, but Fabry disease patients with ESRD receiving ERT might need careful long-term follow-up in cases with cerebrovascular manifestations.

    DOI: 10.2169/internalmedicine.0185-22

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  4. Predicting oxygen requirements in patients with coronavirus disease 2019 using an artificial intelligence-clinician model based on local non-image data 査読有り

    Muto, R; Fukuta, S; Watanabe, T; Shindo, Y; Kanemitsu, Y; Kajikawa, S; Yonezawa, T; Inoue, T; Ichihashi, T; Shiratori, Y; Maruyama, S

    FRONTIERS IN MEDICINE   9 巻   頁: 1042067   2022年11月

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    担当区分:筆頭著者, 責任著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Frontiers in Medicine  

    Background: When facing unprecedented emergencies such as the coronavirus disease 2019 (COVID-19) pandemic, a predictive artificial intelligence (AI) model with real-time customized designs can be helpful for clinical decision-making support in constantly changing environments. We created models and compared the performance of AI in collaboration with a clinician and that of AI alone to predict the need for supplemental oxygen based on local, non-image data of patients with COVID-19. Materials and methods: We enrolled 30 patients with COVID-19 who were aged >60 years on admission and not treated with oxygen therapy between December 1, 2020 and January 4, 2021 in this 50-bed, single-center retrospective cohort study. The outcome was requirement for oxygen after admission. Results: The model performance to predict the need for oxygen by AI in collaboration with a clinician was better than that by AI alone. Sodium chloride difference >33.5 emerged as a novel indicator to predict the need for oxygen in patients with COVID-19. To prevent severe COVID-19 in older patients, dehydration compensation may be considered in pre-hospitalization care. Conclusion: In clinical practice, our approach enables the building of a better predictive model with prompt clinician feedback even in new scenarios. These can be applied not only to current and future pandemic situations but also to other diseases within the healthcare system.

    DOI: 10.3389/fmed.2022.1042067

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  5. Increased Monocyte/Lymphocyte Ratio as Risk Marker for Cardiovascular Events and Infectious Disease Hospitalization in Dialysis Patients 査読有り 国際共著 国際誌

    Muto, R; Kato, S; Lindholm, B; Qureshi, AR; Ishimoto, T; Kosugi, T; Maruyama, S

    BLOOD PURIFICATION   51 巻 ( 9 ) 頁: 747 - 755   2022年9月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Blood Purification  

    Introduction: In dialysis patients, cardiovascular disease (CVD) and infectious disease contribute to poor clinical outcomes. We investigated if a higher monocyte/lymphocyte ratio (MLR) is associated with an increased risk of CVD events and infectious disease hospitalizations in incident dialysis patients. Methods: In an ongoing observational prospective cohort study, 132 Japanese dialysis patients (age 58.7 ± 11.7 years; 70% men) starting dialysis therapy were enrolled and followed up for a median of 48.7 months. Laboratory biomarkers, including white blood cell count and its differential count, were determined at baseline. Event-free time and relative risks (RRs) were calculated using the Kaplan-Meier curves and Cox models, respectively. Results: When divided into 2 groups according to median MLR (0.35 [range, 0.27-0.46]), the periods without CVD events were significantly shorter in the high MLR group than in the low MLR group (log-rank test = 5.60, p = 0.018). The RR of CVD events, after adjusting for age, sex, and diabetes, was 2.43 (1.22-4.84) in the high MLR group compared to the low MLR group. The periods without infections requiring hospitalization were also shorter (log-rank test = 4.16, p = 0.041). The RR of infections requiring hospitalization was 1.98 (1.02-3.83) after the same adjustments. The number of CVD events was higher in the high MLR group (18.6 events per 100 person-years at risk [pyr]) than the low MLR group (11.1 events per 100 pyr). The duration of infectious disease hospitalization was longer in the high MLR group (6.3 days per pyr) than in the low MLR group (2.8 days per pyr). Conclusion: A higher MLR is associated with increased risks of both CVD events and infectious disease hospitalization in dialysis patients.

    DOI: 10.1159/000519289

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  6. The 30-year Natural History of Non-classic Fabry Disease with an R112H Mutation 査読有り

    Muto, R; Inagaki, K; Kato, N; Maruyama, S; Akahori, T

    INTERNAL MEDICINE   61 巻 ( 11 ) 頁: 1727 - 1730   2022年6月

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    担当区分:筆頭著者, 責任著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:一般社団法人 日本内科学会  

    Fabry disease is a rare X-linked lysosomal storage disorder caused by mutations in the alpha-galactosidase A (GLA) gene that results in deficiency of the enzyme GLA and leads to the accumulation of globotriaosylceramide (GL-3) in cells. The accumulation of GL-3 may lead to life-threatening complications. Significant advances in genetic sequencing technology have led to a better understanding of genotype-phenotype interactions in Fabry disease. Fabry disease with an R112H mutation is known as the non-classic type. However, the long-term clinical course of the disease remains unknown. We herein report a patient with a 30-year natural history of non-classic Fabry disease with an R112H mutation.

    DOI: 10.2169/internalmedicine.8213-21

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  7. Ectopic Relapse of Anti-neutrophil Cytoplasmic Antibody-associated Pituitary Vasculitis with No Elevation of Anti-neutrophil Cytoplasmic Antibodies after Renal Remission 査読有り

    Muto, R; Inagaki, K; Sato, N; Sameshima, T; Nagakura, Y; Baba, S; Kato, N; Maruyama, S; Akahori, T

    INTERNAL MEDICINE   59 巻 ( 24 ) 頁: 3187 - 3193   2020年12月

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    担当区分:筆頭著者, 責任著者   記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:一般社団法人 日本内科学会  

    The relationship between anti-neutrophil cytoplasmic antibody (ANCA) titer levels and relapse risk in patients with ANCA-associated vasculitis (AAV) following clinical remission remains controversial. We herein report a case showing ectopic relapse of AAV in the pituitary with no ANCA elevation after renal remission. Magnetic resonance imaging revealed an enlarged pituitary gland. A pituitary biopsy showed geographic necrosis with multinucleated giant cells. We diagnosed this case as relapse of AAV in the pituitary. One month after rituximab therapy, the pituitary gland volume had decreased. The intensification of therapy due to the possibility of vasculitis relapse may facilitate better control of AAV.

    DOI: 10.2169/internalmedicine.4731-20

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講演・口頭発表等 10

  1. 膜性腎症の抗PLA2R抗体と予後規定因子が寛解導入に与える影響

    第56回日本腎臓学会学術総会  2013年5月11日 

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  2. 腎臓内科医の観点を組み込んだ機械学習モデルによる日本人COVID-19患者の重症化予測

    AI-MAILs & Clinical AI 第3回合同シンポジウム  2023年12月2日 

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  3. 腎臓内科医の観点を組み込んだ人工知能による日本人COVID-19患者の重症化予測

    第121回日本内科学会総会  2024年4月13日 

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  4. 性差に着目した透析患者胸部X線画像の解析 招待有り

    第69回日本透析医学会学術集会総会 学会委員会企画  2024年6月9日 

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    会議種別:口頭発表(招待・特別)  

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  5. 当院におけるFabry病症例 招待有り

    2013年6月8日 

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  6. マウスモデルを用いた慢性腎臓病カヘキシアの分子機序の解明

    第95回日本生化学会大会  2022年11月11日 

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  7. R112H変異を持つ男性腎ファブリー病の30年間の経過 招待有り

    ファブリー病 ZOOM講演会 in 静岡  2020年2月13日 

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  8. Fabry病による慢性腎不全で長期に安定した腹膜透析施行中の一例

    第21回東海腹膜透析研究会  2013年2月3日 

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  9. Fabry病による慢性腎不全で長期に安定した腹膜透析(PD)施行中の一例

    第58回日本透析医学会学術集会・総会  2013年6月22日 

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  10. ANTI-PHOSPHOLIPASE A2 RECEPTOR ANTIBODIES FOR MEMBRANOUS NEPHROPATHY WITH NEPHROTIC SYNDROME IN JAPAN

    World Congress of Nephrology 2013  2013年6月2日 

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担当経験のある科目 (本学) 1

  1. 名古屋大学医学部附属病院看護師特定行為研修 (10期生), 循環動態薬剤

    2024

 

社会貢献活動 2

  1. マウスモデルを用いた慢性腎臓病カヘキシアの分子機序の解明

    役割:講師

    QIAGEN  QIAGEN IPA ユーザーグループミーティング  2023年5月

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  2. 少量の尿検査や採血でわかる様々な病気のおさらい〜糖尿病・高血圧から稀少疾患まで〜

    役割:講師

    公益財団法人母子衛生研究会  公益財団法人母子衛生研究会母子保健指導者セミナー  2022年1月

学術貢献活動 1

  1. npj Digital Medicine

    役割:査読

    2023年

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